K. von Figura

发表

Targeted disruption of the lysosomal alpha-mannosidase gene results in mice resembling a mild form of human alpha-mannosidosis.

S. Stinchi, R. Lüllmann-Rauch, D. Hartmann, 1999, Human molecular genetics.

Neurocognitive and Psychotiform Behavioral Alterations and Enhanced Hippocampal Long-Term Potentiation in Transgenic Mice Displaying Neuropathological Features of Human α-Mannosidosis

R. D'Hooge, T. Beckers, D. Balschun, 2005, The Journal of Neuroscience.

Molecular Characterization of the Human Cα-formylglycine-generating Enzyme*

T. Dierks, K. von Figura, D. Wenzel, 2005, Journal of Biological Chemistry.

Crystal structure of human arylsulfatase A: the aldehyde function and the metal ion at the active site suggest a novel mechanism for sulfate ester hydrolysis.

G. Lukatela, K. von Figura, W. Saenger, 1998, Biochemistry.

Structure of the human arylsulfatase B gene.

C. Peters, K. von Figura, S. Modaressi, 1993, Biological chemistry Hoppe-Seyler.

Late infantile metachromatic leukodystrophy in Israel.

K. von Figura, J. Zlotogora, V. Gieselman, 1994, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

Autophagic Vacuoles with Sarcolemmal Features Delineate Danon Disease and Related Myopathies

I. Nonaka, I. Nishino, K. von Figura, 2005, Journal of neuropathology and experimental neurology.

Sanfilippo B disease: serum assays for detection of homozygous and heterozygous individuals in three families.

K. von Figura, H. Kresse, M. Lögering, 1973, The Journal of pediatrics.

Participation of autophagy in storage of lysosomes in neurons from mouse models of neuronal ceroid-lipofuscinoses (Batten disease).

C. Peters, T. Gotow, K. von Figura, 2005, The American journal of pathology.

Effect of lectins on the metabolism of sulfated glycosaminolycans in cultured fibroblasts.

K. von Figura, K. Ullrich, J. Wortmann, 1979, Biochimica et biophysica acta.

Crystal structure of an enzyme-substrate complex provides insight into the interaction between human arylsulfatase A and its substrates during catalysis.

T. Dierks, K. von Figura, I. Usón, 2001, Journal of molecular biology.

The 46-kDa Mannose 6-Phosphate Receptor Contains Multiple Binding Sites for Clathrin Adaptors*

K. von Figura, S. Höning, A. Hille-Rehfeld, 1997, The Journal of Biological Chemistry.

Characterization of phosphorylation sites in the cytoplasmic domain of the 300 kDa mannose-6-phosphate receptor.

K. von Figura, O. Issinger, T. Braulke, 1993, Biochemical Journal.

A di‐leucine‐based motif in the cytoplasmic tail of LIMP‐II and tyrosinase mediates selective binding of AP‐3

K. von Figura, I. Sandoval, S. Höning, 1998, The EMBO journal.

Identification of formylglycine in sulfatases by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.

T. Dierks, K. von Figura, Jianhe Peng, 2003, Journal of mass spectrometry : JMS.

Enzymic diagnosis of the genetic mucopolysaccharide storage disorders.

K. von Figura, K. Figura, H. Kresse, 1982, Methods in enzymology.

Congenital disorder of glycosylation-Ic: case report and genetic defect.

F. Hanefeld, K. von Figura, C. Körner, 2000, Neuropediatrics.

Phosphorylation of the AP2 μ subunit by AAK1 mediates high affinity binding to membrane protein sorting signals

Sandra L. Schmid, S. Schmid, K. von Figura, 2002, The Journal of cell biology.

The Two Mannose 6-Phosphate Receptors Transport Distinct Complements of Lysosomal Proteins (*)

K. von Figura, M. Boeker, R. Pohlmann, 1995, The Journal of Biological Chemistry.

Multiple sulfatase deficiency: catalytically inactive sulfatases are expressed from retrovirally introduced sulfatase cDNAs.

K. von Figura, W. Rommerskirch, 1992, Proceedings of the National Academy of Sciences of the United States of America.

Conversion of cysteine to formylglycine: a protein modification in the endoplasmic reticulum.

T. Dierks, K. von Figura, K. Figura, 1997, Proceedings of the National Academy of Sciences of the United States of America.

Posttranslational Formation of Formylglycine in Prokaryotic Sulfatases by Modification of Either Cysteine or Serine*

T. Dierks, K. von Figura, M. Kertesz, 1998, The Journal of Biological Chemistry.

Sulfatases, Trapping of the Sulfated Enzyme Intermediate by Substituting the Active Site Formylglycine *

T. Dierks, K. von Figura, T. Selmer, 1998, The Journal of Biological Chemistry.

A novel protein modification generating an aldehyde group in sulfatases: its role in catalysis and disease

T. Dierks, K. von Figura, T. Selmer, 1998, Bioessays.

Conversion of cysteine to formylglycine in eukaryotic sulfatases occurs by a common mechanism in the endoplasmic reticulum

T. Dierks, K. von Figura, M. Lecca, 1998, FEBS letters.

The Iron Sulfur Protein AtsB Is Required for Posttranslational Formation of Formylglycine in the Klebsiella Sulfatase*

T. Dierks, K. von Figura, B. Schmidt, 1999, The Journal of Biological Chemistry.

Characterization of Posttranslational Formylglycine Formation by Luminal Components of the Endoplasmic Reticulum*

T. Dierks, K. von Figura, B. Schmidt, 2001, The Journal of Biological Chemistry.

The human SUMF1 gene, required for posttranslational sulfatase modification, defines a new gene family which is conserved from pro- to eukaryotes.

T. Dierks, K. von Figura, J. Landgrebe, 2003, Gene.

Expression, Localization, Structural, and Functional Characterization of pFGE, the Paralog of the Cα-Formylglycine-generating Enzyme*

T. Dierks, K. von Figura, D. Wenzel, 2005, Journal of Biological Chemistry.

Paralog of the formylglycine‐generating enzyme – retention in the endoplasmic reticulum by canonical and noncanonical signals

Tom H. Pringle, T. Dierks, K. von Figura, 2008, The FEBS journal.

ERp44 Mediates a Thiol-independent Retention of Formylglycine-generating Enzyme in the Endoplasmic Reticulum*

T. Dierks, K. von Figura, M. Mariappan, 2008, Journal of Biological Chemistry.

The Non-catalytic N-terminal Extension of Formylglycine-generating Enzyme Is Required for Its Biological Activity and Retention in the Endoplasmic Reticulum*

T. Dierks, K. von Figura, M. Mariappan, 2008, Journal of Biological Chemistry.

Molecular basis of multiple sulfatase deficiency, mucolipidosis II/III and Niemann-Pick C1 disease - Lysosomal storage disorders caused by defects of non-lysosomal proteins.

T. Dierks, K. von Figura, M. Frese, 2009, Biochimica et biophysica acta.

Phosphorylation of arylsulphatase A occurs through multiple interactions with the UDP-N-acetylglucosamine-1-phosphotransferase proximal and distal to its retrieval site by the KDEL receptor.

K. von Figura, F. Dittmer, 1999, The Biochemical journal.

Physical properties and biological activities of two forms of alpha-N-acetylglucosaminidase from bovine spleen.

K. von Figura, E. Buddecke, G. Mersmann, 1974, Biochimica et biophysica acta.

A New Type of Carbohydrate-deficient Glycoprotein Syndrome Due to a Decreased Import of GDP-fucose into the Golgi*

K. von Figura, T. Marquardt, C. Körner, 1999, The Journal of Biological Chemistry.

Carbohydrate deficient glycoprotein syndrome type IV: deficiency of dolichyl‐P‐Man:Man5 GlcNAc2‐PP‐dolichyl mannosyltransferase

U. Stephani, K. von Figura, T. Marquardt, 1999, The EMBO journal.

Carbohydrate-deficient glycoprotein syndrome type V: deficiency of dolichyl-P-Glc:Man9GlcNAc2-PP-dolichyl glucosyltransferase.

