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Volumn 42, Issue 5, 1997, Pages 311-316

Quantitative analysis of leukocyte mitochondrial DNA deletion in affective disorders

Author keywords

Bipolar disorder; Depression; Mitochondrial DNA; Molecular genetics; Mood disorder; Quantitative polymerase chain reaction

Indexed keywords

MITOCHONDRIAL DNA;

EID: 0030852481     PISSN: 00063223     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0006-3223(96)00377-0     Document Type: Article
Times cited : (16)

References (32)
  • 2
    • 0019423856 scopus 로고
    • Sequence and organization of the human mitochondrial genome
    • Anderson S, Bankier AT, Barrel BG, et al (1981): Sequence and organization of the human mitochondrial genome. Nature 290:457-465.
    • (1981) Nature , vol.290 , pp. 457-465
    • Anderson, S.1    Bankier, A.T.2    Barrel, B.G.3
  • 3
    • 0001090629 scopus 로고
    • Multiple deletions of mitochondrial DNA
    • abstract
    • Ciafaloni E, Shanske S, Apostolski S, et al (1991): Multiple deletions of mitochondrial DNA [abstract]. Neurology 41: 207.
    • (1991) Neurology , vol.41 , pp. 207
    • Ciafaloni, E.1    Shanske, S.2    Apostolski, S.3
  • 5
    • 0027933135 scopus 로고
    • Marked changes in mitochondrial DNA deletion levels in Alzheimer brains
    • Corral-Debrinski M, Horton T, Lott MT, et al (1994): Marked changes in mitochondrial DNA deletion levels in Alzheimer brains. Genomics 23:471-476.
    • (1994) Genomics , vol.23 , pp. 471-476
    • Corral-Debrinski, M.1    Horton, T.2    Lott, M.T.3
  • 6
    • 0028344352 scopus 로고
    • The neuropathological basis of affective disorders: Neuroanatomical insights
    • Guze BH, Giltin M (1994): The neuropathological basis of affective disorders: Neuroanatomical insights. J Neuropsychiatry Clin Neurosci 6:114-121.
    • (1994) J Neuropsychiatry Clin Neurosci , vol.6 , pp. 114-121
    • Guze, B.H.1    Giltin, M.2
  • 7
    • 0023883150 scopus 로고
    • Deletions of mitochondrial DNA in patients with mitochondrial myopathies
    • Holt IJ, Harding AE, Morgan-Hughes JA (1988): Deletions of mitochondrial DNA in patients with mitochondrial myopathies. Nature 331:717-719.
    • (1988) Nature , vol.331 , pp. 717-719
    • Holt, I.J.1    Harding, A.E.2    Morgan-Hughes, J.A.3
  • 8
    • 0024798264 scopus 로고
    • Mitochondrial myopathies: Clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNA
    • Holt IJ, Harding AE, Cooper JM, et al (1989): Mitochondrial myopathies: Clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNA. Ann Neurol 26:699-708.
    • (1989) Ann Neurol , vol.26 , pp. 699-708
    • Holt, I.J.1    Harding, A.E.2    Cooper, J.M.3
  • 9
    • 0029431871 scopus 로고
    • Marked increase in mitochondrial DNA deletion levels in the cerebral cortex of Huntington's disease patients
    • Horton TM, Graham BH, Corral-Debrinski M, et al (1995): Marked increase in mitochondrial DNA deletion levels in the cerebral cortex of Huntington's disease patients. Neurology 45:1879-1883.
    • (1995) Neurology , vol.45 , pp. 1879-1883
    • Horton, T.M.1    Graham, B.H.2    Corral-Debrinski, M.3
  • 10
    • 0024577638 scopus 로고
    • Identical mitochondrial DNA deletion in blood and muscle
