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Results: 1-21 |
Results: 21
T-antigen regulated expression reduces apoptosis of Tag-transformed human myoblasts
Authors: Corti, S Salani, S Del Bo, R Torrente, Y Strazzer, S Belicchi, M Paganoni, S Li, Z Comi, GP Bresolin, N Paulin, D Scarlato, G
Citation: S. Corti et al., T-antigen regulated expression reduces apoptosis of Tag-transformed human myoblasts, CELL MOL L, 58(1), 2001, pp. 135-140
In vitro and in vivo tetracycline-controlled myogenic conversion of NIH-3T3 cells: Evidence of programmed cell death after muscle cell transplantation
Authors: Del Bo, R Torrente, Y Corti, S D'Angelo, MG Comi, GP Fagiolari, G Salani, S Cova, A Pisati, F Moggio, M Ausenda, C Scarlato, G Bresolin, N
Citation: R. Del Bo et al., In vitro and in vivo tetracycline-controlled myogenic conversion of NIH-3T3 cells: Evidence of programmed cell death after muscle cell transplantation, CELL TRANSP, 10(2), 2001, pp. 209-221
Primary beta-sarcoglycanopathy manifesting as recurrent exercise-induced myoglobinuria
Authors: Cagliani, R Comi, GP Tancredi, L Sironi, M Fortunato, F Giorda, R Bardoni, A Moggio, M Prelle, A Bresolin, N Scarlato, G
Citation: R. Cagliani et al., Primary beta-sarcoglycanopathy manifesting as recurrent exercise-induced myoglobinuria, NEUROMUSC D, 11(4), 2001, pp. 389-394
Leigh disease: Clinical, neuroradiologic, and biochemical study of three new cases with cytochrome c oxidase deficiency
Authors: Savasta, S Comi, GP Perini, MP Lupi, A Strazzer, S Rognoni, F Rossoni, R
Citation: S. Savasta et al., Leigh disease: Clinical, neuroradiologic, and biochemical study of three new cases with cytochrome c oxidase deficiency, J CHILD NEU, 16(8), 2001, pp. 608-613
beta-enolase deficiency, a new metabolic myopathy of distal glycolysis
Authors: Comi, GP Fortunato, F Lucchiari, S Bordoni, A Prelle, A Jann, S Keller, A Ciscato, P Galbiati, S Chiveri, L Torrente, Y Scarlato, G Bresolin, N
Citation: Gp. Comi et al., beta-enolase deficiency, a new metabolic myopathy of distal glycolysis, ANN NEUROL, 50(2), 2001, pp. 202-207
Down's syndrome fibroblasts anticipate the accumulation of specific ageing-related mtDNA mutations
Authors: Del Bo, R Comi, GP Perini, MP Strazzer, S Bresolin, N Scarlato, G
Citation: R. Del Bo et al., Down's syndrome fibroblasts anticipate the accumulation of specific ageing-related mtDNA mutations, ANN NEUROL, 49(1), 2001, pp. 137-138
Analysis of splicing parameters in the dystrophin gene: relevance for physiological and pathogenetic splicing mechanisms
Authors: Sironi, M Pozzoli, U Cagliani, R Comi, GP Bardoni, A Bresolin, N
Citation: M. Sironi et al., Analysis of splicing parameters in the dystrophin gene: relevance for physiological and pathogenetic splicing mechanisms, HUM GENET, 109(1), 2001, pp. 73-84
Retrospective study of patients affected of a large population with mitochondrial disorders: clinical, morphological and molecular genetic evaluation
Authors: Sciacco, M Prelle, A Comi, GP Napoli, L Battistel, A Bresolin, N Tancredi, L Lamperti, C Bordoni, A Fagiolari, G Ciscato, P Chiveri, L Perini, MP Fortunato, F Adobbati, L Messina, S Toscano, A Martinelli-Boneschi, F Papadimitriou, A Scarlato, G Moggio, M
Citation: M. Sciacco et al., Retrospective study of patients affected of a large population with mitochondrial disorders: clinical, morphological and molecular genetic evaluation, J NEUROL, 248(9), 2001, pp. 778-788
Lack of apoptosis in mitochondrial encephalomyopathies
Authors: Sciacco, M Fagiolari, G Lamperti, C Messina, S Bazzi, P Napoli, L Chiveri, L Prelle, A Comi, GP Bresolin, N Scarlato, G Moggio, M
Citation: M. Sciacco et al., Lack of apoptosis in mitochondrial encephalomyopathies, NEUROLOGY, 56(8), 2001, pp. 1070-1074
Transcriptional activation of the non-muscle, full-length dystrophin isoforms in Duchenne muscular dystrophy skeletal muscle
Authors: Sironi, M Bardoni, A Felisari, G Cagliani, R Robotti, M Comi, GP Moggio, M Bresolin, N
Citation: M. Sironi et al., Transcriptional activation of the non-muscle, full-length dystrophin isoforms in Duchenne muscular dystrophy skeletal muscle, J NEUR SCI, 186(1-2), 2001, pp. 51-57
