| Title | Author(s) | Year | View Count |
 | A systematic analysis of intronic sequences downstream of 5′ splice sites reveals a widespread role for U-rich motifs and TIA1/TIAL1 proteins in alternative splicing regulation | Aznarez, I; Barash, Y; Shai, O; He, D; Zielenski, J; Tsui, LC; Parkinson, J; Frey, BJ; Rommens, JM; Blencowe, BJ | 2008 | 359 |
 | Exon skipping through the creation of a putative exonic splicing silencer as a consequence of the cystic fibrosis mutation R553X | Aznarez, I; Zielenski, J; Rommens, JM; Blencowe, BJ; Tsui, LC | 2007 | 176 |
| Human chromosome 7: DNA sequence and biology | Scherer, SW; Cheung, J; MacDonald, JR; Osborne, LR; Nakabayashi, K; Herbrick, JA; Carson, AR; ParkerKatiraee, L; Skaug, J; Khaja, R; Zhang, J; Hudek, AK; Li, M; Haddad, M; Duggan, GE; Fernandez, BA; Kanematsu, E; Gentles, S; Christopoulos, CC; Choufani, S; Kwasnicka, D; Zheng, XH; Lai, Z; Nusskern, D; Zhang, Q; Gu, Z; Lu, F; Zeesman, S; Nowaczyk, MJ; Teshima, I; Chitayat, D; Shuman, C; Weksberg, R; Zackai, EH; Grebe, TA; Cox, SR; Kirkpatrick, SJ; Rahman, N; Friedman, JM; Heng, HHQ; Pelicci, PG; LoCoco, F; Belloni, E; Shaffer, LG; Pober, B; Morton, CC; Gusella, JF; Bruns, GAP; Korf, BR; Quade, BJ; Ligon, AH; Ferguson, H; Higgins, AW; Leach, NT; Herrick, SR; Lemyre, E; Farra, CG; Kim, HG; Summers, AM; Gripp, KW; Roberts, W; Szatmari, P; Winsor, EJT; Grzeschik, KH; Teebi, A; Minassian, BA; Kere, J; Armengol, L; Pujana, MA; Estivill, X; Wilson, MD; Koop, BF; Tosi, S; Moore, GE; Boright, AP; Zlotorynski, E; Kerem, B; Kroisel, PM; Petek, E; Oscier, DG; Mould, SJ; Döhner, H; Döhner, K; Rommens, JM; Vincent, JB; Venter, JC; Li, PW; Mural, RJ; Adams, MD; Tsui, LC | 2003 | 679 |
 | Cloning and characterization of two cytoplasmic dynein intermediate chain genes in mouse and human | Crackower, MA; Snasac, DS; Xia, J; Motoyama, J; Prochazka, M; Rommens, JM; Sbherer, SW; Tsui, LC | 1999 | 222 |
| The XRCC2 DNA repair gene: Identification of a positional candidate | Tambini, CE; George, AM; Rommens, JM; Tsui, LC; Scherer, SW; Thacker, J | 1997 | 482 |
| Translocation breakpoint maps 5 kb 3' from TWIST in a patient affected with Saethre-Chotzen syndrome | Krebs, I; Weis, I; Hudler, M; Rommens, JM; Roth, H; Scherer, SW; Tsui, LC; Füchtbauer, EM; Grzeschik, KH; Tsuji, K; Kunz, J | 1997 | 402 |
| Amplification of CFTR exon 9 sequences to multiple locations in the human genome | Rozmahel, R; Heng, HHQ; Duncan, AMV; Shi, XM; Rommens, JM; Tsui, LC | 1997 | 285 |
| Permeability of wild-type and mutant cystic fibrosis transmembrane conductance regulator chloride channels to polyatomic anions | Linsdell, P; Tabcharani, JA; Rommens, JM; Hou, YX; Chang, XB; Tsui, LC; Riordan, JR; Hanrahan, JW | 1997 | 281 |
| Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly. | Belloni, E; Muenke, M; Roessler, E; Traverso, G; SiegelBartelt, J; Frumkin, A; Mitchell, HF; DonisKeller, H; Helms, C; Hing, AV; Heng, HH; Koop, B; Martindale, D; Rommens, JM; Tsui, LC; Scherer, SW | 1996 | 282 |
| Episomal expression of wild-type CFTR corrects cAMP-dependent chloride transport in respiratory epithelial cells | Lei, DC; Kunzelmann, K; Koslowsky, T; Yezzi, MJ; Escobar, LC; Xu, Z; Ellison, AR; Rommens, JM; Tsui, LC; Tykocinski, M; Gruenert, DC | 1996 | 350 |
| Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development | Crackower, MA; Scherer, SW; Rommens, JM; Hui, CC; Poorkaj, P; Soder, S; Cobben, JM; Hudgins, L; Evans, JP; Tsui, LC | 1996 | 630 |
| Cloning and characterization of PDK4 on 7q21.3 encoding a fourth pyruvate dehydrogenase kinase isoenzyme in human | Rowles, J; Scherer, SW; Xi, T; Majer, M; Nickle, DC; Rommens, JM; Popov, KM; Harris, RA; Riebow, NL; Xia, J; Tsui, LC; Bogardus, C; Prochazka, M | 1996 | 461 |
| Phosphatase inhibitors activate normal and defective CFTR chloride channels | Becq, F; Jensen, TJ; Chang, XB; Savoia, A; Rommens, JM; Tsui, LC; Buchwald, M; Riordan, JR; Hanrahan, JW | 1994 | 244 |
| Analysis of CFTR transcripts in nasal epithelial cells and lymphoblasts of a cystic fibrosis patient with 621 + 1G → T and 711 + 1G → T mutations | Zielenski, J; Bozon, D; Markiewicz, D; Aubin, G; Simard, F; Rommens, JM; Tsui, LC | 1993 | 285 |
| Refined localization and yeast artificial chromosome (YAC) contig-mapping of genes and DNA segments in the 7q21-q32 region | Scherer, SW; Rommens, JM; Soder, S; Wong, E; Plavsic, N; Tompkins, BJF; Beattie, A; Kim, J; Tsui, LC | 1993 | 377 |
| Multi-ion pore behaviour in the CFTR chloride channel | Tabcharani, JA; Rommens, JM; Hou, YX; Chang, XB; Tsui, LC; Riordan, JR; Hanrahan, JW | 1993 | 186 |
| Identification of mutations in exons 1 through 8 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene | Zielenski, J; Bozon, D; Kerem, BS; Markiewicz, D; Durie, P; Rommens, JM; Tsui, LC | 1991 | 336 |
| Expression of the cystic fibrosis gene in non-epithelial invertebrate cells produces a regulated anion conductance | Kartner, N; Hanrahan, JW; Jensen, TJ; Naismith, AL; Shizhang, S; Ackerley, CA; Reyes, EF; Tsui, LC; Rommens, JM; Bear, CE; Riordan, JR | 1991 | 231 |
| cAMP-inducible chloride conductance in mouse fibroblast lines stably expressing the human cystic fibrosis transmembrane conductance regulator | Rommens, JM; Dho, S; Bear, CE; Kartner, N; Kennedy, D; Riordan, JR; Tsui, LC; Foskett, JK | 1991 | 265 |
| Identification of mutations in regions corresponding to the two putative nucleotide (ATP)-binding folds of the cystic fibrosis gene | Kerem, B; Zielenski, J; Markiewicz, D; Bozon, D; Gazit, E; Yahav, J; Kennedy, D; Riordan, JR; Collins, FS; Rommens, JM; Tsui, LC | 1990 | 297 |
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