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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
1996-7-26
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pubmed:abstractText |
Several human diseases have been mapped to Xp22.3 on the distal short arm of the human X chromosome, and many genes in this area have been found to be expressed from the inactive X chromosome. To facilitate physical mapping and characterization of this interesting region, we have constructed a battery of radiation hybrids containing human X chromosomal fragments, and isolated two hybrid clones A with overlapping fragments of Xp22.3. Alu-PCR on these hybrids and identification of sequences common to both hybrids allowed the isolation of six sequences-tagged sites (STSs) from Xp22.3. Five of the STSs were mapped+ to individual YACs comprising a recently constructed contig of this region. These novel STSs are useful markers for further physical characterization of this part of the genome.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0340-6717
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
97
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
604-10
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:8655139-Animals,
pubmed-meshheading:8655139-Base Sequence,
pubmed-meshheading:8655139-Chromosome Mapping,
pubmed-meshheading:8655139-Chromosomes, Artificial, Yeast,
pubmed-meshheading:8655139-Cricetinae,
pubmed-meshheading:8655139-DNA Primers,
pubmed-meshheading:8655139-Genetic Diseases, Inborn,
pubmed-meshheading:8655139-Genetic Markers,
pubmed-meshheading:8655139-Humans,
pubmed-meshheading:8655139-Hybrid Cells,
pubmed-meshheading:8655139-In Situ Hybridization, Fluorescence,
pubmed-meshheading:8655139-Molecular Sequence Data,
pubmed-meshheading:8655139-Oligonucleotide Probes,
pubmed-meshheading:8655139-Polymerase Chain Reaction,
pubmed-meshheading:8655139-Sequence Tagged Sites,
pubmed-meshheading:8655139-X Chromosome
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pubmed:year |
1996
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pubmed:articleTitle |
Generation of sequence-tagged sites from Xp22.3 by isolating common Alu-PCR products of radiation hybrids retaining overlapping human X chromosome fragments.
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pubmed:affiliation |
Department of Pediatrics, University of California, San Francisco, California 94143, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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