Chemotactic factors enhance myogenic cell migration across an endothelial monolayer
Authors: Corti, S Salani, S Del Bo, R Sironi, M Strazzer, S D'Angelo, MG Comi, GP Bresolin, N Scarlato, G
Citation: S. Corti et al., Chemotactic factors enhance myogenic cell migration across an endothelial monolayer, EXP CELL RE, 268(1), 2001, pp. 36-44
Transplacental injection of somite-derived cells in mdx mouse embryos for the correction of dystrophin deficiency
Authors: Torrente, Y D'Angelo, MG Li, Z Del Bo, R Corti, S Mericskay, M DeLiso, A Fassati, A Paulin, D Comi, GP Scarlato, G Bresolin, N
Citation: Y. Torrente et al., Transplacental injection of somite-derived cells in mdx mouse embryos for the correction of dystrophin deficiency, HUM MOL GEN, 9(12), 2000, pp. 1843-1852
A sporadic, atypical case of desminopathy: morphological and immunologicalcharacterization
Authors: Prelle, A Sciacco, M Comi, GP Messina, S Carpo, M Ciscato, P Orazio, EN Fortunato, F Mora, G Bignotti, V Fagiolari, G Moggio, M Scarlato, G
Citation: A. Prelle et al., A sporadic, atypical case of desminopathy: morphological and immunologicalcharacterization, CLIN NEUR, 19(4), 2000, pp. 208-212
Role of adenine nucleotide translocator 1 in mtDNA maintenance
Authors: Kaukonen, J Juselius, JK Tiranti, V Kyttala, A Zeviani, M Comi, GP Keranen, S Peltonen, L Suomalainen, A
Citation: J. Kaukonen et al., Role of adenine nucleotide translocator 1 in mtDNA maintenance, SCIENCE, 289(5480), 2000, pp. 782-785
Loss of Dp140 dystrophin isoform and intellectual impairment in Duchenne dystrophy
Authors: Felisari, G Boneschi, FM Bardoni, A Sironi, M Comi, GP Robotti, M Turconi, AC Lai, M Corrao, G Bresolin, N
Citation: G. Felisari et al., Loss of Dp140 dystrophin isoform and intellectual impairment in Duchenne dystrophy, NEUROLOGY, 55(4), 2000, pp. 559-564
Intragenic inversion of mtDNA: A new type of pathogenic mutation in a patient with mitochondrial myopathy
Authors: Musumeci, O Andreu, AL Shanske, S Bresolin, N Comi, GP Rothstein, R Schon, EA DiMauro, S
Citation: O. Musumeci et al., Intragenic inversion of mtDNA: A new type of pathogenic mutation in a patient with mitochondrial myopathy, AM J HU GEN, 66(6), 2000, pp. 1900-1904
Extracorporeal circulation as a new experimental pathway for myoblast implantation in mdx mice
Authors: Torrente, Y D'Angelo, MG Del Bo, R DeLiso, A Casati, R Benti, R Corti, S Comi, GP Gerundini, P Anichini, A Scarlato, G Bresolin, N
Citation: Y. Torrente et al., Extracorporeal circulation as a new experimental pathway for myoblast implantation in mdx mice, CELL TRANSP, 8(3), 1999, pp. 247-258
Loss-of-function mutations of SURF-1 are specifically associated with Leigh syndrome with cytochrome c oxidase deficiency
Authors: Tiranti, V Jaksch, M Hofmann, S Galimberti, C Hoertnagel, K Lulli, L Freisinger, P Bindoff, L Gerbitz, KD Comi, GP Uziel, G Zeviani, M Meitinger, T
Citation: V. Tiranti et al., Loss-of-function mutations of SURF-1 are specifically associated with Leigh syndrome with cytochrome c oxidase deficiency, ANN NEUROL, 46(2), 1999, pp. 161-166
Novel donor splice site mutations of AGL gene in glycogen storage disease type IIIa
Authors: Hadjigeorgiou, GM Comi, GP Bordoni, A Shen, J Chen, YT Salani, S Toscano, A Fortunato, F Lucchiari, S Bresolin, N Rodolico, C Piscaglia, MG Franceschina, L Papadimitriou, A Scarlato, G
Citation: Gm. Hadjigeorgiou et al., Novel donor splice site mutations of AGL gene in glycogen storage disease type IIIa, J INH MET D, 22(6), 1999, pp. 762-763
Absence of brain Dp140 isoform and cognitive impairment in Becker musculardystrophy
Authors: Bardoni, A Sironi, M Felisari, G Comi, GP Bresolin, N
Citation: A. Bardoni et al., Absence of brain Dp140 isoform and cognitive impairment in Becker musculardystrophy, LANCET, 353(9156), 1999, pp. 897-898
A third locus predisposing to multiple deletions of mtDNA in autosomal dominant progressive external ophthalmoplegia
Authors: Kaukonen, J Zeviani, M Comi, GP Piscaglia, MG Peltonen, L Suomalainen, A
Citation: J. Kaukonen et al., A third locus predisposing to multiple deletions of mtDNA in autosomal dominant progressive external ophthalmoplegia, AM J HU GEN, 65(1), 1999, pp. 256-261
Risultati: 1-21 |