Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
1994-10-20
pubmed:abstractText
Over a period of many years, germ-cell mutagenesis experiments using the mouse specific-locus test have generated numerous radiation- and chemical-induced alleles of the brown (b; Tyrp 1) locus in mouse chromosome 4. We describe here the origin, maintenance and initial molecular characterization of 28 b mutations that are prenatally lethal when homozygous. Each of these mutations is deleted for Tyrp 1 sequences, and each of 25 mutations tested further is deleted for at least one other locus defined by molecular clones previously found to be closely linked to b by interspecific backcross analysis. A panel of DNAs from mice carrying a lethal b mutation and a Mus spretus chromosome 4 was used in the fine structure mapping of these molecularly defined loci. The deletional nature of each of these prenatally lethal mutations is consistent with the hypothesis that the null phenotype at b has an effect only on the quality (color) of eumelanin produced in melanocytes. The resulting deletion map provides a framework on which to build future molecular-genetic and biological analyses of this region of mouse chromosome 4.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/7916309-1033984, http://linkedlifedata.com/resource/pubmed/commentcorrection/7916309-1409609, http://linkedlifedata.com/resource/pubmed/commentcorrection/7916309-1427844, http://linkedlifedata.com/resource/pubmed/commentcorrection/7916309-14942747, http://linkedlifedata.com/resource/pubmed/commentcorrection/7916309-1684331, http://linkedlifedata.com/resource/pubmed/commentcorrection/7916309-1748094, http://linkedlifedata.com/resource/pubmed/commentcorrection/7916309-1799812, http://linkedlifedata.com/resource/pubmed/commentcorrection/7916309-1952626, http://linkedlifedata.com/resource/pubmed/commentcorrection/7916309-2003334, http://linkedlifedata.com/resource/pubmed/commentcorrection/7916309-2245916, http://linkedlifedata.com/resource/pubmed/commentcorrection/7916309-2245917, http://linkedlifedata.com/resource/pubmed/commentcorrection/7916309-2304907, http://linkedlifedata.com/resource/pubmed/commentcorrection/7916309-2457811, http://linkedlifedata.com/resource/pubmed/commentcorrection/7916309-2806116, http://linkedlifedata.com/resource/pubmed/commentcorrection/7916309-2813427, http://linkedlifedata.com/resource/pubmed/commentcorrection/7916309-3008090, http://linkedlifedata.com/resource/pubmed/commentcorrection/7916309-3132713, http://linkedlifedata.com/resource/pubmed/commentcorrection/7916309-36985, http://linkedlifedata.com/resource/pubmed/commentcorrection/7916309-574104, http://linkedlifedata.com/resource/pubmed/commentcorrection/7916309-680379, http://linkedlifedata.com/resource/pubmed/commentcorrection/7916309-7117820, http://linkedlifedata.com/resource/pubmed/commentcorrection/7916309-791749, http://linkedlifedata.com/resource/pubmed/commentcorrection/7916309-8088529, http://linkedlifedata.com/resource/pubmed/commentcorrection/7916309-8095339, http://linkedlifedata.com/resource/pubmed/commentcorrection/7916309-8141802, http://linkedlifedata.com/resource/pubmed/commentcorrection/7916309-8307327, http://linkedlifedata.com/resource/pubmed/commentcorrection/7916309-8358168, http://linkedlifedata.com/resource/pubmed/commentcorrection/7916309-8389469
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0016-6731
pubmed:author
pubmed:issnType
Print
pubmed:volume
137
pubmed:geneSymbol
Tyrp1
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
845-54
pubmed:dateRevised
2010-6-10
pubmed:meshHeading
pubmed-meshheading:7916309-Alleles, pubmed-meshheading:7916309-Animals, pubmed-meshheading:7916309-Base Sequence, pubmed-meshheading:7916309-Blotting, Southern, pubmed-meshheading:7916309-Chromosome Mapping, pubmed-meshheading:7916309-Crosses, Genetic, pubmed-meshheading:7916309-DNA Mutational Analysis, pubmed-meshheading:7916309-DNA Primers, pubmed-meshheading:7916309-Deoxyribonucleases, Type II Site-Specific, pubmed-meshheading:7916309-Female, pubmed-meshheading:7916309-Gene Deletion, pubmed-meshheading:7916309-Genes, Lethal, pubmed-meshheading:7916309-Germ-Line Mutation, pubmed-meshheading:7916309-Hair Color, pubmed-meshheading:7916309-Male, pubmed-meshheading:7916309-Melanins, pubmed-meshheading:7916309-Membrane Glycoproteins, pubmed-meshheading:7916309-Mice, pubmed-meshheading:7916309-Mice, Inbred C3H, pubmed-meshheading:7916309-Molecular Sequence Data, pubmed-meshheading:7916309-Muridae, pubmed-meshheading:7916309-Mutagenesis, pubmed-meshheading:7916309-Oxidoreductases, pubmed-meshheading:7916309-Polymerase Chain Reaction, pubmed-meshheading:7916309-Polymorphism, Restriction Fragment Length, pubmed-meshheading:7916309-Proteins, pubmed-meshheading:7916309-Spermatogonia
pubmed:year
1994
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