Mitochondrial DNA polymorphisms in bipolar disorder

Journal of Affective Disorders

Volumn 62, Issue 3, 2001, Pages 151-164

  Kato, Tadafumi ^a   Kunugi, Hiroshi ^b   Nanko, Shinichiro ^b   Kato, Nobumasa ^a,c  

^a UNIVERSITY OF TOKYO   (Japan)

^b TEIKYO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^c SHIGA UNIVERSITY OF MEDICAL SCIENCE   (Japan)

Author keywords

Bipolar disorder; Genetics; Mitochondrial DNA; Risk factors

Indexed keywords

ADENOSINE TRIPHOSPHATASE; MITOCHONDRIAL DNA;

ADULT; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE ASSOCIATION; DNA POLYMORPHISM; DNA REPLICATION ORIGIN; DNA SEQUENCE; FAMILY HISTORY; FEMALE; GENE MUTATION; GENOTYPE; HAPLOTYPE; HUMAN; MALE; MANIC DEPRESSIVE PSYCHOSIS; PATHOPHYSIOLOGY; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; RISK FACTOR; SINGLE STRAND CONFORMATION POLYMORPHISM;

ADULT; AMINO ACID SEQUENCE; BASE SEQUENCE; BIPOLAR DISORDER; CASE-CONTROL STUDIES; CHI-SQUARE DISTRIBUTION; DNA, MITOCHONDRIAL; HUMANS; MALE; MIDDLE AGED; MOLECULAR SEQUENCE DATA; MUTATION; POLYMERASE CHAIN REACTION; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; RNA, TRANSFER;

EID: 0035109413     PISSN: 01650327     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-0327(99)00173-1     Document Type: Article

References (53)

1. Sequence and organization of the human mitochondrial genome
2. Southeast Asian mitochondrial DNA analysis reveals genetic continuity of ancient mongoloid migrations
3. Fast and sensitive silver staining of DNA in polyacrylamide gels
4. Molecular genetics of bipolar disorder
5. Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutations
6. Multiple deletions of mitochondrial DNA
7. Maternal inheritance and chromosome 18 allele sharing in unilineal bipolar pedigrees
8. Clinical evidence for genomic imprinting in bipolar I disorder
9. Patterns of parental transmission and familial aggregation models in bipolar affective disorder
10. Mitochondrial DNA 3394 mutation in the NADH dehydrogenase subunit 1 associated with non-insulin-dependent diabetes mellitus
11. Both the conserved stem-loop and divergent 5′-flanking sequences are required for initiation at the human mitochondrial origin of light-strand DNA replication
12. Brain phosphorous metabolism in depressive disorders detected by phosphorous-31 magnetic resonance spectroscopy
13. 7Li magnetic resonance spectroscopy
14. Reduction of brain phosphocreatine in bipolar II disorder detected by phosphorus-31 magnetic resonance spectroscopy
15. Phosphorus-31 magnetic resonance spectroscopy and ventricular enlargement in bipolar disorder
16. 31P-MRS
17. Deletion of leukocyte mitochondrial DNA in bipolar disorder
18. Parent-of-origin effect in the transmission of bipolar disorder
19. Increased levels of a mitochondrial DNA deletion in the brains in patients with bipolar disorder
20. Association between manic-depressive illness and the 5178 polymorphism in mitochondrial DNA
21. Magnetic resonance spectroscopy in affective disorders
22. Failure to demonstrate parent-of-origin effect in transmission of bipolar II disorder
23. Association of bipolar disorder with the S178 polymorphism in mitochondrial DNA
24. Human cells lacking mtDNA: Repopulation with exogenous mitochondria by complementation
25. Mitochondrial genetic analysis suggest selection against maternal liniages in bipolar affective disorder
26. A variant of Leber hereditary optic neuropathy characterized by recovery of vision and by an unusual mitochondrial genetic etiology
27. Normal variants of human mitochondrial DNA and translation products: The building of a reference data base
28. Patterns of maternal transmission in bipolar affective disorder
29. Mitochondrial DNA sequence variation in probands with bipolar affective disorder
30. Mental disorders in diabetic patients with mitochondrial transfer RNALeu(UUR) mutation at position 3243
31. 31P-MRS in bipolar disorder
32. Evalution of linkage of bipolar affective disorder to chromosome 18 in a sample of 57 German families
33. Depressive disorder due to mitochondrial tRNALeu(UUR) mutation
34. Rapid and sensitive detection of point mutation and DNA polymorphisms using the polymerase chain reaction
35. Sensitivity of single-strand conformation polymorphism and heteroduplex method for mutation detection in the cystic fibrosis gene
36. MELAS point mutation with unusual clinical presentation
37. 2+ regulation in neuronal and glial cell signaling
38. Intracellular phosphatidylinositol pathway abnormalities in bipolar disorder patients
39. Exhaustive scanning approach to screen all the mitochondrial tRNA genes for mutations and its application to the investigation of 35 independent patients with mitochondrial disorders
40. Manic-depressive psychosis in a patient with mitochondrial myopathy - A case report
41. Evidence for linkage of bipolar disorder to chromosome 18 with a parent-of-origin effect
42. Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia
43. Mitochondrial myopathy associated with sudden death in young adults and a novel mutation in the mitochondrial DNA leucine transfer RNA(UUR) gene
44. Mitochondrial genotype associated with longevity
45. Mitochondria and aging
46. The detection of mitochondrial DNA mutations using single stranded conformation polymorphism (SSCP) analysis and heteroduplex analysis
47. A new manifestation of Leber's disease and a new explanation for the agency responsible for its unusual pattern of inheritance
48. Two genetic factors in manic-depressive disease