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N Kadhom

Showing results (11-20 of 16) with videos related to

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Cell Biology and Toxicology|August 1, 1994
Periodic fluctuations in proliferation of SV-40 transformed human skin fibroblast lines with prolonged lifespanC Wolfrom, N Raynaud, J Maigne, et al.
The Biochemical Journal|May 1, 1995
Substitution of aspartic acid for glycine at position 310 in type II collagen produces achondrogenesis II, and substitution of serine at position 805 produces hypochondrogenesis: analysis of genotype-phenotype relationshipsJ Bonaventure, L Cohen-Solal, P Ritvaniemi, et al.
Lancet (London, England)|September 6, 2000
Quinone-responsive multiple respiratory-chain dysfunction due to widespread coenzyme Q10 deficiencyA Rötig, E L Appelkvist, V Geromel, et al.
American Journal of Human Genetics|May 12, 2001
Large-scale deletion and point mutations of the nuclear NDUFV1 and NDUFS1 genes in mitochondrial complex I deficiencyP Bénit, D Chretien, N Kadhom, 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.
Molecular Genetics and Metabolism|May 15, 2001
Molecular and enzymatic characterization of a unique carnitine palmitoyltransferase 1A mutation in the Hutterite communityC Prip-Buus, L Thuillier, N Abadi, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Cell Biology and Toxicology|August 1, 1994
Periodic fluctuations in proliferation of SV-40 transformed human skin fibroblast lines with prolonged lifespanC Wolfrom, N Raynaud, J Maigne, et al.
The Biochemical Journal|May 1, 1995
Substitution of aspartic acid for glycine at position 310 in type II collagen produces achondrogenesis II, and substitution of serine at position 805 produces hypochondrogenesis: analysis of genotype-phenotype relationshipsJ Bonaventure, L Cohen-Solal, P Ritvaniemi, et al.
Lancet (London, England)|September 6, 2000
Quinone-responsive multiple respiratory-chain dysfunction due to widespread coenzyme Q10 deficiencyA Rötig, E L Appelkvist, V Geromel, et al.
American Journal of Human Genetics|May 12, 2001
Large-scale deletion and point mutations of the nuclear NDUFV1 and NDUFS1 genes in mitochondrial complex I deficiencyP Bénit, D Chretien, N Kadhom, 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.
Molecular Genetics and Metabolism|May 15, 2001
Molecular and enzymatic characterization of a unique carnitine palmitoyltransferase 1A mutation in the Hutterite communityC Prip-Buus, L Thuillier, N Abadi, et al.
Pageof 2