Authors:
Mansour, I
Delague, V
Cazeneuve, C
Dode, C
Chouery, E
Pecheux, C
Medlej-Hashim, M
Salem, N
El Zein, L
Levan-Petit, I
Lefranc, G
Goossens, M
Delpech, M
Amselem, S
Loiselet, J
Grateau, G
Megarbane, A
Naman, R
Citation: I. Mansour et al., Familial Mediterranean fever in Lebanon: mutation spectrum, evidence for cases in Maronites, Creek orthodoxes, Creek catholics, Syriacs and Chiites and for an association between amyloidosis and M694V and M6941 mutations, EUR J HUM G, 9(1), 2001, pp. 51-55
Authors:
Baghdiguian, S
Richard, I
Martin, M
Coopman, P
Beckmann, JS
Mangeat, P
Lefranc, G
Citation: S. Baghdiguian et al., Pathophysiology of limb girdle muscular dystrophy type 2A: hypothesis and new insights into the I kappa B alpha/NF-kappa B survival pathway in skeletal muscle, J MOL MED-J, 79(5-6), 2001, pp. 254-261
Authors:
Tishkoff, SA
Varkonyi, R
Cahinhinan, N
Abbes, S
Argyropoulos, G
Destro-Bisol, G
Drousiotou, A
Dangerfield, B
Lefranc, G
Loiselet, J
Piro, A
Stoneking, M
Tagarelli, A
Tagarelli, G
Touma, EH
Williams, SM
Clark, AG
Citation: Sa. Tishkoff et al., Haplotype diversity and linkage disequilibrium at human G6PD: Recent origin of alleles that confer malarial resistance, SCIENCE, 293(5529), 2001, pp. 455-462
Authors:
Sanchez-Mazas, A
Butler-Brunner, E
Butler, R
Calderon, R
Chaventre, A
Dugoujon, JM
Hammond, M
Lefranc, G
Matsumoto, H
Osipova, L
Politis, C
Pullmann, R
Langaney, A
Citation: A. Sanchez-mazas et al., A worldwide analysis of AG molecular diversity inferred from serology, HUMAN BIOL, 73(5), 2001, pp. 637-659
Authors:
Comas, D
Calafell, F
Benchemsi, N
Helal, A
Lefranc, G
Stoneking, M
Batzer, MA
Bertranpetit, J
Sajantila, A
Citation: D. Comas et al., Alu insertion polymorphisms in NW Africa and the Iberian Peninsula: evidence for a strong genetic boundary through the Gibraltar Straits, HUM GENET, 107(4), 2000, pp. 312-319
Authors:
Richard, I
Roudaut, C
Marchand, S
Baghdiguian, S
Herasse, M
Stockholm, D
Ono, Y
Suel, L
Bourg, N
Sorimachi, H
Lefranc, G
Fardeau, M
Sebille, A
Beckmann, JS
Citation: I. Richard et al., Loss of calpain 3 proteolytic activity leads to muscular dystrophy and to apoptosis-associated I kappa B alpha/nuclear factor kappa B pathway perturbation in mice, J CELL BIOL, 151(7), 2000, pp. 1583-1590
Authors:
Baghdiguian, S
Martin, M
Richard, I
Pons, F
Astier, C
Bourg, N
Hay, RT
Chemaly, R
Halaby, G
Loiselet, J
Anderson, LVB
de Munain, AL
Fardeau, M
Mangeat, P
Beckmann, JS
Lefranc, G
Citation: S. Baghdiguian et al., Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the IkBa/NF-kB pathway in limb-girdle muscular dystrophy type 2A (vol 5, pg 503, 1999), NAT MED, 5(7), 1999, pp. 849-849
Authors:
Baghdiguian, S
Martin, M
Richard, I
Pons, F
Astier, C
Bourg, N
Hay, RT
Chemaly, R
Halaby, G
Loiselet, J
Anderson, LVB
de Munain, AL
Fardeau, M
Mangeat, P
Beckmann, JS
Lefranc, G
Citation: S. Baghdiguian et al., Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the I kappa B alpha/NF-kappa B pathway in limb-girdle muscular dystrophy type 2A, NAT MED, 5(5), 1999, pp. 503-511
Authors:
Osipova, LP
Posukh, OL
Wiebe, VP
Miyazaki, T
Matsumoto, H
Lefranc, G
Lefranc, MP
Citation: Lp. Osipova et al., BamHI-SacI RFLP and Gm analysis of the immunoglobulin IGHG genes in the Northern Selkups (west Siberia): new haplotypes with deletion, duplication and triplication, HUM GENET, 105(6), 1999, pp. 530-541