Isolation of a partial candidate gene for Menkes disease by positional cloning
Tóm tắt
Từ khóa
Tài liệu tham khảo
Menkes, J.H., Alter, M., Steigleder, G.K., Weakley, D.R. & Sung, J.H. A sex-linked disorder with retardation of growth, peculiar hair and focal cerebral arid cerebellar degeneration. Pediatrics 29, 764–779 (1962).
Danks, D.M. in Metabolic Basis of inherited Disease. (eds Scriver, C.R. et al.) 1411–1462 (Me Graw Hill, New York, 1989).
Kapur, S., Higgins, J.V., Delph, K. & Rogers, B. Menkes Syndrome in a girl with X-autosome translocation. Am. J. med. Genet. 26, 503–510 (1987).
Tonnesen, T., Peterson, A., Kruse, T.A., Gerdes, A.-M. & Horn, N. Am. J. hum. Genet. 50, 1012–1017 (1992).
Keer, J.T. et al. Genetic mapping in the region of the mouse inactivation center. Genomics 7, 566–572 (1990).
Verga, V. et al. Localization of the translocation breakpoint in a female with Menkes syndrome to Xq13.2-q13.3 proximal to PGK-1. J. hum. Genet. 48, 1133–1138 (1991).
Green, E. D. & Olson, M.V. Systematic screening of yeast artificaial-chromosome libraries by use of the polymerase chain reaction. Proc. natn. Acad. Sci. U.S.A. 87, 1213–1217 (1990).
Pieretti, M., Tonlorenzi, R. & Ballabio, A. Rapid assembly of lambda contigs within YAC clones. Nucl. Acids Res. 19, 2795–2796 (1991).
Saburo, S., Shanske, S., Salvatore, D.-M. & Schon, E.A. Isolation of a cDNA encoding the B isozyme of human phosphoglycerate mutase (PGAM) and charavterization of the PGAM gene family. J. biol. Chem. 263, 16899–16705 (1988).
Turner, Z. et al. Characterization of a 1.0 MB YAC contig spanning two chromosome breakpoints related to Menkes disease. Hum. molec. Genet. 483–489 (1992).
Gonsales, G.G. et al. Fine mapping and cloning of the breakpoint associated clone with Menkes syndrome in a female patient. Genomics 14, 557–561 (1992).
Silver, S. & Misra, T.K. Plasmid-mediated heavy metal resistances. Ann. Rev. Microbiol. 42, 717–743 (1988).
Silver, S. et al. Bacterial resistance ATPases: primary pumps for exporting toxic cations and anions. TIBS 14, 76–80 (1989).
Camakaris, J. et al. Altered copper metabolism in cultured cells from Menkes syndrome and mottled mouse mutants. Biochem. Genet. 18, 117–131 (1980).
Sambrook, J., Fritsch, E.F. & Maniatis, T. Molecular Cloning, A Laboratory Manual 2nd edn (Cold Spring Harbor Laboratory Press, New York, 1989).
Piechaczyk, M. et al. Post transcriptional regulation of glyceraldehyde-3-phosphate dehydrogenase gene expression in rat tissues. Nucl. Acids Res. 12, 6951–6963 (1984).
Keith, D.H., Singer-Sam, J. & Riggs, A.D. Active X-chromosome DNA is unmethylated at eight CCGG sites clustered in a guanine-plus-cytosine rich island at the 5′ end of the gene for phosphoglycerate kinase. Molec. cell Biol. 6, 4122–4125 (1986).
Kuwano, A. & Kajii, T. High-resolution banding in chromosomes of B lymphoblastoid cells and cultured skin fibroblasts. Cytogenet. Cell Genet. 56, 212–213 (1991).
Franco, B. et al. A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules. Nature 353, 529–536 (1991).
Lengauer, C., Green, E.D. & Cremer, T. Fluorescence in situ hybridization of YAC clones after Alu-PCR amplification. Genomics 13, 826–828 (1992).