(Q28216564)

12 December 2020

Initiation of platelet adhesion by arrest onto fibrinogen or translocation on von Willebrand factor

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12 December 2020

Localization and characterization of an alpha-thrombin-binding site on platelet glycoprotein Ib alpha

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12 December 2020

A revised classification of von Willebrand disease. For the Subcommittee on von Willebrand Factor of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis.

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12 December 2020

Nonsense mutation in the glycoprotein Ib alpha coding sequence associated with Bernard-Soulier syndrome

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12 December 2020

Platelet-type von Willebrand disease

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12 December 2020

A revised model of platelet aggregation

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12 December 2020

Structural characterization and chromosomal location of the gene encoding human platelet glycoprotein Ib beta

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12 December 2020

A three-base deletion removing a leucine residue in a leucine-rich repeat of platelet glycoprotein Ib alpha associated with a variant of Bernard-Soulier syndrome (Nancy I)

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12 December 2020

Generation and rescue of a murine model of platelet dysfunction: the Bernard-Soulier syndrome

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12 December 2020

Congenital platelet function disorders: survey findings and pathophysiology

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12 December 2020

Evidence that DDAVP transiently improves hemostasis in Bernard-Soulier syndrome independent of von Willebrand-factor

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12 December 2020

Naturally occurring mutations in glycoprotein Ibalpha that result in defective ligand binding and synthesis of a truncated protein.

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12 December 2020

Gray platelet syndrome. A variety of qualitative platelet disorder

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12 December 2020

Characterization of the gene encoding human platelet glycoprotein IX

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12 December 2020

Identification of a patient with Bernard-Soulier syndrome and a deletion in the DiGeorge/velo-cardio-facial chromosomal region in 22q11.2.

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12 December 2020

Missense mutations of the glycoprotein (GP) Ib beta gene impairing the GPIb alpha/beta disulfide linkage in a family with giant platelet disorder

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12 December 2020

Analysis of the megakaryocyte glycoprotein IX promoter identifies positive and negative regulatory domains and functional GATA and Ets sites

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12 December 2020

Specific synergy of multiple substrate-receptor interactions in platelet thrombus formation under flow.

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12 December 2020

Cys209 Ser mutation in the platelet membrane glycoprotein Ib alpha gene is associated with Bernard-Soulier syndrome

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12 December 2020

Platelet glycoprotein ibalpha is a counterreceptor for the leukocyte integrin Mac-1 (CD11b/CD18)

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12 December 2020

Vulnerable mutation Trp126-->stop of glycoprotein IX in Japanese Bernard-Soulier syndrome

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12 December 2020

Variant Bernard-Soulier syndrome type bolzano. A congenital bleeding disorder due to a structural and functional abnormality of the platelet glycoprotein Ib-IX complex

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12 December 2020

The 5' flanking region and chromosomal localization of the gene encoding human platelet membrane glycoprotein Ib alpha

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12 December 2020

Regulation of von Willebrand factor binding to the platelet glycoprotein Ib-IX by a membrane skeleton-dependent inside-out signal

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12 December 2020

Identification of a mutation in a GATA binding site of the platelet glycoprotein Ibbeta promoter resulting in the Bernard-Soulier syndrome

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12 December 2020

Mutations in the NMMHC-A gene cause autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly/Sebastian syndrome).

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12 December 2020

A phenylalanine-55 to serine amino-acid substitution in the human glycoprotein IX leucine-rich repeat is associated with Bernard-Soulier syndrome

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12 December 2020

Bernard-Soulier syndrome: common ancestry in two African American families with the GP Ib alpha Leu129Pro mutation

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12 December 2020

Cytoskeletal regulation of the platelet glycoprotein Ib/V/IX-von willebrand factor interaction.

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12 December 2020

Cytoplasmic domains of GpIbalpha and GpIbbeta regulate 14-3-3zeta binding to GpIb/IX/V

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12 December 2020

Cys97-->Tyr mutation in the glycoprotein IX gene associated with Bernard-Soulier syndrome

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12 December 2020

Identification of essential GATA and Ets binding motifs within the promoter of the platelet glycoprotein Ib alpha gene

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12 December 2020

The vascular biology of the glycoprotein Ib-IX-V complex

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12 December 2020

Structure of the human blood platelet membrane glycoprotein Ib alpha gene

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12 December 2020

Complex conotruncal heart defect, severe bleeding disorder and 22q11 deletion: a new case of Bernard-Soulier syndrome and of 22q11 deletion syndrome?

