About: Diverse somatic mutation patterns and pathway alterations in human cancers

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About: Diverse somatic mutation patterns and pathway alterations in human cancers Goto Sponge Distinct Permalink

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scientific article (publication date: 12 August 2010)

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description	artículu científicu espublizáu en 2010 (ast) наукова стаття, опублікована в серпні 2010 (uk) 2010 թուականի Օգոստոսին հրատարակուած գիտական յօդուած (hyw) 2010 թվականի օգոստոսին հրատարակված գիտական հոդված (hy) article publié dans la revue scientifique Nature (fr) wetenschappelijk artikel (gepubliceerd op 2010/08/12) (nl) مقالة علمية (نشرت في 12-8-2010) (ar) im Juli 2010 veröffentlichter wissenschaftlicher Artikel (de) scientific article (publication date: 12 August 2010) (en) artykuł naukowy opublikowany w Nature 28 lipca 2010 (pl)
publication date	wds:Q29619825-34897D2F-E25C-483D-B039-6960D7231C8D
publication date	2010-07-28 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q29619825-0AC449A4-38E6-405A-9C16-7DE5816BA2BA
language of work or name	English
cites work	wds:Q29619825-0F772C60-37ED-4FCD-8422-1E14FD103997 wds:Q29619825-17C366EB-835A-4BC1-BCF9-9196C1E41CD5 wds:Q29619825-1FEFF2F2-8D83-4C42-86DE-B0FA258E90BE wds:Q29619825-28C7FF62-F527-4314-ACE0-E2DBBC306EED wds:Q29619825-2B04F1C8-DEFB-4B0F-B955-9835310D72E0 wds:Q29619825-387F64AB-4FEB-45E6-9152-09483CFDBB81 wds:Q29619825-3A629D6C-613F-4B74-AA67-F1F9CA118153 wds:Q29619825-3BC2EBC9-ED84-4D67-8218-EEE2B876BA80 wds:Q29619825-40422CF5-ED10-4ACE-9041-33D6B1081CE8 wds:Q29619825-448244F1-5DE4-44A0-BB6A-5F7DEAD664EA wds:Q29619825-4662D42D-5203-451B-8C06-E34410FA3729 wds:Q29619825-4D3EBC0C-1073-444A-B296-BEEE8B764E57 wds:Q29619825-56CAD0E3-D697-47A8-9D23-A68F9BC2E858 wds:Q29619825-618B7EF4-5EB8-4A39-AF65-67925058E128 wds:Q29619825-62AAA73B-0348-4151-ACBE-B70969961554 wds:Q29619825-64B42BF7-F14E-4C74-82F5-C31FEE000778 wds:Q29619825-69F8DB0F-64A5-44CE-9D1A-AF7EEEC4C371 wds:Q29619825-6BAF9EB2-FC85-43A5-9838-4A07904BEA4F wds:Q29619825-7517E21D-2DD9-4A51-A789-1F0E53B7710F wds:Q29619825-79A1A379-AE05-4B26-AF89-DF2E52E89E5D wds:Q29619825-7C725CEF-3351-4BC1-92B6-EAA94E950ACE wds:Q29619825-8327386C-8BCC-4DB9-867B-EB85D489F27B wds:Q29619825-84107471-E8C3-4B77-8712-8342E5CAF2C7 wds:Q29619825-951DB56E-75C0-45D3-94DC-A73770081014 wds:Q29619825-97A344F8-96D3-4BEF-A682-3B77B1C03856 wds:Q29619825-A4AE0FB5-FB04-43CD-9C17-E20D79C79196 wds:Q29619825-AB552384-0163-40D9-8835-606BFE770D9A wds:Q29619825-B5D0D915-1CB6-482E-91A7-E29BF31D223B wds:Q29619825-BA7A1769-61A8-4644-931E-FD46F61234DA wds:Q29619825-C3577449-2F44-484F-82EC-1AC6A7D9B5E5 wds:Q29619825-C3E9D364-7F63-4F1B-9B80-B52065DD80FA wds:Q29619825-C817677F-BA92-44EA-B758-FB48C64EEBFC wds:Q29619825-CC86BA98-4826-4A4C-A33E-0AFE48B01ACE wds:Q29619825-D4F8B33F-C21C-423D-B6D8-BAD31F54812D wds:Q29619825-DAB00942-6C2B-4389-B1CD-5292020237E9 wds:Q29619825-DD1A74CC-BDC6-452C-B062-12E29D27DCFF wds:Q29619825-DF6F6438-491E-4EC1-9F9D-18B154BF834E wds:Q29619825-E1326235-D1D5-4ACE-B6DA-CCAEBD75A19E wds:Q29619825-E8521B0B-63D0-46BE-8054-891016AEF7D1 wds:Q29619825-EE9FB44A-D007-4028-9DAC-DCA969E86EF7 wds:Q29619825-F205B33B-B815-4D7E-9BC6-4CE7D17886EE wds:Q29619825-F53A6057-697A-48B7-8EE1-285A20FC4D0C wds:Q29619825-FB40F5DF-F28A-4319-B188-570F1C6FF794
