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http://purl.uniprot.org/citations/7670465http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/7670465http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/7670465http://www.w3.org/2000/01/rdf-schema#comment"We report the generation and characterization of mice lacking adenosine deaminase (ADA). In humans, absence of ADA causes severe combined immunodeficiency. In contrast, ADA-deficient mice die perinatally with marked liver-cell degeneration, but lack abnormalities in the thymus. The ADA substrates, adenosine and deoxyadenosine, are increased in ADA-deficient mice. Adenine deoxyribonucleotides are only modestly elevated, whereas S-adenosylhomocysteine hydrolase activity is reduced more than 85%. Consequently, the ratio of S-adenosylhomocysteine (AdoMet) to S-adenosyl homocysteine (AdoHcy) is reduced threefold in liver. We conclude that ADA plays a more critical role in murine than human fetal development. The murine liver pathology may be due to AdoHcy-mediated inhibition of AdoMet-dependent transmethylation reactions."xsd:string
http://purl.uniprot.org/citations/7670465http://purl.org/dc/terms/identifier"doi:10.1038/ng0795-279"xsd:string
http://purl.uniprot.org/citations/7670465http://purl.org/dc/terms/identifier"doi:10.1038/ng0795-279"xsd:string
http://purl.uniprot.org/citations/7670465http://purl.uniprot.org/core/author"Hershfield M.S."xsd:string
http://purl.uniprot.org/citations/7670465http://purl.uniprot.org/core/author"Hershfield M.S."xsd:string
http://purl.uniprot.org/citations/7670465http://purl.uniprot.org/core/author"Zurcher C."xsd:string
http://purl.uniprot.org/citations/7670465http://purl.uniprot.org/core/author"Zurcher C."xsd:string
http://purl.uniprot.org/citations/7670465http://purl.uniprot.org/core/author"Berns A."xsd:string
http://purl.uniprot.org/citations/7670465http://purl.uniprot.org/core/author"Berns A."xsd:string
http://purl.uniprot.org/citations/7670465http://purl.uniprot.org/core/author"Breuer M.L."xsd:string
http://purl.uniprot.org/citations/7670465http://purl.uniprot.org/core/author"Breuer M.L."xsd:string
http://purl.uniprot.org/citations/7670465http://purl.uniprot.org/core/author"Migchielsen A.A."xsd:string
http://purl.uniprot.org/citations/7670465http://purl.uniprot.org/core/author"Migchielsen A.A."xsd:string
http://purl.uniprot.org/citations/7670465http://purl.uniprot.org/core/author"Ossendorp F."xsd:string
http://purl.uniprot.org/citations/7670465http://purl.uniprot.org/core/author"Ossendorp F."xsd:string
http://purl.uniprot.org/citations/7670465http://purl.uniprot.org/core/author"Toutain S."xsd:string
http://purl.uniprot.org/citations/7670465http://purl.uniprot.org/core/author"Toutain S."xsd:string
http://purl.uniprot.org/citations/7670465http://purl.uniprot.org/core/author"Valerio D."xsd:string
http://purl.uniprot.org/citations/7670465http://purl.uniprot.org/core/author"Valerio D."xsd:string
http://purl.uniprot.org/citations/7670465http://purl.uniprot.org/core/author"te Riele H."xsd:string
http://purl.uniprot.org/citations/7670465http://purl.uniprot.org/core/author"te Riele H."xsd:string
http://purl.uniprot.org/citations/7670465http://purl.uniprot.org/core/author"van Roon M.A."xsd:string
http://purl.uniprot.org/citations/7670465http://purl.uniprot.org/core/author"van Roon M.A."xsd:string