rdf:type |
|
lifeskim:mentions |
umls-concept:C0007082,
umls-concept:C0015295,
umls-concept:C0204727,
umls-concept:C0205409,
umls-concept:C0456389,
umls-concept:C0936012,
umls-concept:C1514562,
umls-concept:C1517488,
umls-concept:C1561491,
umls-concept:C1880389,
umls-concept:C1883204,
umls-concept:C1883221
|
pubmed:issue |
3
|
pubmed:dateCreated |
1989-4-3
|
pubmed:databankReference |
|
pubmed:abstractText |
Five members of the human CEA gene family [human pregnancy-specific beta 1-glycoprotein (PS beta G); hsCGM1, 2, 3 and 4] have been isolated and identified through sequencing the exons containing their N-terminal domains. Sequence comparisons with published data for CEA and related molecules reveal the existence of highly-conserved gene subgroups within the CEA family. Together with published data eleven CEA family members have so far been determined. Apart from the highly conserved coding sequences, these genes also show strong sequence conservation in their introns, indicating a duplication of whole gene units during the evolution of the CEA gene family.
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pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Neoplasm,
http://linkedlifedata.com/resource/pubmed/chemical/Carcinoembryonic Antigen,
http://linkedlifedata.com/resource/pubmed/chemical/Cell Adhesion Molecules,
http://linkedlifedata.com/resource/pubmed/chemical/DNA, Recombinant,
http://linkedlifedata.com/resource/pubmed/chemical/DNA Probes,
http://linkedlifedata.com/resource/pubmed/chemical/DNA Restriction Enzymes,
http://linkedlifedata.com/resource/pubmed/chemical/Glycoproteins,
http://linkedlifedata.com/resource/pubmed/chemical/Pregnancy-Specific beta...,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger
|
pubmed:status |
MEDLINE
|
pubmed:month |
Feb
|
pubmed:issn |
0006-291X
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:day |
15
|
pubmed:volume |
158
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
996-1004
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:2537643-Amino Acid Sequence,
pubmed-meshheading:2537643-Animals,
pubmed-meshheading:2537643-Antigens,
pubmed-meshheading:2537643-Antigens, Neoplasm,
pubmed-meshheading:2537643-Bacteriophage lambda,
pubmed-meshheading:2537643-Base Sequence,
pubmed-meshheading:2537643-Carcinoembryonic Antigen,
pubmed-meshheading:2537643-Cell Adhesion Molecules,
pubmed-meshheading:2537643-Cosmids,
pubmed-meshheading:2537643-DNA, Recombinant,
pubmed-meshheading:2537643-DNA Probes,
pubmed-meshheading:2537643-DNA Restriction Enzymes,
pubmed-meshheading:2537643-Exons,
pubmed-meshheading:2537643-Glycoproteins,
pubmed-meshheading:2537643-Humans,
pubmed-meshheading:2537643-Introns,
pubmed-meshheading:2537643-Mice,
pubmed-meshheading:2537643-Mice, Nude,
pubmed-meshheading:2537643-Molecular Sequence Data,
pubmed-meshheading:2537643-Neoplasm Transplantation,
pubmed-meshheading:2537643-Neoplasms, Experimental,
pubmed-meshheading:2537643-Nucleic Acid Hybridization,
pubmed-meshheading:2537643-Pregnancy-Specific beta 1-Glycoproteins,
pubmed-meshheading:2537643-RNA, Messenger
|
pubmed:year |
1989
|
pubmed:articleTitle |
Analysis of the size of the carcinoembryonic antigen (CEA) gene family: isolation and sequencing of N-terminal domain exons.
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pubmed:affiliation |
Institute of Immunobiology, University of Freiburg, FRG.
|
pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
|