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Human Molecular Genetics|July 1, 1993
Microsatellite haplotypes for cystic fibrosis: mutation frameworks and evolutionary tracersN Morral, V Nunes, T Casals, et al.Diabetes Research and Clinical Practice|April 27, 2001
Hepatic insulin expression improves glycemic control in type 1 diabetic ratsH Dong, N Morral, R McEvoy, et al.American Journal of Human Genetics|November 1, 1994
Independent origins of cystic fibrosis mutations R334W, R347P, R1162X, and 3849 + 10kbC-->T provide evidence of mutation recurrence in the CFTR geneN Morral, R Llevadot, T Casals, et al.Human Genetics|January 1, 1992
Dinucleotide (CA/GT) repeat polymorphism in intron 17B of the cystic fibrosis transmembrane conductance regulator (CFTR) geneN Morral, E Girbau, J Zielenski, et al.Human Genetics|March 1, 1993
Cystic fibrosis in Spain: high frequency of mutation G542X in the Mediterranean coastal areaT Casals, V Nunes, A Palacio, et al.Medicina Clinica|March 31, 1990
[Use of the polymerase chain reaction technic in the genetic analysis of cystic fibrosis]M Chillón, T Casals, F J Giménez, et al.Human Genetics|April 1, 1994
Analysis of the CFTR gene confirms the high genetic heterogeneity of the Spanish population: 43 mutations account for only 78% of CF chromosomesM Chillón, T Casals, J Giménez, et al.Human Genetics|February 1, 1994
Cystic fibrosis in a low-incidence population: two major mutations in FinlandJ Kere, X Estivill, M Chillón, et al.Molecular Medicine (Cambridge, Mass.)|August 31, 2000
Toxicity associated with repeated administration of first-generation adenovirus vectors does not occur with a helper-dependent vectorW K O'Neal, H Zhou, N Morral, et al.Genomics|May 1, 1991
The search for south European cystic fibrosis mutations: identification of two new mutations, four variants, and intronic sequencesP Gasparini, V Nunes, A Savoia, et al.Pageof 3