Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia - Wikidata - wikimedia - TriplyDB

Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia

Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia

http://www.wikidata.org/entity/Q28943308

about

Acute lymphoblastic leukaemia Nuclear receptor coregulators: modulators of pathology and therapeutic targets Redefining ALL classification: toward detecting high-risk ALL and implementing precision medicine Making the genomic leap in HCT: application of second-generation sequencing to clinical advances in hematopoietic cell transplantation Using germline genomics to individualize pediatric cancer treatments Germline pharmacogenomics in oncology: decoding the patient for targeting therapy Pharmacogenomics of chemotherapeutic susceptibility and toxicity Childhood acute lymphoblastic leukemia: Integrating genomics into therapy Childhood Acute Lymphoblastic Leukemia: Progress Through Collaboration Modeling mechanisms of in vivo variability in methotrexate accumulation and folate pathway inhibition in acute lymphoblastic leukemia cells Multi-agent chemotherapy overcomes glucocorticoid resistance conferred by a BIM deletion polymorphism in pediatric acute lymphoblastic leukemia Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia High-risk childhood acute lymphoblastic leukemia Minireview: the SRC family of coactivators: an entrée to understanding a subset of polygenic diseases?The Eleventh International Childhood Acute Lymphoblastic Leukemia Workshop Report: Ponte di Legno, Italy, 6-7 May 2009.Thiopurine pharmacogenomics: association of SNPs with clinical response and functional validation of candidate genes.Long-term results of St Jude Total Therapy Studies 11, 12, 13A, 13B, and 14 for childhood acute lymphoblastic leukemia.Children's Oncology Group's 2013 blueprint for research: acute lymphoblastic leukemia.Genome-wide transcriptional analysis of T cell activation reveals differential gene expression associated with psoriasis.The role of interleukin-15 polymorphisms in adult acute lymphoblastic leukemia Genetics of ancestry-specific risk for relapse in acute lymphoblastic leukemia Genome-wide association study SNPs in the human genome diversity project populations: does selection affect unlinked SNPs with shared trait associations?A phase I/II study of the safety and efficacy of the addition of sirolimus to tacrolimus/methotrexate graft versus host disease prophylaxis after allogeneic haematopoietic cell transplantation in paediatric acute lymphoblastic leukaemia (ALL).Clinical implementation of germ line cancer pharmacogenetic variants during the next-generation sequencing era.An 8q24 gene desert variant associated with prostate cancer risk confers differential in vivo activity to a MYC enhancer.ARID5B genetic polymorphisms contribute to racial disparities in the incidence and treatment outcome of childhood acute lymphoblastic leukemia.Genetically InFormed therapies--a "GIFT" for children with cancer Pharmacogenomics and individualized medicine: translating science into practice.Pediatric eosinophilic esophagitis is associated with changes in esophageal microRNAs.Genetic variations in GRIA1 on chromosome 5q33 related to asparaginase hypersensitivity.Genome-wide association studies in pharmacogenomics: successes and lessons.Immunologic minimal residual disease detection in acute lymphoblastic leukemia: a comparative approach to molecular testing Biology of childhood acute lymphoblastic leukemia.The biology of relapsed acute lymphoblastic leukemia: opportunities for therapeutic interventions.Pharmacokinetic, pharmacodynamic, and pharmacogenetic determinants of osteonecrosis in children with acute lymphoblastic leukemia.Biology, risk stratification, and therapy of pediatric acute leukemias: an update.A genome-wide integrative study of microRNAs in human liver.The use of genomic information to optimize cancer chemotherapy Pharmacogenomics: the genetics of variable drug responses.A genome-wide association study of susceptibility to acute lymphoblastic leukemia in adolescents and young adults.

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P2860

Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia

http://www.wikidata.org/entity/Q28943308

description

2009 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի հունվարին հրատարակված գիտական հոդված

@hy

article publié dans la revue scientifique Journal of the American Medical Association

@fr

artículu científicu espublizáu en 2009

@ast

im Januar 2009 veröffentlichter wissenschaftlicher Artikel

@de

scientific journal article

@en

wetenschappelijk artikel (gepubliceerd op 2009/01/28)

@nl

наукова стаття, опублікована в січні 2009

@uk

مقالة علمية (نشرت في 28-1-2009)

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name

Genome-wide interrogation of g ...... d acute lymphoblastic leukemia

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Genome-wide interrogation of g ...... d acute lymphoblastic leukemia

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type

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Genome-wide interrogation of g ...... d acute lymphoblastic leukemia

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Genome-wide interrogation of g ...... d acute lymphoblastic leukemia

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Genome-wide interrogation of g ...... d acute lymphoblastic leukemia

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Genome-wide interrogation of g ...... d acute lymphoblastic leukemia

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Journal of the American Medical Association

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Genome-wide interrogation of g ...... d acute lymphoblastic leukemia

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Bruce M. Camitta

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Cheng Cheng

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Cheryl L. Willman

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Dario Campana

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Deborah French

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Deqing Pei

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Geoffrey Neale

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James R. Downing

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Jun J. Yang

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Lisa R. Treviño

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P2860

A fast and flexible statistical model for large-scale population genotype data: applications to inferring missing genotypes and haplotypic phase

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

Genomewide association analysis of coronary artery disease

Principal components analysis corrects for stratification in genome-wide association studies

Newly identified loci that influence lipid concentrations and risk of coronary artery disease

Genome-wide association scan identifies a prostaglandin-endoperoxide synthase 2 variant involved in risk of knee osteoarthritis

Assessing the probability that a positive report is false: an approach for molecular epidemiology studies

Statistical significance threshold criteria for analysis of microarray gene expression data.

Preponderance of thiopurine S-methyltransferase deficiency and heterozygosity among patients intolerant to mercaptopurine or azathioprine.

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10.1001/JAMA.2009.7

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Stephen P Hunger

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