Related Content
Search Google Scholar for:
|
|
Science 29 November 1985: Vol. 230. no. 4729, pp. 1054 - 1057 DOI: 10.1126/science.2997931
|
|
Articles
Science, Vol 230, Issue 4729, 1054-1057
Copyright © 1985 by American Association for the Advancement of Science
Cystic fibrosis locus defined by a genetically linked polymorphic DNA marker
LC Tsui,
M Buchwald,
D Barker,
JC Braman,
R Knowlton,
JW Schumm,
H Eiberg,
J Mohr,
D Kennedy,
N Plavsic,
and
al. et
A polymorphic DNA marker has been found genetically linked, in a set of 39 human families, to an autosomal recessive gene that causes cystic fibrosis (CF), a disease affecting one in 2000 Caucasian children. The DNA marker (called D0CRI-917) is also linked to the PON locus, which by independent evidence is linked to the CF locus. The best estimates of the genetic distances are 5 centimorgans between the DNA marker and PON and 15 centimorgans between the DNA marker and the CF locus, meaning that the location of the disease gene has been narrowed to about 1 percent of the human genome (about 30 million base pairs). Although the data are consistent with the interpretation that a single locus causes cystic fibrosis, the possibility of genetic heterogeneity remains. The discovery of a linked DNA polymorphism is the first step in molecular analysis of the CF gene and its causative role in the disease.
THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
- Changing Models of Biomedical Research.
- W. F. Crowley Jr. and J. F. Gusella (2009)
Science Translational Medicine
1, 1cm1
| Full Text »
| PDF »
- Human chromosome 7 circa 2004: a model for structural and functional studies of the human genome.
- S. W. Scherer and E. D. Green (2004)
Hum. Mol. Genet.
13, R303-R313
| Abstract »
| Full Text »
| PDF »
- Advanced glossary on genetic epidemiology.
- N Malats and F Calafell (2003)
J Epidemiol Community Health
57, 562-564
| Abstract »
| Full Text »
| PDF »
- Variant Cystic Fibrosis Phenotypes in the Absence of CFTR Mutations.
- J. D. Groman, M. E. Meyer, R. W. Wilmott, P. L. Zeitlin, and G. R. Cutting (2002)
N. Engl. J. Med.
347, 401-407
| Abstract »
| Full Text »
| PDF »
- Primer on Medical Genomics Part I: History of Genetics and Sequencing of the Human Genome.
- C. P. Lorentz, E. D. Wieben, A. Tefferi, D. A. H. Whiteman, and G. W. Dewald (2002)
Mayo Clin. Proc.
77, 773-782
| Abstract »
| PDF »
- Lung Infections Associated with Cystic Fibrosis.
- J. B. Lyczak, C. L. Cannon, and G. B. Pier (2002)
Clin. Microbiol. Rev.
15, 194-222
| Abstract »
| Full Text »
| PDF »
- Specific and Rapid Detection by Fluorescent In Situ Hybridization of Bacteria in Clinical Samples Obtained from Cystic Fibrosis Patients.
- M. Hogardt, K. Trebesius, A. M. Geiger, M. Hornef, J. Rosenecker, and J. Heesemann (2000)
J. Clin. Microbiol.
38, 818-825
| Abstract »
| Full Text »
| PDF »
- Physiological Basis of Cystic Fibrosis: A Historical Perspective.
- P. M. QUINTON (1999)
Physiol Rev
79, 3-22
| Abstract »
| Full Text »
| PDF »
- Delta F508 in cystic fibrosis: willing but not able.
- K. W Southern (1997)
Arch. Dis. Child.
76, 278-282
| Full Text »
- Congenital Bilateral Absence of the Vas Deferens: A Primarily Genital Form of Cystic Fibrosis.
- A. Anguiano, R. D. Oates, J. A. Amos, M. Dean, B. Gerrard, C. Stewart, T. A. Maher, M. B. White, and A. Milunsky (1992)
JAMA
267, 1794-1797
| Abstract »
| PDF »
- Identification of mutations in the COL4A5 collagen gene in Alport syndrome.
- D. Barker, S. Hostikka, J Zhou, L. Chow, A. Oliphant, S. Gerken, M. Gregory, M. Skolnick, C. Atkin, and K Tryggvason (1990)
Science
248, 1224-1227
| Abstract »
| PDF »
- High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones.
