Inherited coding variants at the CDKN2A locus influence susceptibility to acute lymphoblastic leukaemia in children. - Wikidata - awgldk - TriplyDB

Inherited coding variants at the CDKN2A locus influence susceptibility to acute lymphoblastic leukaemia in children.

Inherited coding variants at the CDKN2A locus influence susceptibility to acute lymphoblastic leukaemia in children.

http://www.wikidata.org/entity/Q34482019

about

Genetic abnormalities associated with acute lymphoblastic leukemia NUDT15 polymorphisms alter thiopurine metabolism and hematopoietic toxicity Regulatory network of GATA3 in pediatric acute lymphoblastic leukemia Germline genetic variation in ETV6 and risk of childhood acute lymphoblastic leukaemia: a systematic genetic study.Association Between PIP4K2A Polymorphisms and Acute Lymphoblastic Leukemia Susceptibility.Impact of NUDT15 polymorphisms on thiopurines-induced myelotoxicity and thiopurines tolerance dose.Confirmation of involvement of new variants at CDKN2A/B in pediatric acute lymphoblastic leukemia susceptibility in the Spanish population Functional single nucleotide polymorphisms within the cyclin-dependent kinase inhibitor 2A/2B region affect pancreatic cancer risk A genome-wide association study identifies risk loci for childhood acute lymphoblastic leukemia at 10q26.13 and 12q23.1.Novel Gene and Network Associations Found for Acute Lymphoblastic Leukemia Using Case-Control and Family-Based Studies in Multiethnic Populations.Family-based exome-wide assessment of maternal genetic effects on susceptibility to childhood B-cell acute lymphoblastic leukemia in hispanics.Whole-transcriptome sequencing identifies a distinct subtype of acute lymphoblastic leukemia with predominant genomic abnormalities of EP300 and CREBBP.Genetic susceptibility in childhood acute lymphoblastic leukemia.Power Analysis for Genetic Association Test (PAGEANT) provides insights to challenges for rare variant association studies.Regional evaluation of childhood acute lymphoblastic leukemia genetic susceptibility loci among Japanese.TP53 Germline Variations Influence the Predisposition and Prognosis of B-Cell Acute Lymphoblastic Leukemia in Children.GWAS in childhood acute lymphoblastic leukemia reveals novel genetic associations at chromosomes 17q12 and 8q24.21.Combination of common and novel rare NUDT15 variants improves predictive sensitivity of thiopurine-induced leukopenia in children with acute lymphoblastic leukemia.Association of the independent polymorphisms in CDKN2A with susceptibility of acute lymphoblastic leukemia.

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P2860

Inherited coding variants at the CDKN2A locus influence susceptibility to acute lymphoblastic leukaemia in children.

http://www.wikidata.org/entity/Q34482019

description

2015 nî lūn-bûn

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2015 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2015 թվականի հունիսին հրատարակված գիտական հոդված

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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Inherited coding variants at t ...... blastic leukaemia in children.

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Inherited coding variants at t ...... blastic leukaemia in children.

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Inherited coding variants at t ...... blastic leukaemia in children.

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Inherited coding variants at t ...... blastic leukaemia in children.

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Inherited coding variants at t ...... blastic leukaemia in children.

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Inherited coding variants at t ...... blastic leukaemia in children.

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Inherited coding variants at t ...... blastic leukaemia in children.

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Inherited coding variants at t ...... blastic leukaemia in children.

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Nature Communications

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Elaine Mardis

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Elizabeth Raetz

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Jun J Yang

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P2860

An integrated encyclopedia of DNA elements in the human genome

Structural basis for inhibition of the cyclin-dependent kinase Cdk6 by the tumour suppressor p16INK4a

Inference of population structure using multilocus genotype data

Gene targeting of Desrt, a novel ARID class DNA-binding protein, causes growth retardation and abnormal development of reproductive organs

An updated view on transcription factor GATA3-mediated regulation of Th1 and Th2 cell differentiation

Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia

Germline genomic variants associated with childhood acute lymphoblastic leukemia

Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype

Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations

A framework for variation discovery and genotyping using next-generation DNA sequencing data

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