|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
5961
|
|
pubmed:dateCreated |
1984-5-30
|
|
pubmed:databankReference |
|
|
pubmed:abstractText |
In rats with hereditary hypothalamic diabetes insipidus (Brattleboro rats) the gene for the vasopressin precursor lacks a single G residue in the protein-coding region. The mutation gives rise to an open reading frame predicting a hormone precursor having a different C-terminus.
|
|
pubmed:language |
eng
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:issn |
0028-0836
|
|
pubmed:author |
|
|
pubmed:issnType |
Print
|
|
pubmed:volume |
308
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
705-9
|
|
pubmed:dateRevised |
2006-11-15
|
|
pubmed:meshHeading |
pubmed-meshheading:6717565-Amino Acid Sequence,
pubmed-meshheading:6717565-Animals,
pubmed-meshheading:6717565-Base Sequence,
pubmed-meshheading:6717565-Chromosome Deletion,
pubmed-meshheading:6717565-Diabetes Insipidus,
pubmed-meshheading:6717565-Genes,
pubmed-meshheading:6717565-Hypothalamus,
pubmed-meshheading:6717565-Liver,
pubmed-meshheading:6717565-Mutation,
pubmed-meshheading:6717565-Nucleic Acid Hybridization,
pubmed-meshheading:6717565-Protein Biosynthesis,
pubmed-meshheading:6717565-RNA, Messenger,
pubmed-meshheading:6717565-Rabbits,
pubmed-meshheading:6717565-Rats,
pubmed-meshheading:6717565-Rats, Brattleboro,
pubmed-meshheading:6717565-Rats, Mutant Strains,
pubmed-meshheading:6717565-Reticulocytes,
pubmed-meshheading:6717565-Vasopressins
|
|
pubmed:articleTitle |
Single base deletion in the vasopressin gene is the cause of diabetes insipidus in Brattleboro rats.
|
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|
