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Journal of Pharmaceutical and Biomedical Analysis|April 1, 1995
Capillary electrophoretic analysis of DNA restriction fragments and PCR products for polymorphism and mutation studies in cystic fibrosis and Gaucher's diseaseC Bory, C Chantin, D BozonHuman Mutation|April 21, 2005
Identification and characterization of three large deletions and a deletion/polymorphism in the CFTR geneF Chevalier-Porst, G Souche, D BozonThe Biochemical Journal|August 15, 1997
Characterization of iduronate sulphatase mutants affecting N-glycosylation sites and the cysteine-84 residueG Millat, R Froissart, I Maire, et al.Experimental Cell Research|February 1, 1997
IDS transfer from overexpressing cells to IDS-deficient cellsG Millat, R Froissart, I Maire, et al.Human Mutation|June 22, 2000
Identification of 5 novel mutations in the AGXT geneO Basmaison, M O Rolland, P Cochat, et al.Archives of Biochemistry and Biophysics|September 1, 1986
Characterization of cellular oligosaccharides from normal and cystic fibrotic fibroblasts using sequential endoglycosidase digestionsD Bozon, A L Tarentino, R B Trimble, et al.The Biochemical Journal|July 15, 1995
Processing of iduronate 2-sulphatase in human fibroblastsR Froissart, G Millat, M Mathieu, et al.Biochimica Et Biophysica Acta|September 29, 1999
The 2.1-, 5.4- and 5.7-kb transcripts of the IDS gene are generated by different polyadenylation signalsS Cudry, R Froissart, O Bouton, et al.Journal of Medical Genetics|February 1, 1997
Germline and somatic mosaicism in a female carrier of Hunter diseaseR Froissart, I Maire, V Bonnet, et al.Human Mutation|January 1, 1996
IDS gene-pseudogene exchange responsible for an intragenic deletion in a Hunter patientA M Birot, O Bouton, R Froissart, et al.Pageof 4