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Results: 1-6 |
Results: 6

Authors: Santucci-Darmanin, S Vidal, F Scimeca, JC Turc-Carel, C Paquis-Flucklinger, V
Citation: S. Santucci-darmanin et al., Family of SRY/Sox proteins is involved in the regulation of the mouse Msh4(MutS Homolog 4) gene expression, MOL REPROD, 60(2), 2001, pp. 172-180

Authors: Guillausseau, PJ Massin, P Dubois-LaForgue, D Timsit, J Virally, M Gin, H Bertin, E Blickle, JF Bouhanick, B Cahen, J Caillat-Zucman, S Charpentier, G Chedin, P Derrien, C Ducluzeau, PH Grimaldi, A Guerci, B Kaloustian, E Murat, A Olivier, F Paques, M Paquis-Flucklinger, V Porokhov, B Samuel-Lajeunesse, J Vialettes, B
Citation: Pj. Guillausseau et al., Maternally inherited diabetes and deafness: A multicenter study, ANN INT MED, 134(9), 2001, pp. 721-728

Authors: Paul, R Desnuelle, C Pouget, J Pellissier, JF Richelme, C Monfort, MF Butori, C Saunieres, A Paquis-Flucklinger, V
Citation: R. Paul et al., Importance of searching for associated mitochondrial DNA alterations in patients with multiple deletions, EUR J HUM G, 8(5), 2000, pp. 331-338

Authors: Santucci-Darmanin, S Walpita, D Lespinasse, F Desnuelle, C Ashley, T Paquis-Flucklinger, V
Citation: S. Santucci-darmanin et al., MSH4 acts in conjunction with MLH1 during mammalian meiosis, FASEB J, 14(11), 2000, pp. 1539-1547

Authors: Perucca-Lostanlen, D Narbonne, H Hernandez, JB Staccini, P Saunieres, A Paquis-Flucklinger, V Vialettes, B Desnuelle, C
Citation: D. Perucca-lostanlen et al., Mitochondrial DNA variations in patients with maternally inherited diabetes and deafness syndrome, BIOC BIOP R, 277(3), 2000, pp. 771-775

Authors: Santucci-Darmanin, S Paul, R Michiels, JF Saunieres, A Desnuelle, C Paquis-Flucklinger, V
Citation: S. Santucci-darmanin et al., Alternative splicing of hMSH4: two isoforms in testis and abnormal transcripts in somatic tissues, MAMM GENOME, 10(4), 1999, pp. 423-427
Risultati: 1-6 |