Hepatitis, Drug-Induced
|
0.300 |
Biomarker
|
disease |
CTD_human |
Characteristic molecular and proteomic signatures of drug-induced liver injury in a rat model.
|
25231249 |
2015 |
Mammary Neoplasms
|
0.300 |
Biomarker
|
group |
CTD_human |
An integrative approach to identify YB-1-interacting proteins required for cisplatin resistance in MCF7 and MDA-MB-231 breast cancer cells.
|
21466612 |
2011 |
Leigh Syndrome Due To Mitochondrial Complex II Deficiency
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndrome.
|
14729820 |
2004 |
Leigh Syndrome Due To Mitochondrial Complex II Deficiency
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Mutation screening of 75 candidate genes in 152 complex I deficiency cases identifies pathogenic variants in 16 genes including NDUFB9.
|
22200994 |
2012 |
Leigh Syndrome Due To Mitochondrial Complex II Deficiency
|
0.300 |
Biomarker
|
disease |
CLINGEN |
cDNA of eight nuclear encoded subunits of NADH:ubiquinone oxidoreductase: human complex I cDNA characterization completed.
|
9878551 |
1998 |
Leigh Syndrome Due To Mitochondrial Complex II Deficiency
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Mitochondrial NDUFS3 regulates the ROS-mediated onset of metabolic switch in transformed cells.
|
23519235 |
2013 |
Leigh Syndrome Due To Mitochondrial Complex II Deficiency
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Granzyme A cleaves a mitochondrial complex I protein to initiate caspase-independent cell death.
|
18485875 |
2008 |
Leigh Syndrome Due To Mitochondrial Complex II Deficiency
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Regulation of Mitochondrial Complex I Biogenesis in Drosophila Flight Muscles.
|
28683319 |
2017 |
Leigh Syndrome Due To Mitochondrial Complex II Deficiency
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Subunits of mitochondrial complex I exist as part of matrix- and membrane-associated subcomplexes in living cells.
|
18826940 |
2008 |
Leigh Syndrome Due To Mitochondrial Complex II Deficiency
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Early complex I assembly defects result in rapid turnover of the ND1 subunit.
|
22653752 |
2012 |
Leigh Syndrome Due To Mitochondrial Complex II Deficiency
|
0.300 |
Biomarker
|
disease |
CLINGEN |
A Novel NDUFS3 mutation in a Chinese patient with severe Leigh syndrome.
|
30140060 |
2018 |
Leigh Syndrome Due To Mitochondrial Complex II Deficiency
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Progressive loss of dopaminergic neurons in the ventral midbrain of adult mice heterozygote for Engrailed1.
|
17267560 |
2007 |
Leigh Syndrome due to Mitochondrial Complex III Deficiency
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Progressive loss of dopaminergic neurons in the ventral midbrain of adult mice heterozygote for Engrailed1.
|
17267560 |
2007 |
Leigh Syndrome due to Mitochondrial Complex III Deficiency
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Early complex I assembly defects result in rapid turnover of the ND1 subunit.
|
22653752 |
2012 |
Leigh Syndrome due to Mitochondrial Complex III Deficiency
|
0.300 |
Biomarker
|
disease |
CLINGEN |
cDNA of eight nuclear encoded subunits of NADH:ubiquinone oxidoreductase: human complex I cDNA characterization completed.
|
9878551 |
1998 |
Leigh Syndrome due to Mitochondrial Complex III Deficiency
|
0.300 |
Biomarker
|
disease |
CLINGEN |
A Novel NDUFS3 mutation in a Chinese patient with severe Leigh syndrome.
|
30140060 |
2018 |
Leigh Syndrome due to Mitochondrial Complex III Deficiency
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Regulation of Mitochondrial Complex I Biogenesis in Drosophila Flight Muscles.
|
28683319 |
2017 |
Leigh Syndrome due to Mitochondrial Complex III Deficiency
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Mitochondrial NDUFS3 regulates the ROS-mediated onset of metabolic switch in transformed cells.
|
23519235 |
2013 |
Leigh Syndrome due to Mitochondrial Complex III Deficiency
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndrome.
|
14729820 |
2004 |
Leigh Syndrome due to Mitochondrial Complex III Deficiency
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Mutation screening of 75 candidate genes in 152 complex I deficiency cases identifies pathogenic variants in 16 genes including NDUFB9.
|
22200994 |
2012 |
Leigh Syndrome due to Mitochondrial Complex III Deficiency
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Granzyme A cleaves a mitochondrial complex I protein to initiate caspase-independent cell death.
|
18485875 |
2008 |
Leigh Syndrome due to Mitochondrial Complex III Deficiency
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Subunits of mitochondrial complex I exist as part of matrix- and membrane-associated subcomplexes in living cells.
|
18826940 |
2008 |
Leigh Syndrome due to Mitochondrial Complex IV Deficiency
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndrome.
|
14729820 |
2004 |
Leigh Syndrome due to Mitochondrial Complex IV Deficiency
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Mutation screening of 75 candidate genes in 152 complex I deficiency cases identifies pathogenic variants in 16 genes including NDUFB9.
|
22200994 |
2012 |
Leigh Syndrome due to Mitochondrial Complex IV Deficiency
|
0.300 |
Biomarker
|
disease |
CLINGEN |
A Novel NDUFS3 mutation in a Chinese patient with severe Leigh syndrome.
|
30140060 |
2018 |