Nduf

Differential expression of the Atp5 Cox6 or Nduf family genes

| Accessory subunits NDUFA6, NDUFAB1-α, NDUFB9, and NDUFAB1-β in ...

Accessory subunits NDUFA6 NDUFAB1 NDUFB9 and NDUFAB1 in

Electron leak from NDUFA13 within mitochondrial complex I attenuates

Structural insights into respiratory complex I deficiency and assembly

Emerging Roles of NDUFS8 Located in Mitochondrial Complex I in

Molecular docking of NDUFV3L isoform at mitochondrial complex I A

Structural insights into respiratory complex I deficiency and assembly

Nature CommunicationsNDUFS4

Low abundance of NDUFV2 and NDUFS4 subunits of the hydrophilic complex

Accessory subunits NDUFA6 NDUFAB1 NDUFB9 and NDUFAB1 in

NDUFS3 depletion permits complex I maturation and reveals TMEM126AOPA7

Nduf21 Cys366 mediates complex I ROS induced increase in locomotion a

nduf7et19 is a partial lossoffunction allele of the nduf7 gene

CMTR1 RNA methyltransferase mutations activate widespread expression

Accessory subunits NDUFV3 and NDUFA2 NDUFV3S short isoform

Mammalian Mitochondrial Complex I Structure and DiseaseCausing

NDUFAF5 Hydroxylates NDUFS7 at an Early Stage in the Assembly of Human

Mitochondrial Complex I Plays an Essential Role in Human Respirasome

Ndufs2 a Core Subunit of Mitochondrial Complex I Is Essential for

Accessory Subunits of the Matrix Arm of Mitochondrial Complex I with a

NDUFS6 gene Semantic Scholar

Mitochondrial respiratory chain component NDUFA4 a promising

Identification of Mitochondrial Complex I Assembly Intermediates by

Induction of the Mitochondrial NDUFA4L2 Protein by HIF-1α Decreases ...

