Leber's hereditary optic neuropathy (LHON) pathogenic mutations induce mitochondrial-dependent apoptotic death in transmitochondrial cells incubated with galactose medium (Q44226125)

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English	Leber's hereditary optic neuropathy (LHON) pathogenic mutations induce mitochondrial-dependent apoptotic death in transmitochondrial cells incubated with galactose medium	scientific article

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scholarly article

1 reference

Europe PubMed Central

1 December 2017

Leber's hereditary optic neuropathy (LHON) pathogenic mutations induce mitochondrial-dependent apoptotic death in transmitochondrial cells incubated with galactose medium (English)

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Europe PubMed Central

1 December 2017

apoptotic process

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hereditary optic neuropathy

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based on heuristic

inferred from title

Andrea Martinuzzi

5

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Europe PubMed Central

1 December 2017

object named as

Michela Rugolo

7

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Valerio Carelli

object named as

Valerio Carelli

6

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Anthony H V Schapira

4

object named as

Anthony H V Schapira

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Europe PubMed Central

1 December 2017

author name string

Anna Ghelli

1

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Europe PubMed Central

1 December 2017

Claudia Zanna

2

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Europe PubMed Central

1 December 2017

Anna Maria Porcelli

3

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Europe PubMed Central

1 December 2017

language of work or name

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publication date

21 November 2002

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Europe PubMed Central

1 December 2017

Journal of Biological Chemistry

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Europe PubMed Central

1 December 2017

278

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Europe PubMed Central

1 December 2017

6

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Europe PubMed Central

1 December 2017

4145-4150

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Europe PubMed Central

1 December 2017

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

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https://api.crossref.org/works/10.1074%2FJBC.M210285200

21 January 2018

Optic nerve degeneration and mitochondrial dysfunction: genetic and acquired optic neuropathies

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https://api.crossref.org/works/10.1074%2FJBC.M210285200

21 January 2018

The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210285200

21 January 2018

The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210285200

21 January 2018

Mitochondrial DNA C4171A/ND1 is a novel primary causative mutation of Leber's hereditary optic neuropathy with a good prognosis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210285200

21 January 2018

Mitochondrial DNA nucleotide changes C14482G and C14482A in the ND6 gene are pathogenic for Leber's hereditary optic neuropathy.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210285200

21 January 2018

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/10.1074%2FJBC.M210285200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210285200

21 January 2018

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/10.1074%2FJBC.M210285200

21 January 2018

mtDNA mutations confer cellular sensitivity to oxidant stress that is partially rescued by calcium depletion and cyclosporin A.

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https://api.crossref.org/works/10.1074%2FJBC.M210285200

21 January 2018

Differentiation-specific effects of LHON mutations introduced into neuronal NT2 cells

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210285200

21 January 2018

Effect of L-carnitine treatment for valproate-induced hepatotoxicity

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210285200

21 January 2018

Leber hereditary optic neuropathy: how do mitochondrial DNA mutations cause degeneration of the optic nerve?

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210285200

21 January 2018

TUNEL-positive ganglion cells in human primary open-angle glaucoma.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210285200

21 January 2018

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/10.1074%2FJBC.M210285200

21 January 2018

Nonviability of cells with oxidative defects in galactose medium: a screening test for affected patient fibroblasts

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https://api.crossref.org/works/10.1074%2FJBC.M210285200

21 January 2018

The mitochondrial apoptosome: a killer unleashed by the cytochrome seas

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210285200

21 January 2018

Cells bearing mutations causing Leber's hereditary optic neuropathy are sensitized to Fas-Induced apoptosis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210285200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210285200

21 January 2018

Targeting of reporter molecules to mitochondria to measure calcium, ATP, and pH.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210285200

21 January 2018

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210285200

21 January 2018

Control of the Initiation of DNA Synthesis in 3T3 Cells: Low-Molecular-Weight Nutrients

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210285200

21 January 2018

A unique glucose-dependent apoptotic pathway induced by c-Myc

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210285200

21 January 2018

Growth factors can influence cell growth and survival through effects on glucose metabolism

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210285200

21 January 2018

Cell metabolism in the regulation of programmed cell death

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210285200

21 January 2018

Mitochondria as the central control point of apoptosis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210285200

21 January 2018

The Bcl-2 protein family: arbiters of cell survival

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210285200

21 January 2018

Double identity for proteins of the Bcl-2 family

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210285200

21 January 2018

Regulation of the permeability transition pore in skeletal muscle mitochondria. Modulation By electron flow through the respiratory chain complex i.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210285200

21 January 2018

Molecular ordering of the Fas-apoptotic pathway: the Fas/APO-1 protease Mch5 is a CrmA-inhibitable protease that activates multiple Ced-3/ICE-like cysteine proteases

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210285200

21 January 2018

Cleavage of BID by caspase 8 mediates the mitochondrial damage in the Fas pathway of apoptosis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210285200

21 January 2018

Bid, a Bcl2 interacting protein, mediates cytochrome c release from mitochondria in response to activation of cell surface death receptors

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210285200

21 January 2018

A Ubiquinone-binding Site Regulates the Mitochondrial Permeability Transition Pore

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210285200

21 January 2018

Human mitochondrial diseases: answering questions and questioning answers

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210285200

21 January 2018

The enigmatic relationship between mitochondrial dysfunction and Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210285200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210285200

21 January 2018

Use of fibroblast and lymphoblast cultures for detection of respiratory chain defects

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210285200

21 January 2018

The influence of nuclear background on the biochemical expression of 3460 Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M210285200

21 January 2018

Role of hypoxia-induced Bax translocation and cytochrome c release in reoxygenation injury

1 reference

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21 January 2018

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

1 reference

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21 January 2018

Identifiers

10.1074/JBC.M210285200

1 reference

Europe PubMed Central

1 December 2017

1 reference

Europe PubMed Central

1 December 2017

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