Identification of the cystic fibrosis gene: chromosome walking and jumping.
نویسندگان
چکیده
An understanding of the basic defect in the inherited disorder cystic fibrosis requires cloning of the cystic fibrosis gene and definition of its protein product. In the absence of direct functional information, chromosomal map position is a guide for locating the gene. Chromosome walking and jumping and complementary DNA hybridization were used to isolate DNA sequences, encompassing more than 500,000 base pairs, from the cystic fibrosis region on the long arm of human chromosome 7. Several transcribed sequences and conserved segments were identified in this cloned region. One of these corresponds to the cystic fibrosis gene and spans approximately 250,000 base pairs of genomic DNA.
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tion of the cystic fibrosis gene: chromosome walking and jumping. Science 245:1059-1065. 5.Tsui, L.C. 1992. Mutations and sequence variations detected in the cystic fibrosis transmembrane conductance regulator (CFTR) gene: a report from the Cystic Fibrosis Genetic Analysis Consortium. Hum. Mutat. 1:197-203. 6.Ballabio, A., R.A. Gibbs, and C.T. Caskey. 1990. PCR test for cystic fibrosis deletion...
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1 Scanlin TF. Cystic fibrosis. In: Fishman AP, ed. Pulmonary diseases and disorders. 2nd ed. New York: McGraw-Hill, 1988:1273-94 2 Rommens JM, lanuzzi MC, Kerem B, Drumm ML, Melmer G, Dean M, et al. Identification of the cystic fibrosis gene: chromosome walking and jumping. Science 1989; 245:1059-65 3 Kerem B, Rommens JM, Buchanan JA, Markiewicz D, Cos TK, Chakvarti A, et al. Identification of ...
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ورودعنوان ژورنال:
- Science
دوره 245 4922 شماره
صفحات -
تاریخ انتشار 1989