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Results: 1-7 |
Results: 7

Authors: Bykhovskaya, Y Yang, HY Taylor, K Hang, T Tun, RYM Estivill, X Casano, RAMS Majamaa, K Shohat, M Fischel-Ghodsian, N
Citation: Y. Bykhovskaya et al., Modifier locus for mitochondrial DNA disease: Linkage and linkage disequilibrium mapping of a nuclear modifier gene for maternally inherited deafness, GENET MED, 3(3), 2001, pp. 177-180

Authors: Johnson, KR Zheng, QY Bykhovskaya, Y Spirina, O Fischel-Ghodsian, N
Citation: Kr. Johnson et al., A nuclear-mitochondrial DNA interaction affecting hearing impairment in mice, NAT GENET, 27(2), 2001, pp. 191-194

Authors: Spirina, O Bykhovskaya, Y Kajava, AV O'Brien, TW Nierlich, DP Mougey, EB Sylvester, JE Graack, HR Wittmann-Liebold, B Fischel-Ghodsian, N
Citation: O. Spirina et al., Heart-specific splice-variant of a human mitochondrial ribosomal protein (mRNA processing; tissue specific splicing), GENE, 261(2), 2000, pp. 229-234

Authors: Chen, XG Bykhovskaya, Y Tidow, N Hamon, M Bercovitz, Z Spirina, O Fischel-Ghodsian, N
Citation: Xg. Chen et al., The Familial Mediterranean Fever protein interacts and colocalizes with a putative Golgi transporter, P SOC EXP M, 224(1), 2000, pp. 32-40

Authors: Bykhovskaya, Y Estivill, X Taylor, K Hang, T Hamon, M Casano, RAMS Yang, HY Rotter, JI Shohat, M Fischel-Ghodsian, N
Citation: Y. Bykhovskaya et al., Candidate locus for a nuclear modifier gene for maternally inherited deafness, AM J HU GEN, 66(6), 2000, pp. 1905-1910

Authors: Casano, RAMS Johnson, DF Bykhovskaya, Y Torricelli, F Bigozzi, M Fischel-Ghodsian, N
Citation: Rams. Casano et al., Inherited susceptibility to aminoglycoside ototoxicity: Genetic heterogeneity and clinical implications, AM J OTOLAR, 20(3), 1999, pp. 151-156

Authors: Friedman, RA Bykhovskaya, Y Sue, CM DiMauro, S Bradley, R Fallis-Cunningham, R Paradies, N Pensak, ML Smith, RJ Groden, J Li, XYC Fischel-Ghodsian, N
Citation: Ra. Friedman et al., Maternally inherited nonsyndromic hearing loss, AM J MED G, 84(4), 1999, pp. 369-372
Risultati: 1-7 |