Assignment of human 17β-hydroxysteroid dehydrogenase IV to chromosome 5q2 by fluorescence in situ hybridization

Genomics

Volumn 37, Issue 3, 1996, Pages 403-404

  Leenders, Frauke ^a   Prescher, Gabriele ^b   Dolez, Vincent ^a   Begue, Agnès ^a   De Launoit, Yvan ^a   Adamski, Jerzy ^c,d  

^a INSTITUT PASTEUR DE LILLE   (France)

^b UNIVERSITY HOSPITAL ESSEN   (Germany)

^c MAX PLANCK INSTITUTE FOR BIOPHYSICAL CHEMISTRY   (Germany)

^d INSTITUTE OF EPIDEMIOLOGY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

TESTOSTERONE 17BETA DEHYDROGENASE;

ARTICLE; CHROMOSOME 5Q; FLUORESCENCE IN SITU HYBRIDIZATION; GENE ASSIGNMENT; GENE MAPPING; HUMAN; PRIORITY JOURNAL;

EID: 0006165816     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1996.0578     Document Type: Article

References (11)

1. 1. Adamski, J., Normand, T., Leenders, F., Monte, D., Begue, A., Stehelin, D., Jungblut, P. W., and de Launoit, Y. (1995). Molecular cloning of a novel videly expressed human 80 kDa 17β-hydroxysteroid dehydrogenase IV. Biochem. J. 311: 437-443.
2. 2. Andersson, S. (1995). 17β-hydroxysteroid dehydrogenases: Isozymes and mutations. J. Endocrinol. 146: 197-200.
3. 3. Bonney, R. C., Reed, M. J., Davidson, K., Beranek, P. A., and James, V. H. T. (1983). The relationship between 17β-hydroxysteroid dehydrogenase activity and oestrogen concentrations in human breast tumours and in normal breast tissue. Clin. Endocrinol. 19: 727-739.
4. 4. ISCN (1995). "An International System for Human Cytogenetic Nomenclature" (F. Mitelman, Ed.), Krager, Basel.
5. 5. Lazarow, P. B., and Moser, H. W. (1995). Disorders of peroxisome biogenesis. In "The Metabolic and Molecular Basis of Inherited Disease" (C. R. Scriver, A. L. Beaudet, W. S. Sly, and D. Valle, Eds.), pp. 2287-2316. McGraw-Hill, New York.
6. 6. Leenders, F., Tesdorpf, J. G., Markus, M., Engel, T., Seedorf, U., and Adamski, J. (1996). Porcine 80 kDa protein reveals intrinsic 17β-hydroxysteroid dehydrogenase, fatty acyl-CoA-hydratase/dehydrogenase and sterol transfer activities. J. Biol. Chem. 271: 5438-5442.
7. 7. Lichter, P., and Cremer, T. (1992). Chromosome analysis by non-isotopic in situ hybridization. In "Human Cytogenetics" (D. E. Rooney and B. H. Czepulkowski, Eds.), Vol. I, pp. 157-192. IRL, Oxford/New York/Tokyo.
8. 8. Mitelman, F. (1991). "Catalog of Chromosome Aberrations in Cancer." Wiley-Liss, New York.
9. 9. Nishisho, I., Nakamura, Y., Miyoshi, Y., Miki, Y., Ando, H., Horii, A., Koyama, K., Utsunomiya, J., Baba, S., and Hedge, P. (1991). Mutations of chromosome 5q21 genes in FAP and colorectal cancer patients. Science 253: 665-669.
10. 10. Ried, T., Lengauer, C., Cremer, T., Wiegant, J., Raap, A. K., van der Ploeg, M., Groitl, P., and Lipp, M. (1992). Specific metaphase and interphase detection of the breakpoint region in 8q24 of Burkitt lymphoma cells by triple-color fluorescence in situ hybridization. Genes Chromosomes Cancer 4: 69-74.
11. 11. Thomson, A. M., Morris, R. G., Wallace, M., Wyllie, A. H., Steel, C. M., and Carter, D. C. (1993). Allele loss from 5q21 (APC/ MCC) and 18q21 (DCC) and DCC mRNA expression in breast cancer. Br. J. Cancer 68: 61-68.