Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia - Test2 - elhamkhani - TriplyDB

Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia

Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia

http://www.wikidata.org/entity/Q28255147

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The spectrum of SWI/SNF mutations, ubiquitous in human cancers Chapter 14: Cancer genome analysis Exome sequencing identifies a novel mutation in PIK3R1 as the cause of SHORT syndrome The splicing factor SRSF6 is amplified and is an oncoprotein in lung and colon cancers Structure of human Sp140 PHD finger: an atypical fold interacting with Pin1 NCG 4.0: the network of cancer genes in the era of massive mutational screenings of cancer genomes Aberrant Promoter Hypomethylation in CLL: Does It Matter for Disease Development?The clinical implications of gene mutations in chronic lymphocytic leukaemia Chronic Lymphocytic Leukemia in the Elderly, Which Investigations Are Necessary: A Map for the Practicing Oncologist Is lineage decision-making restricted during tumoral reprograming of haematopoietic stem cells?Targeting ATM-deficient CLL through interference with DNA repair pathways Defects in spliceosomal machinery: a new pathway of leukaemogenesis The significance of spliceosome mutations in chronic lymphocytic leukemia Deciphering the molecular landscape in chronic lymphocytic leukemia: time frame of disease evolution Clinical implications of the molecular genetics of chronic lymphocytic leukemia Mutational signatures: the patterns of somatic mutations hidden in cancer genomes Breaking bad: R-loops and genome integrity Mechanisms of epigenetic regulation of leukemia onset and progression Regulation of the Epigenome by Vitamin C Regulation of the Ras-MAPK and PI3K-mTOR Signalling Pathways by Alternative Splicing in Cancer Misregulation of pre-mRNA alternative splicing in cancer Emerging patterns of somatic mutations in cancer The biology and clinical significance of acquired genomic copy number aberrations and recurrent gene mutations in chronic lymphocytic leukemia The pathogenesis of chronic lymphocytic leukemia Clinical impact of recurrently mutated genes on lymphoma diagnostics: state-of-the-art and beyond Characterization of a new chronic lymphocytic leukemia cell line for mechanistic in vitro and in vivo studies relevant to disease SF3B1 mutations in chronic lymphocytic leukemia.Therapeutic targeting of a robust non-oncogene addiction to PRKDC in ATM-defective tumors.Recurrent mutations refine prognosis in chronic lymphocytic leukemia.SF3B1 mutations constitute a novel therapeutic target in breast cancer.Clinical impact of clonal and subclonal TP53, SF3B1, BIRC3, NOTCH1, and ATM mutations in chronic lymphocytic leukemia.The genetics of uveal melanoma: current insights Next-generation sequencing: advances and applications in cancer diagnosis Emerging concepts of epigenetic dysregulation in hematological malignancies Identifying High-Risk Chronic Lymphocytic Leukemia: A Pathogenesis-Oriented Appraisal of Prognostic and Predictive Factors in Patients Treated with Chemotherapy with or without Immunotherapy Defective control of pre-messenger RNA splicing in human disease Chronic lymphocytic leukemia: 2015 Update on diagnosis, risk stratification, and treatment The biology behind PI3K inhibition in chronic lymphocytic leukaemia Genomic and epigenomic heterogeneity in chronic lymphocytic leukemia Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy

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Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia

http://www.wikidata.org/entity/Q28255147

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2011 nî lūn-bûn

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2011 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

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2011 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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Exome sequencing identifies re ...... n chronic lymphocytic leukemia

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Exome sequencing identifies re ...... n chronic lymphocytic leukemia

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Exome sequencing identifies re ...... n chronic lymphocytic leukemia

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Exome sequencing identifies re ...... n chronic lymphocytic leukemia

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Exome sequencing identifies re ...... n chronic lymphocytic leukemia

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Exome sequencing identifies re ...... n chronic lymphocytic leukemia

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Exome sequencing identifies re ...... n chronic lymphocytic leukemia

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Exome sequencing identifies re ...... n chronic lymphocytic leukemia

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Exome sequencing identifies re ...... n chronic lymphocytic leukemia

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Nature Genetics

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Alejandra Martínez-Trillos

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Alfonso Valencia

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Andrew J Ramsay

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Armando López-Guillermo

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Diana A Puente

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Eva Giné

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Gonzalo R Ordóñez

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Ivo Gut

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Jorge Zamora

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José M C Tubío

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Gene ontology: tool for the unification of biology

A small-cell lung cancer genome with complex signatures of tobacco exposure

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International network of cancer genome projects.

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Initial genome sequencing and analysis of multiple myeloma

Accurate whole human genome sequencing using reversible terminator chemistry

KEGG for representation and analysis of molecular networks involving diseases and drugs

MUSTER: Improving protein sequence profile-profile alignments by using multiple sources of structure information

Fast and accurate short read alignment with Burrows-Wheeler transform

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47-52

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scholarly article

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2089773

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10.1038/NG.1032

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1

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44

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Carlos López Otín

Víctor Quesada

Josep Lluís Gelpí

Marcos Gonzalez Díaz

Heinz Himmelbauer

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2011-12-11T00:00:00Z

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51868519

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22158541

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