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P Rustin

Showing results (141-150 of 157) with videos related to

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Nature Genetics|January 23, 1999
Dilated cardiomyopathy and atrioventricular conduction blocks induced by heart-specific inactivation of mitochondrial DNA gene expressionJ Wang, H Wilhelmsson, C Graff, et al.
British Journal of Cancer|October 27, 2004
Investigation of the role of SDHB inactivation in sporadic phaeochromocytoma and neuroblastomaD Astuti, M Morris, C Krona, et al.
Cell Death and Differentiation|March 1, 2008
The molecular archaeology of a mitochondrial death effector: AIF in DrosophilaN Joza, K Galindo, J A Pospisilik, et al.
Molecular Biology of the Cell|May 4, 2000
Branched chain amino acids induce apoptosis in neural cells without mitochondrial membrane depolarization or cytochrome c release: implications for neurological impairment associated with maple syrup urine diseaseP Jouvet, P Rustin, D L Taylor, et al.
Journal of Medical Genetics|March 8, 2003
The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiencyM Chol, S Lebon, P Bénit, et al.
Lancet (London, England)|October 6, 1999
Persistent mitochondrial dysfunction and perinatal exposure to antiretroviral nucleoside analoguesS Blanche, M Tardieu, P Rustin, et al.
Journal of Inherited Metabolic Disease|April 5, 2001
Sequence variations in the NDUFA1 gene encoding a subunit of complex I of the respiratory chainI Wittig, P Augstein, G K Brown, et al.
Archives of Disease in Childhood|January 24, 2006
Wide clinical variability among 13 new Cockayne syndrome cases confirmed by biochemical assaysL Pasquier, V Laugel, L Lazaro, et al.
Prenatal Diagnosis|August 9, 2001
Prenatal diagnosis of respiratory chain deficiency by direct mutation screeningJ Amiel, N Gigarel, A Benacki, et al.
Nature Genetics|August 31, 2001
A mutant mitochondrial respiratory chain assembly protein causes complex III deficiency in patients with tubulopathy, encephalopathy and liver failureP de Lonlay, I Valnot, A Barrientos, et al.
Pageof 16

Showing results (141-150 of 157) with videos related to

Sort By:
Pageof 16
Nature Genetics|January 23, 1999
Dilated cardiomyopathy and atrioventricular conduction blocks induced by heart-specific inactivation of mitochondrial DNA gene expressionJ Wang, H Wilhelmsson, C Graff, et al.
British Journal of Cancer|October 27, 2004
Investigation of the role of SDHB inactivation in sporadic phaeochromocytoma and neuroblastomaD Astuti, M Morris, C Krona, et al.
Cell Death and Differentiation|March 1, 2008
The molecular archaeology of a mitochondrial death effector: AIF in DrosophilaN Joza, K Galindo, J A Pospisilik, et al.
Molecular Biology of the Cell|May 4, 2000
Branched chain amino acids induce apoptosis in neural cells without mitochondrial membrane depolarization or cytochrome c release: implications for neurological impairment associated with maple syrup urine diseaseP Jouvet, P Rustin, D L Taylor, et al.
Journal of Medical Genetics|March 8, 2003
The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiencyM Chol, S Lebon, P Bénit, et al.
Lancet (London, England)|October 6, 1999
Persistent mitochondrial dysfunction and perinatal exposure to antiretroviral nucleoside analoguesS Blanche, M Tardieu, P Rustin, et al.
Journal of Inherited Metabolic Disease|April 5, 2001
Sequence variations in the NDUFA1 gene encoding a subunit of complex I of the respiratory chainI Wittig, P Augstein, G K Brown, et al.
Archives of Disease in Childhood|January 24, 2006
Wide clinical variability among 13 new Cockayne syndrome cases confirmed by biochemical assaysL Pasquier, V Laugel, L Lazaro, et al.
Prenatal Diagnosis|August 9, 2001
Prenatal diagnosis of respiratory chain deficiency by direct mutation screeningJ Amiel, N Gigarel, A Benacki, et al.
Nature Genetics|August 31, 2001
A mutant mitochondrial respiratory chain assembly protein causes complex III deficiency in patients with tubulopathy, encephalopathy and liver failureP de Lonlay, I Valnot, A Barrientos, et al.
Pageof 16