Results 111 to 120 of about 1,959 (184)

472 - NUDT15 Variants Contribute to Thiopurine-Induced Myelosuppression in European Populations

open access: yes, 2018
472 - NUDT15 Variants Contribute to Thiopurine-Induced Myelosuppression in European ...
Gareth J Walker (18617842)   +15 more
core  

Clinically Relevant Pharmacogenomic Variant Frequencies in Kazakh, Russian, and Uzbek Population Groups Residing in Kazakhstan. [PDF]

open access: yesBiology (Basel)
Zhaniyazov Z   +11 more
europepmc   +1 more source

Severe Thiopurine-Induced Myelosuppression in a Pediatric ALL Patient with the NUDT15 *1/*6 Genotype

open access: yes
Introduction: Genetic variants in TPMT and NUDT15 that affect the metabolism of mercaptopurine (6MP) are routinely tested for to guide 6MP dosing. Nudix hydroxylase 15 (NUDT15) deficiency can cause myelosuppression when affected patients are treated with
August, Keith   +3 more
core  

S0730 TPMT and NUDT15 Pharmacogenetics in a Diverse Hispanic IBD Population

open access: yesAmerican Journal of Gastroenterology, 2020
Ryan M. Dauer   +14 more
openaire   +2 more sources

CAN NUDT15 BE PHARMACOGENETIC OR PHARMACOTRANSRIPTOMIC MARKER FOR 6- MERCAPTOPURINE IN CHILDREN WITH ACUTE LYMPHOBLASTIC LEUKEMIA IN SERBIA

open access: yes
Background: 6-mercaptopurine is a drug used in therapeutic protocol for the treatment of children with acute lymphoblastic leukemia (ALL), mostly during the phase of maintenance therapy.
Jelovac, Marina   +10 more
core  

Population frequencies of thiopurine-related pharmacogenes in healthy individuals from Kosovo. [PDF]

open access: yesHum Genome Var
Pasha F   +6 more
europepmc   +1 more source

Prevalence of TPMT and NUDT15 diplotypes in Mexican children with B-cell acute lymphoblastic leukemia. [PDF]

open access: yesPharmacogenet Genomics
Garcia-Solorio J   +28 more
europepmc   +1 more source

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