Inherited genetic variation in childhood acute lymphoblastic leukemia.
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Ewing's Sarcoma as a Second Malignancy in Long-Term Survivors of Childhood Hematologic MalignanciesNon-infectious chemotherapy-associated acute toxicities during childhood acute lymphoblastic leukemia therapy.Thiopurine S-methyltransferase polymorphisms in acute lymphoblastic leukemia, inflammatory bowel disease and autoimmune disorders: influence on treatment responseABCB1 genetic variants in leukemias: current insights into treatment outcomesRegulatory network of GATA3 in pediatric acute lymphoblastic leukemiaPolymorphisms in methotrexate transporters and their relationship to plasma methotrexate levels, toxicity of high-dose methotrexate, and outcome of pediatric acute lymphoblastic leukemia.Germline genetic variation in ETV6 and risk of childhood acute lymphoblastic leukaemia: a systematic genetic study.Old and New Prognostic Markers in Pediatric ALL.Common genetic variants associated with telomere length confer risk for neuroblastoma and other childhood cancersFine-tuning patient-derived xenograft models for precision medicine approaches in leukemia.Therapies on the horizon for childhood acute lymphoblastic leukemia.Targeting asparagine and autophagy for pulmonary adenocarcinoma therapy.Predispositions to Leukemia in Down Syndrome and Other Hereditary Disorders.Safety and Pharmacodynamics of the PDE4 Inhibitor Roflumilast in Advanced B-cell Malignancies.GATA3 rs3824662 gene polymorphism as possible risk factor in a cohort of Egyptian patients with pediatric acute lymphoblastic leukemia and its prognostic impact.A novel xenograft model to study the role of TSLP-induced CRLF2 signals in normal and malignant human B lymphopoiesis.Stroke-like encephalopathy following high-dose intravenous methotrexate in an adolescent with osteosarcoma: a case report.Metachronous T-Lymphoblastic Lymphoma and Burkitt Lymphoma in a Child With Constitutional Mismatch Repair Deficiency Syndrome.Rare gene variants in a patient with azathioprine-induced lethal myelosuppression.Genetic susceptibility in childhood acute lymphoblastic leukemia.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.Constitutional abnormalities of IDH1 combined with secondary mutations predispose a patient with Maffucci syndrome to acute lymphoblastic leukemia.Subclonal mutation selection in mouse lymphomagenesis identifies known cancer loci and suggests novel candidates.
P2860
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P2860
Inherited genetic variation in childhood acute lymphoblastic leukemia.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
Inherited genetic variation in childhood acute lymphoblastic leukemia.
@ast
Inherited genetic variation in childhood acute lymphoblastic leukemia.
@en
type
label
Inherited genetic variation in childhood acute lymphoblastic leukemia.
@ast
Inherited genetic variation in childhood acute lymphoblastic leukemia.
@en
prefLabel
Inherited genetic variation in childhood acute lymphoblastic leukemia.
@ast
Inherited genetic variation in childhood acute lymphoblastic leukemia.
@en
P2860
P1433
P1476
Inherited genetic variation in childhood acute lymphoblastic leukemia.
@en
P2093
Mary V Relling
P2860
P304
P356
10.1182/BLOOD-2014-12-580001
P407
P577
2015-05-21T00:00:00Z