Abstract Aims Phenoconversion, a genotype‐phenotype mismatch, challenges a successful implementation of personalized medicine. The aim of this study was to detect and determine phenoconversion using the solanidine metabolites 3,4‐seco‐solanidine‐3,4‐dioic acid (SSDA) and 4‐OH‐solanidine as diet‐derived cytochrome P450 2D6 (CYP2D6) biomarkers in a ...
Jens Andreas Sarömba+9 more
wiley +1 more source
Abstract Aims The aim of this study was to assess differences between Chinese and White patients in pharmacokinetics (PK) of, and clinical response to, acalabrutinib and its pharmacologically active major metabolite, ACP‐5862, to support recommended dosing in Chinese patients with B‐cell malignancies.
Tingting Yao+5 more
wiley +1 more source
Identification of four single nucleotide polymorphisms in DNA repair genes: XPA and XPB (ERCC3) in Polish population Communicated by: R.G.H. Cotton Online Citation: Human Mutation, Mutation in Brief #329 (2000) Online http://journals.wiley.com/1059-7794/pdf/mutation/329.pdf [PDF]
Dorota Butkiewicz+3 more
openalex +1 more source
Cattle Genomics: Aurochs Admixture in East Asia
Animal Research and One Health, EarlyView.
James A. Ward, David E. MacHugh
wiley +1 more source
Abstract Aim Heart transplantation (HT) is frequently complicated by chronic kidney disease, of which tacrolimus‐related nephrotoxicity is an important cause. In kidney and liver transplant recipients, fast tacrolimus metabolism (defined as a low concentration‐to‐dose [C0/D] ratio), negatively affects kidney function.
Maaike R. Schagen+9 more
wiley +1 more source
Efficient and Cost-Effective Single Nucleotide Polymorphism Detection with Different Fluorescent Applications [PDF]
Ahmet Aydın+4 more
openalex +1 more source
Severe myelosuppression and alopecia after thiopurine initiation in a patient with NUDT15 deficiency
Thiopurines are a class of immunosuppressant and antineoplastic agents. They are widely used in the treatment of inflammatory bowel disease, haematological malignancies and autoimmune diseases, but can cause significant toxicity. Inherited gene mutations are now recognized as independent risk factors for severe adverse drug reactions to thiopurines ...
Annie Siyu Wu+3 more
wiley +1 more source
Analysis of ABCG2 gene rs2231142 single nucleotide polymorphism and risk factors in hyperuricemia. [PDF]
Liang M+10 more
europepmc +1 more source
Relationship between NAFLD and coronary artery disease: A Mendelian randomization study
Abstract Background and Aims There is an ongoing debate on whether NAFLD is an active contributor or an innocent bystander in the pathogenesis of coronary artery disease (CAD). The aim of the present study was to assess the causal relationship between NAFLD and CAD.
Zhewen Ren+4 more
wiley +1 more source
UGT2B15 single nucleotide polymorphism reduces dabigatran acylglucuronide formation in humans. [PDF]
Park JW+5 more
europepmc +1 more source