    • Johns DR, Drachman DB, Hurko O (1989): Identical mitochondrial DNA deletion in blood and muscle. Lancet i:393-394.
    • (1989) Lancet , vol.1 , pp. 393-394
    • Johns, D.R.1    Drachman, D.B.2    Hurko, O.3
  • 11
    • 0029978356 scopus 로고    scopus 로고
    • Deletion of leukocyte mitochondrial DNA in bipolar disorder
    • Kato T, Takahashi Y (1996): Deletion of leukocyte mitochondrial DNA in bipolar disorder. J Affect Disord 37:67-73.
    • (1996) J Affect Disord , vol.37 , pp. 67-73
    • Kato, T.1    Takahashi, Y.2
  • 12
    • 0028352678 scopus 로고
    • Reduction of brain phosphocreatine in bipolar II disorder detected by phosphorus-31 magnetic resonance spectroscopy
    • Kato T, Takahashi S, Shioiri T, Murashita J, Hamakawa H, Inubushi T (1994): Reduction of brain phosphocreatine in bipolar II disorder detected by phosphorus-31 magnetic resonance spectroscopy. J Affect Disord 31:125-133.
    • (1994) J Affect Disord , vol.31 , pp. 125-133
    • Kato, T.1    Takahashi, S.2    Shioiri, T.3    Murashita, J.4    Hamakawa, H.5    Inubushi, T.6
  • 14
    • 0028349234 scopus 로고
    • Defferential accumulations of 4,977 bp deletion in mitochondrial DNA of various tissues in human ageing
    • Lee HC, Pang CY, Hsu HS, Wei YH (1994): Defferential accumulations of 4,977 bp deletion in mitochondrial DNA of various tissues in human ageing. Biochim Biophys Acta 1226:37-43.
    • (1994) Biochim Biophys Acta , vol.1226 , pp. 37-43
    • Lee, H.C.1    Pang, C.Y.2    Hsu, H.S.3    Wei, Y.H.4
  • 16
    • 0025889031 scopus 로고
    • Detection of platelet mitochondrial DNA deletions in Kearns-Sayre syndrome
    • Ota Y, Tanaka M, Sato W, et al (1991): Detection of platelet mitochondrial DNA deletions in Kearns-Sayre syndrome. Invest Ophthalmol Vis Sci 32:2667-2675.
    • (1991) Invest Ophthalmol Vis Sci , vol.32 , pp. 2667-2675
    • Ota, Y.1    Tanaka, M.2    Sato, W.3
  • 17
    • 0024582466 scopus 로고
    • Non-invasive diagnosis of mitochondrial myopathy
    • Poulton J, Gardiner RM (1989): Non-invasive diagnosis of mitochondrial myopathy. Lancet i:961.
    • (1989) Lancet , vol.1 , pp. 961
    • Poulton, J.1    Gardiner, R.M.2
  • 18
    • 0025961538 scopus 로고
    • Detection of mitochondrial DNA deletions in blood using the polymerase chain reaction: Noninvasive diagnosis of mitochondrial myopathy
    • Poulton J, Deadman ME, Turnbull DM, Lake B, Gardiner RM (1991): Detection of mitochondrial DNA deletions in blood using the polymerase chain reaction: Noninvasive diagnosis of mitochondrial myopathy. Clin Genet 39:33-38.
    • (1991) Clin Genet , vol.39 , pp. 33-38
    • Poulton, J.1    Deadman, M.E.2    Turnbull, D.M.3    Lake, B.4    Gardiner, R.M.5
  • 19
    • 0027397842 scopus 로고
    • PCR analysis of platelet mtDNA: Lack of specific changes in Parkinson's disease
    • Sandy MS, Langston JW, Smith MT, Di Monte DA (1993): PCR analysis of platelet mtDNA: Lack of specific changes in Parkinson's disease. Mov Disord 8:74-82.
    • (1993) Mov Disord , vol.8 , pp. 74-82
    • Sandy, M.S.1    Langston, J.W.2    Smith, M.T.3    Di Monte, D.A.4
  • 21
    • 0027021442 scopus 로고
    • Mosaicism for a specific somatic mitochondrial DNA mutation in adult human brain
    • Soong NW, Hinton DR, Cortopassi G, Arnheim N (1992): Mosaicism for a specific somatic mitochondrial DNA mutation in adult human brain. Nat Genet 2:318-323.
