Literature DB >> 1673565

The cDNA of the human neuromedin B gene (NMB) mapped to 15q11-qter recognizes an XbaI RFLP.

C A Gregory1, J S Schwartz.   

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Year:  1991        PMID： 1673565      PMCID： PMC333823          DOI： 10.1093/nar/19.5.1167

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN： 0305-1048            Impact factor:   16.971


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  1 in total

1.  Molecular cloning of cDNAs encoding the human bombesin-like peptide neuromedin B. Chromosomal localization and comparison to cDNAs encoding its amphibian homolog ranatensin.

Authors:  I M Krane; S L Naylor; D Helin-Davis; W W Chin; E R Spindel
Journal:  J Biol Chem       Date:  1988-09-15       Impact factor: 5.157
  1 in total
  1 in total

1.  Somatic recombination rather than uniparental disomy suggested as another mechanism by which genetic imprinting may play a role in the etiology of Prader-Willi syndrome.

Authors:  C A Gregory; J Schwartz; A J Kirkilionis; N Rudd; J L Hamerton
Journal:  Hum Genet       Date:  1991-11       Impact factor: 4.132
  1 in total

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