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P Seibel

Showing results (11-20 of 49) 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.
Neuromuscular Disorders : NMD|July 1, 1995
Sarcoid myopathy and mitochondrial respiratory chain defects: clinicopathological, biochemical and molecular biological analysesH Reichmann, B Schalke, P Seibel, et al.
European Journal of Biochemistry|November 1, 1993
Expression of human cytochrome c oxidase subunits during fetal developmentG Bonne, P Seibel, S Possekel, et al.
Journal of Neurology|April 1, 1996
Investigation on the mitochondrial transfer RNA(Leu)(UUR) in blood cells from patients with cluster headacheP Seibel, T Grünewald, A Gundolla, et al.
American Journal of Medical Genetics|April 24, 1996
VACTERL with the mitochondrial np 3243 point mutationM S Damian, P Seibel, W Schachenmayr, et al.
Journal of Personality Assessment|January 1, 1990
Further evidence concerning motivational distortion on the Sixteen Personality Factor primaries by male felonsH P Seibel, F H Wallbrown, E K Reuter, et al.
Archives of Oral Biology|February 13, 2001
Differential expression of myosin heavy-chain mRNA in muscles of mastication during functional advancement of the mandible in pigsT Gedrange, O Luck, G Hesske, et al.
Nucleic Acids Research|January 11, 1995
Transfection of mitochondria: strategy towards a gene therapy of mitochondrial DNA diseasesP Seibel, J Trappe, G Villani, et al.
Virchows Archiv : an International Journal of Pathology|December 31, 1998
Immunohistochemical detection of human mtDNA polymerase gamma and of human mitochondrial transcription factor A in cytochrome-c-oxidase-deficient oxyphil cells of hyperfunctional parathyroidsJ Müller-Höcker, S Schäfer, W C Copeland, et al.
Biochemical and Biophysical Research Communications|October 28, 1994
Chronic progressive external ophthalmoplegia is associated with a novel mutation in the mitochondrial tRNA(Asn) geneP Seibel, J Lauber, T Klopstock, et al.
Pageof 5

Showing results (11-20 of 49) with videos related to

Sort By:
Pageof 5
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.
Neuromuscular Disorders : NMD|July 1, 1995
Sarcoid myopathy and mitochondrial respiratory chain defects: clinicopathological, biochemical and molecular biological analysesH Reichmann, B Schalke, P Seibel, et al.
European Journal of Biochemistry|November 1, 1993
Expression of human cytochrome c oxidase subunits during fetal developmentG Bonne, P Seibel, S Possekel, et al.
Journal of Neurology|April 1, 1996
Investigation on the mitochondrial transfer RNA(Leu)(UUR) in blood cells from patients with cluster headacheP Seibel, T Grünewald, A Gundolla, et al.
American Journal of Medical Genetics|April 24, 1996
VACTERL with the mitochondrial np 3243 point mutationM S Damian, P Seibel, W Schachenmayr, et al.
Journal of Personality Assessment|January 1, 1990
Further evidence concerning motivational distortion on the Sixteen Personality Factor primaries by male felonsH P Seibel, F H Wallbrown, E K Reuter, et al.
Archives of Oral Biology|February 13, 2001
Differential expression of myosin heavy-chain mRNA in muscles of mastication during functional advancement of the mandible in pigsT Gedrange, O Luck, G Hesske, et al.
Nucleic Acids Research|January 11, 1995
Transfection of mitochondria: strategy towards a gene therapy of mitochondrial DNA diseasesP Seibel, J Trappe, G Villani, et al.
Virchows Archiv : an International Journal of Pathology|December 31, 1998
Immunohistochemical detection of human mtDNA polymerase gamma and of human mitochondrial transcription factor A in cytochrome-c-oxidase-deficient oxyphil cells of hyperfunctional parathyroidsJ Müller-Höcker, S Schäfer, W C Copeland, et al.
Biochemical and Biophysical Research Communications|October 28, 1994
Chronic progressive external ophthalmoplegia is associated with a novel mutation in the mitochondrial tRNA(Asn) geneP Seibel, J Lauber, T Klopstock, et al.
Pageof 5