    • (1992) Nat Genet , vol.2 , pp. 318-323
    • Soong, N.W.1    Hinton, D.R.2    Cortopassi, G.3    Arnheim, N.4
  • 23
    • 0018082913 scopus 로고
    • Research diagnostic criteria: Rationale and reliability
    • Spitzer RL, Endicott J, Robins E (1978): Research diagnostic criteria: Rationale and reliability. Arch Gen Psychiatry 35: 837-844.
    • (1978) Arch Gen Psychiatry , vol.35 , pp. 837-844
    • Spitzer, R.L.1    Endicott, J.2    Robins, E.3
  • 25
    • 0025262101 scopus 로고
    • Manic-depressive psychosis in a patient with mitochondrial myopathy - A case report
    • Stewart JB, Naylor GJ (1990): Manic-depressive psychosis in a patient with mitochondrial myopathy - A case report. Med Sci Res 18:265-266.
    • (1990) Med Sci Res , vol.18 , pp. 265-266
    • Stewart, J.B.1    Naylor, G.J.2
  • 26
    • 0027409599 scopus 로고
    • The possible association between affective disorder and partially deleted mitochondrial DNA
    • Stine OC, Luu SU, Zito M, Casanova M (1993): The possible association between affective disorder and partially deleted mitochondrial DNA. Biol Psychiatry 33:141-142.
    • (1993) Biol Psychiatry , vol.33 , pp. 141-142
    • Stine, O.C.1    Luu, S.U.2    Zito, M.3    Casanova, M.4
  • 27
    • 0028875316 scopus 로고
    • Evidence for linkage of bipolar disorder to chromosome 18 with a parent-of-origin effect
    • Stine OC, Xu J, Koskela R, et al (1995): Evidence for linkage of bipolar disorder to chromosome 18 with a parent-of-origin effect. Am J Hum Genet 57:1384-1394.
    • (1995) Am J Hum Genet , vol.57 , pp. 1384-1394
    • Stine, O.C.1    Xu, J.2    Koskela, R.3
  • 28
    • 0026637067 scopus 로고
    • Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia
    • Suomalainen A, Majander A, Haltia M, et al (1992): Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia. J Clin Invest 90:61-66.
    • (1992) J Clin Invest , vol.90 , pp. 61-66
    • Suomalainen, A.1    Majander, A.2    Haltia, M.3
  • 30
    • 0014706751 scopus 로고
    • A new manifestation of Leber's disease and a new explanation for the agency responsible for its unusual pattern of inheritance
    • Wallace DC (1970): A new manifestation of Leber's disease and a new explanation for the agency responsible for its unusual pattern of inheritance. Brain 93:121-132.
    • (1970) Brain , vol.93 , pp. 121-132
    • Wallace, D.C.1
  • 31
    • 0342686213 scopus 로고
    • The current status of genetic linkage studies of alcoholism and unipolar depression
    • Wilson AF, Elston RC, Mallott DB, Tran LD, Winokur G (1991): The current status of genetic linkage studies of alcoholism and unipolar depression. Psychiatr Genet 2:107-124.
    • (1991) Psychiatr Genet , vol.2 , pp. 107-124
    • Wilson, A.F.1    Elston, R.C.2    Mallott, D.B.3    Tran, L.D.4    Winokur, G.5
  • 32
    • 0016204773 scopus 로고
    • The division of depressive illness into depression spectrum disease and pure depressive disease
    • Winokur G (1974): The division of depressive illness into depression spectrum disease and pure depressive disease. Int Pharmacopsychiatry 9:5-13.
    • (1974) Int Pharmacopsychiatry , vol.9 , pp. 5-13
    • Winokur, G.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.