Decreased mRNA and protein stability of W1282X limits response to modulator therapy von Aksit, M.A, Bowling, A.D, Evans, T.A, Joynt, A.T, Osorio, D, Patel, S, West, N, Merlo, C, Sosnay, P.R, Cutting, G.R, Sharma, N

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A susceptibility gene for type 2 diabetes confers substantial risk for diabetes complicating cystic fibrosis von Blackman, S. M., Hsu, S., Ritter, S. E., Naughton, K. M., Wright, F. A., Drumm, M. L., Knowles, M. R., Cutting, G. R.

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The diagnosis of cystic fibrosis: A consensus statement von Rosenstein, Beryl J., Cutting, Garry R.

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The human embryonic genome is karyotypically complex, with chromosomally abnormal cells preferentially located away from the developing fetus von Griffin, D K, Brezina, P R, Tobler, K, Zhao, Yulian, Silvestri, G, Mccoy, R C, Anchan, R, Benner, A, Cutting, G R, Kearns, W G

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The genetics and genomics of cystic fibrosis von Sharma, N., Cutting, G.R.

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Single-tube multiplex-PCR screen for common deletional determinants of α-thalassemia von CHONG, S. S, BOEHM, C. D, HIGGS, D. R, CUTTING, G. R

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Assessing the Disease-Liability of Mutations in CFTR von Ferec, Claude, Cutting, Garry R

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ECFS standards of care on CFTR-related disorders: Diagnostic criteria of CFTR dysfunction von Sermet-Gaudelus, I., Girodon, E., Vermeulen, F., Solomon, G.M., Melotti, P., Graeber, S.Y., Bronsveld, I., Rowe, S.M., Wilschanski, M., Tümmler, B., Cutting, G.R., Gonska, T.

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Understanding the population structure of North American patients with cystic fibrosis von Li, W, Sun, L, Corey, M, Zou, F, Lee, S, Cojocaru, AL, Taylor, C, Blackman, SM, Stephenson, A, Sandford, AJ, Dorfman, R, Drumm, ML, Cutting, GR, Knowles, MR, Durie, P, Wright, FA, Strug, LJ

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Comparison of the clinical manifestations of cystic fibrosis in black and white patients von Hamosh, Ada, FitzSimmons, Stacey C., Macek, Milan, Knowles, Michael R., Rosenstein, Beryl J., Cutting, Garry R.

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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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Recommendations for the classification of diseases as CFTR-related disorders von Bombieri, C, Claustres, M, De Boeck, K, Derichs, N, Dodge, J, Girodon, E, Sermet, I, Schwarz, M, Tzetis, M, Wilschanski, M, Bareil, C, Bilton, D, Castellani, C, Cuppens, H, Cutting, G.R, Drevínek, P, Farrell, P, Elborn, J.S, Jarvi, K, Kerem, B, Kerem, E, Knowles, M, Macek, M, Munck, A, Radojkovic, D, Seia, M, Sheppard, D.N, Southern, K.W, Stuhrmann, M, Tullis, E, Zielenski, J, Pignatti, P.F, Ferec, C

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Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in allergic bronchopulmonary aspergillosis von MILLER, P. W, HAMOSH, A, MACEK, M. JR, GREENBERGER, P. A, MACLEAN, J, WALDEN, S. M, SLAVIN, R. G, CUTTING, G. R

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Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practice von Castellani, C, Cuppens, H, Macek, M, Cassiman, J.J, Kerem, E, Durie, P, Tullis, E, Assael, B.M, Bombieri, C, Brown, A, Casals, T, Claustres, M, Cutting, G.R, Dequeker, E, Dodge, J, Doull, I, Farrell, P, Ferec, C, Girodon, E, Johannesson, M, Kerem, B, Knowles, M, Munck, A, Pignatti, P.F, Radojkovic, D, Rizzotti, P, Schwarz, M, Stuhrmann, M, Tzetis, M, Zielenski, J, Elborn, J.S

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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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Modifier genetics: cystic fibrosis von Cutting, Garry R

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Both the wild type and a functional isoform of CFTR are expressed in kidney von Morales, M. M, Carroll, T. P, Morita, T, Schwiebert, E. M, Devuyst, O, Wilson, P. D, Lopes, A. G, Stanton, B. A, Dietz, H. C, Cutting, G. R, Guggino, W. B

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The Skipping of Constitutive Exons in Vivo Induced by Nonsense Mutations von Dietz, Harry C., Valle, David, Francomano, Clair A., Kendzior, Raymond J., Pyeritz, Reed E., Cutting, Garry R.

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Cystic fibrosis transmembrane conductance regulator gene mutations: do they play a role in the aetiology of allergic bronchopulmonary aspergillosis? von Eaton, T. E., Weiner Miller, P., Garrett, J. E., Cutting, G. R.

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In vivo model of adeno-associated virus vector persistence and rescue von Afione, S A, Conrad, C K, Kearns, W G, Chunduru, S, Adams, R, Reynolds, T C, Guggino, W B, Cutting, G R, Carter, B J, Flotte, T R

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