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Journal of Neurology, Neurosurgery, and Psychiatry
|
December 20, 2005
Leigh syndrome caused by mutations in the flavoprotein (Fp) subunit of succinate dehydrogenase (SDHA)
R Horváth, A Abicht, E Holinski-Feder, et al.
The Journal of Biological Chemistry
|
November 14, 2000
The external calcium-dependent NADPH dehydrogenase from Neurospora crassa mitochondria
A M Melo, M Duarte, I M Møller, et al.
Nucleic Acids Research
|
December 10, 1998
MITOP: database for mitochondria-related proteins, genes and diseases
C Scharfe, P Zaccaria, K Hoertnagel, et al.
Neuropediatrics
|
June 24, 2010
Leigh disease with brainstem involvement in complex I deficiency due to assembly factor NDUFAF2 defect
M Herzer, J Koch, H Prokisch, et al.
Nucleic Acids Research
|
December 11, 1999
MITOP, the mitochondrial proteome database: 2000 update
C Scharfe, P Zaccaria, K Hoertnagel, et al.
Biochemical and Biophysical Research Communications
|
October 15, 2008
Mitochondrial 12S rRNA susceptibility mutations in aminoglycoside-associated and idiopathic bilateral vestibulopathy
M Elstner, C Schmidt, V C Zingler, et al.
Genes, Brain, and Behavior
|
December 31, 2009
DJ-1-deficient mice show less TH-positive neurons in the ventral tegmental area and exhibit non-motoric behavioural impairments
T T Pham, F Giesert, A Röthig, et al.
Journal of Medical Genetics
|
November 25, 2011
Defective NDUFA9 as a novel cause of neonatally fatal complex I disease
B J C van den Bosch, M Gerards, W Sluiter, et al.
Allergy
|
March 26, 2014
A common atopy-associated variant in the Th2 cytokine locus control region impacts transcriptional regulation and alters SMAD3 and SP1 binding
A Kretschmer, G Möller, H Lee, et al.
Molecular Psychiatry
|
November 16, 2016
A DNA methylation biomarker of alcohol consumption
C Liu, R E Marioni, Å K Hedman, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 20) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 20 results.
Journal of Neurology, Neurosurgery, and Psychiatry
|
December 20, 2005
Leigh syndrome caused by mutations in the flavoprotein (Fp) subunit of succinate dehydrogenase (SDHA)
R Horváth, A Abicht, E Holinski-Feder, et al.
The Journal of Biological Chemistry
|
November 14, 2000
The external calcium-dependent NADPH dehydrogenase from Neurospora crassa mitochondria
A M Melo, M Duarte, I M Møller, et al.
Nucleic Acids Research
|
December 10, 1998
MITOP: database for mitochondria-related proteins, genes and diseases
C Scharfe, P Zaccaria, K Hoertnagel, et al.
Neuropediatrics
|
June 24, 2010
Leigh disease with brainstem involvement in complex I deficiency due to assembly factor NDUFAF2 defect
M Herzer, J Koch, H Prokisch, et al.
Nucleic Acids Research
|
December 11, 1999
MITOP, the mitochondrial proteome database: 2000 update
C Scharfe, P Zaccaria, K Hoertnagel, et al.
Biochemical and Biophysical Research Communications
|
October 15, 2008
Mitochondrial 12S rRNA susceptibility mutations in aminoglycoside-associated and idiopathic bilateral vestibulopathy
M Elstner, C Schmidt, V C Zingler, et al.
Genes, Brain, and Behavior
|
December 31, 2009
DJ-1-deficient mice show less TH-positive neurons in the ventral tegmental area and exhibit non-motoric behavioural impairments
T T Pham, F Giesert, A Röthig, et al.
Journal of Medical Genetics
|
November 25, 2011
Defective NDUFA9 as a novel cause of neonatally fatal complex I disease
B J C van den Bosch, M Gerards, W Sluiter, et al.
Allergy
|
March 26, 2014
A common atopy-associated variant in the Th2 cytokine locus control region impacts transcriptional regulation and alters SMAD3 and SP1 binding
A Kretschmer, G Möller, H Lee, et al.
Molecular Psychiatry
|
November 16, 2016
A DNA methylation biomarker of alcohol consumption
C Liu, R E Marioni, Å K Hedman, et al.
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of 2