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Connors, T D; Burn, T C; VanRaay, T et al. (1997) Evaluation of DNA sequencing ambiguities using tetramethylammonium chloride hybridization conditions. Biotechniques 22:1088-90
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Connors, T D; Van Raay, T J; Petry, L R et al. (1997) The cloning of a human ABC gene (ABC3) mapping to chromosome 16p13.3. Genomics 39:231-4
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Van Raay, T J; Foskett, S M; Connors, T D et al. (1997) The NTN2L gene encoding a novel human netrin maps to the autosomal dominant polycystic kidney disease region on chromosome 16p13.3. Genomics 41:279-82
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Burn, T C; Connors, T D; Van Raay, T J et al. (1996) Generation of a transcriptional map for a 700-kb region surrounding the polycystic kidney disease type 1 (PKD1) and tuberous sclerosis type 2 (TSC2) disease genes on human chromosome 16p3.3. Genome Res 6:525-37
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Van Raay, T J; Burn, T C; Connors, T D et al. (1996) A 2.5 kb polypyrimidine tract in the PKD1 gene contains at least 23 H-DNA-forming sequences. Microb Comp Genomics 1:317-27
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Van Raay, T J; Connors, T D; Klinger, K W et al. (1996) A novel ribosomal protein L3-like gene (RPL3L) maps to the autosomal dominant polycystic kidney disease gene region. Genomics 37:172-6
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Dackowski, W R; Connors, T D; Bowe, A E et al. (1996) The region surrounding the PKD1 gene: a 700-kb P1 contig from a YAC-deficient interval. Genome Res 6:515-24
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Burn, T C; Connors, T D; Klinger, K W et al. (1995) Increased exon-trapping efficiency through modifications to the pSPL3 splicing vector. Gene 161:183-7
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Burn, T C; Connors, T D; Dackowski, W R et al. (1995) Analysis of the genomic sequence for the autosomal dominant polycystic kidney disease (PKD1) gene predicts the presence of a leucine-rich repeat. The American PKD1 Consortium (APKD1 Consortium). Hum Mol Genet 4:575-82
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