(Q53283772)

13 May 2018

title

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

1 reference

13 May 2018

author name string

Farzaneh Fesahat

1

1 reference

13 May 2018

Massoud Houshmand

2

1 reference

13 May 2018

Mehdi Shafa Shariat Panahi

3

1 reference

13 May 2018

Kurosh Gharagozli

4

1 reference

13 May 2018

Farzaneh Mirzajani

5

1 reference

13 May 2018

publication date

21 December 2006

1 reference

13 May 2018

Cellular and Molecular Neurobiology

published in

1 reference

13 May 2018

volume

27

1 reference

13 May 2018

issue

3

1 reference

13 May 2018

page(s)

329-334

1 reference

13 May 2018

https://scigraph.springernature.com/pub.10.1007/s10571-006-9126-9

exact match

0 references

cites work

Sequence and organization of the human mitochondrial genome

1 reference

12 December 2020

Distinct clustering of point mutations in mitochondrial DNA among patients with mitochondrial encephalomyopathies and with Parkinson's disease

1 reference

12 December 2020

Alzheimer's brains harbor somatic mtDNA control-region mutations that suppress mitochondrial transcription and replication

1 reference

12 December 2020

Evolutionary correlation between control region sequence and restriction polymorphisms in the mitochondrial genome of a large Senegalese Mandenka sample

1 reference

12 December 2020

Are substitutions in the first hypervariable region of the mitochondrial DNA displacement-loop in sudden infant death syndrome due to maternal inheritance?

1 reference

12 December 2020

Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484.

1 reference

12 December 2020

Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutations

1 reference

12 December 2020

Amyloid-beta, tau alterations and mitochondrial dysfunction in Alzheimer disease: the chickens or the eggs?

1 reference

12 December 2020

Features of mtDNA mutation patterns in European pedigrees and sporadic cases with Leber hereditary optic neuropathy.

1 reference

12 December 2020

Analysis of European mitochondrial haplogroups with Alzheimer disease risk

1 reference

12 December 2020

Alzheimer's disease: role of aging in pathogenesis

1 reference

12 December 2020

Classification of European mtDNAs from an analysis of three European populations

1 reference

12 December 2020

Neurofibrillary tangles mediate the association of amyloid load with clinical Alzheimer disease and level of cognitive function.

1 reference

12 December 2020

Mitochondrial DNA polymorphism in disease: a possible contributor to respiratory dysfunction

1 reference

12 December 2020

Genetic bases for common polygenic diseases

1 reference

12 December 2020

Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients.

1 reference

12 December 2020

Mitochondrial D-loop variation in Persian multiple sclerosis patients: K and A haplogroups as a risk factor!!

1 reference

12 December 2020

Cytochrome c oxidase and mitochondrial F1F0-ATPase (ATP synthase) activities in platelets and brain from patients with Alzheimer's disease

1 reference

12 December 2020

The emerging tree of West Eurasian mtDNAs: a synthesis of control-region sequences and RFLPs

1 reference

12 December 2020

The role of cytochrome c oxidase deficient hippocampal neurones in Alzheimer's disease

1 reference

12 December 2020

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

12 December 2020

10.1007/S10571-006-9126-9

Identifiers

DOI

1 reference

13 May 2018

PubMed ID

17186363

1 reference

13 May 2018