Mapping of the genes encoding human inducible and endothelial nitric oxide synthase (NOS2 and NOS3) to the pericentric region of chromosome 17 and to chromosome 7, respectively.
- Publication Type:
- Journal Article
- Citation:
- Genomics, 1994, 21 (2), pp. 419 - 422
- Issue Date:
- 1994-05-15
Closed Access
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2009004798OK.pdf | 256.98 kB | Adobe PDF |
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Full metadata record
Field | Value | Language |
---|---|---|
dc.contributor.author | Xu, W | en_US |
dc.contributor.author | Charles, IG | en_US |
dc.contributor.author | Moncada, S | en_US |
dc.contributor.author | Gorman, P | en_US |
dc.contributor.author | Sheer, D | en_US |
dc.contributor.author | Liu, L | en_US |
dc.contributor.author | Emson, P | en_US |
dc.date.issued | 1994-05-15 | en_US |
dc.identifier.citation | Genomics, 1994, 21 (2), pp. 419 - 422 | en_US |
dc.identifier.issn | 0888-7543 | en_US |
dc.identifier.uri | http://hdl.handle.net/10453/13396 | |
dc.description.abstract | Nitric oxide (NO) is an important molecular messenger regulating the functions of a wide variety of cells and tissues. NO is synthesized from L-arginine by a variety of isoforms of the enzyme nitric oxide synthase (NOS). We have used Southern blotting analysis on DNAs obtained from a panel of human-rodent hybrid cell lines to map the gene encoding the inducible NOS (NOS2) to chromosome 17cen-17q11 and the gene encoding the endothelial form of NOS (NOS3) to chromosome 7. Fluorescence in situ hybridization using a NOS2 probe gave several signals in the 17p11-q11 pericentromeric region. | en_US |
dc.language | eng | en_US |
dc.relation.ispartof | Genomics | en_US |
dc.relation.isbasedon | 10.1006/geno.1994.1286 | en_US |
dc.subject.classification | Genetics & Heredity | en_US |
dc.subject.mesh | Cartilage, Articular | en_US |
dc.subject.mesh | Hybrid Cells | en_US |
dc.subject.mesh | Chromosomes, Human, Pair 7 | en_US |
dc.subject.mesh | Chromosomes, Human, Pair 17 | en_US |
dc.subject.mesh | Animals | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Isoenzymes | en_US |
dc.subject.mesh | Amino Acid Oxidoreductases | en_US |
dc.subject.mesh | RNA, Messenger | en_US |
dc.subject.mesh | DNA Primers | en_US |
dc.subject.mesh | Blotting, Southern | en_US |
dc.subject.mesh | Chromosome Banding | en_US |
dc.subject.mesh | Chromosome Mapping | en_US |
dc.subject.mesh | Restriction Mapping | en_US |
dc.subject.mesh | Polymerase Chain Reaction | en_US |
dc.subject.mesh | Base Sequence | en_US |
dc.subject.mesh | Genomic Library | en_US |
dc.subject.mesh | Cosmids | en_US |
dc.subject.mesh | Molecular Sequence Data | en_US |
dc.subject.mesh | Nitric Oxide Synthase | en_US |
dc.title | Mapping of the genes encoding human inducible and endothelial nitric oxide synthase (NOS2 and NOS3) to the pericentric region of chromosome 17 and to chromosome 7, respectively. | en_US |
dc.type | Journal Article | |
utslib.citation.volume | 2 | en_US |
utslib.citation.volume | 21 | en_US |
utslib.location.activity | United States | en_US |
utslib.for | 0604 Genetics | en_US |
utslib.for | 0806 Information Systems | en_US |
pubs.embargo.period | Not known | en_US |
pubs.organisational-group | /University of Technology Sydney | |
pubs.organisational-group | /University of Technology Sydney/Faculty of Science | |
pubs.organisational-group | /University of Technology Sydney/Strength - ithree - Institute of Infection, Immunity and Innovation | |
utslib.copyright.status | closed_access | |
pubs.issue | 2 | en_US |
pubs.publication-status | Published | en_US |
pubs.volume | 21 | en_US |
Abstract:
Nitric oxide (NO) is an important molecular messenger regulating the functions of a wide variety of cells and tissues. NO is synthesized from L-arginine by a variety of isoforms of the enzyme nitric oxide synthase (NOS). We have used Southern blotting analysis on DNAs obtained from a panel of human-rodent hybrid cell lines to map the gene encoding the inducible NOS (NOS2) to chromosome 17cen-17q11 and the gene encoding the endothelial form of NOS (NOS3) to chromosome 7. Fluorescence in situ hybridization using a NOS2 probe gave several signals in the 17p11-q11 pericentromeric region.
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