Search research articles
Contact Us
Filters
Showing results (1-10 of 14) with videos related to
Page
of 2
Sort By:
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 15, 1992
Purification of electron transfer flavoprotein from pig liver mitochondria and its application to the diagnosis of deficiencies of acyl-CoA dehydrogenases in human fibroblasts
C Bertrand, R Dumoulin, P Divry, et al.
Molecular & General Genetics : MGG
|
November 27, 1996
Accumulation of mitochondrial DNA deletions in myotubes cultured from muscles of patients with mitochondrial myopathies
J M Collombet, G Mandon, R Dumoulin, et al.
Molecular and Cellular Probes
|
October 1, 1996
A novel gly290asp mitochondrial cytochrome b mutation linked to a complex III deficiency in progressive exercise intolerance
R Dumoulin, I Sagnol, T Ferlin, et al.
Molecular and Cellular Biochemistry
|
October 6, 1997
Detection of mitochondrial DNA deletions by a screening procedure using the polymerase chain reaction
T Ferlin, G Guironnet, M C Barnoux, et al.
The Journal of Pediatrics
|
November 5, 1997
Segregation of the G8993 mutant mitochondrial DNA through generations and embryonic tissues in a family at risk of Leigh syndrome
T Ferlin, P Landrieu, C Rambaud, et al.
Acta Neuropathologica
|
January 1, 1996
Molecular histology of mitochondrial and nuclear transcripts in the muscle of patients harbouring a single mitochondrial DNA deletion
H Carrier, B Burt-Pichat, F Flocard, et al.
Neuromuscular Disorders : NMD
|
September 1, 1993
Cardiac transplantation in an incomplete Kearns-Sayre syndrome with mitochondrial DNA deletion
C Tranchant, B Mousson, M Mohr, et al.
Molecular and Cellular Biochemistry
|
March 1, 1997
Expression of oxidative phosphorylation genes in muscle cell cultures from patients with mitochondrial myopathies
J M Collombet, H Faure-Vigny, G Mandon, et al.
Molecular and Cellular Probes
|
June 1, 1995
Fine mapping of randomly distributed multiple deletions of mitochondrial DNA in a case of chronic progressive external ophthalmoplegia
T Ville-Ferlin, R Dumoulin, G Stepien, et al.
Pediatrie
|
December 1, 1984
[Cysteamine in the treatment of cystinosis in children. In vitro and in vivo studies]
J J Louis, P Guibaud, R Dumoulin, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 15, 1992
Purification of electron transfer flavoprotein from pig liver mitochondria and its application to the diagnosis of deficiencies of acyl-CoA dehydrogenases in human fibroblasts
C Bertrand, R Dumoulin, P Divry, et al.
Molecular & General Genetics : MGG
|
November 27, 1996
Accumulation of mitochondrial DNA deletions in myotubes cultured from muscles of patients with mitochondrial myopathies
J M Collombet, G Mandon, R Dumoulin, et al.
Molecular and Cellular Probes
|
October 1, 1996
A novel gly290asp mitochondrial cytochrome b mutation linked to a complex III deficiency in progressive exercise intolerance
R Dumoulin, I Sagnol, T Ferlin, et al.
Molecular and Cellular Biochemistry
|
October 6, 1997
Detection of mitochondrial DNA deletions by a screening procedure using the polymerase chain reaction
T Ferlin, G Guironnet, M C Barnoux, et al.
The Journal of Pediatrics
|
November 5, 1997
Segregation of the G8993 mutant mitochondrial DNA through generations and embryonic tissues in a family at risk of Leigh syndrome
T Ferlin, P Landrieu, C Rambaud, et al.
Acta Neuropathologica
|
January 1, 1996
Molecular histology of mitochondrial and nuclear transcripts in the muscle of patients harbouring a single mitochondrial DNA deletion
H Carrier, B Burt-Pichat, F Flocard, et al.
Neuromuscular Disorders : NMD
|
September 1, 1993
Cardiac transplantation in an incomplete Kearns-Sayre syndrome with mitochondrial DNA deletion
C Tranchant, B Mousson, M Mohr, et al.
Molecular and Cellular Biochemistry
|
March 1, 1997
Expression of oxidative phosphorylation genes in muscle cell cultures from patients with mitochondrial myopathies
J M Collombet, H Faure-Vigny, G Mandon, et al.
Molecular and Cellular Probes
|
June 1, 1995
Fine mapping of randomly distributed multiple deletions of mitochondrial DNA in a case of chronic progressive external ophthalmoplegia
T Ville-Ferlin, R Dumoulin, G Stepien, et al.
Pediatrie
|
December 1, 1984
[Cysteamine in the treatment of cystinosis in children. In vitro and in vivo studies]
J J Louis, P Guibaud, R Dumoulin, et al.
Page
of 2