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12 December 2020

Bernard-Soulier syndrome: quantitative characterization of megakaryocytes and platelets by flow cytometric and platelet kinetic measurements

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12 December 2020

A point mutation in glycoprotein IX coding sequence (Cys73 (TGT) to Tyr(TAT)) causes impaired surface expression of GPIb/IX/V complex in two families with Bernard-Soulier syndrome

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12 December 2020

Mutation in the gene encoding the alpha chain of platelet glycoprotein Ib in platelet-type von Willebrand disease

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12 December 2020

Heterogeneous expression of glycoprotein Ib, IX and V in platelets from two patients with Bernard-Soulier syndrome caused by different genetic abnormalities

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12 December 2020

The genetic defect in two well-studied cases of Bernard-Soulier syndrome: a point mutation in the fifth leucine-rich repeat of platelet glycoprotein Ib alpha.

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12 December 2020

An acquired Bernard-Soulier-like platelet defect associated with juvenile myelodysplastic syndrome

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12 December 2020

A missense mutation (Tyr88 to Cys) in the platelet membrane glycoprotein Ibbeta gene affects GPIb/IX complex expression--Bernard-Soulier syndrome in the homozygous form and giant platelets in the heterozygous form

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12 December 2020

Micropipette aspiration of human blood platelets: a defect in Bernard-Soulier's syndrome.

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12 December 2020

Autosomal dominant macrothrombocytopenia in Italy is most frequently a type of heterozygous Bernard-Soulier syndrome

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12 December 2020

Compound heterozygosity (554-589 del, C515-T transition) in the platelet glycoprotein Ib alpha gene in a patient with a severe bleeding tendency

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12 December 2020

Gene cloning of rat and mouse platelet glycoprotein V: identification of megakaryocyte-specific promoters and demonstration of functional thrombin cleavage

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12 December 2020

Platelet ultrastructural abnormalities in three patients with type 2B von Willebrand disease

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12 December 2020

Bernard-Soulier syndrome with severe bleeding: absent platelet glycoprotein Ib alpha due to a homozygous one-base deletion.

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12 December 2020

Role of glycoprotein V in the formation of the platelet high-affinity thrombin-binding site.

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12 December 2020

Bernard-Soulier syndrome

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12 December 2020

The cytoplasmic domain of the alpha-subunit of glycoprotein (GP) Ib mediates attachment of the entire GP Ib-IX complex to the cytoskeleton and regulates von Willebrand factor-induced changes in cell morphology

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12 December 2020

The role of von Willebrand factor and fibrinogen in platelet aggregation under varying shear stress

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12 December 2020

Molecular and genetic analysis of two patients with Bernard-Soulier syndrome--identification of new mutations in glycoprotein Ib alpha gene

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12 December 2020

Homozygous Pro74-->Arg mutation in the platelet glycoprotein Ibbeta gene associated with Bernard-Soulier syndrome

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12 December 2020

Occurrence of the Asn45Ser mutation in the GPIX gene in a Belgian patient with Bernard Soulier syndrome

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12 December 2020

The platelet glycoprotein Ib-IX complex

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12 December 2020

Influence of monoclonal antiplatelet glycoprotein antibodies on in vitro human megakaryocyte colony formation and proplatelet formation

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12 December 2020

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.

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12 December 2020

Novel heterozygous missense mutation in the platelet glycoprotein Ib beta gene associated with isolated giant platelet disorder

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12 December 2020

The glycoprotein Ib-IX-V complex is a platelet counterreceptor for P-selectin

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12 December 2020

Bernard-Soulier syndrome in a patient doubly heterozygous for two frameshift mutations in the glycoprotein ib alpha gene

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12 December 2020

Double heterozygosity for mutations in the platelet glycoprotein IX gene in three siblings with Bernard-Soulier syndrome

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12 December 2020

The von Willebrand factor-binding domain of platelet membrane glycoprotein Ib. Characterization by monoclonal antibodies and partial amino acid sequence analysis of proteolytic fragments

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12 December 2020

Human platelet glycoproteins V and IX: mapping of two leucine-rich glycoprotein genes to chromosome 3 and analysis of structures

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12 December 2020

De novo mutation of the platelet glycoprotein Ib alpha gene in a patient with pseudo-von Willebrand disease

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12 December 2020

DDAVP shortens bleeding time in Bernard-Soulier syndrome

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12 December 2020

Bernard-Soulier syndrome Karlstad: Trp 498Stop mutation resulting in a truncated glycoprotein Ibalpha that contains part of the transmembranous domain

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12 December 2020

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12 December 2020

Platelet thrombus formation on collagen at high shear rates is mediated by von Willebrand factor-glycoprotein Ib interaction and inhibited by von Willebrand factor-glycoprotein IIb/IIIa interaction

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12 December 2020

Role of the leucine-rich domain of platelet GPIbalpha in correct post-translational processing--the Nancy I Bernard-Soulier mutation expressed on CHO cells

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12 December 2020

Efficient plasma membrane expression of a functional platelet glycoprotein Ib-IX complex requires the presence of its three subunits

