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M F Bauer

Showing results (21-30 of 28) with videos related to

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Journal of Inherited Metabolic Disease|August 7, 2001
Detection of neonatal argininosuccinate lyase deficiency by serum tandem mass spectrometryS Stadler, K Gempel, I Bieger, et al.
European Journal of Pediatrics|October 5, 2001
"Adult" form of muscular carnitine palmitoyltransferase II deficiency: manifestation in a 2-year-old childK Gempel, C von Praun, J Baumkötter, et al.
FEBS Letters|December 28, 1999
The mitochondrial TIM22 preprotein translocase is highly conserved throughout the eukaryotic kingdomM F Bauer, U Rothbauer, N Mühlenbein, et al.
The Journal of Biological Chemistry|August 8, 2001
Role of the deafness dystonia peptide 1 (DDP1) in import of human Tim23 into the inner membrane of mitochondriaU Rothbauer, S Hofmann, N Mühlenbein, et al.
Cell|June 1, 2000
Tim23 links the inner and outer mitochondrial membranesM Donzeau, K Káldi, A Adam, et al.
Journal of Molecular Biology|May 26, 1999
Genetic and structural characterization of the human mitochondrial inner membrane translocaseM F Bauer, K Gempel, A S Reichert, et al.
Journal of Inherited Metabolic Disease|May 10, 2002
Screening for carnitine palmitoyltransferase II deficiency by tandem mass spectrometryK Gempel, S Kiechl, S Hofmann, et al.
European Journal of Pediatrics|November 14, 2015
A novel mutation in BCS1L associated with deafness, tubulopathy, growth retardation and microcephalyC B Jackson, M F Bauer, A Schaller, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Journal of Inherited Metabolic Disease|August 7, 2001
Detection of neonatal argininosuccinate lyase deficiency by serum tandem mass spectrometryS Stadler, K Gempel, I Bieger, et al.
European Journal of Pediatrics|October 5, 2001
"Adult" form of muscular carnitine palmitoyltransferase II deficiency: manifestation in a 2-year-old childK Gempel, C von Praun, J Baumkötter, et al.
FEBS Letters|December 28, 1999
The mitochondrial TIM22 preprotein translocase is highly conserved throughout the eukaryotic kingdomM F Bauer, U Rothbauer, N Mühlenbein, et al.
The Journal of Biological Chemistry|August 8, 2001
Role of the deafness dystonia peptide 1 (DDP1) in import of human Tim23 into the inner membrane of mitochondriaU Rothbauer, S Hofmann, N Mühlenbein, et al.
Cell|June 1, 2000
Tim23 links the inner and outer mitochondrial membranesM Donzeau, K Káldi, A Adam, et al.
Journal of Molecular Biology|May 26, 1999
Genetic and structural characterization of the human mitochondrial inner membrane translocaseM F Bauer, K Gempel, A S Reichert, et al.
Journal of Inherited Metabolic Disease|May 10, 2002
Screening for carnitine palmitoyltransferase II deficiency by tandem mass spectrometryK Gempel, S Kiechl, S Hofmann, et al.
European Journal of Pediatrics|November 14, 2015
A novel mutation in BCS1L associated with deafness, tubulopathy, growth retardation and microcephalyC B Jackson, M F Bauer, A Schaller, et al.
Pageof 3