Jean-Claude Kaplan

Dystrophinopathy caused by mid-intronic substitutions activating cryptic exons in the DMD gene

Christophe Béroud, Alain Carrié, Chérif Beldjord et al. · Neuromuscular Disorders · 2003 · 59 citations

Life Sciences, Genetics, Molecular Genetics +11

Absence of γ‐sarcoglycan (35 DAG) in autosomal recessive muscular dystrophy linked to chromosome 13q12

Daniel Jung, France Leturcq, Yoshihide Sunada et al. · FEBS Letters · 1996 · 53 citations

Medicine, Genetics, Molecular Biology +13

A T to G mutation in the polypyrimidine tract of the second intron of the human β-globin gene reduces<i>in vitro</i>splicing efficiency: evidence for an increased hnRNP C interaction

Pascale Sébillon, Chérif Beldjord, Jean-Claude Kaplan et al. · Nucleic Acids Research · 1995 · 29 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Three novel sequence variations in the 5? upstream region of the cystic fibrosis transmembrane conductance regulator (CFTR) gene: two polymorphisms and one putative molecular defect

Thierry Bienvenu, Virginie Penard‐Lacronique, Michel Raymondjean et al. · Human Genetics · 1995 · 23 citations

Life Sciences, Genetics, Molecular Genetics +10

Illegitimate (or ectopic) transcription proceeds through the usual promoters

Jamel Chelly, Jean-Philippe Hugnot, Jean‐Paul Concordet et al. · Biochemical and Biophysical Research Communications · 1991 · 23 citations

Life Sciences, Genetics, Molecular Biology +14