(Q39420582)

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Biogenesis of Weibel-Palade bodies in von Willebrand's disease variants with impaired von Willebrand factor intrachain or interchain disulfide bond formation

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Europe PubMed Central

PMC publication ID

11 September 2017

Biogenesis of Weibel-Palade bodies in von Willebrand's disease variants with impaired von Willebrand factor intrachain or interchain disulfide bond formation (English)

1 reference

Europe PubMed Central

PMC publication ID

11 September 2017

von Willebrand's disease

1 reference

based on heuristic

inferred from title

author name string

Jiong-Wei Wang

1

1 reference

Europe PubMed Central

PMC publication ID

11 September 2017

Dafna J Groeneveld

2

1 reference

Europe PubMed Central

PMC publication ID

11 September 2017

Guy Cosemans

3

1 reference

Europe PubMed Central

PMC publication ID

11 September 2017

Richard J Dirven

4

1 reference

Europe PubMed Central

PMC publication ID

11 September 2017

Karine M Valentijn

5

1 reference

Europe PubMed Central

PMC publication ID

11 September 2017

Jan Voorberg

6

1 reference

Europe PubMed Central

PMC publication ID

11 September 2017

Pieter H Reitsma

7

1 reference

Europe PubMed Central

PMC publication ID

11 September 2017

Jeroen Eikenboom

8

1 reference

Europe PubMed Central

PMC publication ID

11 September 2017

publication date

29 December 2011

1 reference

Europe PubMed Central

PMC publication ID

11 September 2017

1 reference

Europe PubMed Central

PMC publication ID

11 September 2017

97

1 reference

Europe PubMed Central

PMC publication ID

11 September 2017

6

1 reference

Europe PubMed Central

PMC publication ID

11 September 2017

859-866

1 reference

Europe PubMed Central

PMC publication ID

11 September 2017

A pH-regulated dimeric bouquet in the structure of von Willebrand factor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366651

11 September 2017

Biology and physics of von Willebrand factor concatamers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366651

11 September 2017

Phylogenetic and functional analysis of histidine residues essential for pH-dependent multimerization of von Willebrand factor.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366651

11 September 2017

Functional architecture of Weibel-Palade bodies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366651

11 September 2017

Structural organization of Weibel-Palade bodies revealed by cryo-EM of vitrified endothelial cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366651

11 September 2017

Assembly of Weibel-Palade body-like tubules from N-terminal domains of von Willebrand factor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366651

11 September 2017

Two Cys residues essential for von Willebrand factor multimer assembly in the Golgi

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366651

11 September 2017

Mutations C1157F and C1234W of von Willebrand factor cause intracellular retention with defective multimerization and secretion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366651

11 September 2017

Re-establishment of VWF-dependent Weibel-Palade bodies in VWD endothelial cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366651

11 September 2017

Endoplasmic reticulum retention and prolonged association of a von Willebrand's disease-causing von Willebrand factor variant with ERp57 and calnexin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366651

11 September 2017

The CXXCXXC motif determines the folding, structure and stability of human Ero1-Lalpha

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366651

11 September 2017

Biochemistry and genetics of von Willebrand factor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366651

11 September 2017

Defective dimerization of von Willebrand factor subunits due to a Cys-> Arg mutation in type IID von Willebrand disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366651

11 September 2017

New variant of von Willebrand disease type II with markedly increased levels of von Willebrand factor antigen and dominant mode of inheritance: von Willebrand disease type IIC Miami.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366651

11 September 2017

Inducible secretion of large, biologically potent von Willebrand factor multimers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366651

11 September 2017

Cell biology of von Willebrand factor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366651

11 September 2017

Expression of a human proprotein processing enzyme: correct cleavage of the von Willebrand factor precursor at a paired basic amino acid site

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366651

11 September 2017

Assembly and routing of von Willebrand factor variants: the requirements for disulfide-linked dimerization reside within the carboxy-terminal 151 amino acids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366651

11 September 2017

Dimerization and multimerization defects of von Willebrand factor due to mutated cysteine residues

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366651

14 September 2017

Analysis of intracellular storage and regulated secretion of 3 von Willebrand disease-causing variants of von Willebrand factor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366651

14 September 2017

Type 1 von Willebrand disease mutation Cys1149Arg causes intracellular retention and degradation of heterodimers: a possible general mechanism for dominant mutations of oligomeric proteins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366651

25 September 2017

Localization of endogenous furin in cultured cell lines

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366651

25 September 2017

Dominant type 1 von Willebrand disease caused by mutated cysteine residues in the D3 domain of von Willebrand factor.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366651

25 September 2017

Intracellular storage and regulated secretion of von Willebrand factor in quantitative von Willebrand disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366651

15 June 2018

Basal secretion of von Willebrand factor from human endothelial cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366651

15 June 2018

Furin is a subtilisin-like proprotein processing enzyme in higher eukaryotes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366651

15 June 2018

A cluster of mutations in the D3 domain of von Willebrand factor correlates with a distinct subgroup of von Willebrand disease: type 2A/IIE.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366651

21 August 2018

Detailed von Willebrand factor multimer analysis in patients with von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 von Willebrand disease (MCMDM-1VWD).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366651

21 August 2018

Response to desmopressin is influenced by the genotype and phenotype in type 1 von Willebrand disease (VWD): results from the European Study MCMDM-1VWD.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366651

21 August 2018

Cysteine-mutations in von Willebrand factor associated with increased clearance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366651

21 August 2018

Real-time imaging of the dynamics and secretory behavior of Weibel-Palade bodies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366651

21 August 2018

Expression of 14 von Willebrand factor mutations identified in patients with type 1 von Willebrand disease from the MCMDM-1VWD study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366651

21 August 2018

Characterization of the genetic defects in recessive type 1 and type 3 von Willebrand disease patients of Italian origin

1 reference

https://pubmed.ncbi.nlm.nih.gov/22207689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homozygous C2362F von Willebrand factor induces intracellular retention of mutant von Willebrand factor resulting in autosomal recessive severe von Willebrand disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/22207689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Differential effects of the loss of intrachain- versus interchain-disulfide bonds in the cystine-knot domain of von Willebrand factor on the clinical phenotype of von Willebrand disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/22207689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenotype and genotype of a cohort of families historically diagnosed with type 1 von Willebrand disease in the European study, Molecular and Clinical Markers for the Diagnosis and Management of Type 1 von Willebrand Disease (MCMDM-1VWD)

1 reference

https://pubmed.ncbi.nlm.nih.gov/22207689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new look at Weibel-Palade body structure in endothelial cells using electron tomography

1 reference

https://pubmed.ncbi.nlm.nih.gov/22207689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of Disulfide Bonds in the Cystine Knot Domain of Human von Willebrand Factor

1 reference

https://pubmed.ncbi.nlm.nih.gov/22207689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aberrant dimerization of von Willebrand factor as the result of mutations in the carboxy-terminal region: identification of 3 mutations in members of 3 different families with type 2A (phenotype IID) von Willebrand disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/22207689

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/22207689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.3324/HAEMATOL.2011.057216

1 reference

Europe PubMed Central

PMC publication ID

11 September 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

11 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

11 September 2017

ResearchGate publication ID

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