| scholarly article | Q13442814 |
| P2093 | author name string | Renhao Li | |
| Xi Mo | |||
| Vahid Afshar-Kharghan | |||
| José A López | |||
| Sankaranarayanan Srinivasan | |||
| Shi-Zhong Luo | |||
| P2860 | cites work | Oligomerization of the integrin alphaIIbbeta3: roles of the transmembrane and cytoplasmic domains | Q24291812 |
| Glycoproteins V and Ib-IX form a noncovalent complex in the platelet membrane | Q24297475 | ||
| Structures of glycoprotein Ibalpha and its complex with von Willebrand factor A1 domain | Q24304907 | ||
| Crystal structure of the platelet glycoprotein Ib(alpha) N-terminal domain reveals an unmasking mechanism for receptor activation | Q27639267 | ||
| How to measure and predict the molar absorption coefficient of a protein | Q27860551 | ||
| Cytoplasmic domains of GpIbalpha and GpIbbeta regulate 14-3-3zeta binding to GpIb/IX/V | Q28142238 | ||
| Preferential heterodimer formation by isolated leucine zippers from fos and jun | Q28244227 | ||
| Binding of purified 14-3-3 zeta signaling protein to discrete amino acid sequences within the cytoplasmic domain of the platelet membrane glycoprotein Ib-IX-V complex | Q28258514 | ||
| Human signaling protein 14-3-3zeta interacts with platelet glycoprotein Ib subunits Ibalpha and Ibbeta | Q28260927 | ||
| Identification of a binding sequence for the 14-3-3 protein within the cytoplasmic domain of the adhesion receptor, platelet glycoprotein Ib alpha | Q28278900 | ||
| Purification and preliminary characterization of the glycoprotein Ib complex in the human platelet membrane | Q28291722 | ||
| Glycoprotein Ib and glycoprotein IX are fully complexed in the intact platelet membrane | Q28304653 | ||
| A minimal peptide scaffold for beta-turn display: optimizing a strand position in disulfide-cyclized beta-hairpins. | Q30689039 | ||
| Cytoplasmic truncation of glycoprotein Ib alpha weakens its interaction with von Willebrand factor and impairs cell adhesion | Q31131970 | ||
| Synthesis of GPIb beta with novel transmembrane and cytoplasmic sequences in a Bernard-Soulier patient resulting in GPIb-defective signaling in CHO cells. | Q33369895 | ||
| Identification of the disulphide bonds in human platelet glycocalicin | Q34131135 | ||
| Regulation of glycoprotein Ib-IX-von Willebrand factor interaction by cAMP-dependent protein kinase-mediated phosphorylation at Ser 166 of glycoprotein Ib(beta). | Q34152904 | ||
| von Willebrand factor binding to platelet GpIb initiates signals for platelet activation | Q34208569 | ||
| Nuclear magnetic resonance of membrane-associated peptides and proteins | Q34313197 | ||
| Use of thiol-disulfide equilibria to measure the energetics of assembly of transmembrane helices in phospholipid bilayers | Q34385274 | ||
| Polymorphism of human glycoprotein Ib alpha results from a variable number of tandem repeats of a 13-amino acid sequence in the mucin-like macroglycopeptide region. Structure/function implications | Q34404510 | ||
| Acquired Bernard-Soulier syndrome. Evidence for the role of a 210,000-molecular weight protein in the interaction of platelets with von Willebrand factor | Q34556332 | ||
| The cytoplasmic domain of glycoprotein (GP) Ibalpha constrains the lateral diffusion of the GP Ib-IX complex and modulates von Willebrand factor binding | Q36892126 | ||
| Interaction between platelet glycoprotein Ibalpha and filamin-1 is essential for glycoprotein Ib/IX receptor anchorage at high shear | Q38294908 | ||
| The glycoprotein Ib complex of human blood platelets | Q38349632 | ||
| The platelet glycoprotein Ib-IX complex | Q40751091 | ||
| A critical role for 14-3-3zeta protein in regulating the VWF binding function of platelet glycoprotein Ib-IX and its therapeutic implications | Q42092628 | ||
| Determination of membrane protein stability via thermodynamic coupling of folding to thiol-disulfide interchange | Q42109644 | ||
| Regulation of von Willebrand factor binding to the platelet glycoprotein Ib-IX by a membrane skeleton-dependent inside-out signal | Q43559368 | ||
| Role of the intracellular domains of GPIb in controlling the adhesive properties of the platelet GPIb/V/IX complex | Q44274490 | ||
