15219888

Source:http://linkedlifedata.com/resource/pubmed/id/15219888

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0005516, umls-concept:C0162340, umls-concept:C0302592, umls-concept:C0441712, umls-concept:C0919457, umls-concept:C1527148
pubmed:issue	5
pubmed:dateCreated	2004-6-28
pubmed:abstractText	Loss of the fragile histidine triad (Fhit) protein has been documented in cervical cancer and dysplasia. The goal of this study was to confirm the utility of homozygous deletions, aberrant methylation, and immunohistochemical evaluations of FHIT as functionally relevant determinants of FHIT expression.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9433806
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Acid Anhydride Hydrolases, http://linkedlifedata.com/resource/pubmed/chemical/Biological Markers, http://linkedlifedata.com/resource/pubmed/chemical/Dinucleoside Phosphates, http://linkedlifedata.com/resource/pubmed/chemical/Neoplasm Proteins, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger, http://linkedlifedata.com/resource/pubmed/chemical/cytidylyl-3'-5'-guanosine, http://linkedlifedata.com/resource/pubmed/chemical/fragile histidine triad protein
pubmed:status	MEDLINE
pubmed:month	Jul
pubmed:issn	1071-5576
pubmed:author	pubmed-author:AshfaqRaheelaR, pubmed-author:BurbeeDavid GDG, pubmed-author:LeaJayanthi SJS, pubmed-author:MillerDavid SDS, pubmed-author:MinnaJohn DJD, pubmed-author:MullerCarolyn YCY, pubmed-author:MuneerSabeehaS
pubmed:issnType	Print
pubmed:volume	11
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	329-37
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:15219888-Acid Anhydride Hydrolases, pubmed-meshheading:15219888-Base Sequence, pubmed-meshheading:15219888-Biological Markers, pubmed-meshheading:15219888-Cell Line, Tumor, pubmed-meshheading:15219888-Chromosome Mapping, pubmed-meshheading:15219888-Chromosomes, Human, Pair 3, pubmed-meshheading:15219888-DNA Methylation, pubmed-meshheading:15219888-Dinucleoside Phosphates, pubmed-meshheading:15219888-Female, pubmed-meshheading:15219888-HeLa Cells, pubmed-meshheading:15219888-Humans, pubmed-meshheading:15219888-Neoplasm Proteins, pubmed-meshheading:15219888-Polymerase Chain Reaction, pubmed-meshheading:15219888-RNA, Messenger, pubmed-meshheading:15219888-Reverse Transcriptase Polymerase Chain Reaction, pubmed-meshheading:15219888-Sequence Deletion, pubmed-meshheading:15219888-Transcription, Genetic, pubmed-meshheading:15219888-Uterine Cervical Neoplasms
pubmed:year	2004
pubmed:articleTitle	Understanding the mechanisms of FHIT inactivation in cervical cancer for biomarker development.
pubmed:affiliation	Department of Obstetrics and Gynecology, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390-9032, USA.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't