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NDUFB6 gene

Known as: NADH-UBIQUINONE OXIDOREDUCTASE 1 BETA SUBCOMPLEX, 6, CI, NDUFB6 
National Institutes of Health

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NDUFB7 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Porcine epidemic diarrhea virus infection blocks cell cycle and induces apoptosis in pig intestinal epithelial cells
2019
2019
Pathogenic variants in NUBPL result in failure to assemble the matrix arm of complex I and cause a complex leukoencephalopathy with thalamic involvement.
2015
2015
Gene expression analysis of plasmablastic lymphoma identifies downregulation of B-cell receptor signaling and additional unique transcriptional programs
Gene expression analysis of plasmablastic lymphoma identifies downregulation of B-cell receptor signaling and additional unique… 
Highly Cited
2013
Highly Cited
2013
Pioglitazone leads to an inactivation and disassembly of complex I of the mitochondrial respiratory chain
BackgroundThiazolidinediones are antidiabetic agents that increase insulin sensitivity but reduce glucose oxidation, state 3… 
2011
2011
The NDUFB6 subunit of the mitochondrial respiratory chain complex I is required for electron transfer activity: a proof of principle study on stable and controlled RNA interference in human cell…
2011
2011
Defective mitochondrial translation differently affects the live cell dynamics of complex I subunits.
Highly Cited
2010
Highly Cited
2010
Weight gain induced by an isocaloric pair-fed high fat diet: a nutriepigenetic study on FASN and NDUFB6 gene promoters.
Highly Cited
2009
Highly Cited
2009
Short-Term Exercise Training Does Not Stimulate Skeletal Muscle ATP Synthesis in Relatives of Humans With Type 2 Diabetes
OBJECTIVE We tested the hypothesis that short-term exercise training improves hereditary insulin resistance by stimulating ATP… 
Highly Cited
2008
Highly Cited
2008
Subunits of Mitochondrial Complex I Exist as Part of Matrix- and Membrane-associated Subcomplexes in Living Cells*
Mitochondrial complex I (CI) is a large assembly of 45 different subunits, and defects in its biogenesis are the most frequent… 
Highly Cited
2003
Highly Cited
2003
Clinical and genetic heterogeneity in chromosome 9p associated hereditary inclusion body myopathy: exclusion of GNE and three other candidate genes
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