cites work	Pfam: clans, web tools and services The genomic landscapes of human breast and colorectal cancers G protein mutations in human disease Predicting deleterious amino acid substitutions Human non-synonymous SNPs: server and survey The consensus coding sequences of human breast and colorectal cancers Distinct classes of chromosomal rearrangements create oncogenic ETS gene fusions in prostate cancer Core signaling pathways in human pancreatic cancers revealed by global genomic analyses Patterns of somatic mutation in human cancer genomes Analysis of array CGH data: from signal ratio to gain and loss of DNA regions Lung cancer: intragenic ERBB2 kinase mutations in tumours Somatic mutations affect key pathways in lung adenocarcinoma Somatic mutations in p85alpha promote tumorigenesis through class IA PI3K activation Comment on "The consensus coding sequences of human breast and colorectal cancers". Comment on "The consensus coding sequences of human breast and colorectal cancers" An integrated genomic analysis of human glioblastoma multiforme Comprehensive genomic characterization defines human glioblastoma genes and core pathways Developing a SNP panel for forensic identification of individuals A census of human cancer genes CanPredict: a computational tool for predicting cancer-associated missense mutations Systematic sequencing of renal carcinoma reveals inactivation of histone modifying genes Distinguishing cancer-associated missense mutations from common polymorphisms Human mitogen-activated protein kinase kinase 4 as a candidate tumor suppressor A multiplex assay with 52 single nucleotide polymorphisms for human identification Colorectal cancer: mutations in a signalling pathway Swiss-Prot: juggling between evolution and stability. Expression of TTF-1 and cytokeratins in primary and secondary epithelial lung tumours: correlation with histological type and grade Disruption of MKK4 signaling reveals its tumor-suppressor role in embryonic stem cells Insights into ErbB signaling from the structure of the ErbB2-pertuzumab complex Large-scale analysis of non-synonymous coding region single nucleotide polymorphisms Design and analysis issues in genome-wide somatic mutation studies of cancer An open-and-shut case? Recent insights into the activation of EGF/ErbB receptors Cloning and characterization of BAI2 and BAI3, novel genes homologous to brain-specific angiogenesis inhibitor 1 (BAI1) Melanoma mouse model implicates metabotropic glutamate signaling in melanocytic neoplasia. The Catalogue of Somatic Mutations in Cancer (COSMIC) Frequent somatic mutations of GNAQ in uveal melanoma and blue naevi Inferring the functional effects of mutation through clusters of mutations in homologous proteins Stat3-mediated transformation of NIH-3T3 cells by the constitutively active Q205L Galphao protein. Role of mitogen-activated protein kinase kinase 4 in cancer SNP discovery in pooled samples with mismatch repair detection Highly efficient somatic-mutation identification using Escherichia coli mismatch-repair detection High-throughput, high-accuracy array-based resequencing

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