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12 December 2020

Mutation of leucine-57 to phenylalanine in a platelet glycoprotein Ib alpha leucine tandem repeat occurring in patients with an autosomal dominant variant of Bernard-Soulier disease

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12 December 2020

Platelets from "giant platelet syndrome (BSS)" are discocytes and normal sized

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12 December 2020

von Willebrand factor binding to platelet GpIb initiates signals for platelet activation

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12 December 2020

Severe bleeding tendency in a patient with Bernard-Soulier syndrome associated with a homozygous single base pair deletion in the gene coding for the human platelet glycoprotein Ibalpha

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12 December 2020

Bernard-Soulier syndrome caused by a dinucleotide deletion and reading frameshift in the region encoding the glycoprotein Ib alpha transmembrane domain

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12 December 2020

Molecular characterization of two mutations in platelet glycoprotein (GP) Ib alpha in two Finnish Bernard-Soulier syndrome families.

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12 December 2020

Bernard-Soulier syndrome Kagoshima: Ser 444-->stop mutation of glycoprotein (GP) Ib alpha resulting in circulating truncated GPIb alpha and surface expression of GPIb beta and GPIX

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12 December 2020

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12 December 2020

The critical interaction of glycoprotein (GP) IBbeta with GPIX-a genetic cause of Bernard-Soulier syndrome

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12 December 2020

Pseudo-von Willebrand disease: a mutation in the platelet glycoprotein Ib alpha gene associated with a hyperactive surface receptor.

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12 December 2020

Acquired Bernard-Soulier syndrome. Evidence for the role of a 210,000-molecular weight protein in the interaction of platelets with von Willebrand factor

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12 December 2020

Recurrent mutation Asn45-->Ser of glycoprotein IX in Bernard-Soulier syndrome

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12 December 2020

Point mutation in a leucine-rich repeat of platelet glycoprotein Ib alpha resulting in the Bernard-Soulier syndrome

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12 December 2020

Surface expression of glycoprotein ib alpha is dependent on glycoprotein ib beta: evidence from a novel mutation causing Bernard-Soulier syndrome

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12 December 2020

Compound heterozygosity of the GPIbalpha gene associated with Bernard-Soulier syndrome.

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12 December 2020

Platelet characteristics in patients with X-linked macrothrombocytopenia because of a novel GATA1 mutation

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12 December 2020

Substantial expression of glycoproteins IX and V on the platelet surface from a patient with Bernard-Soulier syndrome

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12 December 2020

Identification of a homozygous single base pair deletion in the gene coding for the human platelet glycoprotein Ib alpha causing Bernard-Soulier syndrome

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12 December 2020

Variant Bernard-Soulier syndrome due to homozygous Asn45Ser mutation in the platelet glycoprotein (GP) IX in seven patients of five unrelated Finnish families.

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12 December 2020

Megakaryocyte-targeted synthesis of the integrin beta(3)-subunit results in the phenotypic correction of Glanzmann thrombasthenia

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12 December 2020

Recombinant activated factor VII (NovoSeven) treatment of platelet-related bleeding disorders. International Registry on Recombinant Factor VIIa and Congenital Platelet Disorders Group.

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12 December 2020

Transmembrane calcium influx associated with von Willebrand factor binding to GP Ib in the initiation of shear-induced platelet aggregation

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12 December 2020

Identification of a new mutation in platelet glycoprotein IX (GPIX) in a patient with Bernard-Soulier syndrome

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12 December 2020

Studies on the megakaryocytes of a patient with the Bernard-Soulier syndrome

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12 December 2020

Substitution of Val for Met at residue 239 of platelet glycoprotein Ib alpha in Japanese patients with platelet-type von Willebrand disease

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12 December 2020

Bernard-Soulier syndrome associated with 22q11.2 microdeletion

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12 December 2020

Pseudo-Bernard-Soulier syndrome: thrombocytopenia caused by autoantibody to platelet glycoprotein Ib.

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12 December 2020

The glycoprotein Ib/IX complex regulates cell proliferation

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12 December 2020

A new variant of Bernard-Soulier syndrome characterized by dysfunctional glycoprotein (GP) Ib and severely reduced amounts of GPIX and GPV

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12 December 2020

Novel point mutation in the leucine-rich motif of the platelet glycoprotein IX associated with Bernard-Soulier syndrome

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12 December 2020

Identification of the region in actin-binding protein that binds to the cytoplasmic domain of glycoprotein IBalpha

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12 December 2020

Familial dyserythropoietic anaemia and thrombocytopenia due to an inherited mutation in GATA1

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12 December 2020

Velocardiofacial syndrome patients with a heterozygous chromosome 22q11 deletion have giant platelets

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12 December 2020