About: Richard J. Thompson

Facets (new session)
Description
Metadata
Settings
- owl:sameAs
- Inference Rule:

About: Richard J. Thompson Goto Sponge NotDistinct Permalink

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

English professor of molecular hepatology

Attributes	Values
rdf:type	Item
description	forskare (sv) 연구원 (ko) গবেষক (bn) 研究者 (ja) ഗവേഷകൻ (ml) araştırmacı (tr) wetenschapper (nl) дослідник (uk) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq) English professor of molecular hepatology (en)
rdfs:label	Richard J. Thompson (en) Richard J. Thompson (es) Richard J. Thompson (nl) Richard J. Thompson (sl) Richard J. Thompson (ast) রিচার্ড জে টম্পসন (bn)
skos:prefLabel	Richard J. Thompson (en) Richard J. Thompson (es) Richard J. Thompson (nl) Richard J. Thompson (sl) Richard J. Thompson (ast) রিচার্ড জে টম্পসন (bn)
name	Richard J. Thompson (en) Richard J. Thompson (es) Richard J. Thompson (nl) Richard J. Thompson (sl) Richard J. Thompson (ast) রিচার্ড জে টম্পসন (bn)
LinkedIn personal profile ID	wds:Q42219340-3d9277b1-44f9-984a-d9e6-3bc63c7839b8
LinkedIn personal profile ID	richard-thompson-657a101a
Scopus author ID	wds:Q42219340-78E1990F-0860-4A1F-ADC6-C75F717A2122
Scopus author ID	55482229800
given name	wds:Q42219340-14C24AEC-3334-4701-B22E-27065732781E
given name	Richard
instance of	wds:Q42219340-C74C0BDD-02FF-4FBE-9F02-D71A0BB54B0F
instance of	Homo sapiens
skos:altLabel	Richard Thompson (en)
occupation	wds:Q42219340-21e6462b-4be7-6e35-38f6-ebd9c2e42156 wds:Q42219340-C7841E4E-B4C5-4F62-BEA5-B7C05102BEDD
employer	wds:Q42219340-F8F677E5-D4D9-4BE0-A713-745B0A4C6DC7
sex or gender	wds:Q42219340-4F419A78-2415-439D-800F-9AF85BD3A7AF
country of citizenship	wds:Q42219340-66bd3fb5-4fec-489c-903b-fcc0d3ff62c6
educated at	wds:Q42219340-5BFB8E1E-829C-4F05-BFF5-065E179A99C5 wds:Q42219340-E465E80B-1F2F-402B-BD10-30640AA106B8
family name	wds:Q42219340-E6E13E7B-8038-4DE3-8DE0-FDFD0764DE70
occupation	hepatologist researcher
employer	King's College London
sex or gender	male
country of citizenship	United Kingdom
educated at	Abingdon School Pembroke College
family name	Thompson
ORCID iD	wds:Q42219340-5ED5225D-E8EA-4756-B984-BBC7E6145EAC
ORCID iD	https://orcid.org/0000-0001-5652-0150
ORCID iD	0000-0001-5652-0150
ResearcherID	wds:Q42219340-E56739AC-20C0-4877-B0A3-46A2C8690426
Publons author ID	wds:Q42219340-46fb2992-c3dc-4b86-b46a-c0813ef3af90
ResearcherID	B-7954-2009
Publons author ID	2865280
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q42219340
is author of	Hepatocellular carcinoma in ten children under five years of age with bile salt export pump deficiency Severe bile salt export pump deficiency: 82 different ABCB11 mutations in 109 families. Mutations in bile salt export pump (ABCB11) in two children with progressive familial intrahepatic cholestasis and cholangiocarcinoma Contribution of variant alleles of ABCB11 to susceptibility to intrahepatic cholestasis of pregnancy A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasis Hepatocanalicular bile salt export pump deficiency in patients with progressive familial intrahepatic cholestasis Progressive familial intrahepatic cholestasis, type 1, is associated with decreased farnesoid X receptor activity Gene structure of the human amiloride-sensitive epithelial sodium channel beta subunit Lack of hepatocellular CD10 along bile canaliculi is physiologic in early childhood and persistent in Alagille syndrome. Exocrine pancreatic function in children with progressive familial intrahepatic cholestasis type 2 Mutations in VPS33B, encoding a regulator of SNARE-dependent membrane fusion, cause arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome Effect of ischemic preconditioning on the genomic response to reperfusion injury in deceased donor liver transplantation BSEP: function and role in progressive familial intrahepatic cholestasis Characterization of mutations in ATP8B1 associated with hereditary cholestasis Genetic defects in hepatocanalicular transport. Novel mutations responsible for autosomal recessive multisystem pseudohypoaldosteronism and sequence variants in epithelial sodium channel alpha-, beta-, and gamma-subunit genes VPS33B mutation with ichthyosis, cholestasis, and renal dysfunction but without arthrogryposis: incomplete ARC syndrome phenotype Mutations in TJP2 cause progressive cholestatic liver disease Massive gene amplification drives paediatric hepatocellular carcinoma caused by bile salt export pump deficiency Multiple β-catenin mutations in hepatocellular lesions arising in Abernethy malformation. Localisation of pseudohypoaldosteronism genes to chromosome 16p12.2-13.11 and 12p13.1-pter by homozygosity mapping Bile composition in Alagille Syndrome and PFIC patients having Partial External Biliary Diversion An expanded role for heterozygous mutations of ABCB4, ABCB11, ATP8B1, ABCC2 and TJP2 in intrahepatic cholestasis of pregnancy Mutations in DCDC2 (doublecortin domain containing protein 2) in neonatal sclerosing cholangitis. Recurrent low gamma-glutamyl transpeptidase cholestasis following liver transplantation for bile salt export pump (BSEP) disease (posttransplant recurrent BSEP disease) Healy's law and the pediatric liver allograft Heterogeneity of the egammadeltabeta-thalassaemias: characterization of three novel English deletions Hepatocellular carcinoma associated with tight-junction protein 2 deficiency Progressive Familial Intrahepatic Cholestasis Mutations in TJP2, encoding zona occludens 2, and liver disease. Microvilli as markers of disordered apical-membrane trafficking and assembly: bowel and liver. Anti-CD20 Monoclonal Antibody Therapy in Functional Bile Salt Export Pump Deficiency After Liver Transplantation Pediatric liver disease Pediatric liver disease.

Faceted Search & Find service v1.16.117 as of May 05 2024

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 07.20.3239 as of May 5 2024, on Linux (x86_64-centos_6-linux-gnu), Single-Server Edition (378 GB total memory, 180 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2025 OpenLink Software