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Your search keyword '"Donlon, T A"' showing total 8 results
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8 results on '"Donlon, T A"'

1. Report of the fourth international workshop on human chromosome 15 mapping 1997.

Author

Morton CC, Christian SL, Donlon TA, Driscoll DJ, Fink JK, Gabriel JM, Gotway G, Greally JM, Hitchins MP, Howard HC, Ji Y, Leonard S, Lerner T, Magenis E, Malcolm S, Ohta T, Rainier S, Rees M, Riley B, Robinson WP, Saitoh S, Schultz R, Sell S, Sharp JD, and Nicholls RD

Subjects
Angelman Syndrome genetics, Animals, DNA Methylation, Female, Gene Deletion, Gene Duplication, Gene Expression, Genomic Imprinting, Humans, Male, Mice, Physical Chromosome Mapping, Prader-Willi Syndrome genetics, Chromosome Mapping, Chromosomes, Human, Pair 15 genetics
Published
1999
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2. Report and abstracts of the Second International Workshop on Human Chromosome 15 Mapping. England, February 18-20, 1994.

Author

Malcolm S and Donlon TA

Subjects
Base Sequence, Chromosome Aberrations genetics, Chromosome Disorders, Chromosome Mapping, Chromosomes, Artificial, Yeast, DNA Primers chemistry, DNA Replication, Female, Genetic Markers, Humans, Male, Molecular Sequence Data, Polymorphism, Genetic, Repetitive Sequences, Nucleic Acid, Chromosomes, Human, Pair 15
Published
1994
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4. Localization of the human T lymphocyte activation gene 519 (D2S69E) to chromosome 2p12----q11.

Author

Donlon TA, Krensky AM, and Clayberger C

Subjects
Chromosome Mapping, DNA genetics, DNA Probes, DNA-Binding Proteins genetics, Humans, Nucleic Acid Hybridization, Chromosomes, Human, Pair 2, Lymphocyte Activation, T-Lymphocytes physiology
Abstract

In situ hybridization was used to localize the lymphocyte activation gene 519 (D2S69E) on human metaphase chromosomes. A significant proportion of the grains were situated over chromosome 2p12----q11, a region which contains other genes involved in immunologic functions.

Published
1990
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7. Highly polymorphic DNA sequences in the distal region of the long arm of human chromosome 18.

Author

Müller U, Donlon TA, Harris P, Rose E, Hoffman E, Bruns GP, and Latt SA

Subjects
Animals, Chromosome Banding, Cricetinae, Genetic Markers, Humans, Hybrid Cells, Nucleic Acid Hybridization, Chromosomes, Human, Pair 18, DNA genetics, Polymorphism, Genetic, Polymorphism, Restriction Fragment Length, Repetitive Sequences, Nucleic Acid
Abstract

Highly polymorphic repeated DNA sequences were detected at the end of the long arm of human chromosome 18 by a recombinant DNA probe containing 56 bp of human DNA (pERT25). This was shown by hybridization of pERT25 to DNA from a panel of human X rodent somatic cell hybrids, by dot blot hybridization to flow-sorted human chromosomes, and by in situ hybridization to metaphase chromosomes. The high degree of polymorphism detected by this 18q DNA fragment makes it potentially useful for various applications, including investigations into the genetics of trisomy 18 (Edwards syndrome), linkage studies, and paternity testing.

Published
1987
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