About: P.vincent Jenkins

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

Attributes	Values
rdf:type	Item
description	forskare (sv) researcher (en) 연구원 (ko) গবেষক (bn) 研究者 (ja) ഗവേഷകൻ (ml) araştırmacı (tr) дослідник (uk) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq) investigador britànic (ca) ikertzaile britainiarra (eu) Brits onderzoeker (nl) investigador británico (es) investigador británicu (ast) chercheur britannique (fr) investigador británico (gl) investigador britânico (pt) ricercatore britannico (it)
rdfs:label	P.vincent Jenkins (ca) P.vincent Jenkins (en) P.vincent Jenkins (es) P.vincent Jenkins (nl) P.vincent Jenkins (sl) P.vincent Jenkins (ast)
skos:prefLabel	P.vincent Jenkins (ca) P.vincent Jenkins (en) P.vincent Jenkins (es) P.vincent Jenkins (nl) P.vincent Jenkins (sl) P.vincent Jenkins (ast)
name	P.vincent Jenkins (ca) P.vincent Jenkins (en) P.vincent Jenkins (es) P.vincent Jenkins (nl) P.vincent Jenkins (sl) P.vincent Jenkins (ast)
LinkedIn personal profile ID	wds:Q42767460-9D4333D4-94CC-4474-9D1B-4B5BD49CD625
LinkedIn personal profile ID	vince-jenkins-4251864
instance of	wds:Q42767460-3E712A58-4F4D-4B48-AEA2-E2D56AC4E855
instance of	Homo sapiens
skos:altLabel	Vince Jenkins (en)
occupation	wds:Q42767460-3AA4DD7C-0C01-4DD5-8F77-AE43CA4A71E5
employer	wds:Q42767460-17F90EE7-6ABF-408F-ADE4-C33E6E00960C
languages spoken, written or signed	wds:Q42767460-8C1F32F1-B9C9-43E7-946A-005407E2B0E4
sex or gender	wds:Q42767460-C869FF53-C31B-43B5-9993-787F72ECAA99
country of citizenship	wds:Q42767460-09E42285-2EA3-47A9-A15A-875F1106B520
educated at	wds:Q42767460-6B73C9BD-04DA-41B1-890E-A2F3331FEA97 wds:Q42767460-BAE2BBA6-29B9-48F9-9771-434CB6B9045E
family name	wds:Q42767460-15CA9884-002A-41F1-B14F-D934EE0BA718
occupation	researcher
employer	University Hospital of Wales
languages spoken, written or signed	English
sex or gender	male
country of citizenship	United Kingdom
educated at	University College London University of London
family name	Jenkins
ORCID iD	wds:Q42767460-68B6BDF7-815C-42E1-B10B-D32C3430472F
ORCID iD	https://orcid.org/0000-0001-5301-464X
ORCID iD	0000-0001-5301-464X
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q42767460
is author of	The effects of the 32-bp CCR-5 deletion on HIV transmission and HIV disease progression in individuals with haemophilia Elevated factor VIII levels and risk of venous thrombosis. Molecular modeling of ligand and mutation sites of the type A domains of human von Willebrand factor and their relevance to von Willebrand's disease. Mutations associated with hemophilia A in the 558-565 loop of the factor VIIIa A2 subunit alter the catalytic activity of the factor Xase complex Severe Plasmodium falciparum malaria is associated with circulating ultra-large von Willebrand multimers and ADAMTS13 inhibition 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 Factor VIII gene inversions in severe hemophilia A: results of an international consortium study. Low risk of inhibitor formation in haemophilia A patients following en masse switch in treatment to a third generation full length plasma and albumin-free recombinant factor VIII product (ADVATE®). ABO blood group determines plasma von Willebrand factor levels: a biologic function after all? Mutation analysis of haemophilia B in the Irish population: increased prevalence caused by founder effect Identification of type 2 von Willebrand disease in previously diagnosed type 1 patients: a reappraisal using phenotypes, genotypes and molecular modelling. Role of P1 residues Arg336 and Arg562 in the activated-Protein-C-catalysed inactivation of Factor VIIIa. Platelet factor 4 impairs the anticoagulant activity of activated protein C. Low-molecular weight and unfractionated heparins induce a downregulation of inflammation: decreased levels of proinflammatory cytokines and nuclear factor-kappaB in LPS-stimulated human monocytes. A recurrent F8 mutation in Irish haemophilia A patients: evidence for a founder effect Clustered basic residues within segment 484-510 of the factor VIIIa A2 subunit contribute to the catalytic efficiency for factor Xa generation. Contribution of factor VIIIa A2 and A3-C1-C2 subunits to the affinity for factor IXa in factor Xase Protamine sulfate down-regulates thrombin generation by inhibiting factor V activation Screening for Candidate Mutations Causing von Willebrand's Disease (vWD). Galectin-1 and Galectin-3 Constitute Novel-Binding Partners for Factor VIII. Lack of activated protein C resistance in healthy Hong Kong Chinese blood donors--correlation with absence of Arg506-Gln mutation of factor V gene Use of the collagen-binding assay for von Willebrand factor in the analysis of type 2M von Willebrand disease: a comparison with the ristocetin cofactor assay Networks of enzymatically oxidized membrane lipids support calcium-dependent coagulation factor binding to maintain hemostasis. Laboratory coagulation tests and emicizumab treatment A United Kingdom Haemophilia Centre Doctors' Organisation guideline Survival of von Willebrand factor released following DDAVP in a type 1 von Willebrand disease cohort: Influence of glycosylation, proteolysis and gene mutations Comparison of a fluorogenic anti-FXa assay with a central laboratory chromogenic anti-FXa assay for measuring LMWH activity in patient plasmas. Concentration-dependent roles for heparin in modifying liopolysaccharide-induced activation of mononuclear cells in whole blood Inversion mutation analysis in hemophilia a by restriction enzyme analysis and southern blotting Intron 22 inversions and haemophilia Thrombin generation in haemophilia A patients with mutations causing factor VIII assay discrepancy X-linked moyamoya syndrome associated with severe haemophilia A. Analysis of intron 22 inversions of the factor VIII gene in severe hemophilia A: implications for genetic counseling. Clinical utility gene card for: haemophilia A. Value of DNA analysis with multiple DNA probes for the detection of hemophilia A carriers.

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