Chromosomal assignment of seven genes on canine chromosomes by fluorescence in situ hybridization

Mammalian Genome

Volumn 7, Issue 4, 1996, Pages 268-270

  Guevara Fujita, M L ^a   Loechel, R ^a   Venta, P J ^b   Yuzbasiyan Gurkan, V ^b   Brewer, G J ^a  

^a UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

^b MICHIGAN STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CANIS FAMILIARIS;

ADENINE PHOSPHORIBOSYLTRANSFERASE; COLONY STIMULATING FACTOR RECEPTOR; CREATINE KINASE; GLUCOSE TRANSPORTER; GLUCOSE TRANSPORTER 2; ISOENZYME; PYRUVATE KINASE;

ANIMAL; ARTICLE; CHROMOSOME MAP; COSMID; DNA PROBE; DOG; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC MARKER; GENETICS; TUMOR SUPPRESSOR GENE;

ADENINE PHOSPHORIBOSYLTRANSFERASE; ANIMALS; CHROMOSOME MAPPING; COSMIDS; CREATINE KINASE; DNA PROBES; DOGS; GENES, P53; GENETIC MARKERS; GLUCOSE TRANSPORTER TYPE 2; IN SITU HYBRIDIZATION, FLUORESCENCE; ISOENZYMES; MONOSACCHARIDE TRANSPORT PROTEINS; PYRUVATE KINASE; RECEPTOR, MACROPHAGE COLONY-STIMULATING FACTOR;

EID: 0030124520     PISSN: 09388990     EISSN: None     Source Type: Journal    
DOI: 10.1007/s003359900080     Document Type: Article

References (13)

1. Fratini, A., Simmers, R.N., Callen, D.F., Hyland, V.J., Tischfield, J.A., Stambrook, P.J., Sutherland, G.R. (1986). A new location for the human adenine phosphoribosyltransferase gene (APRT) distal to the haptoglobin (HP) and fra (16) (q23) (FRA16D) loci. Cytogenet. Cell Genet. 43, 10-13.
2. Fukumoto, H., Seino, S., Imura, H., Seino, Y., Eddy, R.L., Fukushima, Y., Byers, M.G., Shows, T.B., Bell, G.I. (1988). Sequence, tissue distribution, and chromosomal localization of mRNA encoding a human glucose transporter-like protein. Proc. Natl. Acad. Sci. USA 85, 5434-5438.
3. Isobe, M., Emanuel, B.S. Givol, D., Oren, M., Croce, C.M. (1986). Localization of gene for human p53 tumour antigen to band 17p13. Nature 320, 84-85.
4. Le Beau, M.M., Westbrook, C.A., Diaz, M.O., Larson, R.A., Rowley, J.D., Gasson, J.C., Golde, D.W., Scherr, C.J. (1986). Evidence for the involvement of GM-CSF and FMS in the deletion (5q) in myeloid disorders. Science 231, 984-987.
5. Mouse Genome Database (MGD) (July, 1995), Mouse Genome Informatics Project, The Jackson Laboratory, Bar Harbor, Maine, World Wide Web (URL: http://www.informatics.jax.org).
6. Nigro, J.M., Schweinfest, C.W., Rajkovic, A., Pavlovic, J., Jamal, S., Dottin, R.P., Hart, J.T., Kamarck, M.E., Rae, P.M.M., Carty, M.D., Martin-DeLeon, P. (1987). cDNA cloning and mapping of the human creatine kinase M gene to 19q13. Am. J. Hum. Genet. 40, 115-125.
7. Sambrook, J., Fristch, E.F., Maniatis, T. (1989). Molecular Cloning: A Laboratory Manual, 2nd ed. (Cold Spring Harbor, N.Y.: Cold Spring Harbor Laboratory Press).
8. Satoh, H., Tani, K., Yoshida, M.C., Sasaki, M., Miwa, S., Fuji, H. (1988). The human liver-type pyruvate kinase (PKL) gene is on chromosome 1 at band q21. Cytogenet. Cell Genet. 47,132-133.
9. Selden, J.R., Moorhead, P.S., Oehlert, M.L., Patterson, D.F. (1975). The Giemsa handing pattern of the canine karyotype. Cytogenet. Cell Genet. 15, 380-387.
10. Silver, L.M. (1993). Master locus list (Encyclopedia of the Mouse Genome III) Mamm. Genome 4 (Suppl.), S2-S9.
11. Stone, D.M., Jacky, P.B., Prieur, D.J. (1991). The giemsa banding pattern of canine chromosomes, using a cell synchronization technique. Genome 34, 407-412.
12. Verga, V., Hall, B.K., Wang, S., Johnson, S., Higgins, J.V., Glover, T.W. (1991). Localization of the translocation breakpoint in a female with Menkes syndrome to Xq13.2-q13.3 proximal to PGK-1. Am. J. Hum. Genet. 48, 1133-1138.
13. Yu, J., Tong, S., Yang-Feng, T., Kao, F-T. (1992). Construction and characterization of a region-specific microdissection library from human chromosome 2q35-q37. Genomics 14, 769-774.