Structure of pre-pro-von Willebrand factor and its expression in heterologous cells
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The relationship of N-linked glycosylation and heavy chain-binding protein association with the secretion of glycoproteinsA cloned human CCAAT-box-binding factor stimulates transcription from the human hsp70 promoterThe LAR transmembrane protein tyrosine phosphatase and a coiled-coil LAR-interacting protein co-localize at focal adhesionsCloning and characterization of mouse CCAAT binding factorExpression of the receptor-linked protein tyrosine phosphatase LAR: proteolytic cleavage and shedding of the CAM-like extracellular regionExpression of a human proprotein processing enzyme: correct cleavage of the von Willebrand factor precursor at a paired basic amino acid siteA family of receptor-linked protein tyrosine phosphatases in humans and DrosophilaAssembly and routing of von Willebrand factor variants: the requirements for disulfide-linked dimerization reside within the carboxy-terminal 151 amino acidsHuman fur gene encodes a yeast KEX2-like endoprotease that cleaves pro-beta-NGF in vivoThe mouse tectorins. Modular matrix proteins of the inner ear homologous to components of the sperm-egg adhesion systemThe molecular defect in type IIB von Willebrand disease. Identification of four potential missense mutations within the putative GpIb binding domainMolecular characterization and developmental expression of a retinoid- and fatty acid-binding glycoprotein from Drosophila. A putative lipophorin.The linker between the D3 and A1 domains of vWF suppresses A1-GPIbα catch bonds by site-specific binding to the A1 domain.Platelet adhesion involves a novel interaction between vimentin and von Willebrand factor under high shear stressEpitope mapping by cDNA expression of a monoclonal antibody which inhibits the binding of von Willebrand factor to platelet glycoprotein IIb/IIIa.Characterization of gill-specific genes of the acorn worm Ptychodera flava.Apolipocrustacein, formerly vitellogenin, is the major egg yolk precursor protein in decapod crustaceans and is homologous to insect apolipophorin II/I and vertebrate apolipoprotein B.Insights into von Willebrand factor proteolysis: clinical implications.Regulation of VWF expression, and secretion in health and disease.Molecular basis of human von Willebrand disease: analysis of platelet von Willebrand factor mRNA.The thrombin receptor extracellular domain contains sites crucial for peptide ligand-induced activation.Glanzmann thrombasthenia secondary to a Gly273-->Asp mutation adjacent to the first calcium-binding domain of platelet glycoprotein IIb.The molecular biology of von Willebrand disease.Structure, tissue distribution and genomic organization of the murine RRM-type RNA binding proteins TIA-1 and TIAR.Highly inducible expression from vectors containing multiple GRE's in CHO cells overexpressing the glucocorticoid receptor.Genetic linkage of two intragenic restriction fragment length polymorphisms with von Willebrand's disease type IIA. Evidence for a defect in the von Willebrand factor geneN-terminal flanking region of A1 domain in von Willebrand factor stabilizes structure of A1A2A3 complex and modulates platelet activation under shear stress.Sequence and structure relationships within von Willebrand factorComposition of the von Willebrand factor storage organelle (Weibel-Palade body) isolated from cultured human umbilical vein endothelial cellsCytoplasmic and transmembrane domains of integrin beta 1 and beta 3 subunits are functionally interchangeable.The phosphorylation state of eucaryotic initiation factor 2 alters translational efficiency of specific mRNAs.Effect of von Willebrand factor coexpression on the synthesis and secretion of factor VIII in Chinese hamster ovary cells.Cloning and analysis of human gastric mucin cDNA reveals two types of conserved cysteine-rich domains.Promoter-cDNA-directed heterologous protein expression in Xenopus laevis oocytes.Methods for genetic modification of megakaryocytes and platelets.Acquired von Willebrand syndrome associated with left ventricular assist device.The molecular genetics of von Willebrand diseaseChanges in thermodynamic stability of von Willebrand factor differentially affect the force-dependent binding to platelet GPIbalpha.von Willebrand factor biosynthesis and processing.Development of new cell lines for animal cell biotechnology.
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Structure of pre-pro-von Willebrand factor and its expression in heterologous cells
description
article publié dans la revue scientifique Nature
@fr
scientific article published in Nature
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована в Nature в листопаді 1986
@uk
name
Structure of pre-pro-von Willebrand factor and its expression in heterologous cells
@en
Structure of pre-pro-von Willebrand factor and its expression in heterologous cells
@nl
type
label
Structure of pre-pro-von Willebrand factor and its expression in heterologous cells
@en
Structure of pre-pro-von Willebrand factor and its expression in heterologous cells
@nl
prefLabel
Structure of pre-pro-von Willebrand factor and its expression in heterologous cells
@en
Structure of pre-pro-von Willebrand factor and its expression in heterologous cells
@nl
P2093
P2860
P356
P1433
P1476
Structure of pre-pro-von Willebrand factor and its expression in heterologous cells
@en
P2093
Bruce Ewenstein
David Ginsburg
David T. Bonthron
Elizabeth C. Orr
Lisa M. Mitsock
Louise C. Wasley
Randal J. Kaufman
Robert I. Handin
Stuart H. Orkin
P2860
P2888
P304
P356
10.1038/324270A0
P407
P577
1986-11-01T00:00:00Z
P6179
1029006732