Do common in silico tools predict the clinical consequences of amino-acid substitutions in the CFTR gene? von Dorfman, R, Nalpathamkalam, T, Taylor, C, Gonska, T, Keenan, K, Yuan, XW, Corey, M, Tsui, L-C, Zielenski, J, Durie, P

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A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome von Scherer, Stephen W, Osborne, Lucy R, Li, Martin, Pober, Barbara, Chitayat, David, Bodurtha, Joann, Mandel, Ariane, Costa, Teresa, Grebe, Theresa, Cox, Sarah, Tsui, Lap-Chee

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Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly von Belloni, E, Muenke, M, Roessler, E, Traverse, G, Siegel-Bartelt, J, Frumkin, A, Mitchell, H.F, Donis-Keller, H, Helms, C, Hing, A.V, Heng, H.H.Q, Koop, B, Martindale, D, Rommens, J.M, Tsui, L.-C, Scherer, S.W

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Dysregulation of cyclin dependent kinase 6 expression in splenic marginal zone lymphoma through chromosome 7q translocations von CORCORAN, M. M, MOULD, S. J, ORCHARD, J. A, IBBOTSON, R. E, CHAPMAN, R. M, BORIGHT, A. P, PLATT, C, TSUI, L.-C, SCHERER, S. W, OSCIER, D. G

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Molecular consequences of cystic fibrosis transmembrane regulator (CFTR) gene mutations in the exocrine pancreas von Ahmed, N, Corey, M, Forstner, G, Zielenski, J, Tsui, L-C, Ellis, L, Tullis, E, Durie, P

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Arrhythmia and sudden death associated with elevated cardiac chloride channel activity von Ye, L., Zhu, W., Backx, P. H., Cortez, M. A., Wu, J., Chow, Y.‐H., Mckerlie, C., Wang, A., Tsui, L.‐C., Gross, G.J., Hu, J.

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Mutations in the human Sonic Hedgehog gene cause holoprosencephaly von Gaudenz, Karin, Jay, Philippe, Berta, Philippe, Scherer, Stephen W, Belloni, Elena, Roessler, Erich, Tsui, Lap-Chee, Muenke, Maximilian

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Visual Assessment of Contusion-Like Lesions Caused by Live Sharksucker (Echeneis naucrates) Attachment in an Indo-Pacific Humpback Dolphin (Sousa chinensis) von Ho, Heysen H. N, Kot, Brian C. W, Tsui, Henry C. L, Chung, Tabris Y. T

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Mutations in the C-Terminal Domain of Sonic Hedgehog Cause Holoprosencephaly von Roessler, Erich, Belloni, Elena, Gaudenz, Karin, Vargas, Fernando, Scherer, Stephen W., Tsui, Lap-Chee, Muenke, Maximilian

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Virtopsy as a Revolutionary Tool for Cetacean Stranding Programs: Implementation and Management von Tsui, Henry C. L., Kot, Brian C. W., Chung, Tabris Y. T., Chan, Derek K. P.

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Molecular Analysis of the Pds Gene in Pendred Syndrome (Sensorineural Hearing Loss and Goitre) von Coyle, Beth, Reardon, William, Herbrick, Jo-Anne, Tsui, Lap-Chee, Gausden, Eleanor, Lee, Jeffrey, Coffey, Rebecca, Grueters, Annette, Grossman, Ashley, Phelps, Peter D., Luxon, Linda, Kendall-Taylor, Pat, Scherer, Stephen W., Trembath, Richard C.

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Postmortem Neuroimaging of Cetacean Brains Using Computed Tomography and Magnetic Resonance Imaging von Kot, Brian C. W., Tsui, Henry C. L., Chung, Tabris Y. T., Lau, Amy P. Y.

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A mutation in CFTR produces different phenotypes depending on chromosomal background von Kiesewetter, S, Macek, M, Davis, C, Curristin, S. M, Chu, C.-S, Graham, C, Shrimpton, A. E, Cashman, S. M, Tsui, L.-C, Mickle, J, Amos, J, Highsmith, W. E, Shuber, A, Witt, D. R, Crystal, R. G, Cutting, G. R

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The cystic fibrosis gene: a molecular genetic perspective von Tsui, Lap-Chee, Dorfman, Ruslan

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Fine mapping of the X-linked split-hand/split-foot malformation (SHFM2) locus to a 5.1-Mb region on Xq26.3 and analysis of candidate genes von Faiyaz-Ul-Haque, M, Zaidi, SHE, King, LM, Haque, S, Patel, M, Ahmad, M, Siddique, T, Ahmad, W, Tsui, L-C, Cohn, DH

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Band gaps of wurtzite ScxGa1−xN alloys von Tsui H C L, Rhode, S K, Pereira, S, Beere, H E, Farrer, I, Nicoll, C A, Ritchie, D A, Moram, M A

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Nonsteroidal anti-inflammatory drugs upregulate function of wild-type and mutant CFTR von Li, J, Xiang, Y-Y, Ye, L, Tsui, L-C, MacDonald, J. F, Hu, J, Lu, W-Y

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Proportion of Cystic Fibrosis Gene Mutations Not Detected by Routine Testing in Men With Obstructive Azoospermia von Mak, Victor, Zielenski, Julian, Tsui, Lap-Chee, Durie, Peter, Zini, Armand, Martin, Sheelagh, Longley, Teresa Barry, Jarvi, Keith A

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The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein von Kobayashi, Keiko, Scherer, Stephen W, Sinasac, David S, Iijima, Mikio, Boright, Andrew P, Begum, Laila, Lee, Jeffrey R, Yasuda, Tomotsugu, Ikeda, Sayaka, Hirano, Ryuki, Terazono, Hiroki, Crackower, Michael A, Kondo, Ikuko, Tsui, Lap-Chee, Saheki, Takeyori

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Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13 von Zielenski, Julian, Bal, Jerzy, Cutting, Garry R, Macek, Milan, Palacio, Ana, Ferec, Claude, Larriba, Sara, Marshall, Bruce C, Krebsova, Alice, Markiewicz, Danuta, Casals, Teresa, Claustres, Mirreille, Durie, Peter, Tsui, Lap-Chee, Corey, Mary, Langfelder-Schwind, Elinor, Rozmahel, Richard, DeCelie-Germana, J, Nowakowska, Aleksandra, Mercier, Bernard, Estivill, Xavier, Aznarez, Isabel

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