| Filamin A binding to the cytoplasmic tail of glycoprotein Ibalpha regulates von Willebrand factor-induced platelet activation | Q44468894 | ||
| Identification of a novel 14-3-3zeta binding site within the cytoplasmic tail of platelet glycoprotein Ibalpha | Q44822030 | ||
| Expression of platelet glycoprotein (GP) V in heterologous cells and evidence for its association with GP Ib alpha in forming a GP Ib-IX-V complex on the cell surface. | Q45962782 | ||
| Efficient plasma membrane expression of a functional platelet glycoprotein Ib-IX complex requires the presence of its three subunits | Q46244502 | ||
| Glycoprotein (GP) Ib beta is the critical subunit linking GP Ib alpha and GP IX in the GP Ib-IX complex. Analysis of partial complexes. | Q46485616 | ||
| The transmembrane domain of glycoprotein Ibbeta is critical to efficient expression of glycoprotein Ib-IX complex in the plasma membrane. | Q51807050 | ||
| A novel ligand-binding site in the zeta-form 14-3-3 protein recognizing the platelet glycoprotein Ibalpha and distinct from the c-Raf-binding site. | Q52532830 | ||
| The vascular biology of the glycoprotein Ib-IX-V complex | Q59281509 | ||
| Platelet plasma membrane glycoproteins. Evidence for the presence of nonequivalent disulfide bonds using nonreduced-reduced two-dimensional gel electrophoresis | Q67556563 | ||
| Modulation of platelet function through adhesion receptors. A dual role for glycoprotein IIb-IIIa (integrin alpha IIb beta 3) mediated by fibrinogen and glycoprotein Ib-von Willebrand factor | Q68142029 | ||
| Disulfide bonds as probes of protein folding pathways | Q69647577 | ||
| Molecular characterization of quinine/quinidine drug-dependent antibody platelet interaction using monoclonal antibodies | Q69916943 | ||
| A buried polar interaction can direct the relative orientation of helices in a coiled coil | Q77217036 | ||
| The variable number of tandem repeat polymorphism of platelet glycoprotein Ibalpha and risk of coronary heart disease | Q79236961 | ||
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | cell biology | Q7141 |
| P304 | page(s) | 603-609 | |
| P577 | publication date | 2006-09-28 | |
| P1433 | published in | Blood | Q885070 |
| P1476 | title | Glycoprotein Ibalpha forms disulfide bonds with 2 glycoprotein Ibbeta subunits in the resting platelet | |
| P478 | volume | 109 |
| Q48106594 | A new heterozygous mutation in GP1BA gene responsible for macrothrombocytopenia |
| Q41991691 | Analysis of inter-subunit contacts reveals the structural malleability of extracellular domains in platelet glycoprotein Ib-IX complex |
| Q38990156 | Basic mechanisms of platelet receptor shedding |
| Q28972536 | Bernard-Soulier syndrome |
| Q42641525 | Binding of platelet glycoprotein Ibbeta through the convex surface of leucine-rich repeats domain of glycoprotein IX. |
| Q34712807 | Calmodulin adopts an extended conformation when interacting with L-selectin in membranes. |
| Q42209721 | Copy number analysis of the murine platelet proteome spanning the complete abundance range |
| Q37056698 | Defective Association of the Platelet Glycoprotein Ib-IX Complex with the Glycosphingolipid-Enriched Membrane Domain Inhibits Murine Thrombus and Atheroma Formation |
| Q90572410 | Delimiting the autoinhibitory module of von Willebrand factor |
| Q46356975 | Effect of Xiaoyu Zhixue Tablet on the expression of platelet membrane glycoprotein I b/IX/V complex in patients with chronic renal failure |
| Q41459186 | Epac1-deficient mice have bleeding phenotype and thrombocytes with decreased GPIbβ expression |
| Q33745920 | Exploring the potential of the platelet membrane proteome as a source of peripheral biomarkers for Alzheimer's disease. |
| Q83080871 | Expression of platelet membrane glycoprotein Ib/IX/V complex, a receptor of thrombin, in patients with hemorrhagic thrombopathy |
| Q35762807 | Extracellular matrix proteins in hemostasis and thrombosis |
| Q37382363 | FERM domain of moesin desorbs the basic-rich cytoplasmic domain of l-selectin from the anionic membrane surface. |
