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- Publisher Website: 10.1007/BF00360899
- Scopus: eid_2-s2.0-0027688026
- PMID: 8281012
- WOS: WOS:A1993MF57400002
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Article: Mapping the midkine family of developmentally regulated signaling molecules
Title | Mapping the midkine family of developmentally regulated signaling molecules |
---|---|
Authors | |
Issue Date | 1993 |
Publisher | Springer New York LLC. The Journal's web site is located at http://link.springer.de/link/service/journals/00335/ |
Citation | Mammalian Genome, 1993, v. 4 n. 11, p. 632-638 How to Cite? |
Abstract | Midkine (Mdk) and heparin-binding neurotrophic factor (Hbnf)/pleiotrophin (Ptn) comprise the Midkine family of developmentally regulated signaling molecules. We have determined the chromosomal localization of these genes in the mouse by use of single-strand conformation polymorphisms (SSCPs), which facilitated the typing of Mdk and Hbnf alleles in recombinant inbred (RI) strains and interspecific backcrosses. Mapping was performed relative to other cloned genes, as well as simple sequence length polymorphisms (SSLPs) in the interspecific backcrosses. Mdk maps to mouse Chromosome (Chr) 2, linked to the Hoxd gene cluster. Hbnf maps to proximal mouse Chr 6, linked to the Cftr and Cpa genes. Comparative mapping of human MDK and HBNF employing species-specific polymerase chain reaction (PCR) primers and human monochromosomal somatic cell hybrids assigns MDK to human Chr 11 and HBNF to human Chr 7q32-qter. |
Persistent Identifier | http://hdl.handle.net/10722/44270 |
ISSN | 2023 Impact Factor: 2.7 2023 SCImago Journal Rankings: 0.855 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Peichel, CL | en_HK |
dc.contributor.author | Scherer, SW | en_HK |
dc.contributor.author | Tsui, LC | en_HK |
dc.contributor.author | Beier, DR | en_HK |
dc.contributor.author | Vogt, TF | en_HK |
dc.date.accessioned | 2007-09-12T03:50:20Z | - |
dc.date.available | 2007-09-12T03:50:20Z | - |
dc.date.issued | 1993 | en_HK |
dc.identifier.citation | Mammalian Genome, 1993, v. 4 n. 11, p. 632-638 | en_HK |
dc.identifier.issn | 0938-8990 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/44270 | - |
dc.description.abstract | Midkine (Mdk) and heparin-binding neurotrophic factor (Hbnf)/pleiotrophin (Ptn) comprise the Midkine family of developmentally regulated signaling molecules. We have determined the chromosomal localization of these genes in the mouse by use of single-strand conformation polymorphisms (SSCPs), which facilitated the typing of Mdk and Hbnf alleles in recombinant inbred (RI) strains and interspecific backcrosses. Mapping was performed relative to other cloned genes, as well as simple sequence length polymorphisms (SSLPs) in the interspecific backcrosses. Mdk maps to mouse Chromosome (Chr) 2, linked to the Hoxd gene cluster. Hbnf maps to proximal mouse Chr 6, linked to the Cftr and Cpa genes. Comparative mapping of human MDK and HBNF employing species-specific polymerase chain reaction (PCR) primers and human monochromosomal somatic cell hybrids assigns MDK to human Chr 11 and HBNF to human Chr 7q32-qter. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Springer New York LLC. The Journal's web site is located at http://link.springer.de/link/service/journals/00335/ | en_HK |
dc.relation.ispartof | Mammalian Genome | en_HK |
dc.rights | The original publication is available at www.springerlink.com | en_HK |
dc.subject.mesh | Carrier proteins - genetics | en_HK |
dc.subject.mesh | Chromosomes, human, pair 11 | en_HK |
dc.subject.mesh | Chromosomes, human, pair 7 | en_HK |
dc.subject.mesh | Cytokines - genetics | en_HK |
dc.subject.mesh | Gene expression regulation | en_HK |
dc.title | Mapping the midkine family of developmentally regulated signaling molecules | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0938-8990&volume=4&issue=11&spage=632&epage=638&date=1993&atitle=Mapping+themidkine+family+of+developmentally+regulated+signaling+molecules | en_HK |
dc.identifier.email | Tsui, LC: tsuilc@hkucc.hku.hk | en_HK |
dc.identifier.authority | Tsui, LC=rp00058 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | en_HK |
dc.identifier.doi | 10.1007/BF00360899 | en_HK |
dc.identifier.pmid | 8281012 | en_HK |
dc.identifier.scopus | eid_2-s2.0-0027688026 | en_HK |
dc.identifier.volume | 4 | en_HK |
dc.identifier.issue | 11 | en_HK |
dc.identifier.spage | 632 | en_HK |
dc.identifier.epage | 638 | en_HK |
dc.identifier.isi | WOS:A1993MF57400002 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Peichel, CL=6602163057 | en_HK |
dc.identifier.scopusauthorid | Scherer, SW=35374654500 | en_HK |
dc.identifier.scopusauthorid | Tsui, LC=7102754167 | en_HK |
dc.identifier.scopusauthorid | Beier, DR=7006462014 | en_HK |
dc.identifier.scopusauthorid | Vogt, TF=16154720700 | en_HK |
dc.identifier.issnl | 0938-8990 | - |