N-linked glycosylation and homeostasis of the endoplasmic reticulum.
暂无分享,去创建一个
[1] J. Ling,et al. Role of Magnesium Transporter Subtype 1 (MagT1) in the Osteogenic Differentiation of Rat Bone Marrow Stem Cells , 2016, Biological Trace Element Research.
[2] R. Gilmore,et al. Mammalian cells lacking either the cotranslational or posttranslocational oligosaccharyltransferase complex display substrate-dependent defects in asparagine linked glycosylation , 2016, Scientific Reports.
[3] G. Superti-Furga,et al. Gene essentiality and synthetic lethality in haploid human cells , 2015, Science.
[4] J. Caramelo,et al. A sweet code for glycoprotein folding , 2015, FEBS letters.
[5] J. Shendure,et al. Expanding the Molecular and Clinical Phenotype of SSR4‐CDG , 2015, Human mutation.
[6] J. Irving,et al. Interactions between N‐linked glycosylation and polymerisation of neuroserpin within the endoplasmic reticulum , 2015, The FEBS journal.
[7] F. Förster,et al. Structure of the native Sec61 protein-conducting channel , 2015, Nature Communications.
[8] Nan Yan,et al. Cytosolic Nuclease TREX1 Regulates Oligosaccharyltransferase Activity Independent of Nuclease Activity to Suppress Immune Activation. , 2015, Immunity.
[9] R. Gilmore,et al. Reduced expression of the oligosaccharyltransferase exacerbates protein hypoglycosylation in cells lacking the fully assembled oligosaccharide donor. , 2015, Glycobiology.
[10] Thierry Hennet,et al. Congenital disorders of glycosylation: a concise chart of glycocalyx dysfunction. , 2015, Trends in biochemical sciences.
[11] S. Burns,et al. A case of XMEN syndrome presented with severe auto-immune disorders mimicking autoimmune lymphoproliferative disease. , 2015, Clinical immunology.
[12] Kai Zhang,et al. Association of TUSC3 gene polymorphisms with non-syndromic mental retardation based on nuclear families in the Qinba mountain area of China. , 2015, Genetics and molecular research : GMR.
[13] G. Lederkremer,et al. Glycan regulation of ER-associated degradation through compartmentalization. , 2015, Seminars in cell & developmental biology.
[14] M. Molinari,et al. N-linked sugar-regulated protein folding and quality control in the ER. , 2015, Seminars in cell & developmental biology.
[15] R. Gilmore,et al. Cotranslational and posttranslocational N-glycosylation of proteins in the endoplasmic reticulum. , 2015, Seminars in cell & developmental biology.
[16] L. David,et al. Cotranslational stabilization of Sec62/63 within the ER Sec61 translocon is controlled by distinct substrate-driven translocation events. , 2015, Molecular cell.
[17] Smita Y. Patel,et al. Identification of a Novel Mutation in MAGT1 and Progressive Multifocal Leucoencephalopathy in a 58-Year-Old Man with XMEN Disease , 2014, Journal of Clinical Immunology.
[18] M. Lenardo,et al. X-linked immunodeficiency with magnesium defect, Epstein–Barr virus infection, and neoplasia disease: a combined immune deficiency with magnesium defect , 2014, Current opinion in pediatrics.
[19] K. Takeda,et al. Association of malectin with ribophorin I is crucial for attenuation of misfolded glycoprotein secretion. , 2014, Biochemical and biophysical research communications.
[20] R. Gilmore,et al. Oxidoreductase activity is necessary for N-glycosylation of cysteine-proximal acceptor sites in glycoproteins , 2014, The Journal of cell biology.
[21] J. Christianson,et al. OS-9 facilitates turnover of nonnative GRP94 marked by hyperglycosylation , 2014, Molecular biology of the cell.
[22] W. R. Kobertz,et al. The Middle X Residue Influences Cotranslational N-Glycosylation Consensus Site Skipping , 2014, Biochemistry.
