19820032

Source:http://linkedlifedata.com/resource/pubmed/id/19820032

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0037083, umls-concept:C0170936, umls-concept:C0221099, umls-concept:C0342384, umls-concept:C1524003, umls-concept:C1710082
pubmed:issue	11
pubmed:dateCreated	2009-11-5
pubmed:abstractText	FGFR1 mutations have been identified in about 10% of patients with Kallmann syndrome. Recently cases of idiopathic hypogonadotropic hypogonadism (IHH) with a normal sense of smell (nIHH) have been reported.
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/R01 DE13686-09, http://linkedlifedata.com/resource/pubmed/grant/R01 HD015788-21, http://linkedlifedata.com/resource/pubmed/grant/R01 HD056264-04, http://linkedlifedata.com/resource/pubmed/grant/R01 HD19938, http://linkedlifedata.com/resource/pubmed/grant/U54HD028138-16
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0375362
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/DNA, http://linkedlifedata.com/resource/pubmed/chemical/Estradiol, http://linkedlifedata.com/resource/pubmed/chemical/FGFR1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Fibroblast Growth Factor 2, http://linkedlifedata.com/resource/pubmed/chemical/Phosphotyrosine, http://linkedlifedata.com/resource/pubmed/chemical/Receptor, Fibroblast Growth..., http://linkedlifedata.com/resource/pubmed/chemical/Testosterone
pubmed:status	MEDLINE
pubmed:month	Nov
pubmed:issn	1945-7197
pubmed:author	pubmed-author:ChenHuaibinH, pubmed-author:DwyerAndrewA, pubmed-author:HayesFrances JFJ, pubmed-author:HughesVirginia AVA, pubmed-author:Jacobson-DickmanElkaE, pubmed-author:KaiserUrsula BUB, pubmed-author:LavoieHeleneH, pubmed-author:MaJinghongJ, pubmed-author:MohammadiMoosaM, pubmed-author:MukherjeeAbirA, pubmed-author:PitteloudNellyN, pubmed-author:PlummerLaceyL, pubmed-author:QuintonRichardR, pubmed-author:RaivioTaneliT, pubmed-author:SidisYisraelY, pubmed-author:SparksSusanS, pubmed-author:Van VlietGuyG, pubmed-author:XuShuyunS
pubmed:issnType	Electronic
pubmed:volume	94
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	4380-90
pubmed:dateRevised	2011-4-1
pubmed:meshHeading	pubmed-meshheading:19820032-Animals, pubmed-meshheading:19820032-COS Cells, pubmed-meshheading:19820032-Cercopithecus aethiops, pubmed-meshheading:19820032-Cohort Studies, pubmed-meshheading:19820032-DNA, pubmed-meshheading:19820032-Estradiol, pubmed-meshheading:19820032-Female, pubmed-meshheading:19820032-Fibroblast Growth Factor 2, pubmed-meshheading:19820032-Genotype, pubmed-meshheading:19820032-Humans, pubmed-meshheading:19820032-Hypogonadism, pubmed-meshheading:19820032-Male, pubmed-meshheading:19820032-Mutation, pubmed-meshheading:19820032-Phenotype, pubmed-meshheading:19820032-Phosphotyrosine, pubmed-meshheading:19820032-Puberty, Delayed, pubmed-meshheading:19820032-Receptor, Fibroblast Growth Factor, Type 1, pubmed-meshheading:19820032-Reference Values, pubmed-meshheading:19820032-Testosterone
pubmed:year	2009
pubmed:articleTitle	Impaired fibroblast growth factor receptor 1 signaling as a cause of normosmic idiopathic hypogonadotropic hypogonadism.
pubmed:affiliation	Reproductive Endocrine Unit, Department of Medicine, The Harvard Center for Reproductive Endocrine Sciences, Massachusetts General Hospital, Boston, Massachusetts 02114, USA.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural