Mitochondrial DNA 3644T--&gt;C mutation associated with bipolar disorder (Q45144296)

10 December 2017

Mitochondrial DNA 3644T-->C mutation associated with bipolar disorder (English)

1 reference

10 December 2017

0 references

1 reference

9

1 reference

10 December 2017

20

1 reference

10 December 2017

Norio Ozaki

11

0 references

Kazuo Yamada

18

object named as

Kazuo Yamada

1 reference

10 December 2017

16

Nakao Iwata

1 reference

10 December 2017

17

Masahiko Tatsumi

1 reference

10 December 2017

15

Yoshimi Iijima

1 reference

10 December 2017

14

Takako Fukunaga

1 reference

10 December 2017

8

Shinichiro Nanko

1 reference

10 December 2017

Kae Munakata

1

1 reference

10 December 2017

Masashi Tanaka

2

1 reference

10 December 2017

Kanako Mori

3

1 reference

10 December 2017

Shinsuke Washizuka

4

1 reference

10 December 2017

Makoto Yoneda

5

1 reference

10 December 2017

Osamu Tajima

6

1 reference

10 December 2017

Tsuyoshi Akiyama

7

1 reference

10 December 2017

Kazuyuki Tadokoro

10

1 reference

10 December 2017

Toshiya Inada

12

1 reference

10 December 2017

Kaoru Sakamoto

13

1 reference

10 December 2017

Takeo Yoshikawa

19

1 reference

10 December 2017

1 December 2004

1 reference

10 December 2017

1 reference

10 December 2017

84

1 reference

10 December 2017

1041-1050

1 reference

10 December 2017

6

1 reference

Family-based association study of 76 candidate genes in bipolar disorder: BDNF is a potential risk locus. Brain-derived neutrophic factor

10 December 2017

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

The brain-derived neurotrophic factor gene confers susceptibility to bipolar disorder: evidence from a family-based association study.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

Impaired feedback regulation of XBP1 as a genetic risk factor for bipolar disorder

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

Alterations in brain phosphorous metabolism in bipolar disorder detected by in vivo 31P and 7Li magnetic resonance spectroscopy.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

Molecular evidence for mitochondrial dysfunction in bipolar disorder.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

Autosomal dominant external ophthalmoplegia and bipolar affective disorder associated with a mutation in the ANT1 gene.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

Mitochondrial DNA polymorphisms in bipolar disorder

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

Mitochondrial DNA Sequence Diversity in Bipolar Affective Disorder

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

Association of mitochondrial complex I subunit gene NDUFV2 at 18p11 with bipolar disorder.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

Sequence and organization of the human mitochondrial genome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

Mitochondrial diseases in man and mouse

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

Biochemical evidence for nuclear gene involvement in phenotype of non-syndromic deafness associated with mitochondrial 12S rRNA mutation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

The frequency of point mutations in mitochondrial DNA is elevated in the Alzheimer's brain.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

Mitochondrial Polymorphisms Significantly Reduce the Risk of Parkinson Disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

MITOMAP: a human mitochondrial genome database

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

MITOMAP: a human mitochondrial genome database--1998 update

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

Mitochondrial genome single nucleotide polymorphisms and their phenotypes in the Japanese.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

Cytoplasmic transfer of platelet mtDNA from elderly patients with Parkinson's disease to mtDNA-less HeLa cells restores complete mitochondrial respiratory function

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

Matrilineal inheritance of complex I dysfunction in a multigenerational Parkinson's disease family

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

Calcium homeostasis and reactive oxygen species production in cells transformed by mitochondria from individuals with sporadic Alzheimer's disease.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

Neuropathology of bipolar disorder

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

Cell pathology in bipolar disorder

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

Dementia in affective disorder: a case-register study

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

Depression as a risk factor for Alzheimer disease: the MIRAGE Study.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

Increased risk of developing Parkinson's disease for patients with major affective disorder: a register study

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

The mood-stabilizing agents lithium and valproate robustly increase the levels of the neuroprotective protein bcl-2 in the CNS

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

Psychiatric symptoms in MELAS; a case report

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

Mitochondrial DNA modifies cognition in interaction with the nuclear genome and age in mice.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

Deletion of leukocyte mitochondrial DNA in bipolar disorder

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

Two pathogenic point mutations exist in the authentic mitochondrial genome, not in the nuclear pseudogene.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

A new congenital muscular dystrophy with mitochondrial structural abnormalities.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

Correction of hemophilia B in canine and murine models using recombinant adeno-associated viral vectors

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

Assessment of mitochondrial oxidative phosphorylation in patient muscle biopsies, lymphoblasts, and transmitochondrial cell lines

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2004.08.015

10.1016/J.YGENO.2004.08.015

7 January 2021

Identifiers

DOI

1 reference

10 December 2017

1 reference