F. Hanefeld, K. von Figura, K. Figura, 1998, Proceedings of the National Academy of Sciences of the United States of America.

Abnormal synthesis of mannose 1-phosphate derived carbohydrates in carbohydrate-deficient glycoprotein syndrome type I fibroblasts with phosphomannomutase deficiency.

K. von Figura, C. Körner, L. Lehle, 1998, Glycobiology.

Disturbed cholesterol traffic but normal proteolytic function in LAMP-1/LAMP-2 double-deficient fibroblasts.

R. Lüllmann-Rauch, D. Hartmann, K. von Figura, 2004, Molecular biology of the cell.

Differential involvement of the extracellular 6-O-endosulfatases Sulf1 and Sulf2 in brain development and neuronal and behavioural plasticity

R. D'Hooge, T. Dierks, C. Viebahn, 2008, Journal of cellular and molecular medicine.

Granzyme-mediated Cytotoxicity Does Not Involve the Mannose 6-Phosphate Receptors on Target Cells*

K. von Figura, R. Dressel, S. Raja, 2004, Journal of Biological Chemistry.

Cloning and sequence analysis of human guanidinoacetate N-methyltransferase cDNA.

K. von Figura, D. Isbrandt, 1995, Biochimica et biophysica acta.

Alternative mechanisms for trafficking of lysosomal enzymes in mannose 6-phosphate receptor-deficient mice are cell type-specific.

K. von Figura, K. Figura, W. Schmahl, 1999, Journal of cell science.

Localization of the Insulin-like Growth Factor II Binding Site to Amino Acids 1508–1566 in Repeat 11 of the Mannose 6-Phosphate/Insulin-like Growth Factor II Receptor (*)

K. von Figura, A. Waheed, T. Braulke, 1995, The Journal of Biological Chemistry.

Tartrate-inhibitable acid phosphatase. Purification from placenta, characterization and subcellular distribution in fibroblasts.

K. von Figura, A. Hasilik, V. Gieselmann, 1984, Hoppe-Seyler's Zeitschrift fur physiologische Chemie.

μ1A‐adaptin‐deficient mice: lethality, loss of AP‐1 binding and rerouting of mannose 6‐phosphate receptors

K. von Figura, P. Saftig, E. Eskelinen, 2000, The EMBO journal.

Synthesis of lysosomal alpha-mannosidase in normal and mannosidosis fibroblasts.

K. von Figura, A. Hasilik, B. Winchester, 1983, Biochemical and biophysical research communications.

Overlapping functions of lysosomal acid phosphatase (LAP) and tartrate-resistant acid phosphatase (Acp5) revealed by doubly deficient mice.

Sheila J. Jones, A. Boyde, M. Evans, 2001, Development.

Disease model: LAMP-2 enlightens Danon disease.

R. Lüllmann-Rauch, K. von Figura, P. Saftig, 2001, Trends in molecular medicine.

Conditions for a reliable application of the lysoplate method in the determination of lysozyme.

K. von Figura, A. Hasilik, D. Gupta, 1987, Clinica chimica acta; international journal of clinical chemistry.

Cathepsin D deficiency induces lysosomal storage with ceroid lipofuscin in mouse CNS neurons.

H. Nakanishi, C. Peters, W. Schulz-Schaeffer, 2000, The Journal of neuroscience : the official journal of the Society for Neuroscience.

Mu 1A deficiency induces a profound increase in MPR300/IGF-II receptor internalization rate.

C. Meyer, K. von Figura, E. Eskelinen, 2001, Journal of cell science.

In vitro binding of plasma membrane-coated vesicle adaptors to the cytoplasmic domain of lysosomal acid phosphatase.

K. von Figura, B. Schmidt, A. Hille-Rehfeld, 1993, The Journal of biological chemistry.

Mannose 6-phosphate/insulin-like growth factor II receptor: distinct binding sites for mannose 6-phosphate and insulin-like growth factor II.

K. von Figura, A. Waheed, P. Malý, 1988, Biochemical and biophysical research communications.

Metabolism of sulfated glycosaminoglycans in cultivated bovine arterial cells. II. Quantitative studies on the uptake of 35SO4-labeled proteoglycans.

K. von Figura, H. Kresse, E. Buddecke, 1975, Hoppe-Seyler's Zeitschrift fur physiologische Chemie.

Studies on secretion and endocytosis of macromolecules by cultivated skin fibroblasts. Effects of anti-microtubular agents on secretion and endocytosis of lysosomal hydrolases and of sulphated glycosaminoglycans.

K. von Figura, H. Kresse, U. Meinhard, 1978, The Biochemical journal.

Cell surface-associated lysosomal enzymes in cultured human skin fibroblasts.

K. von Figura, B. Voss, 1979, Experimental cell research.

Lysosomal enzyme precursors in coated vesicles derived from the exocytic and endocytic pathways

K. von Figura, N. Kedersha, A. Hasilik, 1987, The Journal of cell biology.

Cathepsin D Deficiency Induces Lysosomal Storage with Ceroid Lipofuscin in Mouse CNS Neurons

H. Nakanishi, C. Peters, W. Schulz-Schaeffer, 2000, The Journal of Neuroscience.

Brefeldin A affects the cellular distribution of endocytic receptors differentially.

K. von Figura, J. Klumperman, T. Braulke, 1992, Biochemical and biophysical research communications.

Ultrastructural localization of the mannose 6-phosphate receptor in rat liver

J. Slot, H. Geuze, K. von Figura, 1984, The Journal of cell biology.

Proteolytic processing of cathepsin D in prelysosomal organelles.

K. von Figura, C. Desel, A. Hille-Rehfeld, 1994, European journal of cell biology.

Biosynthesis and transport of cathepsin D in cultured human fibroblasts

K. von Figura, A. Hasilik, V. Gieselmann, 1983, The Journal of cell biology.

Quaternary structure of the Mr 46,000 mannose 6-phosphate specific receptor: effect of ligand, pH, and receptor concentration on the equilibrium between dimeric and tetrameric receptor forms.

K. von Figura, A. Waheed, U. Junghans, 1990, Biochemistry.

The ‘cation‐dependent’ mannose 6‐phosphate receptor binds ligands in the absence of divalent cations

K. von Figura, A. Waheed, U. Junghans, 1988, FEBS letters.

Is movement of mannose 6-phosphate-specific receptor triggered by binding of lysosomal enzymes?

K. von Figura, C. Gartung, A. Hasilik, 1987, The Journal of cell biology.

Processing of human cathepsin D in lysosomes in vitro.

K. von Figura, K. Figura, A. Hasilik, 1985, The Journal of biological chemistry.

Translational control of arylsulfatase A expression in mouse testis.

G. Lukatela, K. von Figura, V. Gieselmann, 1994, The Journal of biological chemistry.

Mutations in the arylsulfatase A pseudodeficiency allele causing metachromatic leukodystrophy.

K. von Figura, V. Gieselmann, A. Fluharty, 1991, American journal of human genetics.

Biosynthesis and transport of lysosomal enzymes in human monocytes and macrophages. Effects of ammonium chloride, zymosan and tunicamycin.

K. von Figura, M. Zühlsdorf, A. Hasilik, 1983, The Biochemical journal.

An alternative hypothesis of cellular transport of lysosomal enzymes in fibroblasts. Effect of inhibitors of lysosomal enzyme endocytosis on intra- and extra-cellular lysosomal enzyme activities.

K. von Figura, E. Weber, 1978, The Biochemical journal.

Enhanced degradation of cathepsin D synthesized in the presence of the threonine analog beta-hydroxynorvaline.

K. von Figura, A. Hasilik, M. Hentze, 1984, Archives of biochemistry and biophysics.

Molecular forms of cathepsin D in coated vesicle preparations.

