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G Hofhaus

Showing results (11-20 of 25) with videos related to

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Nucleic Acids Research|June 15, 1997
Comprehensive, rapid and sensitive detection of sequence variants of human mitochondrial tRNA genesY Michikawa, G Hofhaus, L S Lerman, et al.
European Journal of Biochemistry|December 16, 1998
MtDNA mutations associated with sideroblastic anaemia cause a defect of mitochondrial cytochrome c oxidaseS Bröker, B Meunier, P Rich, et al.
European Journal of Cell Biology|June 29, 1999
Highly divergent amino termini of the homologous human ALR and yeast scERV1 gene products define species specific differences in cellular localizationG Hofhaus, G Stein, L Polimeno, et al.
The Journal of Biological Chemistry|May 31, 1996
Respiration and growth defects in transmitochondrial cell lines carrying the 11778 mutation associated with Leber's hereditary optic neuropathyG Hofhaus, D R Johns, O Hurko, et al.
The Journal of Biological Chemistry|April 21, 2001
Yeast ERV2p is the first microsomal FAD-linked sulfhydryl oxidase of the Erv1p/Alrp protein familyJ Gerber, U Mühlenhoff, G Hofhaus, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|May 11, 2001
Mammalian augmenter of liver regeneration protein is a sulfhydryl oxidaseT Lisowsky, J E Lee, L Polimeno, et al.
Biological Chemistry|September 24, 1999
Role of mitochondria in Parkinson diseaseS Kösel, G Hofhaus, A Maassen, et al.
FEBS Letters|June 4, 1990
The same domain motif for ubiquinone reduction in mitochondrial or chloroplast NADH dehydrogenase and bacterial glucose dehydrogenaseT Friedrich, M Strohdeicher, G Hofhaus, et al.
The EMBO Journal|May 1, 1989
Identification and electron microscopic analysis of a chaperonin oligomer from Neurospora crassa mitochondriaE G Hutchinson, W Tichelaar, G Hofhaus, et al.
Cell Death & Disease|February 26, 2016
cBid, Bax and Bcl-xL exhibit opposite membrane remodeling activitiesS Bleicken, G Hofhaus, B Ugarte-Uribe, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Nucleic Acids Research|June 15, 1997
Comprehensive, rapid and sensitive detection of sequence variants of human mitochondrial tRNA genesY Michikawa, G Hofhaus, L S Lerman, et al.
European Journal of Biochemistry|December 16, 1998
MtDNA mutations associated with sideroblastic anaemia cause a defect of mitochondrial cytochrome c oxidaseS Bröker, B Meunier, P Rich, et al.
European Journal of Cell Biology|June 29, 1999
Highly divergent amino termini of the homologous human ALR and yeast scERV1 gene products define species specific differences in cellular localizationG Hofhaus, G Stein, L Polimeno, et al.
The Journal of Biological Chemistry|May 31, 1996
Respiration and growth defects in transmitochondrial cell lines carrying the 11778 mutation associated with Leber's hereditary optic neuropathyG Hofhaus, D R Johns, O Hurko, et al.
The Journal of Biological Chemistry|April 21, 2001
Yeast ERV2p is the first microsomal FAD-linked sulfhydryl oxidase of the Erv1p/Alrp protein familyJ Gerber, U Mühlenhoff, G Hofhaus, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|May 11, 2001
Mammalian augmenter of liver regeneration protein is a sulfhydryl oxidaseT Lisowsky, J E Lee, L Polimeno, et al.
Biological Chemistry|September 24, 1999
Role of mitochondria in Parkinson diseaseS Kösel, G Hofhaus, A Maassen, et al.
FEBS Letters|June 4, 1990
The same domain motif for ubiquinone reduction in mitochondrial or chloroplast NADH dehydrogenase and bacterial glucose dehydrogenaseT Friedrich, M Strohdeicher, G Hofhaus, et al.
The EMBO Journal|May 1, 1989
Identification and electron microscopic analysis of a chaperonin oligomer from Neurospora crassa mitochondriaE G Hutchinson, W Tichelaar, G Hofhaus, et al.
Cell Death & Disease|February 26, 2016
cBid, Bax and Bcl-xL exhibit opposite membrane remodeling activitiesS Bleicken, G Hofhaus, B Ugarte-Uribe, et al.
Pageof 3