(Q45144296)

10 December 2017

title

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

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10 December 2017

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Norio Ozaki

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Kazuo Yamada

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object named as

Kazuo Yamada

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Nakao Iwata

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Masahiko Tatsumi

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Yoshimi Iijima

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Takako Fukunaga

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Shinichiro Nanko

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Kae Munakata

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Masashi Tanaka

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Kanako Mori

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Shinsuke Washizuka

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Makoto Yoneda

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Osamu Tajima

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Tsuyoshi Akiyama

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Kazuyuki Tadokoro

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Toshiya Inada

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Kaoru Sakamoto

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Takeo Yoshikawa

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publication date

1 December 2004

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10 December 2017

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volume

84

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issue

6

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10 December 2017

page(s)

1041-1050

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

10 December 2017

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

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

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Molecular evidence for mitochondrial dysfunction in bipolar disorder

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

7 January 2021

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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

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

7 January 2021

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Mitochondrial DNA polymorphisms in bipolar disorder

7 January 2021

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Mitochondrial DNA Sequence Diversity in Bipolar Affective Disorder

7 January 2021

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

7 January 2021

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Sequence and organization of the human mitochondrial genome

7 January 2021

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Mitochondrial diseases in man and mouse

7 January 2021

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

7 January 2021

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

7 January 2021

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

7 January 2021

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Mitochondrial Polymorphisms Significantly Reduce the Risk of Parkinson Disease

7 January 2021

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

7 January 2021

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7 January 2021

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7 January 2021

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

7 January 2021

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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

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

7 January 2021

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

7 January 2021

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7 January 2021

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Cell pathology in bipolar disorder

7 January 2021

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Dementia in affective disorder: a case-register study

7 January 2021

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

7 January 2021

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

7 January 2021

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

7 January 2021

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7 January 2021

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

7 January 2021

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

7 January 2021

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Deletion of leukocyte mitochondrial DNA in bipolar disorder

7 January 2021

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

7 January 2021

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Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

7 January 2021

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A new congenital muscular dystrophy with mitochondrial structural abnormalities.

7 January 2021

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

7 January 2021

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

7 January 2021

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10.1016/J.YGENO.2004.08.015

7 January 2021

Identifiers

DOI

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10 December 2017

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