(Q34416941)

2 August 2017

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title

The other, forgotten genome: mitochondrial DNA and mental disorders (English)

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2 August 2017

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Kato T

1

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2 August 2017

language of work or name

English

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publication date

1 November 2001

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2 August 2017

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2 August 2017

volume

6

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2 August 2017

issue

6

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2 August 2017

page(s)

625-633

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Sequence and organization of the human mitochondrial genome

2 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies.

21 January 2018

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Mitochondrial oversight of cellular Ca2+ signaling

21 January 2018

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Abnormal calcium homeostasis and mitochondrial polarization in a human encephalomyopathy

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

A calcium signaling defect in the pathogenesis of a mitochondrial DNA inherited oxidative phosphorylation deficiency

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Normal variants of human mitochondrial DNA and translation products: the building of a reference data base

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Functional integrity of mitochondrial genomes in human platelets and autopsied brain tissues from elderly patients with Alzheimer's disease

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

MITOMAP: a human mitochondrial genome database--1998 update

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Fragile mitochondrial DNA: the missing link in the apoptotic neuronal cell death in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

The 'common deletion' is not increased in parkinsonian substantia nigra as shown by competitive polymerase chain reaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Mitochondrial involvement in Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Gene expression of ND4, a subunit of complex I of oxidative phosphorylation in mitochondria, is decreased in temporal cortex of brains of Alzheimer's disease patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Detection of point mutations in codon 331 of mitochondrial NADH dehydrogenase subunit 2 in Alzheimer's brains

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

A mitochondrial DNA clone is associated with increased risk for Alzheimer disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Is a point mutation in the mitochondrial ND2 gene associated with Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

No association of mutations at nucleotide 5460 of mitochondrial NADH dehydrogenase with Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

No association found between Alzheimer's disease and a mitochondrial tRNA glutamine gene variant.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

mtDNA polymorphisms in Japanese sporadic Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Mitochondrial DNA mutations in Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Mutations in mitochondrial cytochrome c oxidase genes segregate with late-onset Alzheimer disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Apparent mtDNA heteroplasmy in Alzheimer's disease patients and in normals due to PCR amplification of nucleus-embedded mtDNA pseudogenes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Ancient mtDNA sequences in the human nuclear genome: a potential source of errors in identifying pathogenic mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Evidence that two reports of mtDNA cytochrome c oxidase "mutations" in Alzheimer's disease are based on nDNA pseudogenes of recent evolutionary origin

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Mitochondria in sporadic amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Characterization of cybrid cell lines containing mtDNA from Huntington's disease patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Mitochondrial DNA deletions in human brain: regional variability and increase with advanced age

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Aging-dependent large accumulation of point mutations in the human mtDNA control region for replication

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

In vivo neurochemistry of the brain in schizophrenia as revealed by magnetic resonance spectroscopy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Sex differences in the familial transmission of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Schizophrenia: gender and familial risk

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Mitochondrial encephalomyopathies: biochemical studies in two cases revealing defects in the respiratory chain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Mitochondrial encephalomyopathy (MELAS) with mental disorder. CT, MRI and SPECT findings

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Psychiatric symptoms in MELAS; a case report

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Psychiatric symptoms in a patient with diabetes mellitus associated with point mutation in mitochondrial DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Mitochondrial involvement in schizophrenia and other functional psychoses

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Superoxide, neuroleptics and the ubiquinone and cytochrome b5 reductases in brain and lymphocytes from normals and schizophrenic patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

A study of altered gene expression in frontal cortex from schizophrenic patients using differential screening

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Decreased cytochrome-c oxidase activity and lack of age-related accumulation of mitochondrial DNA deletions in the brains of schizophrenics.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Normalization of cytochrome-c oxidase activity in the rat brain by neuroleptics after chronic treatment with PCP or methamphetamine

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Mitochondrial function is differentially altered in the basal ganglia of chronic schizophrenics

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Putamen mitochondrial energy metabolism is highly correlated to emotional and intellectual impairment in schizophrenics.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Mitochondrial pathology in human schizophrenic striatum: a postmortem ultrastructural study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Synaptic contacts in schizophrenia: studies using immunocytochemical identification of dopaminergic neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Decreased brain intracellular pH measured by 31P-MRS in bipolar disorder: a confirmation in drug-free patients and correlation with white matter hyperintensity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Reduction of brain phosphocreatine in bipolar II disorder detected by phosphorus-31 magnetic resonance spectroscopy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