K. von Figura, M. Zühlsdorf, H. Robenek, 1983, Hoppe-Seyler's Zeitschrift fur physiologische Chemie.

Transport and processing of lysosomal enzymes by smooth muscle cells and endothelial cells.

K. von Figura, A. Hasilik, B. Voss, 1981, Experimental cell research.

Enzymatic phosphorylation of lysosomal enzymes in the presence of UDP-N-acetylglucosamine. Absence of the activity in I-cell fibroblasts.

K. von Figura, A. Waheed, A. Hasilik, 1981, Biochemical and biophysical research communications.

Phosphorylated oligosaccharides in lysosomal enzymes: identification of alpha-N-acetylglucosamine(1)phospho(6)mannose diester groups.

K. von Figura, A. Waheed, G. Strecker, 1980, Proceedings of the National Academy of Sciences of the United States of America.

Effect of tunicamycin on transport of lysosomal enzymes in cultured skin fibroblasts.

K. von Figura, K. Ullrich, B. Voss, 1979, European journal of biochemistry.

Arylsulfatase from Klebsiella pneumoniae Carries a Formylglycine Generated from a Serine*

T. Dierks, K. von Figura, T. Selmer, 1998, The Journal of Biological Chemistry.

Cloning and expression of human arylsulfatase A.

C. Stein, K. von Figura, K. Figura, 1989, The Journal of biological chemistry.

Structure of the human lysosomal acid phosphatase gene.

K. von Figura, R. Pohlmann, C. Geier, 1989, European journal of biochemistry.

The tyrosine motifs of Lamp 1 and LAP determine their direct and indirect targetting to lysosomes.

K. von Figura, S. Höning, Christina Kiecke, 2002, Journal of cell science.

Structural Requirements for Interactions between Leucine-sorting Signals and Clathrin-associated Adaptor Protein Complex AP3*

K. von Figura, O. Bakke, S. Höning, 2002, The Journal of Biological Chemistry.

Endocytosis of Insulin-like Growth Factor II by a Mini-receptor Based on Repeat 11 of the Mannose 6-Phosphate/Insulin-like Growth Factor II Receptor*

K. von Figura, S. Höning, B. Schmidt, 2000, The Journal of Biological Chemistry.

Immunoelectron-microscopic study on the location of fibronectin in human fibroblast cultures.

K. von Figura, B. Voss, M. Grote, 1982, Journal of ultrastructure research.

Mr 46,000 mannose 6-phosphate receptor. The role of histidine and arginine residues for binding of ligand.

K. von Figura, A. Waheed, M. Wendland, 1991, The Journal of biological chemistry.

The carboxy-terminal peptides of 46 kDa and 300 kDa mannose 6-phosphate receptors share partial sequence homology and contain information for sorting in the early endosomal pathway.

K. von Figura, K. Figura, A. Hille-Rehfeld, 1997, Journal of cell science.

Tail-specific antibodies that block return of 46,000 M(r) mannose 6- phosphate receptor to the trans-Golgi network

K. von Figura, C. Schulze-Garg, A. Hille-Rehfeld, 1993, The Journal of cell biology.

Expression of the two mannose 6-phosphate receptors is spatially and temporally different during mouse embryogenesis.

K. von Figura, K. Figura, U. Matzner, 1992, Development.

Lysosomal enzyme precursors in human fibroblasts. Activation of cathepsin D precursor in vitro and activity of beta-hexosaminidase A precursor towards ganglioside GM2.

K. von Figura, A. Hasilik, K. Sandhoff, 1982, European journal of biochemistry.

An N‐acetylgalactosamine‐4‐sulfatase mutation (ΔG238) results in a severe Maroteaux‐Lamy phenotype

C. P. Morris, C. Peters, K. von Figura, 1992, Human mutation.

Differences in the endosomal distributions of the two mannose 6- phosphate receptors

H. Geuze, K. von Figura, H. Geuze, 1993, The Journal of cell biology.

Low temperature blocks transport and sorting of cathepsin D in fibroblasts.

K. von Figura, A. Hasilik, T. Braulke, 1988, Biological chemistry Hoppe-Seyler.

The Dileucine Motif Within the Tail of MPR46 is Required for Sorting of the Receptor in Endosomes

H. Geuze, K. von Figura, H. Geuze, 2000, Traffic.

Proteolysis of IGFBPs by cathepsin D in vitro and in cathepsin D-deficient mice.

C. Peters, K. von Figura, P. Saftig, 1995, Progress in growth factor research.

Mannose 6-phosphate/insulin-like growth factor II-binding proteins in human serum and urine. Their relation to the mannose 6-phosphate/insulin-like growth factor II receptor.

K. von Figura, K. Figura, A. Waheed, 1988, The Biochemical journal.

Natural killer cell-mediated cytotoxicity does not depend on recognition of mannose 6-phosphate residues.

K. von Figura, A. Hasilik, H. Haubeck, 1985, Journal of immunology.

Identification of the Putative Mannose 6-Phosphate Receptor (MPR 46) Protein in the Invertebrate Mollusc

K. von Figura, Siva Kumar Nadimpalli, 2002, Bioscience reports.

Mutational analysis of disulfide bridges in the Mr 46,000 mannose 6-phosphate receptor. Localization and role for ligand binding.

K. von Figura, M. Wendland, R. Pohlmann, 1991, The Journal of biological chemistry.

UDP-N-acetylglucosamine:lysosomal enzyme precursor N-acetylglucosamine-1-phosphotransferase. Partial purification and characterization of the rat liver Golgi enzyme.

K. von Figura, A. Waheed, A. Hasilik, 1982, The Journal of biological chemistry.

Synthesis of phosphorylated recognition marker in lysosomal enzymes is located in the cis part of Golgi apparatus.

K. von Figura, A. Waheed, A. Hasilik, 1982, The Journal of biological chemistry.

Processing of the phosphorylated recognition marker in lysosomal enzymes. Characterization and partial purification of a microsomal alpha-N-acetylglucosaminyl phosphodiesterase.

K. von Figura, A. Waheed, A. Hasilik, 1981, The Journal of biological chemistry.

46-kDa mannose 6-phosphate-specific receptor: biosynthesis, processing, subcellular location and topology.

K. von Figura, A. Hasilik, T. Braulke, 1987, Biological chemistry Hoppe-Seyler.

Phylogenetic conservation of cysteine proteinases. Cloning and expression of a cDNA coding for human cathepsin S.

C. Peters, K. von Figura, K. Figura, 1992, The Journal of biological chemistry.

Tilorone acts as a lysosomotropic agent in fibroblasts.

K. von Figura, A. Hasilik, V. Gieselmann, 1984, Hoppe-Seyler's Zeitschrift fur physiologische Chemie.

Quantitation of Mr 46000 and Mr 300000 mannose 6-phosphate receptors in human cells and tissues.

K. von Figura, A. Hille, J. Wenk, 1991, Biochemistry international.

The Normal Phenotype of Pmm1-Deficient Mice Suggests that Pmm1 Is Not Essential for Normal Mouse Development

R. D'Hooge, R. Sciot, D. Hartmann, 2006, Molecular and Cellular Biology.

Effects of brefeldin A on the endocytic route. Redistribution of mannose 6-phosphate/insulin-like growth factor II receptors to the cell surface.

K. von Figura, J. Klumperman, T. Braulke, 1991, The Journal of biological chemistry.

Lysosomal enzymes and their receptors.

K. von Figura, K. Figura, A. Hasilik, 1986, Annual review of biochemistry.

Mistargeting of lysosomal enzymes in M(r) 46,000 mannose 6-phosphate receptor-deficient mice is compensated by carbohydrate-specific endocytotic receptors.

