Reactome | Mootha, VK

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Mootha, VK Show undefined attributes

created	[InstanceEdit:3323020] May, B, 2013-05-09
crossReference	[DatabaseIdentifier:9942571] ORCID:0000-0001-9924-642X
dbId	3323073
displayName	Mootha, VK
firstname	Vamsi K
initial	VK
modified	[InstanceEdit:9942575] May, Bruce, 2025-03-17
orcidId	0000-0001-9924-642X
publications	[LiteratureReference:9854858] PGC-1alpha-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes [LiteratureReference:9837181] Functional genomic analysis of human mitochondrial RNA processing [LiteratureReference:8949763] MICU1 and MICU2 play nonredundant roles in the regulation of the mitochondrial calcium uniporter [LiteratureReference:8949781] MCU encodes the pore conducting mitochondrial calcium currents [LiteratureReference:3323031] Proteomic mapping of mitochondria in living cells via spatially restricted enzymatic tagging [LiteratureReference:9857790] Lipoylation is dependent on the ferredoxin FDX1 and dispensable under hypoxia in human cells [LiteratureReference:9936284] A Genome-wide CRISPR Death Screen Identifies Genes Essential for Oxidative Phosphorylation [LiteratureReference:8956338] MICU1 encodes a mitochondrial EF hand protein required for Ca(2+) uptake [LiteratureReference:5696058] Proteomic mapping of the human mitochondrial intermembrane space in live cells via ratiometric APEX tagging [LiteratureReference:9906637] FOXRED1, encoding an FAD-dependent oxidoreductase complex-I-specific molecular chaperone, is mutated in infantile-onset mitochondrial encephalopathy [LiteratureReference:8949218] Integrative genomics identifies MCU as an essential component of the mitochondrial calcium uniporter [LiteratureReference:8956341] EMRE is an essential component of the mitochondrial calcium uniporter complex [LiteratureReference:8949167] MICU2, a paralog of MICU1, resides within the mitochondrial uniporter complex to regulate calcium handling [LiteratureReference:5432420] Mutations in MTFMT underlie a human disorder of formylation causing impaired mitochondrial translation
schemaClass	Person
surname	Mootha

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