31P magnetic resonance spectroscopy in the frontal lobe of major depressed patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Lower levels of nucleoside triphosphate in the basal ganglia of depressed subjects: a phosphorous-31 magnetic resonance spectroscopy study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Photic stimulation-induced alteration of brain energy metabolism measured by 31P-MR spectroscopy in patients with MELAS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Brain activation in normal subjects and in patients affected by mitochondrial disease without clinical central nervous system involvement: a phosphorus magnetic resonance spectroscopy study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Clinical evidence for genomic imprinting in bipolar I disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

A new manifestation of Leber's disease and a new explanation for the agency responsible for its unusual pattern of inheritance

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Depressive disorder due to mitochondrial transfer RNALeu(UUR) mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Mental disorders in diabetic patients with mitochondrial transfer RNA(Leu) (UUR) mutation at position 3243.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

A nuclear defect in the 4p16 region predisposes to multiple mitochondrial DNA deletions in families with Wolfram syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Predisposition of Wolfram syndrome heterozygotes to psychiatric illness.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome)

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

A rare coding variant within the wolframin gene in bipolar and unipolar affective disorder cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Bipolar disorder and variation at a common polymorphism (A1832G) within exon 8 of the Wolfram gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

WFS1 gene mutation search in depressive patients: detection of five missense polymorphisms but no association with depression or bipolar affective disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

WFS1 (Wolfram syndrome 1) gene product: predominant subcellular localization to endoplasmic reticulum in cultured cells and neuronal expression in rat brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Homozygosity mapping identifies an additional locus for Wolfram syndrome on chromosome 4q

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

The possible association between affective disorder and partially deleted mitochondrial DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Increased levels of a mitochondrial DNA deletion in the brain of patients with bipolar disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Mitochondrial genetic analyses suggest selection against maternal lineages in bipolar affective disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Mitochondrial DNA polymorphisms in bipolar disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Mitochondrial dysfunction in bipolar disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Identifying a series of candidate genes for mania and psychosis: a convergent functional genomics approach

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Quantitation and origin of the mitochondrial membrane potential in human cells lacking mitochondrial DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

The occurrence of depressive symptoms in the preclinical phase of AD: a population-based study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Quantitative analysis of leukocyte mitochondrial DNA deletion in affective disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

A locus for bipolar affective disorder on chromosome 4p

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Mitochondrial DNA Sequence Diversity in Bipolar Affective Disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

Investigations on the point mutations at nt 5460 of the mtDNA in different neurodegenerative and neuromuscular diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

7 January 2021

Altered calcium homeostasis in cells transformed by mitochondria from individuals with Parkinson's disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

7 January 2021

Mitochondrial DNA mutations as an important contributor to ageing and degenerative diseases

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

7 January 2021

Mitochondrial genotype associated with longevity

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

7 January 2021

Mitochondrial DNA inherited variants are associated with successful aging and longevity in humans

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

7 January 2021

Psychosis and progressing dementia: presenting features of a mitochondriopathy

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

7 January 2021

Insulin therapy and risk of retinopathy in type 2 diabetes mellitus

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

7 January 2021

Absence of association between a mitochondrial DNA mutation at nucleotide position 3243 and schizophrenia in Japanese

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

7 January 2021

Mitochondrial DNA variants in schizophrenia: association studies

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

7 January 2021

Altered brain energy metabolism in lithium-resistant bipolar disorder detected by photic stimulated 31P-MR spectroscopy

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

7 January 2021

Two genetic factors in manic-depressive disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

7 January 2021

Maternal inheritance and chromosome 18 allele sharing in unilineal bipolar illness pedigrees

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

7 January 2021

Parent-of-origin effect in transmission of bipolar disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

7 January 2021

Patterns of parental transmission and familial aggregation models in bipolar affective disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

7 January 2021

MELAS point mutation with unusual clinical presentation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

7 January 2021

Deletion of leukocyte mitochondrial DNA in bipolar disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

7 January 2021

Mutational analysis of the Wolfram syndrome gene in two families with chromosome 4p-linked bipolar affective disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

7 January 2021

Association of bipolar disorder with the 5178 polymorphism in mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

7 January 2021

Dementia in affective disorder: a case-register study

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000926

7 January 2021

Identifiers

DOI

10.1038/SJ.MP.4000926

1 reference

2 August 2017

1 reference