Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia - Wikidata - wikimedia - TriplyDB

Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia

Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia

http://www.wikidata.org/entity/Q28943326

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Asparaginase treatment side-effects may be due to genes with homopolymeric Asn codons (Review-Hypothesis)Genetic and nongenetic risk factors for childhood cancer Genetic susceptibility in childhood acute leukaemias: a systematic review Childhood Acute Lymphoblastic Leukemia: Progress Through Collaboration Perspectives on the causes of childhood leukemia Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations Nonsyndromic cleft lip with or without cleft palate and cancer: Evaluation of a possible common genetic background through the analysis of GWAS data SNP association mapping across the extended major histocompatibility complex and risk of B-cell precursor acute lymphoblastic leukemia in children.Genomics of racial and ethnic disparities in childhood acute lymphoblastic leukemia.Revealing phenotype-associated functional differences by genome-wide scan of ancient haplotype blocks.Children's Oncology Group's 2013 blueprint for research: acute lymphoblastic leukemia.Pathogenesis of ETV6/RUNX1-positive childhood acute lymphoblastic leukemia and mechanisms underlying its relapse ARID5B, IKZF1 and non-genetic factors in the etiology of childhood acute lymphoblastic leukemia: the ESCALE study.Germline genetic variation in ETV6 and risk of childhood acute lymphoblastic leukaemia: a systematic genetic study.Biology of childhood acute lymphoblastic leukemia.Contribution of polymorphisms in IKZF1 gene to childhood acute leukemia: a meta-analysis of 33 case-control studies.Genome-wide meta-analysis identifies multiple novel associations and ethnic heterogeneity of psoriasis susceptibility.Association between CEBPE Variant and Childhood Acute Leukemia Risk: Evidence from a Meta-Analysis of 22 Studies.Inherited genetic variation in childhood acute lymphoblastic leukemia.A variant at 9p21.3 functionally implicates CDKN2B in paediatric B-cell precursor acute lymphoblastic leukaemia aetiology.Pathway Analysis of Genome-wide Association Study in Childhood Leukemia among Hispanics.ARID5B and IKZF1 variants, selected demographic factors, and childhood acute lymphoblastic leukemia: a report from the Children's Oncology Group.Human leukocyte antigens and epstein-barr virus-associated nasopharyngeal carcinoma: old associations offer new clues into the role of immunity in infection-associated cancers.Genome-wide DNA promoter methylation and transcriptome analysis in human adipose tissue unravels novel candidate genes for obesity.Current evidence for an inherited genetic basis of childhood acute lymphoblastic leukemia.The role of ATP-binding cassette transporter A2 in childhood acute lymphoblastic leukemia multidrug resistance.Genomic and pharmacogenetic studies of childhood acute lymphoblastic leukemia.Novel Gene and Network Associations Found for Acute Lymphoblastic Leukemia Using Case-Control and Family-Based Studies in Multiethnic Populations.Pan-Cancer Mutational and Transcriptional Analysis of the Integrator Complex.The protein tyrosine phosphatase DEP-1/PTPRJ promotes breast cancer cell invasion and metastasis.Association of ARID5B gene variants with acute lymphoblastic leukemia in Yemeni children.GATA3 rs3824662 gene polymorphism as possible risk factor in a cohort of Egyptian patients with pediatric acute lymphoblastic leukemia and its prognostic impact.Association of genetic variation in IKZF1, ARID5B, CDKN2A, and CEBPE with the risk of acute lymphoblastic leukemia in Tunisian children and their contribution to racial differences in leukemia incidence.Family-based exome-wide association study of childhood acute lymphoblastic leukemia among Hispanics confirms role of ARID5B in susceptibility.Replication analysis confirms the association of several variants with acute myeloid leukemia in Chinese population.Maternal reproductive history, fertility treatments and folic acid supplementation in the risk of childhood acute leukemia: the ESTELLE study.Focused screening of a panel of cancer-related genetic polymorphisms reveals new susceptibility loci for pediatric acute lymphoblastic leukemia.TERT polymorphisms modify the risk of acute lymphoblastic leukemia in Chinese children.Genetic susceptibility in childhood acute lymphoblastic leukemia.An analysis of measures of effect size by age of onset in cancer genomewide association studies.

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Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia

http://www.wikidata.org/entity/Q28943326

description

2012 թուականի Մայիսին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի մայիսին հրատարակված գիտական հոդված

@hy

artículu científicu espublizáu en 2012

@ast

im November 2011 veröffentlichter wissenschaftlicher Artikel

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scientific journal article

@en

wetenschappelijk artikel (gepubliceerd op 2012/05/01)

@nl

наукова стаття, опублікована в травні 2012

@uk

مقالة علمية (نشرت في مايو 2012)

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Identification of germline sus ...... d acute lymphoblastic leukemia

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Identification of germline sus ...... d acute lymphoblastic leukemia

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Identification of germline sus ...... d acute lymphoblastic leukemia

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Identification of germline sus ...... d acute lymphoblastic leukemia

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P2860

CD148 is a membrane protein tyrosine phosphatase present in all hematopoietic lineages and is involved in signal transduction on lymphocytes

dbSNP: the NCBI database of genetic variation

TAp63 prevents premature aging by promoting adult stem cell maintenance

A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals

PLINK: a tool set for whole-genome association and population-based linkage analyses

Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome

Ptprj is a candidate for the mouse colon-cancer susceptibility locus Scc1 and is frequently deleted in human cancers

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

p63 Is essential for the proliferative potential of stem cells in stratified epithelia

p63 is essential for regenerative proliferation in limb, craniofacial and epithelial development

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10.1038/LEU.2011.302

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