[23] R. Glockshuber,et al. Structural basis of substrate specificity of human oligosaccharyl transferase subunit N33/Tusc3 and its role in regulating protein N-glycosylation. , 2014, Structure.
[24] J. Shendure,et al. A new congenital disorder of glycosylation caused by a mutation in SSR4, the signal sequence receptor 4 protein of the TRAP complex. , 2014, Human molecular genetics.
[25] P. Horák,et al. TUSC3 Loss Alters the ER Stress Response and Accelerates Prostate Cancer Growth in vivo , 2014, Scientific Reports.
[26] Friedrich Förster,et al. Structure of the mammalian oligosaccharyl-transferase complex in the native ER protein translocon , 2014, Nature Communications.
[27] R. Gilmore,et al. Glycosylation of closely spaced acceptor sites in human glycoproteins , 2013, Journal of Cell Science.
[28] H. Freeze,et al. Mutations in STT3A and STT3B cause two congenital disorders of glycosylation. , 2013, Human molecular genetics.
[29] Claire Redin,et al. XLID-causing mutations and associated genes challenged in light of data from large-scale human exome sequencing. , 2013, American journal of human genetics.
[30] W. R. Kobertz,et al. Molecular determinants of co- and post-translational N-glycosylation of type I transmembrane peptides. , 2013, The Biochemical journal.
[31] S. Pittaluga,et al. Mg2+ Regulates Cytotoxic Functions of NK and CD8 T Cells in Chronic EBV Infection Through NKG2D , 2013, Science.
[32] R. Gilmore,et al. Extreme C-terminal sites are posttranslocationally glycosylated by the STT3B isoform of the OST , 2013, The Journal of cell biology.
[33] D. Pincus,et al. Endoplasmic reticulum stress sensing in the unfolded protein response. , 2013, Cold Spring Harbor perspectives in biology.
[34] H. Freeze. Understanding Human Glycosylation Disorders: Biochemistry Leads the Charge* , 2013, The Journal of Biological Chemistry.
[35] Y. Yamaguchi,et al. Malectin Forms a Complex with Ribophorin I for Enhanced Association with Misfolded Glycoproteins* , 2012, The Journal of Biological Chemistry.
[36] S. High,et al. The oligosaccharyltransferase subunits OST48, DAD1 and KCP2 function as ubiquitous and selective modulators of mammalian N-glycosylation , 2012, Journal of Cell Science.
[37] M. Taura,et al. STT3B-dependent posttranslational N-glycosylation as a surveillance system for secretory protein. , 2012, Molecular cell.
[38] Florian Gnad,et al. Mapping N-glycosylation sites across seven evolutionarily distant species reveals a divergent substrate proteome despite a common core machinery. , 2012, Molecular cell.
[39] M. Hegde,et al. DDOST mutations identified by whole-exome sequencing are implicated in congenital disorders of glycosylation. , 2012, American journal of human genetics.
[40] J. Hirabayashi,et al. Role of malectin in Glc2Man9GlcNAc2-dependent quality control of α1-antitrypsin , 2011, Molecular biology of the cell.
[41] H. Ropers,et al. A novel nonsense mutation in TUSC3 is responsible for non‐syndromic autosomal recessive mental retardation in a consanguineous Iranian family , 2011, American journal of medical genetics. Part A.
[42] D. Douek,et al. Second messenger role for Mg2+ revealed by human T-cell immunodeficiency , 2011, Nature.
[43] Markus Aebi,et al. X-ray structure of a bacterial oligosaccharyltransferase , 2011, Nature.
[44] William R. Kobertz,et al. Post-translational N-Glycosylation of Type I Transmembrane KCNE1 Peptides , 2011, The Journal of Biological Chemistry.
[45] Riccardo Bernasconi,et al. Malectin Participates in a Backup Glycoprotein Quality Control Pathway in the Mammalian ER , 2011, PloS one.
[46] V. Rybin,et al. Analysis of the specific interactions between the lectin domain of malectin and diglucosides. , 2010, Glycobiology.
