Wilms tumor 1 (WT1) gene mutations in pediatric T-cell malignancies. - Wikidata - wikimedia - TriplyDB

Wilms tumor 1 (WT1) gene mutations in pediatric T-cell malignancies.

Wilms tumor 1 (WT1) gene mutations in pediatric T-cell malignancies.

http://www.wikidata.org/entity/Q47268104

about

Prognostification of ALL by Cytogenetics Two hits are better than one: targeting both phosphatidylinositol 3-kinase and mammalian target of rapamycin as a therapeutic strategy for acute leukemia treatment.Single nucleotide polymorphisms in the Wilms' tumour gene 1 in clear cell renal cell carcinoma Clinical and molecular characterization of early T-cell precursor leukemia: a high-risk subgroup in adult T-ALL with a high frequency of FLT3 mutations The NOTCH signaling pathway: role in the pathogenesis of T-cell acute lymphoblastic leukemia and implication for therapy.Cytogenetic and molecular predictors of outcome in acute lymphocytic leukemia: recent developments.The molecular basis of T cell acute lymphoblastic leukemia The Wilms' tumor suppressor WT1 enhances CD95L expression and promotes activation-induced cell death in leukemic T cells.Genetic mutational profiling analysis of T cell acute lymphoblastic leukemia reveal mutant FBXW7 as a prognostic indicator for inferior survival.WT1 loss attenuates the TP53-induced DNA damage response in T-cell acute lymphoblastic leukemia.Acute myeloid leukemia derived from lympho-myeloid clonal hematopoiesis.

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Wilms tumor 1 (WT1) gene mutations in pediatric T-cell malignancies.

http://www.wikidata.org/entity/Q47268104

description

2009 nî lūn-bûn

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2009年の論文

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2009年学术文章

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2009年学术文章

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2009年学术文章

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2009年学术文章

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2009年学术文章

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2009年学术文章

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2009年學術文章

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2009年學術文章

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name

Wilms tumor 1 (WT1) gene mutations in pediatric T-cell malignancies.

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Wilms tumor 1 (WT1) gene mutations in pediatric T-cell malignancies.

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Wilms tumor 1 (WT1) gene mutations in pediatric T-cell malignancies.

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Wilms tumor 1 (WT1) gene mutations in pediatric T-cell malignancies

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A Renneville

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E Clappier

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J-B Micol

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P2860

Wilms' tumor 1 gene mutations independently predict poor outcome in adults with cytogenetically normal acute myeloid leukemia: a cancer and leukemia group B study

Mutation of the Wilms' tumor 1 gene is a poor prognostic factor associated with chemotherapy resistance in normal karyotype acute myeloid leukemia: the United Kingdom Medical Research Council Adult Leukaemia Working Party.

Wilms tumor 1 gene mutations are associated with a higher risk of recurrence in young adults with acute myeloid leukemia: a study from the Acute Leukemia French Association.

Clinical significance of HOX11L2 expression linked to t(5;14)(q35;q32), of HOX11 expression, and of SIL-TAL fusion in childhood T-cell malignancies: results of EORTC studies 58881 and 58951

Activating mutations of NOTCH1 in human T cell acute lymphoblastic leukemia

The SCFFBW7 ubiquitin ligase complex as a tumor suppressor in T cell leukemia

WT1 mutations in T-ALL

Novel WT1 mutation (C388Y) in a female child with Denys-Drash syndrome.

The C-MYB locus is involved in chromosomal translocation and genomic duplications in human T-cell acute leukemia (T-ALL), the translocation defining a new T-ALL subtype in very young children.

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476-480

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scholarly article

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10.1038/LEU.2009.221

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2

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24

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Claude Preudhomme

Brigitte Nelken

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2009-10-22T00:00:00Z

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38028065

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