(Q34904962)

5 August 2017

An inherited mitochondrial DNA disruptive mutation shifts to homoplasmy in oncocytic tumor cells (English)

1 reference

5 August 2017

0 references

Martin Lang

4

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Ivana Kurelac

Ivana Kurelac

6

0 references

Elena Bonora

Elena Bonora

13

0 references

Luisa Iommarini

Luisa Iommarini

2

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Michela Rugolo

Michela Rugolo

15

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Claudio Ceccarelli

Claudio Ceccarelli

14

0 references

Gianandrea Pasquinelli

Gianandrea Pasquinelli

11

0 references

Valerio Carelli

Valerio Carelli

18

0 references

author name string

Giuseppe Gasparre

1

1 reference

5 August 2017

Anna Maria Porcelli

3

1 reference

5 August 2017

Gian Gaetano Ferri

5

1 reference

5 August 2017

Roberta Zuntini

7

1 reference

5 August 2017

Elisa Mariani

8

1 reference

5 August 2017

Lucia Fiammetta Pennisi

9

1 reference

5 August 2017

Ernesto Pasquini

10

1 reference

5 August 2017

Anna Ghelli

12

1 reference

5 August 2017

Nunzio Salfi

16

1 reference

5 August 2017

Giovanni Romeo

17

1 reference

5 August 2017

1 March 2009

1 reference

5 August 2017

1 reference

5 August 2017

30

1 reference

5 August 2017

3

1 reference

5 August 2017

391-396

1 reference

Efficient selection and characterization of mutants of a human cell line which are defective in mitochondrial DNA-encoded subunits of respiratory NADH dehydrogenase

5 August 2017

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20870

Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20870

7 January 2021

Energy converting NADH:quinone oxidoreductase (complex I).

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20870

7 January 2021

High frequency of homoplasmic mitochondrial DNA mutations in human tumors can be explained without selection

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20870

7 January 2021

Mitochondrial DNA mutations in oxyphilic and chief cell parathyroid adenomas

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20870

7 January 2021

Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumors.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20870

7 January 2021

Clonal expansion of mutated mitochondrial DNA is associated with tumor formation and complex I deficiency in the benign renal oncocytoma

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20870

7 January 2021

Mitochondrial complex I: structure, function and pathology

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20870

7 January 2021

The MELAS mutations 3946 and 3949 perturb the critical structure in a conserved loop of the ND1 subunit of mitochondrial complex I.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20870

7 January 2021

Mutations of the mitochondrial ND1 gene as a cause of MELAS.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20870

7 January 2021

Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonus.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20870

7 January 2021

The ND1 subunit constructs the inhibitor binding domain in bovine heart mitochondrial complex I.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20870

7 January 2021

Leber hereditary optic neuropathy mutations in the ND6 subunit of mitochondrial complex I affect ubiquinone reduction kinetics in a bacterial model of the enzyme

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20870

7 January 2021

Somatic mutations of the mitochondrial genome in human colorectal tumours

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20870

7 January 2021

Human non-synonymous SNPs: server and survey

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20870

7 January 2021

Low mitochondrial respiratory chain content correlates with tumor aggressiveness in renal cell carcinoma.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20870

7 January 2021

Mitochondrial complex I is deficient in renal oncocytomas

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20870

7 January 2021

PGC-1alpha/beta upregulation is associated with improved oxidative phosphorylation in cells harboring nonsense mtDNA mutations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20870

7 January 2021

https://api.crossref.org/works/10.1002%2FHUMU.20870

1 reference

7 January 2021

The ND1 gene of complex I is a mutational hot spot for Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20870

7 January 2021

Identifiers

DOI

10.1002/HUMU.20870

1 reference

5 August 2017

1 reference