K. von Figura, R. Pohlmann, A. Köster, 1994, European journal of biochemistry.

Assembly of the ligand-binding conformation of Mr 46,000 mannose 6- phosphate-specific receptor takes place before reaching the Golgi complex

K. von Figura, A. Waheed, A. Hille, 1990, The Journal of cell biology.

Association of the precursor of cathepsin D with coated membranes. Kinetics and carbohydrate processing.

K. von Figura, A. Hasilik, T. Marquardt, 1987, European journal of biochemistry.

46-kDa mannose 6-phosphate-specific receptor: purification, subunit composition, chemical modification.

K. von Figura, A. Hasilik, H. Meyer, 1987, Biological chemistry Hoppe-Seyler.

Sulfated oligosaccharides in human lysosomal enzymes.

W. Huttner, K. von Figura, A. Hasilik, 1987, Biochemical and biophysical research communications.

Synthesis and transport of lysosomal acid phosphatase in normal and I-cell fibroblasts.

K. von Figura, A. Hasilik, V. Gieselmann, 1985, The Journal of biological chemistry.

Deficiency of UDP-N-acetylglucosamine:lysosomal enzyme N-acetylglucosamine-1-phosphotransferase in organs of I-cell patients.

K. von Figura, A. Waheed, A. Hasilik, 1982, Biochemical and biophysical research communications.

Function and Properties of Chimeric MPR 46-MPR 300 Mannose 6-Phosphate Receptors*

K. von Figura, R. Pohlmann, U. Sandholzer, 2000, The Journal of Biological Chemistry.

The oligomeric state of 46-kDa mannose 6-phosphate receptor does not change upon intracellular recycling and binding of ligands.

K. von Figura, A. Hille-Rehfeld, E. Punnonen, 1996, European journal of biochemistry.

Four monoclonal antibodies inhibit the recognition of arylsulphatase A by the lysosomal enzyme phosphotransferase.

K. von Figura, V. Gieselmann, A. Hille-Rehfeld, 1994, The Biochemical journal.

Lysosomal acid phosphatase is not involved in the dephosphorylation of mannose 6-phosphate containing lysosomal proteins.

C. Peters, K. von Figura, R. Bresciani, 1992, European journal of cell biology.

Synthesis of a truncated Mr 46,000 mannose 6-phosphate receptor that is secreted and retains ligand binding.

K. von Figura, A. Waheed, G. Nagel, 1989, The Biochemical journal.

The two mannose 6-phosphate receptors have almost identical subcellular distributions in U937 monocytes.

J. Slot, H. Geuze, K. von Figura, 1988, European journal of cell biology.

Sanfilippo disease type B: presence of material cross reacting with antibodies against alpha-N-acetylglucosaminidase.

K. von Figura, H. Kresse, 1976, European journal of biochemistry.

Evidence for lysosomal enzyme recognition by human fibroblasts via a phosphorylated carbohydrate moiety.

K. von Figura, K. Figura, K. Ullrich, 1978, The Biochemical journal.

Insulin-like growth factor II overexpression does not affect sorting of lysosomal enzymes in NIH-3T3 cells.

K. von Figura, T. Braulke, R. Bresciani, 1991, Biochemical and biophysical research communications.

Mannose 6-phosphate/insulin like growth factor II receptor: the two types of ligands bind simultaneously to one receptor at different sites.

K. von Figura, K. Figura, A. Waheed, 1988, Biochemical and biophysical research communications.

Genetic heterogeneity of steroid sulfatase deficiency revealed with cDNA for human steroid sulfatase.

K. von Figura, A. Hasilik, J. Conary, 1987, Biochemical and biophysical research communications.

Synthesis and processing of alpha-galactosidase A in human fibroblasts. Evidence for different mutations in Fabry disease.

R. Desnick, K. von Figura, A. Hasilik, 1987, The Journal of biological chemistry.

Heterogeneity in late-onset metachromatic leukodystrophy. Effect of inhibitors of cysteine proteinases.

K. von Figura, E. Shaw, A. Hasilik, 1986, American journal of human genetics.

Sequential detection of antigens in Western blots with differently colored products.

K. von Figura, A. Hasilik, N. Theisen, 1986, Analytical biochemistry.

Comparison of biosynthesis and subcellular distribution of lysozyme and lysosomal enzymes in U937 monocytes.

K. von Figura, A. Hasilik, D. Gupta, 1985, Biochimica et biophysica acta.

Synthesis and stability of arylsulfatase A and B in fibroblasts from multiple sulfatase deficiency.

K. von Figura, A. Hasilik, F. Steckel, 1985, European journal of biochemistry.

Biosynthesis and maturation of alpha-N-acetylglucosaminidase in normal and Sanfilippo B-fibroblasts.

K. von Figura, A. Hasilik, J. V. D. van de Kamp, 1984, American journal of human genetics.

Two allelic forms of human arylsulfatase A with different numbers of asparagine-linked oligosaccharides.

K. von Figura, A. Waheed, A. Hasilik, 1983, American journal of human genetics.

Biosynthesis of acid α‐glucosidase in late‐onset forms of glycogenosis type II (Pompe's disease)

K. von Figura, A. Waheed, A. Hasilik, 1982 .

Enhanced breakdown of arylsulfatase A in multiple sulfatase deficiency.

K. von Figura, A. Waheed, A. Hasilik, 1982, European journal of biochemistry.

Impaired phosphorylation of lysosomal enzymes in fibroblasts of patients with mucolipidosis III.

K. von Figura, A. Waheed, A. Hasilik, 1982, European journal of biochemistry.

Involvement of Cathepsin E in Exogenous Antigen Processing in Primary Cultured Murine Microglia*

H. Nakanishi, T. Nishioku, C. Peters, 2002, The Journal of Biological Chemistry.

Cathepsin D precursors in clathrin-coated organelles from human fibroblasts

K. von Figura, E. Schulze-Lohoff, A. Hasilik, 1985, The Journal of cell biology.

Quantitative aspects of pinocytosis and the intracellular fate of N-acetyl-alpha-D-glucosaminidase in Sanfilippo B fibroblasts.

K. von Figura, H. Kresse, Hans Kresse, 1974, The Journal of clinical investigation.

Mannose 6-phosphate receptors, Niemann-Pick C2 protein, and lysosomal cholesterol accumulation Published, JLR Papers in Press, September 21, 2005. DOI 10.1194/jlr.M500131-JLR200

K. von Figura, P. Saftig, E. Eskelinen, 2005, Journal of Lipid Research.

Molecular forms of beta-hexosaminidase and cathepsin D in serum and urine of healthy subjects and patients with elevated activity of lysosomal enzymes.

K. von Figura, M. Zühlsdorf, A. Hasilik, 1983, The Biochemical journal.

Effects of differentiation-inducing agents on synthesis, maturation and secretion of cathepsin D in U937 and HL-60 cells.

K. von Figura, A. Hasilik, T. Braulke, 1987, Biological chemistry Hoppe-Seyler.

Lysosomal acid phosphatase is internalized via clathrin-coated pits.

C. Peters, K. von Figura, H. Geuze, 1992, European journal of cell biology.

Insulin-like growth factors I and II stimulate endocytosis but do not affect sorting of lysosomal enzymes in human fibroblasts.

K. von Figura, T. Braulke, H. Chao, 1990, The Journal of biological chemistry.

Partial purification and characterization of heparan sulfate specific endoglucuronidase.

K. von Figura, U. Klein, 1976, Biochemical and biophysical research communications.

Homologous low density lipoprotein does not affect proteoglycan metabolism of cultured skin fibroblasts and arterial smooth muscle cells.

K. von Figura, E. Buddecke, P. Sudhakaran, 1980, Hoppe-Seyler's Zeitschrift fur physiologische Chemie.

Is an ATPase involved in uncoating of plasma membrane adaptor complex AP‐2?

K. von Figura, A. Hille-Rehfeld, M. Sosa, 1997, FEBS letters.

Heparan sulfate 6-O-endosulfatases: discrete in vivo activities and functional co-operativity.

