Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5338
pubmed:dateCreated
1997-11-10
pubmed:databankReference
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF000979, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF000980, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF000981, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF000982, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF000983, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF000984, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF000985, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF000986, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF000987, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF000988, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF000989, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF000990, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF000991, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF000992, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF000993, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF000994, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF000995, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF000996, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF000997
pubmed:abstractText
A systematic search of the nonrecombining region of the human Y chromosome (NRY) identified 12 novel genes or families, 10 with full-length complementary DNA sequences. All 12 genes, and six of eight NRY genes or families previously isolated by less systematic means, fell into two classes. Genes in the first group were expressed in many organs; these housekeeping genes have X homologs that escape X inactivation. The second group, consisting of Y-chromosomal gene families expressed specifically in testes, may account for infertility among men with Y deletions. The coherence of the NRY's gene content contrasts with the apparently haphazard content of most eukaryotic chromosomes.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
0036-8075
pubmed:author
pubmed:issnType
Print
pubmed:day
24
pubmed:volume
278
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
675-80
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:9381176-Adult, pubmed-meshheading:9381176-Biological Evolution, pubmed-meshheading:9381176-Chromosome Mapping, pubmed-meshheading:9381176-Cloning, Molecular, pubmed-meshheading:9381176-DNA, Complementary, pubmed-meshheading:9381176-Dosage Compensation, Genetic, pubmed-meshheading:9381176-Gene Dosage, pubmed-meshheading:9381176-Gene Expression, pubmed-meshheading:9381176-Genes, pubmed-meshheading:9381176-Humans, pubmed-meshheading:9381176-Infertility, Male, pubmed-meshheading:9381176-Male, pubmed-meshheading:9381176-Molecular Sequence Data, pubmed-meshheading:9381176-Multigene Family, pubmed-meshheading:9381176-Proteins, pubmed-meshheading:9381176-Recombination, Genetic, pubmed-meshheading:9381176-Repetitive Sequences, Nucleic Acid, pubmed-meshheading:9381176-Seminal Plasma Proteins, pubmed-meshheading:9381176-Sequence Analysis, DNA, pubmed-meshheading:9381176-Spermatogenesis, pubmed-meshheading:9381176-Testis, pubmed-meshheading:9381176-X Chromosome, pubmed-meshheading:9381176-Y Chromosome
pubmed:year
1997
pubmed:articleTitle
Functional coherence of the human Y chromosome.
pubmed:affiliation
Howard Hughes Medical Institute, Whitehead Institute, and Department of Biology, Massachusetts Institute of Technology, 9 Cambridge Center, Cambridge, MA 02142, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S.