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F Degoul

Showing results (1-10 of 27) with videos related to

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Biochemical and Biophysical Research Communications|December 14, 1990
Identification of point mutations by mispairing PCR as exemplified in MERRF diseaseP Seibel, F Degoul, N Romero, et al.
British Journal of Pharmacology|August 21, 2007
Alkylation of prohibitin by cyclohexylphenyl-chloroethyl urea on an aspartyl residue is associated with cell cycle G(1) arrest in B16 cellsB Bouchon, J Papon, Y Communal, et al.
Annals of Neurology|March 1, 1994
Myo-leukoencephalopathy in twins: study of 3243-myopathy, encephalopathy, lactic acidosis, and strokelike episodes mitochondrial DNA mutationF Degoul, M Diry, A Pou-Serradell, et al.
Neuropediatrics|August 1, 1992
Kearns-Sayre syndrome with sideroblastic anemia: molecular investigationsI Nelson, G Bonne, F Degoul, et al.
Physica Medica : PM : an International Journal Devoted to the Applications of Physics to Medicine and Biology : Official Journal of the Italian Association of Biomedical Physics (AIFB)|August 3, 2021
CPOP: An open source C++ cell POPulation modeler for radiation biology applicationsL Maigne, A Delsol, G Fois, et al.
Nucleic Acids Research|May 30, 1998
The presence of modified nucleotides is required for cloverleaf folding of a human mitochondrial tRNAM Helm, H Brulé, F Degoul, et al.
Journal of the Neurological Sciences|July 1, 1992
Uneven distribution of mitochondrial DNA mutation in MERRF dizygotic twinsI Penisson-Besnier, F Degoul, C Desnuelle, et al.
Human Molecular Genetics|April 18, 1998
Isoleucylation properties of native human mitochondrial tRNAIle and tRNAIle transcripts. Implications for cardiomyopathy-related point mutations (4269, 4317) in the tRNAIle geneF Degoul, H Brulé, C Cepanec, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Clinical, biochemical, and molecular analysis of a maternally inherited case of Leigh syndrome (MILS) associated with the mtDNA T8993G point mutationF Degoul, M Diry, D Rodriguez, et al.
Annals of Neurology|June 1, 1991
Zidovudine myopathy: a distinctive disorder associated with mitochondrial dysfunctionC Mhiri, M Baudrimont, G Bonne, et al.
Pageof 3

Showing results (1-10 of 27) with videos related to

Sort By:
Pageof 3
Biochemical and Biophysical Research Communications|December 14, 1990
Identification of point mutations by mispairing PCR as exemplified in MERRF diseaseP Seibel, F Degoul, N Romero, et al.
British Journal of Pharmacology|August 21, 2007
Alkylation of prohibitin by cyclohexylphenyl-chloroethyl urea on an aspartyl residue is associated with cell cycle G(1) arrest in B16 cellsB Bouchon, J Papon, Y Communal, et al.
Annals of Neurology|March 1, 1994
Myo-leukoencephalopathy in twins: study of 3243-myopathy, encephalopathy, lactic acidosis, and strokelike episodes mitochondrial DNA mutationF Degoul, M Diry, A Pou-Serradell, et al.
Neuropediatrics|August 1, 1992
Kearns-Sayre syndrome with sideroblastic anemia: molecular investigationsI Nelson, G Bonne, F Degoul, et al.
Physica Medica : PM : an International Journal Devoted to the Applications of Physics to Medicine and Biology : Official Journal of the Italian Association of Biomedical Physics (AIFB)|August 3, 2021
CPOP: An open source C++ cell POPulation modeler for radiation biology applicationsL Maigne, A Delsol, G Fois, et al.
Nucleic Acids Research|May 30, 1998
The presence of modified nucleotides is required for cloverleaf folding of a human mitochondrial tRNAM Helm, H Brulé, F Degoul, et al.
Journal of the Neurological Sciences|July 1, 1992
Uneven distribution of mitochondrial DNA mutation in MERRF dizygotic twinsI Penisson-Besnier, F Degoul, C Desnuelle, et al.
Human Molecular Genetics|April 18, 1998
Isoleucylation properties of native human mitochondrial tRNAIle and tRNAIle transcripts. Implications for cardiomyopathy-related point mutations (4269, 4317) in the tRNAIle geneF Degoul, H Brulé, C Cepanec, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Clinical, biochemical, and molecular analysis of a maternally inherited case of Leigh syndrome (MILS) associated with the mtDNA T8993G point mutationF Degoul, M Diry, D Rodriguez, et al.
Annals of Neurology|June 1, 1991
Zidovudine myopathy: a distinctive disorder associated with mitochondrial dysfunctionC Mhiri, M Baudrimont, G Bonne, et al.
Pageof 3