about
Polymorphic variation in TPMT is the principal determinant of TPMT phenotype: A meta-analysis of three genome-wide association studies.Genetics, epigenetics, and regulation of drug-metabolizing cytochrome p450 enzymes.Gene copy number variation analysis reveals dosage-insensitive expression of CYP2E1.Methyleugenol DNA adducts in human liver are associated with SULT1A1 copy number variations and expression levels.Next-generation personalised medicine for high-risk paediatric cancer patients - The INFORM pilot study.Association between CYP2E1 polymorphisms and risk of differentiated thyroid carcinoma.Genetic variation in human drug-related genes.α2-Adrenergic Receptor in Liver Fibrosis: Implications for the Adrenoblocker MesedinAntifibrotic Effects of Amyloid-Beta and Its Loss in Cirrhotic LiverInfluence of NOD2 Variants on Trichuris suis ova Treatment Outcome in Crohn's DiseaseThe Impact of CYP3A4*22 on Tacrolimus Pharmacokinetics and Outcome in Clinical Practice at a Single Kidney Transplant CenterCopy number variation profiling in pharmacogenes using panel-based exome resequencing and correlation to human liver expression
P50
Q30244222-A28CDBA8-686D-45EB-8CA3-892BEED63301Q38160337-F78BFD14-F6A8-43FE-BD39-242705A1E2FDQ38824701-9FB4A230-B9C5-40B6-A335-6B7C80F25D67Q38888279-B64AC6CC-EA80-4272-BE3F-0A1285BB5CEBQ39538403-DBBC9EBA-2570-4ACE-BB59-F60BFE7C4AC6Q40091055-489B5818-3DA8-42DC-A309-270389DE6F6DQ47564586-C7AD785C-060B-46BB-94D0-1A71A34422BFQ89834185-BA583FDD-C545-42D3-B53A-1F5BE7C80D2CQ89848388-739744B5-93E8-4E2F-9CF0-69E84618CDBBQ90649882-5CCA395F-EDDF-4591-80C7-9E48081FD76BQ90733358-DACD034C-963F-431F-BA6C-CAD8C3D68839Q91574686-5D1F1FAC-E9B9-4C6C-90E2-CF440272C9D0
P50
description
researcher, ORCID id # 0000-0003-1564-0433
@en
wetenschapper
@nl
name
R Tremmel
@ast
R Tremmel
@en
R Tremmel
@nl
type
label
R Tremmel
@ast
R Tremmel
@en
R Tremmel
@nl
prefLabel
R Tremmel
@ast
R Tremmel
@en
R Tremmel
@nl
P106
P31
P496
0000-0003-1564-0433