T. Dierks, K. von Figura, T. V. van Kuppevelt, 2006, The Biochemical journal.

Mannose 6-phosphate-specific receptor is a transmembrane protein with a C-terminal extension oriented towards the cytosol.

K. von Figura, A. Hasilik, V. Gieselmann, 1985, The Biochemical journal.

Evidence for degradation of heparan sulfate by endoglycosidases: glucosamine and hexuronic acid are reducing terminals of intracellular heparan sulfate from human skin fibroblasts.

K. von Figura, H. Kresse, U. Klein, 1976, Biochemical and biophysical research communications.

LIMP-2/LGP85 deficiency causes ureteric pelvic junction obstruction, deafness and peripheral neuropathy in mice.

R. D'Hooge, R. Lüllmann-Rauch, D. Hartmann, 2003, Human molecular genetics.

Mucopolysaccharidosis VI (Maroteaux-Lamy syndrome). An intermediate clinical phenotype caused by substitution of valine for glycine at position 137 of arylsulfatase B.

C. Peters, K. von Figura, K. Figura, 1991, The Journal of biological chemistry.

Role of LAMP-2 in lysosome biogenesis and autophagy.

K. von Figura, P. Saftig, E. Eskelinen, 2002, Molecular biology of the cell.

Phenotype of arylsulfatase A-deficient mice: relationship to human metachromatic leukodystrophy.

R. D'Hooge, C. Peters, G. Nagels, 1996, Proceedings of the National Academy of Sciences of the United States of America.

Molecular basis of different forms of metachromatic leukodystrophy.

K. von Figura, V. Gieselmann, A. Fluharty, 1991, The New England journal of medicine.

Golgi GDP-fucose Transporter-deficient Mice Mimic Congenital Disorder of Glycosylation IIc/Leukocyte Adhesion Deficiency II*

D. Frommhold, M. Sperandio, K. von Figura, 2007, Journal of Biological Chemistry.

Guanidinoacetate methyltransferase deficiency: the first inborn error of creatine metabolism in man.

F. Hanefeld, K. von Figura, K. Figura, 1996, American journal of human genetics.

1.3 A structure of arylsulfatase from Pseudomonas aeruginosa establishes the catalytic mechanism of sulfate ester cleavage in the sulfatase family.

T Dierks, T. Dierks, K. von Figura, 2001, Structure.

Subcellular location of two enzymes involved in the synthesis of phosphorylated recognition markers in lysosomal enzymes.

K. von Figura, A. Waheed, A. Hasilik, 1981, The Journal of biological chemistry.

Endocytosis of lysosomal enzymes by non-parenchymal rat liver cells. Comparative study of lysosomal-enzyme uptake by hepatocytes and non-parenchymal liver cells.

K. von Figura, V. Gieselmann, K. Ullrich, 1979, The Biochemical journal.

Spontaneous Mucolipidosis in a Cat: An Animal Model of Human I-Cell Disease

K. von Figura, R. Gitzelmann, M. Spycher, 1996, Veterinary pathology.

Mannose 6-phosphate specific receptors: structure and function.

K. von Figura, A. Waheed, T. Braulke, 1989, Biochemical Society transactions.

Leukocyte adhesion deficiency II syndrome, a generalized defect in fucose metabolism☆☆☆

H. Freeze, K. von Figura, D. Vestweber, 1999, The Journal of Pediatrics.

Normal Lysosomal Morphology and Function in LAMP-1-deficient Mice*

R. Lüllmann-Rauch, D. Hartmann, K. von Figura, 1999, The Journal of Biological Chemistry.

Cathepsin D and beta-hexosaminidase synthesized in the presence of 1-deoxynojirimycin accumulate in the endoplasmic reticulum.

K. von Figura, A. Hasilik, V. Gieselmann, 1984, The Journal of biological chemistry.

AP‐1 and AP‐3 Mediate Sorting of Melanosomal and Lysosomal Membrane Proteins into Distinct Post‐Golgi Trafficking Pathways

K. von Figura, R. Tikkanen, D. Wenzel, 2008, Traffic.

Cathepsin L deficiency as molecular defect of furless: hyperproliferation of keratinocytes and pertubation of hair follicle cycling

J. Deussing, C. Peters, K. von Figura, 2000, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

The disintegrin/metalloprotease ADAM 10 is essential for Notch signalling but not for alpha-secretase activity in fibroblasts.

B. de Strooper, W. Annaert, D. Hartmann, 2002, Human molecular genetics.

Involvement of Nitric Oxide Released from Microglia–Macrophages in Pathological Changes of Cathepsin D-Deficient Mice

H. Nakanishi, T. Nishioku, C. Peters, 2001, The Journal of Neuroscience.

Primary cultures of rat hepatocytes synthesize fibronectin.

K. von Figura, V. Gieselmann, K. Ullrich, 1979, Biochemical and biophysical research communications.

Phosphorylation of lysosomal enzymes in fibroblasts. Marked deficiency of N-acetylglucosamine-1-phosphotransferase in fibroblasts of patients with mucolipidosis III.

K. von Figura, A. Waheed, A. Hasilik, 1982, Hoppe-Seyler's Zeitschrift fur physiologische Chemie.

N-Acetylglucosamine-6-sulfate sulfatase from human urine.

K. von Figura, H. Kresse, R. Basner, 1979, Journal of Biological Chemistry.

Sanfilippo's disease type A: sulfamidase activity in peripheral leukocytes of normal, heterozygous and homozygous individuals.

K. von Figura, H. Kresse, E. Paschke, 1977, Clinica chimica acta; international journal of clinical chemistry.

Possible pathways for lysosomal enzyme delivery

J. Slot, H. Geuze, K. von Figura, 1985, The Journal of cell biology.

Recognition of human urine alpha-N-acetylglucosaminidase by rat hepatocytes. Involvement of receptors specific for galactose, mannose 6-phosphate and mannose.

K. von Figura, R. Basner, V. Gieselmann, 1979, The Biochemical journal.

Metabolism of cell surface-associated sulfated glycosaminoglycans in cultured human smooth muscle cells.

K. von Figura, D. Zach, F. Middendorf, 1980, Hoppe-Seyler's Zeitschrift fur physiologische Chemie.

Epithelial rat liver cells have cell surface receptors recognizing a phosphorylated carbohydrate on lysosomal enzymes.

K. von Figura, K. Ullrich, G. Mersmann, 1978, Hoppe-Seyler's Zeitschrift fur physiologische Chemie.

Impaired osteoclastic bone resorption leads to osteopetrosis in cathepsin-K-deficient mice.

Sheila J. Jones, A. Boyde, K. von Figura, 1998, Proceedings of the National Academy of Sciences of the United States of America.

Deficiency of dolichyl-P-Man:Man7GlcNAc2-PP-dolichyl mannosyltransferase causes congenital disorder of glycosylation type Ig.

F. Hanefeld, K. von Figura, C. Thiel, 2002, The Biochemical journal.

Human tartrate-inhibitable lysosomal acid phosphatase. Purification, characterization, biosynthesis and intracellular transport.

K. von Figura, A. Waheed, A. Hasilik, 1986, Acta biochimica Polonica.

Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId.

E. Berger, K. von Figura, C. Thiel, 2002, The Journal of clinical investigation.

A 3H-labelled trisaccharide from heparin as substrate for acetyl-CoA: 2-amino-2-deoxy-alpha-D-glucoside N-acetyltransferase.

K. von Figura, U. Klein, 1980, Carbohydrate research.

Steroid sulfatase. Biosynthesis and processing in normal and mutant fibroblasts.

K. von Figura, A. Hasilik, J. Conary, 1986, European journal of biochemistry.

Cloning and expression of human steroid-sulfatase. Membrane topology, glycosylation, and subcellular distribution in BHK-21 cells.

H. Geuze, C. Stein, K. von Figura, 1989, The Journal of biological chemistry.

On the effects of weak bases and monensin on sorting and processing of lysosomal enzymes in human cells.

