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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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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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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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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Genotype and Phenotype in Cystic Fibrosis von Zielenski, Julian

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Cystic fibrosis modifier genes related to Pseudomonas aeruginosa infection von Park, J E, Yung, R, Stefanowicz, D, Shumansky, K, Akhabir, L, Durie, P R, Corey, M, Zielenski, J, Dorfman, R, Daley, D, Sandford, A J

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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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Exon skipping through the creation of a putative exonic splicing silencer as a consequence of the cystic fibrosis mutation R553X von Aznarez, Isabel, Zielenski, Julian, Rommens, Johanna M, Blencowe, Benjamin J, Tsui, Lap-Chee

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Genetic Modifiers of Lung Disease in Cystic Fibrosis von Drumm, Mitchell L, Konstan, Michael W, Schluchter, Mark D, Handler, Allison, Pace, Rhonda, Zou, Fei, Zariwala, Maimoona, Fargo, David, Xu, Airong, Dunn, John M, Darrah, Rebecca J, Dorfman, Ruslan, Sandford, Andrew J, Corey, Mary, Zielenski, Julian, Durie, Peter, Goddard, Katrina, Yankaskas, James R, Wright, Fred A, Knowles, Michael R

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Identification of Mutations in Regions Corresponding to the Two Putative Nucleotide (ATP)-Binding Folds of the Cystic Fibrosis Gene von Kerem, Bat-sheva, Zielenski, Julian, Markiewicz, Danuta, Bozon, Dominique, Gazit, Ephraim, Yahav, Jacob, Kennedy, Dara, Riordan, John R., Collins, Francis S., Rommens, Johanna M., Tsui, Lap-Chee

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Prostaglandin-endoperoxide synthase genes COX1 and COX2 - novel modifiers of disease severity in cystic fibrosis patients von Czerska, K, Sobczynska-Tomaszewska, A, Sands, D, Nowakowska, A, Bak, D, Wertheim, K, Poznanski, J, Zielenski, J, Norek, A, Bal, J

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Higher Proportion of Intact Exon 9 CFTR mRNA in Nasal Epithelium Compared with Vas Deferens von Mak, Victor, Jarvi, Keith A., Zielenski, Julian, Durie, Peter, Tsui, Lap-Chee

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The prevalence and clinical characteristics of cystic fibrosis in South Asian Canadian immigrants von Mei-Zahav, M, Durie, P, Zielenski, J, Solomon, M, Tullis, E, Tsui, L-C, Corey, M

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12 The relation between meconium ileus prevalence score and functional severity of CFTR mutations von Gonska, T, Keenan, K, Dorfman, R, Taylor, C, Sun, L, Ooi, C.Y, Zielenski, J, Corey, M, Rommens, J, Strug, L, Durie, P

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CF diagnosis algorithms: challenging dogma von Ooi, C.Y, Durie, P.R, Gonska, T, Dupuis, A, Ellis, L, Martin, S, Jarvi, K, Schibli, S, Zielenski, J, Tullis, E

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A novel paradigm for attributing the diagnosis of CF disease von Ooi, C.Y, Tullis, E, Dupuis, A, Gonska, T, Ellis, L, Martin, S, Schibli, S, Jarvi, K, Zielenski, J, Durie, P.R

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Genotype and phenotype correlations in patients with cystic fibrosis and pancreatitis von Durno, Carol, Corey, Mary, Zielenski, Julian, Tullis, Elizabeth, Tsui, Lap-Chee, Durie, Peter

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Clinical Manifestations of Cystic Fibrosis Among Patients With Diagnosis in Adulthood von Gilljam, Marita, Ellis, Lynda, Corey, Mary, Zielenski, Julian, Durie, Peter, Tullis, D. Elizabeth

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COX2 as a protective modifier of CF pulmonary disease severity von Czerska, K, Sobczynska-Tomaszewska, A, Sands, D, Nowakowska, A, Wertheim, K, Bak, D, Zielenski, J, Bai, J

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Prostaglandin-endoperoxide synthase genesCOX1 andCOX2 — novel modifiers of disease severity in cystic fibrosis patients von Czerska, K., Sobczyńska-Tomaszewska, A., Sands, D., Nowakowska, A., Bąk, D., Wertheim, K., Poznański, J., Zielenski, J., Norek, A., Bal, J.

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