Tracy D. Connors, Ph.D. - Publications

Affiliations: 
2013 School of Public Service Leadership Capella University, Minneapolis, MN, United States 
Area:
Organization Theory, Organizational

0/18 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
Low-probability matches (unlikely to be authored by this person)
2001 Sood R, Bonner TI, Makalowska I, Stephan DA, Robbins CM, Connors TD, Morgenbesser SD, Su K, Faruque MU, Pinkett H, Graham C, Baxevanis AD, Klinger KW, Landes GM, Trent JM, et al. Cloning and characterization of 13 novel transcripts and the human RGS8 gene from the 1q25 region encompassing the hereditary prostate cancer (HPC1) locus. Genomics. 73: 211-22. PMID 11318611 DOI: 10.1006/Geno.2001.6500  0.01
2001 Bacolla A, Jaworski A, Connors TD, Wells RD. Pkd1 unusual DNA conformations are recognized by nucleotide excision repair. The Journal of Biological Chemistry. 276: 18597-604. PMID 11279140 DOI: 10.1074/Jbc.M100845200  0.01
2000 Sood R, Makalowska I, Carpten JD, Robbins CM, Stephan DA, Connors TD, Morgenbesser SD, Su K, Pinkett HW, Graham CL, Quesenberry MI, Baxevanis AD, Klinger KW, Trent JM, Bonner TI. The human RGL (RalGDS-like) gene: cloning, expression analysis and genomic organization. Biochimica Et Biophysica Acta. 1491: 285-8. PMID 10760592 DOI: 10.1016/S0167-4781(00)00031-2  0.01
2000 Carpten JD, Makalowska I, Robbins CM, Scott N, Sood R, Connors TD, Bonner TI, Smith JR, Faruque MU, Stephan DA, Pinkett H, Morgenbesser SD, Su K, Graham C, Gregory SG, et al. A 6-Mb high-resolution physical and transcription map encompassing the hereditary prostate cancer 1 (HPC1) region. Genomics. 64: 1-14. PMID 10708513 DOI: 10.1006/Geno.1999.6051  0.01
1998 Lee MP, Reeves C, Schmitt A, Su K, Connors TD, Hu RJ, Brandenburg S, Lee MJ, Miller G, Feinberg AP. Somatic mutation of TSSC5, a novel imprinted gene from human chromosome 11p15.5. Cancer Research. 58: 4155-9. PMID 9751628  0.01
1997 Hu RJ, Lee MP, Connors TD, Johnson LA, Burn TC, Su K, Landes GM, Feinberg AP. A 2.5-Mb transcript map of a tumor-suppressing subchromosomal transferable fragment from 11p15.5, and isolation and sequence analysis of three novel genes. Genomics. 46: 9-17. PMID 9403053 DOI: 10.1006/geno.1997.4981  0.01
1997 Connors TD, Burn TC, VanRaay T, Germino GG, Klinger KW, Landes GM. Evaluation of DNA sequencing ambiguities using tetramethylammonium chloride hybridization conditions. Biotechniques. 22: 1088-90. PMID 9187758 DOI: 10.2144/97226bm17  0.01
1997 Ibraghimov-Beskrovnaya O, Dackowski WR, Foggensteiner L, Coleman N, Thiru S, Petry LR, Burn TC, Connors TD, Van Raay T, Bradley J, Qian F, Onuchic LF, Watnick TJ, Piontek K, Hakim RM, et al. Polycystin: in vitro synthesis, in vivo tissue expression, and subcellular localization identifies a large membrane-associated protein. Proceedings of the National Academy of Sciences of the United States of America. 94: 6397-402. PMID 9177229 DOI: 10.1073/pnas.94.12.6397  0.01
1997 Van Raay TJ, Foskett SM, Connors TD, Klinger KW, Landes GM, Burn TC. 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. PMID 9143507 DOI: 10.1006/geno.1997.4659  0.01
1997 Connors TD, Van Raay TJ, Petry LR, Klinger KW, Landes GM, Burn TC. The cloning of a human ABC gene (ABC3) mapping to chromosome 16p13.3. Genomics. 39: 231-4. PMID 9027511 DOI: 10.1006/geno.1996.4500  0.01
1996 Van Raay TJ, Burn TC, Connors TD, Petry LR, Germino GG, Klinger KW, Landes GM. A 2.5 kb polypyrimidine tract in the PKD1 gene contains at least 23 H-DNA-forming sequences. Microbial & Comparative Genomics. 1: 317-27. PMID 9689215  0.01
1996 Van Raay TJ, Connors TD, Klinger KW, Landes GM, Burn TC. A novel ribosomal protein L3-like gene (RPL3L) maps to the autosomal dominant polycystic kidney disease gene region. Genomics. 37: 172-6. PMID 8921388 DOI: 10.1006/geno.1996.0538  0.01
1996 Burn TC, Connors TD, Van Raay TJ, Dackowski WR, Millholland JM, Klinger KW, Landes GM. 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 Research. 6: 525-37. PMID 8828041  0.01
1996 Dackowski WR, Connors TD, Bowe AE, Stanton V, Housman D, Doggett NA, Landes GM, Klinger KW. The region surrounding the PKD1 gene: a 700-kb P1 contig from a YAC-deficient interval. Genome Research. 6: 515-24. PMID 8828040 DOI: 10.1101/Gr.6.6.515  0.01
1996 Wang Q, Curran ME, Splawski I, Burn TC, Millholland JM, VanRaay TJ, Shen J, Timothy KW, Vincent GM, de Jager T, Schwartz PJ, Toubin JA, Moss AJ, Atkinson DL, Landes GM, ... Connors TD, et al. Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias. Nature Genetics. 12: 17-23. PMID 8528244 DOI: 10.1038/Ng0196-17  0.01
1995 Burn TC, Connors TD, Klinger KW, Landes GM. Increased exon-trapping efficiency through modifications to the pSPL3 splicing vector. Gene. 161: 183-7. PMID 7665076 DOI: 10.1016/0378-1119(95)00223-S  0.01
1995 Burn TC, Connors TD, Dackowski WR, Petry LR, Van Raay TJ, Millholland JM, Venet M, Miller G, Hakim RM, Landes GM, Klinger KW, Qian F, Onuchic LF, Watnick T, Germino GG, et al. 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) Human Molecular Genetics. 4: 575-582. PMID 7633406 DOI: 10.1093/hmg/4.4.575  0.01
1989 Ellison KS, Dogliotti E, Connors TD, Basu AK, Essigmann JM. Site-specific mutagenesis by O6-alkylguanines located in the chromosomes of mammalian cells: influence of the mammalian O6-alkylguanine-DNA alkyltransferase. Proceedings of the National Academy of Sciences of the United States of America. 86: 8620-4. PMID 2813414 DOI: 10.1073/Pnas.86.22.8620  0.01
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