about
Oligosaccharyltransferase-subunit mutations in nonsyndromic mental retardationExome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinomaDistinct H3F3A and H3F3B driver mutations define chondroblastoma and giant cell tumor of boneA small-cell lung cancer genome with complex signatures of tobacco exposureData mining using the Catalogue of Somatic Mutations in Cancer BioMartCOSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in CancerInternational network of cancer genome projects.A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardationMutational processes molding the genomes of 21 breast cancersA comprehensive catalogue of somatic mutations from a human cancer genomeMassive genomic rearrangement acquired in a single catastrophic event during cancer developmentComplex landscapes of somatic rearrangement in human breast cancer genomes.COSMIC (the Catalogue of Somatic Mutations in Cancer): a resource to investigate acquired mutations in human cancerThe COSMIC (Catalogue of Somatic Mutations in Cancer) database and websiteMutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus.COSMIC 2005Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencingThe Catalogue of Somatic Mutations in Cancer (COSMIC)Mutations in the gene encoding the Sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardationMutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephalyMutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a Marfanoid habitusSomatic SF3B1 mutation in myelodysplasia with ring sideroblastsGenomic Classification and Prognosis in Acute Myeloid Leukemia.Mutations of the BRAF gene in human cancerThe BioMart community portal: an innovative alternative to large, centralized data repositoriesMutations in CUL4B, which encodes a ubiquitin E3 ligase subunit, cause an X-linked mental retardation syndrome associated with aggressive outbursts, seizures, relative macrocephaly, central obesity, hypogonadism, pes cavus, and tremorMutational signatures of ionizing radiation in second malignanciesSignatures of mutational processes in human cancerPatterns of somatic mutation in human cancer genomesThe landscape of cancer genes and mutational processes in breast cancerThe life history of 21 breast cancersCOSMIC: exploring the world's knowledge of somatic mutations in human cancerSystematic sequencing of renal carcinoma reveals inactivation of histone modifying genesThe patterns and dynamics of genomic instability in metastatic pancreatic cancerSingle-cell paired-end genome sequencing reveals structural variation per cell cycle.cgpCaVEManWrapper: Simple Execution of CaVEMan in Order to Detect Somatic Single Nucleotide Variants in NGS Data.ascatNgs: Identifying Somatically Acquired Copy-Number Alterations from Whole-Genome Sequencing Data.Somatic mutation databases as tools for molecular epidemiology and molecular pathology of cancer: proposed guidelines for improving data collection, distribution, and integration.Recurrent PTPRB and PLCG1 mutations in angiosarcoma.Recurrent mutation of IGF signalling genes and distinct patterns of genomic rearrangement in osteosarcoma.
P50
Q24309324-03E57036-A48B-40AF-BFF8-F6E2E542F228Q24337664-0C7F83A9-7042-4DBD-AE08-CB0B7A5A852BQ24595521-D6D499D1-BE4F-493A-91F1-4908B382BDAEQ24600510-526C2526-FBC8-443A-AAFF-EF6364A1D5DAQ24604621-7109E96F-9A16-4F1E-8491-2FF33AB1A989Q24608391-4FBC7857-BE32-4014-9CEE-B32679D1BFB1Q24611474-CA33FA82-F9D0-4894-A91B-FDE7C93FC653Q24613870-69AC148F-F6F4-4E49-8256-673375EC8693Q24620915-A0E47EA3-B436-4D63-97B2-E29896880DD2Q24628532-13C6D7A9-B952-4DD1-B053-17F18F2F8979Q24631164-68E082DF-C5FB-42A7-A8C0-670E0C907CA5Q24631412-9505D083-CE8E-42F9-AB29-68DAE6673A81Q24644945-EC308950-B783-413C-B38B-F4A0B3743985Q24645514-F0C74F90-F9AA-4E0B-B3CB-6E54D4BEFE0DQ24651919-DDE469C1-3E6D-4BC6-AD7B-BF0352E64F5EQ24652464-7874DC62-1A01-4ED5-BB61-AE937165745EQ24653015-4794295A-FA7C-4CB2-9874-79CC46289FAEQ24653244-D5E16708-426C-44A8-967B-71EDDFF3B37CQ24671723-8F5EAE74-6E28-4A1E-905A-827E6A7FBE37Q24678235-B3CECB4E-916E-4D09-91D9-75261AA48E03Q24682652-9DA72F0F-FD78-4AD1-BDA2-A15BF4FF4CFEQ27851675-176791D3-1B27-437A-A976-F6EC62BA9EC1Q27853389-35A286EF-77BA-4365-AA51-BFA3FA0E8D58Q27860760-7347EA99-13CC-4E6B-B290-BAD2B1B8299FQ27949361-938C427B-2CE1-4EC7-A702-88D9CFD62773Q28284058-C18C8223-ABB0-4B6C-B2AE-D2373C9EA2E9Q28389573-1D95BBD6-33D5-4B3D-914F-DDF272040FABQ29547191-58B827CB-C274-483B-9E4D-2D10072161A0Q29547841-119211A8-DDF0-40E2-930F-011F07752E95Q29614637-D9679118-6DEA-48FF-83F1-FCC0B04E849FQ29614642-940809C2-BFCB-4FE1-B2EB-A878FC02CDD4Q29615725-3D08AE54-F014-4EEE-855A-E8136E878DF4Q29615757-ADAD0C69-DAD1-4031-8081-153C3BBA631EQ29618121-F1F6B128-2E57-4BFC-A136-491A2F98254DQ30453107-33FFAC17-88C4-48F0-A6D5-52565C4CAC28Q31147548-923AC343-EED5-42C4-94F5-B6A0219253DAQ31147553-C4B07A89-7490-4A70-8A4F-F59134643BC3Q33384182-43AF1DE6-9FBB-48C1-9457-0C608B343851Q33657848-DBC0F26B-0082-4A61-BBEA-C5082CA87A5BQ33850534-EB2798AF-35B3-4E1D-A167-C4F5C846D52E
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Jon Teague
@ast
Jon Teague
@en
Jon Teague
@es
Jon Teague
@nl
Jon Teague
@sl
type
label
Jon Teague
@ast
Jon Teague
@en
Jon Teague
@es
Jon Teague
@nl
Jon Teague
@sl
prefLabel
Jon Teague
@ast
Jon Teague
@en
Jon Teague
@es
Jon Teague
@nl
Jon Teague
@sl