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Results: 1-17 |
Results: 17
'CFTR-opathies': disease phenotypes associated with cystic fibrosis transmembrane regulator gene mutations
Authors: Noone, PG Knowles, MR
Citation: Pg. Noone et Mr. Knowles, 'CFTR-opathies': disease phenotypes associated with cystic fibrosis transmembrane regulator gene mutations, RESPIR RES, 2(6), 2001, pp. 328-332
A modified technique for measurement of nasal transepithelial potential difference in infants
Authors: Southern, KW Noone, PG Bosworth, DG LeGrys, VA Knowles, MR Barker, PM
Citation: Kw. Southern et al., A modified technique for measurement of nasal transepithelial potential difference in infants, J PEDIAT, 139(3), 2001, pp. 353-358
Cystic fibrosis gene mutations and pancreatitis risk: Relation to epithelial ion transport and trypsin inhibitor gene mutations
Authors: Noone, PG Zhou, ZQ Silverman, LM Jowell, PS Knowles, MR Cohn, JA
Citation: Pg. Noone et al., Cystic fibrosis gene mutations and pancreatitis risk: Relation to epithelial ion transport and trypsin inhibitor gene mutations, GASTROENTY, 121(6), 2001, pp. 1310-1319
Interpretation of CF gene therapy trial results - Reply
Authors: Noone, PG Knowles, MR
Citation: Pg. Noone et Mr. Knowles, Interpretation of CF gene therapy trial results - Reply, MOL THER, 2(1), 2000, pp. 4-4
Safety and biological efficacy of a lipid-CFTR complex for gene transfer in the nasal epithelium of adult patients with cystic fibrosis
Authors: Noone, PG Hohneker, KW Zhou, ZQ Johnson, LG Foy, C Gipson, C Jones, K Noah, TL Leigh, MW Schwartzbach, C Efthimiou, J Pearlman, R Boucher, RC Knowles, MR
Citation: Pg. Noone et al., Safety and biological efficacy of a lipid-CFTR complex for gene transfer in the nasal epithelium of adult patients with cystic fibrosis, MOL THER, 1(1), 2000, pp. 105-114
Basal nucleotide levels, release, and metabolism in normal and cystic fibrosis airways
Authors: Donaldson, SH Lazarowski, ER Picher, M Knowles, MR Stutts, MJ Boucher, RC
Citation: Sh. Donaldson et al., Basal nucleotide levels, release, and metabolism in normal and cystic fibrosis airways, MOL MED, 6(11), 2000, pp. 969-982
Lung disease associated with the IVS8 5T allele of the CFTR gene
Authors: Noone, PG Pue, CA Zhou, ZQ Friedman, KJ Wakeling, EL Ganeshananthan, M Simon, RH Silverman, LM Knowles, MR
Citation: Pg. Noone et al., Lung disease associated with the IVS8 5T allele of the CFTR gene, AM J R CRIT, 162(5), 2000, pp. 1919-1924
Effect of aerosolized uridine-5 '-triphosphate on airway clearance with cough in patients with primary ciliary dyskinesia
Authors: Noone, PG Bennett, WD Regnis, JA Zeman, KL Carson, JL King, M Boucher, RC Knowles, MR
Citation: Pg. Noone et al., Effect of aerosolized uridine-5 '-triphosphate on airway clearance with cough in patients with primary ciliary dyskinesia, AM J R CRIT, 160(1), 1999, pp. 144-149
Pharmaceutical dry powder aerosols: Correlation of powder properties with dose delivery and implications for pharmacodynamic effect
Authors: Concessio, NM VanOort, MM Knowles, MR Hickey, AJ
Citation: Nm. Concessio et al., Pharmaceutical dry powder aerosols: Correlation of powder properties with dose delivery and implications for pharmacodynamic effect, PHARM RES, 16(6), 1999, pp. 828-834
Discordant organ laterality in monozygotic twins with primary ciliary dyskinesia
Authors: Noone, PG Bali, D Carson, JL Sannuti, A Gipson, CL Ostrowski, LE Bromberg, PA Boucher, RC Knowles, MR
Citation: Pg. Noone et al., Discordant organ laterality in monozygotic twins with primary ciliary dyskinesia, AM J MED G, 82(2), 1999, pp. 155-160
Molecular differentiation of Renibacterium salmoninarum isolates from worldwide locations
Authors: Grayson, TH Cooper, LF Atienzar, FA Knowles, MR Gilpin, ML
Citation: Th. Grayson et al., Molecular differentiation of Renibacterium salmoninarum isolates from worldwide locations, APPL ENVIR, 65(3), 1999, pp. 961-968
Pulmonary epithelial sodium-channel dysfunction and excess airway liquid in pseudohypoaldosteronism
Authors: Kerem, E Bistritzer, T Hanukoglu, A Hofmann, T Zhou, ZQ Bennett, W MacLaughlin, E Barker, P Nash, M Quittell, L Boucher, R Knowles, MR
Citation: E. Kerem et al., Pulmonary epithelial sodium-channel dysfunction and excess airway liquid in pseudohypoaldosteronism, N ENG J MED, 341(3), 1999, pp. 156-162
Mutations of the cystic fibrosis gene and pancreatitis - Reply
Authors: Cohn, JA Silverman, LM Knowles, MR
Citation: Ja. Cohn et al., Mutations of the cystic fibrosis gene and pancreatitis - Reply, N ENG J MED, 340(3), 1999, pp. 239-239
Correction of aberrant splicing of the cystic fibrosis transmembrane conductance regulator (CFTR) gene by antisense oligonucleotides
Authors: Friedman, KJ Kole, J Cohn, JA Knowles, MR Silverman, LM Kole, R
Citation: Kj. Friedman et al., Correction of aberrant splicing of the cystic fibrosis transmembrane conductance regulator (CFTR) gene by antisense oligonucleotides, J BIOL CHEM, 274(51), 1999, pp. 36193-36199
Genetics, diagnosis, and clinical phenotype
Authors: Knowles, MR Friedman, KJ Silverman, LM
Citation: Mr. Knowles et al., Genetics, diagnosis, and clinical phenotype, CYSTIC FIBROSIS IN ADULTS, 1999, pp. 27-42
Standard therapy of cystic fibrosis lung disease
Authors: Noone, PG Knowles, MR
Citation: Pg. Noone et Mr. Knowles, Standard therapy of cystic fibrosis lung disease, CYSTIC FIBROSIS IN ADULTS, 1999, pp. 145-173
New therapeutic strategies for cystic fibrosis lung disease
Authors: Johnson, LG Knowles, MR
Citation: Lg. Johnson et Mr. Knowles, New therapeutic strategies for cystic fibrosis lung disease, CYSTIC FIBROSIS IN ADULTS, 1999, pp. 233-258
Risultati: 1-17 |