(Q57588241)

Fabiana Fattori

4

0 references

Arnaldo Videira

Arnaldo Videira

12

0 references

Fiorella Piemonte

Fiorella Piemonte

10

0 references

Rosalba Carrozzo

Rosalba Carrozzo

15

0 references

Carlo Dionisi-Vici

Carlo Dionisi-Vici

11

0 references

Enrico Bertini

Enrico Bertini

16

0 references

Filippo Maria Santorelli

14

Filippo M. Santorelli

0 references

author name string

Mariana Ferreira

1

0 references

Alessandra Torraco

2

0 references

Teresa Rizza

3

0 references

Maria Chiara Meschini

5

0 references

Cinzia Castana

6

0 references

Nancy E. Go

7

0 references

Frank E. Nargang

8

0 references

Laura Vilarinho

https://scigraph.springernature.com/pub.10.1007/s10048-010-0265-2

13

0 references

publication date

4 January 2011

0 references

published in

Neurogenetics

0 references

volume

12

0 references

issue

1

0 references

page(s)

9-17

0 references

exact match

0 references

cites work

Bovine complex I is a complex of 45 different subunits.

1 reference

https://api.crossref.org/works/10.1007%2FS10048-010-0265-2

Analysis of the assembly profiles for mitochondrial- and nuclear-DNA-encoded subunits into complex I

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-010-0265-2

Human NADH:ubiquinone oxidoreductase

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-010-0265-2

Isolated complex I deficiency in children: clinical, biochemical and genetic aspects

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-010-0265-2

Mutant NDUFV1 subunit of mitochondrial complex I causes leukodystrophy and myoclonic epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-010-0265-2

Clinical and molecular findings in children with complex I deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-010-0265-2

Novel mutations in the NDUFS1 gene cause low residual activities in human complex I deficiencies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-010-0265-2

Large-scale deletion and point mutations of the nuclear NDUFV1 and NDUFS1 genes in mitochondrial complex I deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-010-0265-2

Leigh syndrome associated with mitochondrial complex I deficiency due to a novel mutation in the NDUFS1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-010-0265-2

Rapid screening for nuclear genes mutations in isolated respiratory chain complex I defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-010-0265-2

Complex I from the fungus Neurospora crassa

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-010-0265-2

Progressive cavitating leukoencephalopathy: a novel childhood disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-010-0265-2

Assaying ATP synthesis in cultured cells: a valuable tool for the diagnosis of patients with mitochondrial disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-010-0265-2

Blue Native electrophoresis to study mitochondrial and other protein complexes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-010-0265-2

Structure, functioning, and assembly of the ATP synthase in cells from patients with the T8993G mitochondrial DNA mutation. Comparison with the enzyme in Rho(0) cells completely lacking mtdna

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-010-0265-2

Supramolecular organization of the respiratory chain in Neurospora crassa mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-010-0265-2

The external calcium-dependent NADPH dehydrogenase from Neurospora crassa mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-010-0265-2

Quantification of muscle mitochondrial oxidative phosphorylation enzymes via histochemical staining of blue native polyacrylamide gels.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-010-0265-2

Disruption of the gene encoding the 78-kilodalton subunit of the peripheral arm of complex I in Neurospora crassa by repeat induced point mutation (RIP).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-010-0265-2

Effects of mitochondrial complex III disruption in the respiratory chain of Neurospora crassa.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-010-0265-2

From NADH to ubiquinone in Neurospora mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-010-0265-2

Kinetics of the mitochondrial NADH-ubiquinone oxidoreductase interaction with hexammineruthenium(III).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-010-0265-2

Effects of disrupting the 21 kDa subunit of complex I from Neurospora crassa

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-010-0265-2

Prediction of deleterious human alleles

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-010-0265-2

Neurospora strains harboring mitochondrial disease-associated mutations in iron-sulfur subunits of complex I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-010-0265-2

Structure of the hydrophilic domain of respiratory complex I from Thermus thermophilus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-010-0265-2

Disruption of mitochondrial function during apoptosis is mediated by caspase cleavage of the p75 subunit of complex I of the electron transport chain

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-010-0265-2

Direct evidence for S-nitrosation of mitochondrial complex I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-010-0265-2

Differences in assembly or stability of complex I and other mitochondrial OXPHOS complexes in inherited complex I deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-010-0265-2

Leukodystrophies and other genetic metabolic leukoencephalopathies in children and adults

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-010-0265-2

Leukoencephalopathy with vanishing white matter caused by compound heterozygous mutations in mitochondrial complex I NDUFS1 subunit

21 January 2018

1 reference

12 December 2020

Identification of the TYKY homologous subunit of complex I from Neurospora crassa

1 reference

12 December 2020

Identification of the polypeptide encoded by the URF-1 gene of Neurospora crassa mtDNA

1 reference

12 December 2020

Reversible inhibition of mitochondrial complex I activity following chronic dopaminergic glutathione depletion in vitro: implications for Parkinson's disease

1 reference

12 December 2020

Disruption of the gene coding for the 21.3-kDa subunit of the peripheral arm of complex I from Neurospora crassa.

1 reference

12 December 2020