J. Slot, H. Geuze, K. von Figura, 1987, European journal of cell biology.

Arylsulfatase A pseudodeficiency: loss of a polyadenylylation signal and N-glycosylation site.

K. von Figura, K. Figura, V. Gieselmann, 1989, Proceedings of the National Academy of Sciences of the United States of America.

Mouse cathepsin D gene: molecular organization, characterization of the promoter, and chromosomal localization.

C. Peters, K. von Figura, P. Saftig, 1994, DNA and cell biology.

Proteolytic degradation of glutamate decarboxylase mediates disinhibition of hippocampal CA3 pyramidal cells in cathepsin D‐deficient mice

H. Nakanishi, C. Peters, K. von Figura, 2005, Journal of neurochemistry.

Isolation and analysis of the human 46-kDa mannose 6-phosphate receptor gene.

K. von Figura, K. Figura, R. Pohlmann, 1991, European journal of biochemistry.

Differently labelled glucosamine-precursor pools for the biosynthesis of hyaluronate and heparan sulfate.

K. von Figura, W. Kiowski, E. Buddecke, 1973, European journal of biochemistry.

Mucopolysaccharidosis VI (Maroteaux-Lamy syndrome): six unique arylsulfatase B gene alleles causing variable disease phenotypes.

C. Peters, K. von Figura, K. Figura, 1994, American journal of human genetics.

Restoration of arylsulphatase B activity in human mucopolysaccharidosis-type-VI fibroblasts by retroviral-vector-mediated gene transfer.

C. Peters, K. von Figura, S. Modaressi, 1991, The Biochemical journal.

Phylogenetic conservation of arylsulfatases. cDNA cloning and expression of human arylsulfatase B.

C. Peters, M. Vingron, K. von Figura, 1990, The Journal of biological chemistry.

Restoration of arylsulphatase A activity in human-metachromatic-leucodystrophy fibroblasts via retroviral-vector-mediated gene transfer.

C. Peters, K. von Figura, V. Gieselmann, 1991, The Biochemical journal.

Structure of the mouse arylsulfatase A gene and cDNA.

K. von Figura, F. Steiner, V. Gieselmann, 1994, Genomics.

Thyroid functions of mouse cathepsins B, K, and L.

J. Deussing, C. Peters, T. Reinheckel, 2003, The Journal of clinical investigation.

Conserved cassette structure of vertebrate Mr 300 kDa mannose 6-phosphate receptors: partial cDNA sequence of fish MPR 300.

K. von Figura, A. Hille-Rehfeld, P. Schu, 2000, Comparative biochemistry and physiology. Part B, Biochemistry & molecular biology.

A single origin for the most frequent mutation causing late infantile metachromatic leucodystrophy.

K. von Figura, K. Figura, A. Harris, 1994, Journal of medical genetics.

Structure of the arylsulfatase A gene.

K. von Figura, V. Gieselmann, J. Kreysing, 1990, European journal of biochemistry.

Carbohydrate-deficient glycoprotein syndrome type Ib. Phosphomannose isomerase deficiency and mannose therapy.

H. Freeze, G. Alton, K. von Figura, 1998, The Journal of clinical investigation.

Immuno-electron microscopical demonstration of lysosomes in human blood platelets and megakaryocytes using anti-cathepsin D.

J. Sixma, K. von Figura, H. Geuze, 1985, Blood.

Endocytosis of beta-N-acetylglucosaminidase from sections of mucolipidosis-II and-III fibroblasts by non-parenchymal rat liver cells.

K. von Figura, K. Ullrich, 1979, The Biochemical journal.

Identification of the Putative Mannose 6-phosphate Receptor Protein (MPR 300) in the Invertebrate unio

K. von Figura, A. Hille-Rehfeld, N. S. Kumar, 1999, Bioscience reports.

Mannose 6-phosphate receptors (MPR 300 and MPR 46) from a teleostean fish (trout).

K. von Figura, A. Hille-Rehfeld, S. Nadimpalli, 1999, Comparative biochemistry and physiology. Part B, Biochemistry & molecular biology.

Expression and processing of the activin-A/erythroid differentiation factor precursor: a member of the transforming growth factor-beta superfamily.

H. Stunnenberg, D. Huylebroeck, K. von Figura, 1990, Molecular endocrinology.

Molecular cloning of the mouse 46-kDa mannose 6-phosphate receptor (MPR 46).

K. von Figura, G. Nagel, R. Pohlmann, 1991, Biological chemistry Hoppe-Seyler.

The Leucine-based Sorting Motifs in the Cytoplasmic Domain of the Invariant Chain Are Recognized by the Clathrin Adaptors AP1 and AP2 and their Medium Chains*

K. von Figura, O. Bakke, B. Dobberstein, 1999, The Journal of Biological Chemistry.

Molecular basis of late infantile metachromatic leukodystrophy in the Habbanite Jews

K. von Figura, V. Gieselmann, J. Zlotogora, 1995, Human mutation.

Late‐onset metachromatic leukodystrophy: Molecular pathology in two siblings

K. von Figura, V. Gieselmann, J. Kappler, 1992, Annals of neurology.

Two new arylsulfatase A (ARSA) mutations in a juvenile metachromatic leukodystrophy (MLD) patient.

K. von Figura, K. Figura, V. Gieselmann, 1991, American journal of human genetics.

Unimpaired allorejection of cells deficient for the mannose 6-phosphate receptors Mpr300 and Mpr46.

K. von Figura, R. Dressel, E. Günther, 2004, Transplantation.

Mucolipidosis type II in a domestic shorthair cat.

K. von Figura, M. Haskins, R. Gitzelmann, 1996, The Journal of small animal practice.

Metabolism of sulfated glycosaminoglycans in cultivated bovine arterial cells. I. Characterization of different pools of sulfated glycosaminoglycans.

K. von Figura, H. Kresse, E. Buddecke, 1975, Hoppe-Seyler's Zeitschrift fur physiologische Chemie.

Processing and transport of lysosomal enzymes in human monocyte line U937.

K. von Figura, A. Hasilik, A. Schmidt, 1984, Hoppe-Seyler´s Zeitschrift für physiologische Chemie.

Efficacy of enzyme replacement therapy in alpha-mannosidosis mice: a preclinical animal study.

R. Lüllmann-Rauch, T. Beccari, A. Orlacchio, 2004, Human molecular genetics.

Targeted disruption of the arylsulfatase B gene results in mice resembling the phenotype of mucopolysaccharidosis VI.

C. Peters, K. von Figura, P. Saftig, 1996, Proceedings of the National Academy of Sciences of the United States of America.

Sanfilippo disease type D: deficiency of N-acetylglucosamine-6-sulfate sulfatase required for heparan sulfate degradation.

K. von Figura, K. Figura, H. Kresse, 1980, Proceedings of the National Academy of Sciences of the United States of America.

Sanfilippo syndrome type C: deficiency of acetyl-CoA:alpha-glucosaminide N-acetyltransferase in skin fibroblasts.

K. von Figura, K. Figura, H. Kresse, 1978, Proceedings of the National Academy of Sciences of the United States of America.

Deficiency of arylsulfatase B in 2 brothers aged 40 and 38 years. (Maroteaux‐Lamy syndrome, type B)

H. Goebel, K. von Figura, K. Figura, 1979, Annals of neurology.

Characterization of glycosaminoglycans stored in mucopolysaccharidosis III A: evidence for a generally occuring degradation of heparan sulfate by endoglycosidases.

K. von Figura, U. Klein, A. Kindler, 1977, Hoppe-Seyler's Zeitschrift fur physiologische Chemie.

Prenatal diagnosis of morquio's disease type a (n‐acetylgalactosamine 6‐sulphate sulphatase deficiency)

K. von Figura, M. Niermeijer, J. V. D. van de Kamp, 1982 .

Morquio syndrome (mucopolysaccharidosis IV B) associated with beta-galactosidase deficiency. Report of two cases.

