Neuronal degeneration and mitochondrial dysfunction

[21] Recruitment and activation of caspase-8 by the Huntingtin-interacting protein Hip-1 and a novel partners Hippi [J]. NATURE CELL BIOLOGY, 2002, 4 (02) : 95 - 105

[22] Hereditary spastic paraplegia SPG13 is associated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60 [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 70 (05) : 1328 - 1332

[23] Apoptosis is suspended in muscle of mitochondrial encephalomyopathies [J]. ACTA NEUROPATHOLOGICA, 2002, 103 (06) : 531 - 540

[24] EVIDENCE FOR IMPAIRMENT OF ENERGY-METABOLISM IN-VIVO IN HUNTINGTONS-DISEASE USING LOCALIZED H-1-NMR SPECTROSCOPY [J]. NEUROLOGY, 1993, 43 (12) : 2689 - 2695

[25] A novel X-linked gene, DDP, shows mutations in families with deafness (DFN-1), dystonia, mental deficiency and blindness [J]. NATURE GENETICS, 1996, 14 (02) : 177 - 180

[26] Neuroprotective effects of creatine in a transgenic animal model of amyotrophic lateral sclerosis [J]. NATURE MEDICINE, 1999, 5 (03) : 347 - 350

[27] Kong JM, 1998, J NEUROSCI, V18, P3241

[28] Energy metabolism defects in Huntington's disease and effects of coenzyme Q(10) [J]. ANNALS OF NEUROLOGY, 1997, 41 (02) : 160 - 165

[29] ARC, an inhibitor of apoptosis expressed in skeletal muscle and heart that interacts selectively with caspases [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (09) : 5156 - 5160

[30] Mitochondrial control of cell death [J]. NATURE MEDICINE, 2000, 6 (05) : 513 - 519

[21] Recruitment and activation of caspase-8 by the Huntingtin-interacting protein Hip-1 and a novel partners Hippi [J]. NATURE CELL BIOLOGY, 2002, 4 (02) : 95 - 105

[22] Hereditary spastic paraplegia SPG13 is associated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60 [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 70 (05) : 1328 - 1332

[23] Apoptosis is suspended in muscle of mitochondrial encephalomyopathies [J]. ACTA NEUROPATHOLOGICA, 2002, 103 (06) : 531 - 540

[24] EVIDENCE FOR IMPAIRMENT OF ENERGY-METABOLISM IN-VIVO IN HUNTINGTONS-DISEASE USING LOCALIZED H-1-NMR SPECTROSCOPY [J]. NEUROLOGY, 1993, 43 (12) : 2689 - 2695

[25] A novel X-linked gene, DDP, shows mutations in families with deafness (DFN-1), dystonia, mental deficiency and blindness [J]. NATURE GENETICS, 1996, 14 (02) : 177 - 180

[26] Neuroprotective effects of creatine in a transgenic animal model of amyotrophic lateral sclerosis [J]. NATURE MEDICINE, 1999, 5 (03) : 347 - 350

[27] Kong JM, 1998, J NEUROSCI, V18, P3241

[28] Energy metabolism defects in Huntington's disease and effects of coenzyme Q(10) [J]. ANNALS OF NEUROLOGY, 1997, 41 (02) : 160 - 165

[29] ARC, an inhibitor of apoptosis expressed in skeletal muscle and heart that interacts selectively with caspases [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (09) : 5156 - 5160

[30] Mitochondrial control of cell death [J]. NATURE MEDICINE, 2000, 6 (05) : 513 - 519