Induction of the Mitochondrial NDUFA4L2 Protein by HIF1 Decreases

The patient had mitochondrial complex I deficiency resulted from a

Dissecting the concordant and disparate roles of NDUFAF3 and NDUFAF4 in

Insights into complex I assembly Function of NDUFAF1 and a link with

NDUFS6 mutations are a novel cause of lethal neonatal mitochondrial

nduf7et19 mutant worms are resistant to statins and have activated

Hypoxia and intracomplex genetic suppressors rescue complex I mutants

Protein Nmyristoylation plays a critical role in the mitochondrial

Systematic analysis of NDUFAF6 in complex I assembly and mitochondrial

Accessory subunit NDUFB4 participates in mitochondrial complex I

Systematic analysis of NDUFAF6 in complex I assembly and mitochondrial

Genetic diversity of NDUFV1dependent mitochondrial complex I

Accessory subunit NDUFB4 participates in mitochondrial complex I

Hypoxia and intracomplex genetic suppressors rescue complex I mutants

JCI NDUFS6 mutations are a novel cause of lethal neonatal

Full article Knockdown of NDUFAF6 inhibits breast cancer progression

Systematic analysis of NDUFAF6 in complex I assembly and mitochondrial

Phenotypic Heterogeneity in Patients with Mutations in the

Nduf21 Cys366 effects on hypoxic signaling a Complex I ROS requires

overview of the structure of mouse complex I The 14 core subunits

Figure S1 a Human NDUFA11 subunit darker grey on Complex I light

NDUFAF7 is a soluble mitochondrial protein A Analysis of NDUFAF7

The National Defense University Foundation Names James Schmeling JD

Figure S6 Effect of NDUF11 knockdown on the total and average crista

LargeScale Deletion and Point Mutations of the Nuclear NDUFV1 and

Insights into complex I assembly Function of NDUFAF1 and a link with

Analysis of Human Mutations in the Supernumerary Subunits of Complex I

NDUFAF5 Hydroxylates NDUFS7 at an Early Stage in the Assembly of Human

Studies on Hypoxic Pulmonary Vasoconstriction Detect a Novel Role for

nduf7et19 mutant worms are resistant to statins and have activated

Human mitochondrial complex I assembly is mediated by NDUFAF1 Vogel

LargeScale Deletion and Point Mutations of the Nuclear NDUFV1 and

Identification of Mitochondrial Complex I Assembly Intermediates by

Mitochondrial targeting of human NADH dehydrogenase ubiquinone

NDUFAF5 Hydroxylates NDUFS7 at an Early Stage in the Assembly of Human

Sites of residues in human NDUFS8 and bacterial subunit I of Complex I

Proteomic and Metabolomic Analyses of Mitochondrial Complex Ideficient

Neuroimaging in complex 1 deficiency mutation proven NDUFV2

NDUFAF5 Hydroxylates NDUFS7 at an Early Stage in the Assembly of Human

Hypoxia and intracomplex genetic suppressors rescue complex I mutants

mRNA levels of NDUFV1 NDUFV2 and NDUFS1 subunits of complex I in post

An Overview of Mitochondrial Protein Defects in Neuromuscular Diseases

Mitochondrial complex I activity promotes antigen crosspresentation in

Accessory subunit NDUFB4 participates in mitochondrial complex I

Subunitspecific Incorporation Efficiency and Kinetics in Mitochondrial

New MTND6 and NDUFA1 mutations in mitochondrial respiratory chain

Tissuespecific splicing of an Ndufs6 genetrap insertion generates a

Mitochondrial gene expression ETC function and aging towards

The role of NDUFB3 overexpression in mitochondrial respiration and

Dissecting the Roles of Mitochondrial Complex I Intermediate Assembly

Genetic diversity of NDUFV1dependent mitochondrial complex I

Inherited complex I deficiency is associated with faster protein

NDUFA9 point mutations cause a variable mitochondrial complex I

Human mitochondrial complex I assembly is mediated by NDUFAF1 Vogel

Subunit NDUFV3 is present in two distinct isoforms in mammalian complex

Mitochondrial respiratory chain component NDUFA4 a promising

Mitochondrial Protein Interaction Mapping Identifies Regulators of

Figure 1 from A Mutation in Caenorhabditis elegans NDUF7 Activates the

NDUFAF7 Methylates Arginine 85 in the NDUFS2 Subunit of Human Complex I

Accessory subunits NDUFA6 NDUFAB1 NDUFB9 and NDUFAB1 in

Induction of the Mitochondrial NDUFA4L2 Protein by HIF1 Decreases

Loss of mitochondrial DNAencoded protein ND1 results in disruption of

NDUFA4 Is a Subunit of Complex IV of the Mammalian Electron Transport

Identification of Mitochondrial Complex I Assembly Intermediates by

Human mitochondrial complex I assembly is mediated by NDUFAF1 Vogel

NDUFA13 NADHubiquinone oxidoreductase subunit A13

Figure 11 from Novel mutations in the NDUFS1 gene cause low residual

Frontiers A Novel Variation in the Mitochondrial Complex I Assembly

Mitochondrial complex I deficiency leads to inflammation and retinal

NDUFAF5 Hydroxylates NDUFS7 at an Early Stage in the Assembly of Human

PDF Noninvasive Ophthalmic Imaging Measures Retinal Degeneration and

Human mitochondrial complex I assembly is mediated by NDUFAF1 Vogel

Mitochondrial complex I activity promotes antigen crosspresentation in

PDF A Mutation in Caenorhabditis elegans NDUF7 Activates the

Analysis of Human Mutations in the Supernumerary Subunits of Complex I

Figure 12 from Novel mutations in the NDUFS1 gene cause low residual

NDUFV2 pseudogene NDUFV2P1 contributes to mitochondrial complex I

Expression of mitochondrial complexrelative proteins NDUFV1 ATP5f1

Ndufs2 a Core Subunit of Mitochondrial Complex I Is Essential for

Conserved loop cluster of mitochondrial complex I formed by central

FallWinter 2023 NDU Foundation Newsletter

Ndufs2 a Core Subunit of Mitochondrial Complex I Is Essential for

Accessory subunit NDUFB4 participates in mitochondrial complex I

nduf7et19 is a partial lossoffunction allele of the nduf7 gene

Emerging Roles of NDUFS8 Located in Mitochondrial Complex I in

Identification of Mitochondrial Complex I Assembly Intermediates by

The Upregulation of NDUFB3 Is Implicated in Mitochondrial Dysfunction

Figure 13 from Novel mutations in the NDUFS1 gene cause low residual

Knockdown of Ndufv1 aggravates oxidative stress in TCMK1 cells A B

Ndufs2 a Core Subunit of Mitochondrial Complex I Is Essential for

Mitochondrial complex I activity promotes antigen crosspresentation in

CMTR1 RNA methyltransferase mutations activate widespread expression

Structural insights into respiratory complex I deficiency and assembly

Systematic Expression Analysis of Mitochondrial Complex I Identifies

Figure 11 from Novel mutations in the NDUFS1 gene cause low residual

Dysfunctions of Cellular Oxidative Metabolism in Patients with

Myeloidspecific deletion of the mitochondrial complex I protein Ndufs4

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