K. von Figura, A. Sewell, H. Kresse, 1980, American Journal of Human Genetics.

Biosynthesis and maturation of arylsulfatase B in normal and mutant cultured human fibroblasts.

K. von Figura, A. Hasilik, F. Steckel, 1983, The Journal of biological chemistry.

Identification of novel lysosomal matrix proteins by proteome analysis

K. von Figura, B. Schmidt, Kudzai E. Mutenda, 2005, Proteomics.

A new biochemical subtype of the Sanfilippo syndrome: characterization of the storage material in cultured fibroblasts of Sanfilippo C patients.

K. von Figura, H. Kresse, U. Klein, 1978, European journal of biochemistry.

Serum α-N-acetylglucosaminidase: Determination, Characterization, and Corrective Activity in Sanfilippo B Fibroblasts

K. von Figura, H. Kresse, M. Lögering, 1975 .

Localisation of acetyl-CoA: alpha-glucosaminide N-acetyltransferase in microsomes and lysosomes of rat liver.

K. von Figura, U. Klein, R. Pohlmann, 1981, Hoppe-Seyler's Zeitschrift fur physiologische Chemie.

The sanfilippo B corrective factor: a N-acetyl-alpha-D-glucosamindiase.

K. von Figura, H. Kresse, 1972, Biochemical and biophysical research communications.

Localization of sulfated glycosaminoglycans within cell nuclei by high-resolution autoradiography.

K. von Figura, H. Kresse, E. Buddecke, 1976, Experimental cell research.

Characterization of dermatan sulfate in mucopolysaccharidosis VI. Evidence for the absence of hyaluronidase-like enzymes in human skin fibroblasts.

K. von Figura, U. Klein, 1980, Biochimica et biophysica acta.

Studies on the chemistry of arterial wall, XVI. Topochemical studies on the glycoasaminoglycan and lipid metabolism in bovine arterial tissue.

K. von Figura, E. Buddecke, I. Filipović, 1973, Hoppe-Seyler's Zeitschrift fur physiologische Chemie.

Multiple sulfatase deficiency: degradation of arylsulfatase A and B after endocytosis in fibroblasts.

K. von Figura, A. Hasilik, F. Steckel, 1985, European journal of biochemistry.

Metabolism of sulfated glycosaminoglycans in rat hepatocytes. Synthesis of heparan sulfate and distribution into cellular and extracellular pools.

K. von Figura, K. Ullrich, P. Sudhakaran, 1980, Biochimica et biophysica acta.

Juvenile form of mucopolysaccharidosis VI (Maroteaux-Lamy syndrome). A C-terminal extension causes instability but increases catalytic efficiency of arylsulfatase B.

C. Peters, K. von Figura, D. Brooks, 1994, The Journal of biological chemistry.

[Identification of mutations in the arylsulfatase B gene in Russian mucopolysaccharidosis type VI patients].

K. von Figura, K. D. Krasnopol'skaia, K. Peters, 2000, Genetika.

Adhesion of human skin fibroblasts. Effect of tetravalent, divalent and monovalent concanavalin A.

K. von Figura, R. Prinz, 1978, Experimental cell research.

Receptor-mediated endocytosis of proteoglycans by human fibroblasts involves recognition of the protein core.

J. D. Gregory, K. von Figura, H. Kresse, 1983, The Biochemical journal.

Amyloidogenic Processing of Human Amyloid Precursor Protein in Hippocampal Neurons Devoid of Cathepsin D*

C. Peters, B. de Strooper, K. von Figura, 1996, The Journal of Biological Chemistry.

Occurrence of tyrosine sulfate in proteins--a balance sheet. 1. Secretory and lysosomal proteins.

W. Huttner, K. von Figura, T. Braulke, 1990, European journal of biochemistry.

Effect of lectins on endocytosis and secretion of lysosomal enzymes by cultured fibroblasts.

K. von Figura, K. Ullrich, H. Beeck, 1979, Biochimica et biophysica acta.

Crystal Structure of Human pFGE, the Paralog of the Cα-formylglycine-generating Enzyme*

T. Dierks, M. Rudolph, K. von Figura, 2005, Journal of Biological Chemistry.

Glycosylation of the Mr 46,000 mannose 6-phosphate receptor. Effect on ligand binding, stability, and conformation.

K. von Figura, A. Waheed, B. Schmidt, 1991, The Journal of biological chemistry.

Molecular recognition and targeting of lysosomal proteins.

K. von Figura, 1991, Current opinion in cell biology.

Binding of AP2 to Sorting Signals Is Modulated by AP2 Phosphorylation*

K. von Figura, S. Höning, Stefan Höning, 2001, The Journal of Biological Chemistry.

Sequence determinants directing conversion of cysteine to formylglycine in eukaryotic sulfatases

T. Dierks, K. von Figura, M. Lecca, 1999, The EMBO journal.

Residues critical for formylglycine formation and/or catalytic activity of arylsulfatase A.

T. Dierks, K. von Figura, A. Knaust, 1998, Biochemistry.

Posttranslational Modification of Serine to Formylglycine in Bacterial Sulfatases

T. Dierks, K. von Figura, Jianhe Peng, 2003, The Journal of Biological Chemistry.

Amino Acid Residues Forming the Active Site of Arylsulfatase A

T. Dierks, K. von Figura, B. Schmidt, 1999, The Journal of Biological Chemistry.

Degradation of even-numbered reduced and non-reduced hyaluronate oligosaccharides with D-glucuronic acid or N-acetyl-D-glucosamine as non-reducing terminal by chondroitin ABC and AC lyases.

K. von Figura, U. Klein, H. Ulrich, 1979, Hoppe-Seyler's Zeitschrift fur physiologische Chemie.

Biogenesis of lysosomal membranes

K. von Figura, C. Peters, 1994, FEBS letters.

A New Type of Congenital Disorders of Glycosylation (CDG-Ii) Provides New Insights into the Early Steps of Dolichol-linked Oligosaccharide Biosynthesis*

K. von Figura, Jianhe Peng, M. Grzmil, 2003, Journal of Biological Chemistry.

Arylsulfatase A pseudodeficiency: a common polymorphism which is associated with a unique haplotype.

K. von Figura, V. Gieselmann, J. Zlotogora, 1994, American journal of medical genetics.

Defective Oligomerization of Arylsulfatase A as a Cause of Its Instability in Lysosomes and Metachromatic Leukodystrophy*

T. Dierks, K. von Figura, I. Usón, 2002, The Journal of Biological Chemistry.

Glycosylation and phosphorylation of arylsulfatase A.

K. von Figura, V. Gieselmann, T. Selmer, 1994, The Journal of biological chemistry.

In vitro mutagenesis of potential N-glycosylation sites of arylsulfatase A. Effects on glycosylation, phosphorylation, and intracellular sorting.

K. von Figura, V. Gieselmann, B. Schmidt, 1992, The Journal of biological chemistry.

Deficiency of GDP-Man:GlcNAc2-PP-dolichol mannosyltransferase causes congenital disorder of glycosylation type Ik.

K. von Figura, C. Thiel, T. D. de Koning, 2004, American journal of human genetics.

Biosynthesis of secreted beta-hexosaminidase in Tetrahymena thermophila. A comparison of the wild type with a secretory mutant.

K. von Figura, A. Tiedtke, P. Hünseler, 1988, The Biochemical journal.

A general binding mechanism for all human sulfatases by the formylglycine-generating enzyme.

T. Dierks, M. Rudolph, K. von Figura, 2006, Proceedings of the National Academy of Sciences of the United States of America.

Neither type of mannose 6-phosphate receptor is sufficient for targeting of lysosomal enzymes along intracellular routes

K. von Figura, R. Pohlmann, F. Dittmer, 1996, Journal of Cell Biology.

Identification of N-sulphated disaccharide units in heparin-like polysaccharides.

