HKU Scholars Hub: Browsing DSpace

Browsing "President's Office" by Author durie, p

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 中

or enter first few letters:

Showing results 1 to 20 of 28 next >

Title	Author(s)	Issue Date
Clinical and genetic comparisons of patients with cystic fibrosis, with or without meconium ileus Journal:Journal of Pediatrics	Kerem, E Corey, M Kerem, B Durie, P Tsui, LC Levison, H	1989
Complex two-gene modulation of lung disease severity in children with cystic fibrosis Journal:Journal of Clinical Investigation	Dorfman, R Sandford, A Taylor, C Huang, B Frangolias, D Wang, Y Sang, R Pereira, L Sun, L Berthiaume, Y Tsui, LC Paré, PD Durie, P Corey, M Zielenski, J	2008
Correlation between genotype and phenotype in patients with cystic fibrosis Journal:New England Journal of Medicine	Hamosh, A Rosenstein, BJ Nash, E Curristin, SM Cutting, GR Macek Jr, M McIntosh, I Krasnicanova, H Vavrova, V Zemkova, D Keston, M Brock, DJH Corey, M Durie, P Levison, H Tsui, LC Aubin, G Simard, F Allard, C	1993
Cystic fibrosis gene mutations and infertile men with primary testicular failure Journal:Human Reproduction	Mak, V Zielenski, J Tsui, LC Durie, P Zini, A Martin, S Longley, TB Jarvi, KA	2000
Cystic fibrosis patients bearing both the common missense mutation Gly→Asp at codon 551 and the ΔF508 mutation are clinically indistinguishable from ΔF508 homozygotes, except for decreased risk of meconium ileus Journal:American Journal of Human Genetics	Hamosh, A King, TM Rosenstein, BJ Corey, M Levison, H Durie, P Tsui , LC Mcintosh, I Keston, M Brock, DJH Macek Jr, M Zemkova, D Krasnicanova, H Vavrova, V Macek Sr, M Golder, N Schwarz, MJ Super, M Watson, EK	1992
Cystic fibrosis transmembrane conductance regulator and obstructive azoospermia [21] Journal:Lancet	Jarvi, K Zielenski, J Wilschanski, M Durie, P Buckspan, M Tullis, E Markiewicz, D Tsui, LC	1995
Defining the modifiers of CF pathophysiology Proceeding/Conference:Pediatric Pulmonology	Rozmahel, R Nguyen, V Corey, M Haston, CK Kent, G Bear, C Durie, P Tsui, LC	1998
Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13 [3] Journal:Nature Genetics	Zielenski, J Corey, M Rozmahel, R Markiewicz, D Aznarez, I Casals, T Larriba, S Mercier, B Cutting, GR Krebsova, A Macek M, Jr Langfelder Schwind, E Marshall, BC DecelieGermana, J Claustres, M Palacio, A Bal, J Nowakowska, A Ferec, C Estivill, X Durie, P Tsui, LC	1999
DNA marker haplotype association with pancreatic sufficiency in cystic fibrosis Journal:American Journal of Human Genetics	Kerem, BS Buchanan, JA Durie, P Corey, ML Levison, H Rommens, JM Buchwald, M Tsui, LC	1989
Do common in silico tools predict the clinical consequences of amino-acid substitutions in the CFTR gene? Journal:Clinical Genetics	Dorfman, R Nalpathamkalam, T Taylor, C Gonska, T Keenan, K Yuan, XW Corey, M Tsui, LC Zielenski, J Durie, P	2010
Genetic determination of exocrine pancreatic function in cystic fibrosis Journal:American Journal of Human Genetics	Kristidis, P Bozon, D Corey, M Markiewicz, D Rommens, J Tsui, LC Durie, P	1992
Genotype and phenotype correlations in patients with cystic fibrosis and pancreatitis Journal:Gastroenterology	Durno, C Corey, M Zielenski, J Tullis, E Tsui, LC Durie, P	2002
Genotype and phenotype in cystic fibrosis Journal:Hospital Practice	Tsui, LC Durie, P	1997
Glucose intolerance in children with cystic fibrosis Journal:Journal of Pediatrics	Solomon, MP Wilson, DC Corey, M Kalnins, D Zielenski, J Tsui, LC Pencharz, P Durie, P Sweezey, NB	2003
Heterogeneity of reproductive tract abnormalities in men with absence of the vas deferens: Role of cystic fibrosis transmembrane conductance regulator gene mutations Journal:Fertility and Sterility	Jarvi, K McCallum, S Zielenski, J Durie, P Tullis, E Wilchanski, M Margolis, M Asch, M Ginzburg, B Martin, S Buckspan, MB Tsui, LC	1998
Higher proportion of intact exon 9 CFTR mRNA in nasal epithelium compared with vas deferens Journal:Human Molecular Genetics	Mak, V Jarvi, KA Zielenski, J Durie, P Tsui, LC	1997
Identification of mutations in exons 1 through 8 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene Journal:Genomics	Zielenski, J Bozon, D Kerem, BS Markiewicz, D Durie, P Rommens, JM Tsui, LC	1991
Identification of six mutations (R31L, 441delA, 681delC, 1461ins4, W1089R, E1104X) in the cystic fibrosis transmembrane conductance regulator (CFTR) gene Journal:Human Mutation	Zielenski, J Markiewicz, D Chen, HS Schappert, K Seller, A Durie, P Corey, M Tsui, LC	1995
In vivo measurements of ion transport in long-living CF mice Journal:Biochemical and Biophysical Research Communications	Wilschanski, MA Rozmahel, R Beharry, S Kent, G Li, C Tsui, LC Durie, P Bear, CE	1996
Incomplete rescue of cystic fibrosis transmembrane conductance regulator deficient mice by the human CFTR cDNA Journal:Human Molecular Genetics	Rozmahel, R Gyömörey, K Plyte, S Nguyen, V Wilschanski, M Durie, P Bear, CE Tsui, LC	1997

Showing results 1 to 20 of 28 next >