- P Lichter, C. Tang, K Call, G Hermanson, G. Evans, D Housman, and D. Ward (1990)
Science
247, 64-69
| Abstract »
| PDF »
- Mild Cystic Fibrosis Linked to Chromosome 7q22 Markers with an Uncommon Haplotype.
- A. McConkie-Rosell, Y.-T. Chen, D. Harris, M. C. Speer, M. A. Pericak-Vance, J.-H. Ding, W. E. Highsmith Jr., M. Knowles, and S. G. Kahler (1989)
Ann Intern Med
111, 797-801
| Abstract »
| PDF »
- Identification of the cystic fibrosis gene: chromosome walking and jumping.
- J. Rommens, M. Iannuzzi, B Kerem, M. Drumm, G Melmer, M Dean, R Rozmahel, J. Cole, D Kennedy, N Hidaka, et al. (1989)
Science
245, 1059-1065
| Abstract »
| PDF »
- Identification of the cystic fibrosis gene: genetic analysis.
- B Kerem, J. Rommens, J. Buchanan, D Markiewicz, T. Cox, A Chakravarti, M Buchwald, and L. Tsui (1989)
Science
245, 1073-1080
| Abstract »
| PDF »
- Medical Genetics.
- A. G. Motulsky (1989)
JAMA
261, 2855-2856
| Abstract »
| PDF »
- The human as an experimental system in molecular genetics.
- R White and C. Caskey (1988)
Science
240, 1483-1488
| Abstract »
| PDF »
- Derivation of clones close to met by preparative field inversion gel electrophoresis.
- F Michiels, M Burmeister, and H Lehrach (1987)
Science
236, 1305-1308
| Abstract »
| PDF »
- Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17.
- D Barker, E Wright, K Nguyen, L Cannon, P Fain, D Goldgar, D. Bishop, J Carey, B Baty, J Kivlin, et al. (1987)
Science
236, 1100-1102
| Abstract »
| PDF »
- Variable number of tandem repeat (VNTR) markers for human gene mapping.
- Y Nakamura, M Leppert, P O'Connell, R Wolff, T Holm, M Culver, C Martin, E Fujimoto, M Hoff, E Kumlin, et al. (1987)
Science
235, 1616-1622
| Abstract »
| PDF »
- Construction of a general human chromosome jumping library, with application to cystic fibrosis.
- F. Collins, M. Drumm, J. Cole, W. Lockwood, G. Vande Woude, and M. Iannuzzi (1987)
Science
235, 1046-1049
| Abstract »
| PDF »
- The genetic defect causing familial Alzheimer's disease maps on chromosome 21.
- P. St George-Hyslop, R. Tanzi, R. Polinsky, J. Haines, L Nee, P. Watkins, R. Myers, R. Feldman, D Pollen, D Drachman, et al. (1987)
Science
235, 885-890
| Abstract »
| PDF »
- The search for the cystic fibrosis gene.
- R White (1986)
Science
234, 1054-1055
| PDF »
- New Frontiers in Genetic Medicine.
- L. J. SHAPIRO, D. E. COMINGS, O. W. JONES, and D. L. RIMOIN (1986)
Ann Intern Med
104, 527-539
| Abstract »
| PDF »
- Mapping Complex Genetic Traits in Humans: New Methods Using a Complete RFLP Linkage Map.
- E.S. Lander and D. Botstein (1986)
Cold Spring Harb Symp Quant Biol
51, 49-62
| Abstract »
| PDF »
- Molecular Genetics and the Basic Defect Causing Cystic Fibrosis.
- R. Williamson, G. Bell, J. Bell, G. Bates, K.A. Davies, X. Estivill, M. Farrall, H. Kruyer, H.Y. Law, N. Lench, et al. (1986)
Cold Spring Harb Symp Quant Biol
51, 309-315
| Abstract »
| PDF »
- Highly Polymorphic RFLP Probes as Diagnostic Tools.
- H. Donis-Keller, D.F. Barker, R.G. Knowlton, J.W. Schumm, J.C. Braman, and P. Green (1986)
Cold Spring Harb Symp Quant Biol
51, 317-324
| Abstract »
| PDF »
- Mapping of the Cystic Fibrosis Locus on Chromosome 7.
- L.-C. Tsui, S. Zengerling, H.F. Willard, and M. Buchwald (1986)
Cold Spring Harb Symp Quant Biol
51, 325-335
| Abstract »
| PDF »
|
|