[47] Florian Gnad,et al. Precision Mapping of an In Vivo N-Glycoproteome Reveals Rigid Topological and Sequence Constraints , 2010, Cell.
[48] F. Wolf,et al. Modulation of TRPM6 and Na+/Mg2+ exchange in mammary epithelial cells in response to variations of magnesium availability , 2010, Journal of cellular physiology.
[49] Thierry Hennet,et al. Congenital disorders of glycosylation: an update on defects affecting the biosynthesis of dolichol‐linked oligosaccharides , 2009, Human mutation.
[50] D. Clapham,et al. Mammalian MagT1 and TUSC3 are required for cellular magnesium uptake and vertebrate embryonic development , 2009, Proceedings of the National Academy of Sciences.
[51] R. Glockshuber,et al. Oxidoreductase activity of oligosaccharyltransferase subunits Ost3p and Ost6p defines site-specific glycosylation efficiency , 2009, Proceedings of the National Academy of Sciences.
[52] M. Aebi,et al. Analysis of Glycosylation Site Occupancy Reveals a Role for Ost3p and Ost6p in Site-specific N-Glycosylation Efficiency*S , 2009, Molecular & Cellular Proteomics.
[53] C. Ruiz-Cañada,et al. Cotranslational and Posttranslational N-Glycosylation of Polypeptides by Distinct Mammalian OST Isoforms , 2009, Cell.
[54] T. Gibson,et al. Malectin: a novel carbohydrate-binding protein of the endoplasmic reticulum and a candidate player in the early steps of protein N-glycosylation. , 2008, Molecular biology of the cell.
[55] M. Schweigel,et al. Expression and functional activity of the Na/Mg exchanger, TRPM7 and MagT1 are changed to regulate Mg homeostasis and transport in rumen epithelial cells. , 2008, Magnesium research.
[56] J. Gécz,et al. Oligosaccharyltransferase-subunit mutations in nonsyndromic mental retardation. , 2008, American journal of human genetics.
[57] A. Helenius,et al. More than one glycan is needed for ER glucosidase II to allow entry of glycoproteins into the calnexin/calreticulin cycle. , 2005, Molecular cell.
[58] A. McCormack,et al. Proteomic analysis of mammalian oligosaccharyltransferase reveals multiple subcomplexes that contain Sec61, TRAP, and two potential new subunits. , 2005, Biochemistry.
[59] G. Quamme,et al. Identification and characterization of a novel mammalian Mg2+ transporter with channel-like properties , 2005, BMC Genomics.
[60] D. Karaoglu,et al. Oligosaccharyltransferase isoforms that contain different catalytic STT3 subunits have distinct enzymatic properties. , 2003, Molecular cell.
[61] G. von Heijne,et al. Photocross-linking of nascent chains to the STT3 subunit of the oligosaccharyltransferase complex , 2003, The Journal of cell biology.
[62] M. Aebi,et al. A specific screen for oligosaccharyltransferase mutations identifies the 9 kDa OST5 protein required for optimal activity in vivo and in vitro , 1997, The EMBO journal.
[63] W. Isaacs,et al. Structure and methylation-associated silencing of a gene within a homozygously deleted region of human chromosome band 8p22. , 1996, Genomics.
[64] G. von Heijne,et al. A Nascent Secretory Protein 5 Traverse the Ribosome/Endoplasmic Reticulum Translocase Complex as an Extended Chain (*) , 1996, The Journal of Biological Chemistry.
[65] G von Heijne,et al. Determination of the distance between the oligosaccharyltransferase active site and the endoplasmic reticulum membrane. , 1993, The Journal of biological chemistry.
[66] J. Thevenon,et al. Homozygous Truncating Intragenic Duplication in TUSC3 Responsible for Rare Autosomal Recessive Nonsyndromic Intellectual Disability with No Clinical or Biochemical Metabolic Markers. , 2015, JIMD reports.