16807482

Source:http://linkedlifedata.com/resource/pubmed/id/16807482

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0003097, umls-concept:C0205444, umls-concept:C1337007
pubmed:issue	10
pubmed:dateCreated	2006-6-29
pubmed:abstractText	Werner syndrome (WS) is a segmental progeroid syndrome in which patients display pleiotropic features of aging seen in the normal population. The advent of positional cloning in the 1990s markedly accelerated the identification of human disease-causing genes. In 1996, mutations in WRN, which was shown to encode a new, putative member of the family of RecQ DNA helicases, were identified in four patients as the cause of WS. Ten years after the identification of WRN, what have we learned about its role in WS, and its contribution to normal aging?
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/101146039
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	May
pubmed:issn	1539-6150
pubmed:author	pubmed-author:BohrVilhelm AVA, pubmed-author:HisamaFuki MFM, pubmed-author:OshimaJunkoJ
pubmed:issnType	Electronic
pubmed:day	25
pubmed:volume	2006
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	pe18
pubmed:meshHeading	pubmed-meshheading:16807482-Adult, pubmed-meshheading:16807482-Genes, Recessive, pubmed-meshheading:16807482-Humans, pubmed-meshheading:16807482-Middle Aged, pubmed-meshheading:16807482-Werner Syndrome
pubmed:year	2006
pubmed:articleTitle	WRN's tenth anniversary.
pubmed:affiliation	Department of Neurology, Yale University, New Haven, CT 06520, USA. fuki.hisama@yale.edu
pubmed:publicationType	Journal Article, Review