4
results
for author:"Cure S."
in Literature Citations
| An autosomal-recessive form of cutis laxa is due to homozygous elastin mutations, and the phenotype may be modified by a heterozygous fibulin 5 polymorphism. Megarbane H., Florence J., Oliver Sass J., Schwonbeck S., Foglio M., de Cid R., Cure S., Saker S., Megarbane A., Fischer J. J. Invest. Dermatol. 129:1650-1655(2009) · Mapped (15) |
| Novel mutations in the gene encoding secreted lymphocyte antigen-6/urokinase-type plasminogen activator receptor-related protein-1 (SLURP-1) and description of five ancestral haplotypes in patients with Mal de Meleda. Marrakchi S., Audebert S., Bouadjar B., Has C., Lefevre C., Munro C., Cure S., Jobard F., Morlot S., Hohl D. et al. J. Invest. Dermatol. 120:351-355(2003) · Mapped (1) |
| The DNA sequence and analysis of human chromosome 14. Heilig R., Eckenberg R., Petit J.-L., Fonknechten N., Da Silva C., Cattolico L., Levy M., Barbe V., De Berardinis V., Ureta-Vidal A. et al. Nature 421:601-607(2003) · UniProtKB (542) |
| Novel point mutations, deletions, and polymorphisms in the cathepsin C gene in nine families from Europe and North Africa with Papillon-Lefevre syndrome. Lefevre C., Blanchet-Bardon C., Jobard F., Bouadjar B., Stalder J.-F., Cure S., Hoffmann A., Prud'Homme J.-F., Fischer J. J. Invest. Dermatol. 117:1657-1661(2001) · UniProtKB (1) |
