Sulfatase modifying factor 1 trafficking through the cells: from endoplasmic reticulum to the endoplasmic reticulum
暂无分享,去创建一个
A. Ballabio | T. Dierks | M. Cosma | M. Monti | P. Pucci | E. Surace | S. Pepe | C. Settembre | Ida Annunziata | E. Zito | M. Buono | M. Cozzolino
[1] A. Ballabio,et al. SUMF1 enhances sulfatase activities in vivo in five sulfatase deficiencies. , 2007, The Biochemical journal.
[2] A. Ballabio,et al. Systemic inflammation and neurodegeneration in a mouse model of multiple sulfatase deficiency , 2007, Proceedings of the National Academy of Sciences.
[3] H. Hauri,et al. Cargo Selectivity of the ERGIC‐53/MCFD2 Transport Receptor Complex , 2006, Traffic.
[4] Hong Li,et al. Identification and Validation of Mannose 6-Phosphate Glycoproteins in Human Plasma Reveal a Wide Range of Lysosomal and Non-lysosomal Proteins*S , 2006, Molecular & Cellular Proteomics.
[5] C. Morales,et al. The sorting and trafficking of lysosomal proteins. , 2006, Histology and histopathology.
[6] A. Ballabio,et al. Correction of Hunter syndrome in the MPSII mouse model by AAV2/8-mediated gene delivery. , 2006, Human molecular genetics.
[7] A. Ballabio,et al. Sulfatases and sulfatase modifying factors: an exclusive and promiscuous relationship. , 2005, Human molecular genetics.
[8] I. Nabi,et al. pH-specific sequestration of phosphoglucose isomerase/autocrine motility factor by fibronectin and heparan sulphate , 2005, Journal of Cell Science.
[9] A. Ballabio,et al. Sulfatases and human disease. , 2005, Annual review of genomics and human genetics.
[10] A. Ballabio,et al. Sulphatase activities are regulated by the interaction of sulphatase‐modifying factor 1 with SUMF2 , 2005, EMBO reports.
[11] T. Dierks,et al. Molecular Basis for Multiple Sulfatase Deficiency and Mechanism for Formylglycine Generation of the Human Formylglycine-Generating Enzyme , 2005, Cell.
[12] T. Dierks,et al. Molecular Characterization of the Human Cα-formylglycine-generating Enzyme* , 2005, Journal of Biological Chemistry.
[13] A. Ballabio,et al. Molecular and functional analysis of SUMF1 mutations in multiple sulfatase deficiency , 2004, Human mutation.
[14] T. Dierks,et al. The human SUMF1 gene, required for posttranslational sulfatase modification, defines a new gene family which is conserved from pro- to eukaryotes. , 2003, Gene.
[15] Somasekar Seshagiri,et al. The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment. , 2003, Genome research.
[16] A. Ballabio,et al. The Multiple Sulfatase Deficiency Gene Encodes an Essential and Limiting Factor for the Activity of Sulfatases , 2003, Cell.
[17] T. Dierks,et al. Multiple Sulfatase Deficiency Is Caused by Mutations in the Gene Encoding the Human Cα-Formylglycine Generating Enzyme , 2003, Cell.
[18] M. Desjardins,et al. ER-mediated phagocytosis: a new membrane for new functions , 2003, Nature Reviews Immunology.
[19] M. Nussenzweig,et al. Mannose Receptor-Mediated Regulation of Serum Glycoprotein Homeostasis , 2002, Science.
[20] T Dierks,et al. 1.3 A structure of arylsulfatase from Pseudomonas aeruginosa establishes the catalytic mechanism of sulfate ester cleavage in the sulfatase family. , 2001, Structure.
[21] C. Scriver,et al. The Metabolic and Molecular Bases of Inherited Disease, 8th Edition 2001 , 2001, Journal of Inherited Metabolic Disease.
[22] K. Sandvig,et al. Entry of ricin and Shiga toxin into cells: molecular mechanisms and medical perspectives , 2000, The EMBO journal.
[23] R. Pepperkok,et al. Evidence for a COP-I-independent transport route from the Golgi complex to the endoplasmic reticulum , 1999, Nature Cell Biology.
[24] W. Schneider,et al. Cellular uptake of saposin (SAP) precursor and lysosomal delivery by the low density lipoprotein receptor‐related protein (LRP) , 1998, The EMBO journal.
[25] T. Cox. The metabolic and molecular bases of inherited disease: Vols I, II and III (7th edn): edited by Charles R. Scriver, Arthur L. Beaudet, William S. Sly and David Valle McGraw-Hill, 1995, £195.00 hbk (4605 pages) ISBN 0 07 909826 6 , 1996 .
[26] T. Selmer,et al. A novel amino acid modification in sulfatases that is defective in multiple sulfatase deficiency , 1995, Cell.
[27] A Helenius,et al. How N-linked oligosaccharides affect glycoprotein folding in the endoplasmic reticulum. , 1994, Molecular biology of the cell.
[28] M. Taylor,et al. Structural requirements for high affinity binding of complex ligands by the macrophage mannose receptor. , 1993, The Journal of biological chemistry.
[29] P. Stahl. The macrophage mannose receptor: current status. , 1990, American journal of respiratory cell and molecular biology.
[30] J. Russell,et al. Mannose receptor-mediated uptake of ricin toxin and ricin A chain by macrophages. Multiple intracellular pathways for a chain translocation. , 1986, The Journal of biological chemistry.
[31] C C Howe,et al. Human hepatocellular carcinoma cell lines secrete the major plasma proteins and hepatitis B surface antigen. , 1980, Science.
[32] R. Giugliani,et al. The mucopolysaccharidoses. , 1976, Journal of medical genetics.
[33] Peter Bross,et al. The Metabolic and Molecular Basis of Inherited Disease: Protein Folding and Misfolding: the Role of Cellular Protein Quality Control Systems in Inherited Disorders , 2005 .