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Mvwf, a dominant modifier of murine von Willebrand factor, results from altered lineage-specific expression of a glycosyltransferase
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PubMed
PubMed ID
9989502
retrieved
25 January 2017
title
Mvwf, a dominant modifier of murine von Willebrand factor, results from altered lineage-specific expression of a glycosyltransferase
(English)
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PubMed
PubMed ID
9989502
retrieved
25 January 2017
main subject
Beta-1,4-N-acetyl-galactosaminyl transferase 2
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GOA release 2020-03-11
author name string
K. L. Mohlke
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1
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PubMed
PubMed ID
9989502
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25 January 2017
A. A. Purkayastha
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2
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PubMed
PubMed ID
9989502
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R. J. Westrick
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PubMed
PubMed ID
9989502
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P. L. Smith
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9989502
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B. Petryniak
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9989502
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J. B. Lowe
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PubMed
PubMed ID
9989502
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D. Ginsburg
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PubMed
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9989502
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language of work or name
English
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publication date
8 January 1999
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PubMed
PubMed ID
9989502
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25 January 2017
published in
Cell
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PubMed
PubMed ID
9989502
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volume
96
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PubMed
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9989502
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page(s)
111–120
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PubMed
PubMed ID
9989502
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issue
1
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PubMed ID
9989502
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25 January 2017
cites work
Human von Willebrand factor gene sequences target expression to a subpopulation of endothelial cells in transgenic mice
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DNA rearrangements located over 100 kb 5' of the Steel (Sl)-coding region in Steel-panda and Steel-contrasted mice deregulate Sl expression and cause female sterility by disrupting ovarian follicle development
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Good genes in bad neighbourhoods.
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Variations in the NRAMP1 gene and susceptibility to tuberculosis in West Africans
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https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980964-2
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Structure of pre-pro-von Willebrand factor and its expression in heterologous cells
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https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980964-2
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Recovery from Hemophilia B Leyden: An Androgen-Responsive Element in the Factor IX Promoter
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Neomorphic agouti mutations in obese yellow mice
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A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.
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Ectopic expression of N-acetylglucosaminyltransferase III in transgenic hepatocytes disrupts apolipoprotein B secretion and induces aberrant cellular morphology with lipid storage
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Mechanism of N-acetylgalactosamine binding to a C-type animal lectin carbohydrate-recognition domain
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https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980964-2
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Diseases of abnormal protein glycosylation: an emerging area
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von Willebrand factor: a marker of endothelial dysfunction in vascular disorders?
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The secretory phospholipase A2 gene is a candidate for the Mom1 locus, a major modifier of ApcMin-induced intestinal neoplasia
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https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980964-2
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7 January 2021
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von Willebrand disease and quantitative variation in von Willebrand factor
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https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980964-2
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7 January 2021
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A novel modifier gene for plasma von Willebrand factor level maps to distal mouse chromosome 11
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https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980964-2
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Comparative mapping of distal murine chromosome 11 and human 17q21.3 in a region containing a modifying locus for murine plasma von Willebrand factor level.
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reference URL
https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980964-2
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7 January 2021
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von Willebrand disease
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https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980964-2
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Severe von Willebrand disease due to a defect at the level of von Willebrand factor mRNA expression: detection by exonic PCR-restriction fragment length polymorphism analysis.
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https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980964-2
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7 January 2021
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Mutations in the ER-Golgi intermediate compartment protein ERGIC-53 cause combined deficiency of coagulation factors V and VIII
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Derivation of mouse intestinal crypts from single progenitor cells
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Organ-related differences in binding of Dolichos biflorus agglutinin to vascular endothelium
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Distribution of von Willebrand factor in porcine intima varies with blood vessel type and location
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Initiation of platelet adhesion by arrest onto fibrinogen or translocation on von Willebrand factor
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Uniform vascular-endothelial-cell-specific gene expression in both embryonic and adult transgenic mice
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Cell migration pathway in the intestinal epithelium: an in situ marker system using mouse aggregation chimeras
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Photolabeling of Prostaglandin Endoperoxide H Synthase-1 with 3-Trifluoro-3-(m-Iiodophenyl)diazirine as a Probe of Membrane Association and the Cyclooxygenase Active Site
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Genetic analysis of autoimmune type 1 diabetes mellitus in mice
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The gene controlling the binding sites of Dolichos biflorus agglutinin, Dlb-1, is on chromosome 11 of the mouse
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Biological roles of oligosaccharides: all of the theories are correct
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Gene therapy -- promises, problems and prospects
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Natural resistance to infection with intracellular parasites: isolation of a candidate for Bcg
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Induction of specific storage organelles by von Willebrand factor propolypeptide
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https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980964-2
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7 January 2021
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Identifiers
DOI
10.1016/S0092-8674(00)80964-2
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PubMed ID
9989502
1 reference
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PubMed
PubMed ID
9989502
retrieved
25 January 2017
ResearchGate publication ID
13298970
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