(Q34528381)

English

Subunit composition of plasma von Willebrand factor. Cleavage is present in normal individuals, increased in IIA and IIB von Willebrand disease, but minimal in variants with aberrant structure of individual oligomers (types IIC, IID, and IIE).

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Europe PubMed Central

PubMed publication ID

2 August 2017

Subunit composition of plasma von Willebrand factor. Cleavage is present in normal individuals, increased in IIA and IIB von Willebrand disease, but minimal in variants with aberrant structure of individual oligomers (types IIC, IID, and IIE). (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

author name string

T S Zimmerman

1

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

J A Dent

2

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Z M Ruggeri

3

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

L H Nannini

4

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

language of work or name

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publication date

1 March 1986

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Journal of Clinical Investigation

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Europe PubMed Central

PubMed publication ID

2 August 2017

77

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Europe PubMed Central

PubMed publication ID

2 August 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

947-951

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Aberrant multimeric structure of von Willebrand factor in a new variant of von Willebrand's disease (type IIC)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423489

7 July 2018

Characterization of the human factor VIII procoagulant protein with a heterologous precipitating antibody

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423489

7 July 2018

Properties of human asialo-factor VIII. A ristocetin-independent platelet-aggregating agent

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423489

7 July 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

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423489

7 July 2018

A new variant of dominant type II von Willebrand's disease with aberrant multimeric pattern of factor VIII-related antigen (type IID).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423489

7 July 2018

Platelet aggregation induced by 1-desamino-8-D-arginine vasopressin (DDAVP) in 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=423489

7 July 2018

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423489

7 July 2018

Type IIB Tampa: a variant of von Willebrand disease with chronic thrombocytopenia, circulating platelet aggregates, and spontaneous platelet aggregation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423489

7 July 2018

Effects of plasmin on von Willebrand factor multimers. Degradation in vitro and stimulation of release in vivo

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423489

7 July 2018

In vitro correction of the abnormal multimeric structure of von Willebrand factor in type IIa 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=423489

7 July 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

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=423489

7 July 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=423489

7 July 2018

von Willebrand disease type IIC with different abnormalities of von Willebrand factor in the same sibship

1 reference

https://pubmed.ncbi.nlm.nih.gov/3485111

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/3485111

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The complex multimeric composition of factor VIII/von Willebrand factor

1 reference

https://pubmed.ncbi.nlm.nih.gov/3485111

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A variant of von Willebrand's disease characterized by recessive inheritance and missing triplet structure of von Willebrand factor multimers

1 reference

https://pubmed.ncbi.nlm.nih.gov/3485111

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cleavage of human von Willebrand factor by platelet calcium-activated protease

1 reference

https://pubmed.ncbi.nlm.nih.gov/3485111

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enzymatic degradation of the factor-VIII-von-Willebrand protein: a unique tryptic fragment with ristocetin cofactor activity

1 reference

https://pubmed.ncbi.nlm.nih.gov/3485111

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1172/JCI112394

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

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