Molecular basis of von Willebrand disease type IIB. Candidate mutations cluster in one disulfide loop between proposed platelet glycoprotein Ib binding sequences (Q28776606)

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scientific article (publication date: April 1991)

Language	Label	Description	Also known as
English	Molecular basis of von Willebrand disease type IIB. Candidate mutations cluster in one disulfide loop between proposed platelet glycoprotein Ib binding sequences	scientific article (publication date: April 1991)

Statements

scholarly article

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Molecular basis of von Willebrand disease type IIB. Candidate mutations cluster in one disulfide loop between proposed platelet glycoprotein Ib binding sequences (English)

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author name string

A M Randi

1

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I Rabinowitz

2

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D J Mancuso

3

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P M Mannucci

4

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J E Sadler

5

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language of work or name

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publication date

April 1991

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Journal of Clinical Investigation

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87

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4

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1220-6

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Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

1 reference

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16 March 2017

Establishing homologies in protein sequences

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7 April 2017

Pseudo-von Willebrand's disease. An intrinsic platelet defect with aggregation by unmodified human factor VIII/von Willebrand factor and enhanced adsorption of its high-molecular-weight multimers

1 reference

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3 June 2018

Variant von Willebrand's disease: characterization of two subtypes by analysis of multimeric composition of factor VIII/von Willebrand factor in plasma and platelets

1 reference

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3 June 2018

Platelet aggregation induced by 1-desamino-8-D-arginine vasopressin (DDAVP) in Type IIB von Willebrand's disease

1 reference

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3 June 2018

Carrier detection of Hemophilia B by using a restriction site polymorphism associated with the coagulation Factor IX gene

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3 June 2018

DNA methylation and the frequency of CpG in animal DNA.

1 reference

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3 June 2018

Base composition-independent hybridization in tetramethylammonium chloride: a method for oligonucleotide screening of highly complex gene libraries

1 reference

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3 June 2018

Type IIB von Willebrand's disease presenting as thrombocytopenia during pregnancy

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3 June 2018

Type IIB von Willebrand's disease with probable autosomal recessive inheritance and presenting as thrombocytopenia in infancy

1 reference

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3 June 2018

Recurrent mutations in haemophilia A give evidence for CpG mutation hotspots

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295140

3 June 2018

Gene deletions correlate with the development of alloantibodies in von Willebrand disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295140

3 June 2018

Thrombocytopenia associated with pregnancy in a patient with type IIB von Willebrand's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295140

3 June 2018

von Willebrand factor. A reduced and alkylated 52/48-kDa fragment beginning at amino acid residue 449 contains the domain interacting with platelet glycoprotein Ib.

1 reference

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3 June 2018

Interaction of purified type IIB von Willebrand factor with the platelet membrane glycoprotein Ib induces fibrinogen binding to the glycoprotein IIb/IIIa complex and initiates aggregation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295140

3 June 2018

Cloning and characterization of two cDNAs coding for human von Willebrand factor.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295140

3 June 2018

Molecular basis of human von Willebrand disease: analysis of platelet von Willebrand factor mRNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295140

3 June 2018

Spontaneous platelet aggregation in type IIB Tampa von Willebrand disease is inhibited by the 52/48-kDa fragment of normal von Willebrand factor, which contains the GPIb binding domain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295140

3 June 2018

von Willebrand factor synthesized by endothelial cells from a patient with type IIB von Willebrand disease supports platelet adhesion normally but has an increased affinity for platelets

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295140

3 June 2018

Structure of the gene for human von Willebrand factor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295140

3 June 2018

Isolation of the von Willebrand factor domain interacting with platelet glycoprotein Ib, heparin, and collagen and characterization of its three distinct functional sites

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295140

3 June 2018

Haemophilia B: database of point mutations and short additions and deletions

1 reference

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3 June 2018

Postoperative thrombocytopenia in type IIB von Willebrand disease

1 reference

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3 June 2018

Human von Willebrand factor gene and pseudogene: structural analysis and differentiation by polymerase chain reaction

1 reference

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3 June 2018

Molecular basis of base substitution hotspots in Escherichia coli

1 reference

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3 June 2018

Structure of the von Willebrand factor domain interacting with glycoprotein Ib.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=295140

26 November 2018

Heterogeneity in type IIB von Willebrand disease: two unrelated cases with no family history and mild abnormalities of ristocetin-induced interaction between von Willebrand factor and platelets

1 reference

https://pubmed.ncbi.nlm.nih.gov/2010538

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of disulfide-bridged substructures within human von Willebrand factor

1 reference

https://pubmed.ncbi.nlm.nih.gov/2010538

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cross-linking of a monomeric 39/34-kDa dispase fragment of von Willebrand factor (Leu-480/Val-481-Gly-718) to the N-terminal region of the alpha-chain of membrane glycoprotein Ib on intact platelets with bis(sulfosuccinimidyl) suberate

1 reference

https://pubmed.ncbi.nlm.nih.gov/2010538

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multimeric composition of factor VIII/von Willebrand factor following administration of DDAVP: implications for pathophysiology and therapy of von Willebrand's disease subtypes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2010538

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Platelet-type von Willebrand's disease: characterization of a new bleeding disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/2010538

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Type IIB von Willebrand's disease: differential clearance of endogenous versus transfused large multimer von willebrand factor

1 reference

https://pubmed.ncbi.nlm.nih.gov/2010538

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heightened interaction between platelets and factor VIII/von Willebrand factor in a new subtype of von Willebrand's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/2010538

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1172/JCI115122

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