(Q36846397)

16 August 2017

Genetic regulation of plasma von Willebrand factor levels: quantitative trait loci analysis in a mouse model (English)

1 reference

16 August 2017

quantitative trait locus

1 reference

H L Lemmerhirt

1

1 reference

16 August 2017

K W Broman

series ordinal

2

1 reference

16 August 2017

J A Shavit

series ordinal

3

1 reference

16 August 2017

D Ginsburg

series ordinal

4

1 reference

16 August 2017

28 November 2006

1 reference

Journal of Thrombosis and Haemostasis

16 August 2017

1 reference

16 August 2017

5

1 reference

16 August 2017

2

1 reference

16 August 2017

329-335

1 reference

Enhanced VWF biosynthesis and elevated plasma VWF due to a natural variant in the murine Vwf gene

16 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3654791

Modifier genes and protective alleles in humans and mice

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3654791

R/qtl: QTL mapping in experimental crosses

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3654791

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3654791

Murine equivalent of the human histo-blood group ABO gene is a cis-AB gene and encodes a glycosyltransferase with both A and B transferase activity

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3654791

Modifier genes in mice and humans

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3654791

Mvwf, a dominant modifier of murine von Willebrand factor, results from altered lineage-specific expression of a glycosyltransferase

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3654791

Variations in the NRAMP1 gene and susceptibility to tuberculosis in West Africans

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3654791

A novel modifier gene for plasma von Willebrand factor level maps to distal mouse chromosome 11

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3654791

Natural resistance to infection with intracellular parasites: isolation of a candidate for Bcg

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3654791

Empirical threshold values for quantitative trait mapping

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3654791

Factor VIII and factor IX in a twin population. Evidence for a major effect of ABO locus on factor VIII level

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3654791

Mapping mendelian factors underlying quantitative traits using RFLP linkage maps

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3654791

Genetic determinants of hemostasis phenotypes in Spanish families.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3654791

Genetic linkage and association analysis in type 1 von Willebrand disease: results from the Canadian type 1 VWD study

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3654791

Mice are unsuitable for modelling ABO discordance despite strain-specific A cross-reactive natural IgM.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3654791

SNPs, microarrays and pooled DNA: identification of four loci associated with mild mental impairment in a sample of 6000 children.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3654791

An association of candidate gene haplotypes and bleeding severity in von Willebrand disease (VWD) type 1 pedigrees

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3654791

Heritability of plasma concentrations of clotting factors and measures of a prethrombotic state in a protein C-deficient family

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3654791

Epistasis in quantitative trait locus linkage analysis: interaction or main effect?

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3654791

Founder von Willebrand factor haplotype associated with type 1 von Willebrand disease

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3654791

DNA pooling identifies QTLs on chromosome 4 for general cognitive ability in children

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3654791

Obesity QTLs on mouse chromosomes 2 and 17.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3654791

Detection of obesity QTLs on mouse chromosomes 1 and 7 by selective DNA pooling.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3654791

Getting at the variable expressivity of von Willebrand disease

5 September 2018

1 reference

12 December 2020

Universal SNP genotyping assay with fluorescence polarization detection

1 reference

12 December 2020

Significant linkage and non-linkage of type 1 von Willebrand disease to the von Willebrand factor gene

1 reference

12 December 2020

Genome-wide linkage analysis of von Willebrand factor plasma levels: results from the GAIT project

1 reference

12 December 2020

Linkage analysis of factor VIII and von Willebrand factor loci as quantitative trait loci

1 reference

12 December 2020

Associations of factor VIII and von Willebrand factor with age, race, sex, and risk factors for atherosclerosis. The Atherosclerosis Risk in Communities (ARIC) Study

1 reference

12 December 2020

Role of clotting factor VIII in effect of von Willebrand factor on occurrence of deep-vein thrombosis

1 reference

12 December 2020

von Willebrand disease

1 reference

12 December 2020

Linkage analysis in families diagnosed with type 1 von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 VWD

1 reference

12 December 2020

Genetic analysis of 31 Swedish type 1 von Willebrand disease families reveals incomplete linkage to the von Willebrand factor gene and a high frequency of a certain disease haplotype

1 reference

12 December 2020

Inconsistency of association between type 1 von Willebrand disease phenotype and genotype in families identified in an epidemiological investigation

1 reference

12 December 2020

Variation at the von Willebrand factor (vWF) gene locus is associated with plasma vWF:Ag levels: identification of three novel single nucleotide polymorphisms in the vWF gene promoter

1 reference

12 December 2020

High levels of factor VIII and venous thrombosis

1 reference

12 December 2020

The genetics of haemostasis: a twin study

1 reference

12 December 2020

High plasma concentration of factor VIIIc is a major risk factor for venous thromboembolism

1 reference

12 December 2020

A single nucleotide polymorphism at nucleotide -1793 in the von Willebrand factor (VWF) regulatory region is associated with plasma VWF:Ag levels

1 reference

12 December 2020

10.1111/J.1538-7836.2007.02325.X

Identifiers

DOI

1 reference

16 August 2017

1 reference

16 August 2017

PubMed publication ID

17155961

1 reference