(Q40697564)

22 September 2017

Respiratory function in cybrid cell lines carrying European mtDNA haplogroups: implications for Leber's hereditary optic neuropathy (English)

1 reference

22 September 2017

9

1 reference

22 September 2017

Maria Lucia Valentino

object named as

Maria Valentino

6

0 references

Valerio Carelli

object named as

Valerio Carelli

1

0 references

author name string

Lodovica Vergani

2

1 reference

22 September 2017

Barbara Bernazzi

3

1 reference

22 September 2017

Claudia Zampieron

4

1 reference

22 September 2017

Laura Bucchi

5

1 reference

22 September 2017

Chiara Rengo

7

1 reference

22 September 2017

Antonio Torroni

8

1 reference

22 September 2017

1 October 2002

1 reference

Biochimica et Biophysica Acta

22 September 2017

1 reference

22 September 2017

1588

1 reference

22 September 2017

1

1 reference

22 September 2017

7-14

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Mitochondrial DNA and human evolution

22 September 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900097-2

7 January 2021

Mitochondrial DNA variation in human evolution and disease

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900097-2

7 January 2021

Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900097-2

7 January 2021

Cytochrome b mutations in Leber hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900097-2

7 January 2021

Leber's hereditary optic neuropathy: no significant evidence for primary or secondary pathogenicity of the 15257 mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900097-2

7 January 2021

Disease relevance of the so-called secondary Leber hereditary optic neuropathy mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900097-2

7 January 2021

Reply to Hofmann et al.

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900097-2

7 January 2021

Human mitochondrial diseases: answering questions and questioning answers

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900097-2

7 January 2021

Phylogenetic network for European mtDNA.

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900097-2

7 January 2021

Population genetics and disease susceptibility: characterization of central European haplogroups by mtDNA gene mutations, correlation with D loop variants and association with disease

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900097-2

7 January 2021

Leber's hereditary optic neuropathy: correlations between mitochondrial genotype and visual outcome.

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900097-2

7 January 2021

Mitochondrial DNA inherited variants are associated with successful aging and longevity in humans

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900097-2

7 January 2021

Human mtDNA haplogroups associated with high or reduced spermatozoa motility

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900097-2

7 January 2021

Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900097-2

7 January 2021

MtDNA mutations associated with Leber's hereditary optic neuropathy: studies on cytoplasmic hybrid (cybrid) cells.

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900097-2

7 January 2021

Titrating the effects of mitochondrial complex I impairment in the cell physiology

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900097-2

7 January 2021

Respiration and growth defects in transmitochondrial cell lines carrying the 11778 mutation associated with Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900097-2

7 January 2021

Leber's hereditary optic neuropathy: biochemical effect of 11778/ND4 and 3460/ND1 mutations and correlation with the mitochondrial genotype.

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900097-2

7 January 2021

Biochemical features of mtDNA 14484 (ND6/M64V) point mutation associated with Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900097-2

7 January 2021

Functional analysis of lymphoblast and cybrid mitochondria containing the 3460, 11778, or 14484 Leber's hereditary optic neuropathy mitochondrial DNA mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900097-2

7 January 2021

'Secondary' 4216/ND1 and 13708/ND5 Leber's hereditary optic neuropathy mitochondrial DNA mutations do not further impair in vivo mitochondrial oxidative metabolism when associated with the 11778/ND4 mitochondrial DNA mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900097-2

7 January 2021

Ophthalmologic findings in Leber hereditary optic neuropathy, with special reference to mtDNA mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900097-2

7 January 2021

Remarkable recovery of visual function in a patient with Leber's optic neuropathy and multiple mutations of mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900097-2

7 January 2021

Leber's Hereditary Optic Neuropathy (LHON) with 14484/ND6 mutation in a North African patient.

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900097-2

7 January 2021

Predominance of the T14484C mutation in French-Canadian families with Leber hereditary optic neuropathy is due to a founder effect

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900097-2

7 January 2021

Spectrum of pathogenic mitochondrial DNA mutations and clinical features in Japanese families with Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900097-2

7 January 2021

Pedigree analysis of French Canadian families with T14484C Leber's hereditary optic neuropathy.

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900097-2

7 January 2021

The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation.

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2802%2900097-2

7 January 2021

10.1016/S0925-4439(02)00097-2

Identifiers

DOI

1 reference

22 September 2017

1 reference