Huntington's disease and mitochondrial DNA deletions: event or regular mechanism for mutant huntingtin protein and CAG repeats expansion?! (Q45306758)

11 December 2017

title

Huntington's disease and mitochondrial DNA deletions: event or regular mechanism for mutant huntingtin protein and CAG repeats expansion?! (English)

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11 December 2017

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Mohammad Mehdi Banoei

1

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11 December 2017

Massoud Houshmand

2

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11 December 2017

Mehdi Shafa Shariat Panahi

3

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11 December 2017

Parvin Shariati

4

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11 December 2017

Maryam Rostami

5

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11 December 2017

Masoumeh Dehghan Manshadi

6

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11 December 2017

Tayebeh Majidizadeh

7

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11 December 2017

publication date

20 October 2007

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Cellular and Molecular Neurobiology

11 December 2017

published in

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11 December 2017

volume

27

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11 December 2017

issue

7

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11 December 2017

page(s)

867-875

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Marked increase in mitochondrial DNA deletion levels in the cerebral cortex of Huntington's disease patients

11 December 2017

cites work

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https://api.crossref.org/works/10.1007/S10571-007-9206-5

Identification and sizing of GAA trinucleotide repeat expansion, investigation for D-loop variations and mitochondrial deletions in Iranian patients with Friedreich's ataxia

21 January 2018

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https://api.crossref.org/works/10.1007/S10571-007-9206-5

Secondary abnormalities of mitochondrial DNA associated with neurodegeneration

21 January 2018

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https://api.crossref.org/works/10.1007/S10571-007-9206-5

Mitochondrial DNA mutations in human degenerative diseases and aging

21 January 2018

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https://api.crossref.org/works/10.1007/S10571-007-9206-5

Analysis of the trinucleotide CAG repeat from the DNA polymerase gamma gene (POLG) in patients with Parkinson's disease.

21 January 2018

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12 December 2020

TATA-binding protein in neurodegenerative disease.

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12 December 2020

Mutant huntingtin aggregates impair mitochondrial movement and trafficking in cortical neurons

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12 December 2020

Neuronal degeneration and mitochondrial dysfunction

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12 December 2020

Cellular localization and development of neuronal intranuclear inclusions in striatal and cortical neurons in R6/2 transgenic mice

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12 December 2020

Oxidative stress, mitochondrial dysfunction and cellular stress response in Friedreich's ataxia

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12 December 2020

Increased apoptosis of Huntington disease lymphoblasts associated with repeat length-dependent mitochondrial depolarization

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12 December 2020

Mitochondrial involvement in Parkinson's disease, Huntington's disease, hereditary spastic paraplegia and Friedreich's ataxia

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12 December 2020

A century of mitochondrial research: achievements and perspectives

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12 December 2020

Rapid aggregate formation of the huntingtin N-terminal fragment carrying an expanded polyglutamine tract

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12 December 2020

Clonal expansion of mitochondrial DNA with multiple deletions in autosomal dominant progressive external ophthalmoplegia

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12 December 2020

Complex I defect in muscle from patients with Huntington's disease.

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12 December 2020

Do haplogroups H and U act to increase the penetrance of Alzheimer's disease?

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12 December 2020

Transcriptional dysregulation in Huntington's disease

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12 December 2020

Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes

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12 December 2020

Detection of mitochondrial DNA deletion by a modified PCR method in a 60Co radiation-exposed patient.

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12 December 2020

Exclusion of mutations in the PRNP, JPH3, TBP, ATN1, CREBBP, POU3F2 and FTL genes as a cause of disease in Portuguese patients with a Huntington-like phenotype

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12 December 2020

The "new" mitochondrial disorders

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12 December 2020

Huntington aggregates may not predict neuronal death in Huntington's disease

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12 December 2020

Mitochondrial DNA sequence variation in human evolution and disease.

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12 December 2020

Truncated N-terminal fragments of huntingtin with expanded glutamine repeats form nuclear and cytoplasmic aggregates in cell culture.

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12 December 2020

Deranged neuronal calcium signaling and Huntington disease.

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12 December 2020

The Clinical Significance of the POLG Gene Polymorphism in Male Infertility

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12 December 2020

Molecular basis of the neurodegenerative disorders

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12 December 2020

Mitochondrial dysfunction and its role in motor neuron degeneration in ALS.

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12 December 2020

Severe ultrastructural mitochondrial changes in lymphoblasts homozygous for Huntington disease mutation

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12 December 2020

Defects of intergenomic communication: autosomal disorders that cause multiple deletions and depletion of mitochondrial DNA.

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12 December 2020

Mitochondrial DNA deletion mutations colocalize with segmental electron transport system abnormalities, muscle fiber atrophy, fiber splitting, and oxidative damage in sarcopenia

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12 December 2020

Region-specific analysis of mitochondrial DNA deletions in neurodegenerative disorders in humans

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12 December 2020

10.1007/S10571-007-9206-5

Identifiers

DOI

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Dimensions Publication ID

11 December 2017

1022512050

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