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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0007589,
umls-concept:C0015576,
umls-concept:C0017262,
umls-concept:C0017337,
umls-concept:C0018270,
umls-concept:C0025914,
umls-concept:C0026809,
umls-concept:C0084084,
umls-concept:C0128479,
umls-concept:C0185117,
umls-concept:C0443199,
umls-concept:C1148608,
umls-concept:C1511938,
umls-concept:C1521761,
umls-concept:C1527148,
umls-concept:C2911684
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pubmed:issue |
3
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pubmed:dateCreated |
1992-12-17
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pubmed:abstractText |
MK (midkine) and HB-GAM (heparin-binding growth-associated molecule) constitute a new family of heparin-binding growth differentiation factors. The modes of expression of MK and HB-GAM during mouse development were quantitatively examined by mRNA hybridization. The following three distinct patterns of expression were observed in the brain/head region. On the 11th-13th days of gestation, MK was intensely, but HB-GAM relatively weakly expressed; on the 15th-19th days, both MK and HB-GAM expression became weaker; and in the neonatal period, HB-GAM was intensely expressed and MK expression increased slightly. The level of HB-GAM expression was lower than that of MK in the whole embryo on the 11th to 13th days of gestation. HB-GAM mRNA was detected in the kidney of newborn and young mice, where MK was more highly expressed. The identity of the weakly expressed MK and HB-GAM signals was confirmed by means of the polymerase chain reaction in the neonatal brain (MK), the head of 13-day embryos (HB-GAM), and the kidney of 7-day-old mice (HB-GAM). In conclusion, MK and HB-GAM are frequently co-expressed in the same cells and anatomic regions of the fetus or new born mouse, while their modes of expression differ.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Cytokines,
http://linkedlifedata.com/resource/pubmed/chemical/Growth Substances,
http://linkedlifedata.com/resource/pubmed/chemical/Heparin,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/midkine,
http://linkedlifedata.com/resource/pubmed/chemical/pleiotrophin
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0021-924X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
112
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pubmed:geneSymbol |
HB-GAM,
MK
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
346-9
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pubmed:dateRevised |
2007-12-19
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pubmed:meshHeading |
pubmed-meshheading:1343086-Animals,
pubmed-meshheading:1343086-Animals, Newborn,
pubmed-meshheading:1343086-Carrier Proteins,
pubmed-meshheading:1343086-Cytokines,
pubmed-meshheading:1343086-Embryonic and Fetal Development,
pubmed-meshheading:1343086-Female,
pubmed-meshheading:1343086-Gene Expression,
pubmed-meshheading:1343086-Growth Substances,
pubmed-meshheading:1343086-Heparin,
pubmed-meshheading:1343086-Mice,
pubmed-meshheading:1343086-Mice, Inbred ICR,
pubmed-meshheading:1343086-Pregnancy,
pubmed-meshheading:1343086-RNA, Messenger
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pubmed:year |
1992
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pubmed:articleTitle |
A new family of heparin binding growth/differentiation factors: differential expression of the midkine (MK) and HB-GAM genes during mouse development.
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pubmed:affiliation |
Department of Biochemistry, Faculty of Medicine, Kagoshima University.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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