| Q35485719 | Force-induced on-rate switching and modulation by mutations in gain-of-function von Willebrand diseases |
| Q33402780 | Genetics of familial forms of thrombocytopenia |
| Q34974088 | Identification of a juxtamembrane mechanosensitive domain in the platelet mechanosensor glycoprotein Ib-IX complex |
| Q33406532 | Inherited thrombocytopenias frequently diagnosed in adults |
| Q28114988 | Juxtamembrane basic residues in glycoprotein Ibbeta cytoplasmic domain are required for assembly and surface expression of glycoprotein Ib-IX complex. |
| Q34810114 | L-selectin transmembrane and cytoplasmic domains are monomeric in membranes |
| Q37461882 | Membrane skeleton orchestrates the platelet glycoprotein (GP) Ib-IX complex clustering and signaling |
| Q34526248 | Membrane-enabled dimerization of the intrinsically disordered cytoplasmic domain of ADAM10. |
| Q33434155 | Metalloproteolytic receptor shedding…platelets "acting their age". |
| Q42993250 | Modularity of the oncoprotein-like properties of platelet glycoprotein Ibalpha |
| Q33422658 | Molecular basis of inherited thrombocytopenias |
| Q37609911 | Parsing the repertoire of GPIb-IX-V disorders |
| Q37824742 | Platelet adhesion to collagen |
| Q37314944 | Platelet clearance via shear-induced unfolding of a membrane mechanoreceptor |
| Q35065172 | Platelet glycoprotein Ib beta/IX mediates glycoprotein Ib alpha localization to membrane lipid domain critical for von Willebrand factor interaction at high shear |
| Q37273226 | Platelet interaction with von Willebrand factor is enhanced by shear-induced clustering of glycoprotein Ibα. |
| Q37807427 | Platelet physiology and antiplatelet agents |
| Q37175605 | Platelet receptors and signaling in the dynamics of thrombus formation. |
| Q28068448 | Platelets and platelet adhesion molecules: novel mechanisms of thrombosis and anti-thrombotic therapies |
| Q33432917 | Platelets are versatile cells: New discoveries in hemostasis, thrombosis, immune responses, tumor metastasis and beyond |
| Q33404311 | Platelets with a W127X mutation in GPIX express sufficient residual amounts of GPIbα to support adhesion to von Willebrand factor and collagen |
| Q24627629 | Quaternary organization of GPIb-IX complex and insights into Bernard-Soulier syndrome revealed by the structures of GPIbβ and a GPIbβ/GPIX chimera |
| Q89879223 | RNA Sequencing (RNA-Seq) Based Transcriptome Analysis in Immune Response of Holstein Cattle to Killed Vaccine against Bovine Viral Diarrhea Virus Type I |
| Q39033939 | Rare variants in GP1BB are responsible for autosomal dominant macrothrombocytopenia. |
| Q47625174 | Receptor-mediated cell mechanosensing. |
| Q42931957 | Reconstitution of the platelet glycoprotein Ib-IX complex in phospholipid bilayer Nanodiscs. |
| Q43143824 | Role of the transmembrane domain of glycoprotein IX in assembly of the glycoprotein Ib-IX complex |
| Q37540219 | Rolling cell adhesion |
| Q28116998 | Specific heteromeric association of four transmembrane peptides derived from platelet glycoprotein Ib-IX complex |
| Q38220681 | Spectrum of the mutations in Bernard-Soulier syndrome |
| Q36824113 | Structural basis for the specific inhibition of glycoprotein Ibα shedding by an inhibitory antibody |
| Q52338988 | TAILS N-Terminomics and proteomics reveal complex regulation of proteolytic cleavage by O-glycosylation. |
| Q40717707 | The dimerization interface of the glycoprotein Ibβ transmembrane domain corresponds to polar residues within a leucine zipper motif |
| Q37163637 | The membrane-proximal intermolecular disulfide bonds in glycoprotein Ib influence receptor binding to von Willebrand factor. |
| Q34323610 | The organizing principle of the platelet glycoprotein Ib-IX-V complex. |
| Q34186405 | Transmembrane and trans-subunit regulation of ectodomain shedding of platelet glycoprotein Ibalpha. |
| Q34285705 | Transmembrane domains are critical to the interaction between platelet glycoprotein V and glycoprotein Ib-IX complex. |
| Q53061821 | Unravelling the mechanism and significance of thrombin binding to platelet glycoprotein Ib |
| Q33733889 | Zebrafish von Willebrand factor |
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