|
Browning, Kirsteen N; Mendelowitz, David (2003) Musings on the wanderer: what's new in our understanding of vago-vagal reflexes?: II. Integration of afferent signaling from the viscera by the nodose ganglia. Am J Physiol Gastrointest Liver Physiol 284:G8-14
|
|
Orozco, L; Zielenski, J; Markiewicz, D et al. (1997) Two novel frameshift deletions (1924del7, 2055del9-->A) in the CFTR gene in Mexican cystic fibrosis patients. Hum Mutat 10:239-40
|
|
Morral, N; Dork, T; Llevadot, R et al. (1996) Haplotype analysis of 94 cystic fibrosis mutations with seven polymorphic CFTR DNA markers. Hum Mutat 8:149-59
|
|
Zielenski, J; Markiewicz, D; Lin, S P et al. (1995) Skipping of exon 12 as a consequence of a point mutation (1898 + 5G-->T) in the cystic fibrosis transmembrane conductance regulator gene found in a consanguineous Chinese family. Clin Genet 47:125-32
|
|
Zielenski, J; Markiewicz, D; Chen, H S et al. (1995) Identification of six mutations (R31L, 441delA, 681delC, 1461ins4, W1089R, E1104X) in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. Hum Mutat 5:43-7
|
|
Jarvi, K; Zielenski, J; Wilschanski, M et al. (1995) Cystic fibrosis transmembrane conductance regulator and obstructive azoospermia. Lancet 345:1578
|
|
Bozon, D; Zielenski, J; Rininsland, F et al. (1994) Identification of four new mutations in the cystic fibrosis transmembrane conductance regulator gene: I148T, L1077P, Y1092X, 2183AA-->G. Hum Mutat 3:330-2
|
|
Zielenski, J; Bozon, D; Markiewicz, D et al. (1993) Analysis of CFTR transcripts in nasal epithelial cells and lymphoblasts of a cystic fibrosis patient with 621 + 1G-->T and 711 + 1G-->T mutations. Hum Mol Genet 2:683-7
|
|
Tsui, L C (1992) Mutations and sequence variations detected in the cystic fibrosis transmembrane conductance regulator (CFTR) gene: a report from the Cystic Fibrosis Genetic Analysis Consortium. Hum Mutat 1:197-203
|
|
Mornet, E; Chateau, C; Simon-Bouy, B et al. (1992) Carrier detection and prenatal diagnosis of cystic fibrosis using an intragenic TA-repeat polymorphism. Hum Genet 88:479-81
|
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