about
Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardationA systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardationEnsembl's 10th yearIntegrating biological data--the Distributed Annotation SystemMutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephalyMutations 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 tremorThe EBI RDF platform: linked open data for the life sciencesDASMI: exchanging, annotating and assessing molecular interaction dataMyDas, an extensible Java DAS serverX-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment.Mutation analysis of 24 known cancer genes in the NCI-60 cell line set.easyDAS: automatic creation of DAS servers.A hypermutation phenotype and somatic MSH6 mutations in recurrent human malignant gliomas after alkylator chemotherapy.
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description
onderzoeker
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researcher
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հետազոտող
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name
Andy Jenkinson
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Andy Jenkinson
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Andy Jenkinson
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Andy Jenkinson
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Andy Jenkinson
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type
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Andy Jenkinson
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Andy Jenkinson
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Andy Jenkinson
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Andy Jenkinson
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Andy Jenkinson
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Andy Jenkinson
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Andy Jenkinson
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Andy Jenkinson
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Andy Jenkinson
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Andy Jenkinson
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P21
P2456
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0000-0002-0703-6984