The region surrounding the PKD1 gene: A 700-kb P1 contig from a YAC-deficient interval

Genome Research

Volumn 6, Issue 6, 1996, Pages 515-524

  Dackowski, William R ^a   Connors, Timothy D ^a   Bowe, Ann E ^a   Stanton Jr , Vincent ^b   Housman, David ^b   Doggett, Norman A ^c   Landes, Gregory M ^a   Klinger, Katherine W ^a  

^a Intgd Genet ^*  (United States)

^b MASSACHUSETTS INSTITUTE OF TECHNOLOGY   (United States)

^c LOS ALAMOS NATIONAL LABORATORY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALU SEQUENCE; ARTICLE; CHROMOSOME 16P; DNA LIBRARY; DNA PROBE; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC MARKER; HUMAN; KIDNEY POLYCYSTIC DISEASE; MOLECULAR CLONING; NONHUMAN; PRIORITY JOURNAL; RESTRICTION MAPPING; YEAST ARTIFICIAL CHROMOSOME;

ESCHERICHIA COLI;

EID: 0029894804     PISSN: 10549803     EISSN: None     Source Type: Journal    
DOI: 10.1101/gr.6.6.515     Document Type: Article

References (6)

1. American PDK1 Consortium. 1995. Analysis of the genomic sequence for the autosomal dominant polycystic kidney disease (PKD1) gene predicts the presence of a leucine-rich repeat. Hum. Mol. Genet. 4: 575-582.
2. Bellanne-Chantelot, C., B. Lacroix, P. Ougen, A. Billault, S. Beaufils, S. Bertrand, I. Georges, F. Gilbert, I. Gros, G. Lucotte, L. Susini, J.-J. Codani, P. Gesnouin, S. Pook, G. Vaysseix, J. Ried, D. Ward, I. Chumakov, D. LePaslier, and D. Cohen. 1992. Mapping the whole human genome by fingerprinting yeast artificial chromosomes. Cell 70: 1059-1068.
3. Brook-Carter, P.T., B. Peral, C.J. Ward, P. Thompson, J. Hughes, M.M. Maheshwar, M. Nellist, V. Gamble, P.C. Harris, and J.R. Sampson. 1994. Deletion of the TSC2 and PKD genes associated with severe infantile polycystic kidney disease-a contiguous gene syndrome. Nature Genet. 8: 328-332.
4. Burn, T.C., T.D. Connors, T.J. Van Raay, W.R. Dackowski, J.M. Millholland, K.W. Klinger, and G.M. Landes. 1996. Generation of a transcriptional map for a 700 kilobase region surrounding the polycystic kidney disease typel (PKD1) and tuberous sclerosis type 2 (TSC2) disease genes on human chromosome 16p13.3. Genome Res. (this issue).
5. Willard, H.F., F. Cremers, J.L. Mandel, A.P. Monaco, D.L. Nelson, and D. Schlessinger. 1994. Report and abstracts of the Fifth International Workshop on Human X Chromosome Mapping 1994. Heidelberg, Germany, April 24-27, 1994. Cytogenet. Cell Genet. 67: 295-358.
6. Zuo, J., C. Robbins, P. Taillon-Miller, D.R. Cox, and R.M. Myers. 1992. Cloning of the Huntington disease region in yeast artificial chromosomes. Hum. Mol. Genet. 1: 149-159.