Authors:
Broughton, BC
Berneburg, M
Fawcett, H
Taylor, EM
Arlett, CF
Nardo, T
Stefanini, M
Menefee, E
Price, VH
Queille, S
Sarasin, A
Bohnert, E
Krutmann, J
Davidson, R
Kraemer, KH
Lehmann, AR
Citation: Bc. Broughton et al., Two individuals with features of both xeroderma pigmentosum and trichothiodystrophy highlight the complexity of the clinical outcomes of mutations inthe XPD gene, HUM MOL GEN, 10(22), 2001, pp. 2539-2547
Authors:
Queille, S
Drougard, C
Sarasin, A
Daya-Grosjean, L
Citation: S. Queille et al., Effects of XPD mutations on ultraviolet-induced apoptosis in relation to skin cancer-proneness in repair-deficient syndromes, J INVES DER, 117(5), 2001, pp. 1162-1170
Authors:
Bodak, N
Queille, S
Avril, MF
Bouadjar, B
Drougard, C
Sarasin, A
Daya-Grosjean, L
Citation: N. Bodak et al., High levels of patched gene mutations in basal-cell carcinomas from patients with xeroderma pigmentosum, P NAS US, 96(9), 1999, pp. 5117-5122
Authors:
Pillot, T
Drouet, B
Queille, S
Labeur, C
Vandekerckhove, J
Rosseneu, M
Pincon-Raymond, M
Chambaz, J
Citation: T. Pillot et al., The nonfibrillar amyloid beta-peptide induces apoptotic neuronal cell death: Involvement of its C-terminal fusogenic domain, J NEUROCHEM, 73(4), 1999, pp. 1626-1634