K. von Figura, I. Pettersson, O. Larm, 1979, The Biochemical journal.

Carbohydrate-free carboxypeptidase Y is transferred into the lysosome-like yeast vacuole.

K. von Figura, A. Hasilik, A. Wiemken, 1982, Biochemical and biophysical research communications.

Two novel frameshift mutations causing premature stop codons in a patient with the severe form of Maroteaux‐Lamy syndrome

K. von Figura, J. Hopwood, D. Isbrandt, 1996, Human mutation.

Regulation of mannose 6-phosphate/insulin-like growth factor II receptor distribution by activators and inhibitors of protein kinase C.

K. von Figura, T. Braulke, H. Chao, 1990, European journal of biochemistry.

The evolutionary conservation of a novel protein modification, the conversion of cysteine to serinesemialdehyde in arylsulfatase from Volvox carteri.

K. von Figura, A. Hallmann, T. Selmer, 1996, European journal of biochemistry.

The polarized epithelia‐specific μ1B‐adaptin complements μ1A‐deficiency in fibroblasts

C. Meyer, K. von Figura, E. Eskelinen, 2002, EMBO reports.

The 46 kDa mannose-6-phosphate receptor contains a signal for basolateral sorting within the 19 juxtamembrane cytosolic residues.

K. von Figura, R. Bresciani, R. Pohlmann, 1997, The Biochemical journal.

The ligand-binding conformation of Mr 46,000 mannose 6-phosphate-specific receptor. Acquisition of binding activity during in vitro synthesis.

K. von Figura, A. Waheed, A. Hille, 1989, The Journal of biological chemistry.

Targeted Disruption of the Mouse Phosphomannomutase 2 Gene Causes Early Embryonic Lethality

K. von Figura, G. Matthijs, C. Thiel, 2006, Molecular and Cellular Biology.

Carbohydrate-deficient glycoprotein syndrome type 1: correction of the glycosylation defect by deprivation of glucose or supplementation of mannose

K. von Figura, L. Lehle, C. Korner, 1998, Glycoconjugate Journal.

Uptake of hyaluronate by cultured cells.

K. von Figura, H. Kresse, R. Basner, 1977, Biochemical and biophysical research communications.

High residual arylsulfatase A (ARSA) activity in a patient with late-infantile metachromatic leukodystrophy.

N. Baumann, K. von Figura, V. Gieselmann, 1993, American journal of human genetics.

Prostaglandins and fibroblast functions in vitro.

K. von Figura, A. Dembińska-kieć, P. Schönhöfer, 1979, Agents and actions. Supplements.

Functions of cathepsin K in bone resorption. Lessons from cathepsin K deficient mice.

A. Boyde, K. von Figura, P. Saftig, 2000, Advances in experimental medicine and biology.

Molecular characterization of the hypothetical 66.3‐kDa protein in mouse: Lysosomal targeting, glycosylation, processing and tissue distribution

K. von Figura, F. Deuschl, T. Lübke, 2006, FEBS letters.

Complex arylsulfatase A alleles causing metachromatic leukodystrophy

K. von Figura, V. Gieselmann, J. Kappler, 1994, Human mutation.

Synthesis and processing of arylsulfatase A in human skin fibroblasts.

K. von Figura, A. Waheed, A. Hasilik, 1982, Hoppe-Seyler's Zeitschrift fur physiologische Chemie.

Human placenta alpha-N-acetylglucosaminidase: purification, characterization and demonstration of multiple recognition forms.

K. von Figura, W. Röhrborn, 1978, Hoppe-Seyler´s Zeitschrift für physiologische Chemie.

Locating the anomalous scatterer substructures in halide and sulfur phasing.

G. Sheldrick, Z. Dauter, K. von Figura, 2003, Acta crystallographica. Section D, Biological crystallography.

Juvenile and adult metachromatic leukodystrophy: partial restoration of arylsulfatase A (cerebroside sulfatase) activity by inhibitors of thiol proteinases.

K. von Figura, A. Hasilik, F. Steckel, 1983, Proceedings of the National Academy of Sciences of the United States of America.

Synthesis and stability of steroid sulfatase in fibroblasts from multiple sulfatase deficiency.

K. von Figura, A. Hasilik, J. Conary, 1988, Biological chemistry Hoppe-Seyler.

Effect of monensin on intracellular transport and receptor-mediated endocytosis of lysosomal enzymes.

K. von Figura, A. Hasilik, R. Pohlmann, 1984, The Biochemical journal.

Localization of lysosomal acid phosphatase mRNA in mouse tissues.

K. von Figura, R. Pohlmann, J. Kreysing, 1992, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Neutral endopeptidase-24.11 (enkephalinase). Biosynthesis and localization in human fibroblasts.

K. von Figura, A. Hasilik, J. E. Zijderhand-Bleekemolen, 1987, The Biochemical journal.

Antibodies against the cytoplasmic tail can differentiate between the quaternary forms of the M r 46000 mannose 6‐phosphate receptor

K. von Figura, B. Schmidt, S. Nadimpalli, 1991, FEBS letters.

Early Embryonic Death of Mice Deficient in γ-Adaptin*

K. von Figura, P. Saftig, P. Schu, 1999, The Journal of Biological Chemistry.

Mice Deficient in Lysosomal Acid Phosphatase Develop Lysosomal Storage in the Kidney and Central Nervous System*

C. Peters, R. Lüllmann-Rauch, D. Hartmann, 1997, The Journal of Biological Chemistry.

Effect of tunicamycin on the metabolism of low-density lipoproteins by control and low-density-lipoprotein-receptor-deficient human skin fibroblasts.

K. von Figura, I. Filipović, 1980, The Biochemical journal.

Initiation of altered heparan sulphate on beta-D-xyloside in rat hepatocytes.

K. von Figura, P. Sudhakaran, W. Sinn, 1981, Hoppe-Seyler's Zeitschrift fur physiologische Chemie.

Human alpha-n-acetylglucosaminidase. 2. Activity towards natural substrates and multiple recognition forms.

K. von Figura, 1977, European journal of biochemistry.

Dephosphorylation of the mannose-6-phosphate recognition marker is localized in later compartments of the endocytic route. Identification of purple acid phosphatase (uteroferrin) as the candidate phosphatase.

K. von Figura, R. Bresciani, 1996, European journal of biochemistry.

Human alpha-N-acetylglucosaminidase. 1. Purification and properties.

K. von Figura, 1977, European journal of biochemistry.

Lysosomal glycogen storage disease without deficiency of acid alpha-glucosidase.

K. von Figura, R. Korinthenberg, D. von Bassewitz, 1989, Progress in clinical and biological research.

Biosynthesis of acid alpha-glucosidase in late-onset forms of glycogenosis type II (Pompe's disease).

K. von Figura, A. Waheed, A. Hasilik, 1982, FEBS letters.

Genetics of metachromatic leukodystrophy.

K. von Figura, V. Gieselmann, J. Kreysing, 1994, Gene therapy.

Synthesis, transport and processing of cathepsin C in Morris hepatoma 7777 cells and rat hepatocytes.

K. von Figura, R. Wattiaux, F. Mainferme, 1985, European journal of biochemistry.

Oligosaccharides in lysosomal enzymes. Distribution of high-mannose and complex oligosaccharides in cathepsin D and beta-hexosaminidase.

K. von Figura, A. Hasilik, 1981, European Journal of Biochemistry.

The Non-catalytic N-terminal Extension of Formylglycine-generating Enzyme Is Required for Its Biological Activity and Retention in the Endoplasmic Reticulum*

T. Dierks, K. von Figura, M. Mariappan, 2008, Journal of Biological Chemistry.

Paralog of the formylglycine‐generating enzyme – retention in the endoplasmic reticulum by canonical and noncanonical signals

Tom H. Pringle, T. Dierks, K. von Figura, 2008, The FEBS journal.