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Volumn 543, Issue 1, 2014, Pages 1-7

Epigenetics and migraine complex mitochondrial interactions contributing to disease susceptibility

Author keywords

Disease susceptibility; Epigenetics; Migraine; Mitochondrial methylation

Indexed keywords

CELL NUCLEUS DNA; MITOCHONDRIAL DNA; UNTRANSLATED RNA;

EID: 84899647287     PISSN: 03781119     EISSN: 18790038     Source Type: Journal    
DOI: 10.1016/j.gene.2014.04.001     Document Type: Review
Times cited : (19)

References (84)
  • 2
    • 77957993889 scopus 로고    scopus 로고
    • Lessons from genome-wide studies: an integrated definition of the coactivator function of histone acetyl transferases
    • Anamika K., et al. Lessons from genome-wide studies: an integrated definition of the coactivator function of histone acetyl transferases. Epigenetics & Chromatin 2010, 3(1):18.
    • (2010) Epigenetics & Chromatin , vol.3 , Issue.1 , pp. 18
    • Anamika, K.1
  • 3
    • 79958737573 scopus 로고    scopus 로고
    • Nuclear outsourcing of RNA interference components to human mitochondria
    • Bandiera S., et al. Nuclear outsourcing of RNA interference components to human mitochondria. PLoS One 2011, 6(6):e20746.
    • (2011) PLoS One , vol.6 , Issue.6
    • Bandiera, S.1
  • 4
    • 34249337761 scopus 로고    scopus 로고
    • Perceptions of epigenetics
    • Bird A. Perceptions of epigenetics. Nature 2007, 447(7143):396-398.
    • (2007) Nature , vol.447 , Issue.7143 , pp. 396-398
    • Bird, A.1
  • 5
    • 33846968150 scopus 로고    scopus 로고
    • Supramolecular structure of the mitochondrial oxidative phosphorylation system
    • Boekema E.J., Braun H.P. Supramolecular structure of the mitochondrial oxidative phosphorylation system. The Journal of Biological Chemistry 2007, 282(1):1-4.
    • (2007) The Journal of Biological Chemistry , vol.282 , Issue.1 , pp. 1-4
    • Boekema, E.J.1    Braun, H.P.2
  • 6
    • 0028788493 scopus 로고
    • Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutations
    • Brown M.D., et al. Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutations. Human Mutation 1995, 6(4):311-325.
    • (1995) Human Mutation , vol.6 , Issue.4 , pp. 311-325
    • Brown, M.D.1
  • 7
    • 33747322165 scopus 로고    scopus 로고
    • Tagging mammalian transcription complexity
    • Carninci P. Tagging mammalian transcription complexity. Trends in Genetics 2006, 22(9):501-510.
    • (2006) Trends in Genetics , vol.22 , Issue.9 , pp. 501-510
    • Carninci, P.1
  • 8
    • 0038204415 scopus 로고    scopus 로고
    • The diverse functions of histone acetyltransferase complexes
    • Carrozza M.J., et al. The diverse functions of histone acetyltransferase complexes. Trends in Genetics 2003, 19(6):321-329.
    • (2003) Trends in Genetics , vol.19 , Issue.6 , pp. 321-329
    • Carrozza, M.J.1
  • 9
    • 81255143014 scopus 로고    scopus 로고
    • Epigenetic regulation of motor neuron cell death through DNA methylation
    • Chestnut B.A., et al. Epigenetic regulation of motor neuron cell death through DNA methylation. Journal of Neuroscience 2011, 31(46):16619-16636.
    • (2011) Journal of Neuroscience , vol.31 , Issue.46 , pp. 16619-16636
    • Chestnut, B.A.1
  • 10
    • 0034705419 scopus 로고    scopus 로고
    • The mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episode syndrome-associated human mitochondrial tRNALeu(UUR) mutation causes aminoacylation deficiency and concomitant reduced association of mRNA with ribosomes
    • Chomyn A., et al. The mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episode syndrome-associated human mitochondrial tRNALeu(UUR) mutation causes aminoacylation deficiency and concomitant reduced association of mRNA with ribosomes. The Journal of Biological Chemistry 2000, 275(25):19198-19209.
    • (2000) The Journal of Biological Chemistry , vol.275 , Issue.25 , pp. 19198-19209
    • Chomyn, A.1
  • 11
    • 84859421209 scopus 로고    scopus 로고
    • A mitochondrial etiology of Alzheimer and Parkinson disease
    • Coskun P., et al. A mitochondrial etiology of Alzheimer and Parkinson disease. Biochimica et Biophysica Acta 2012, 1820(5):553-564.
    • (2012) Biochimica et Biophysica Acta , vol.1820 , Issue.5 , pp. 553-564
    • Coskun, P.1
  • 12
    • 0345863901 scopus 로고    scopus 로고
    • MitoProteome: mitochondrial protein sequence database and annotation system
    • (Database issue)
    • Cotter D., et al. MitoProteome: mitochondrial protein sequence database and annotation system. Nucleic Acids Research 2004, 32:D463-D467. (Database issue).
    • (2004) Nucleic Acids Research , vol.32
    • Cotter, D.1
  • 13
    • 67650641262 scopus 로고    scopus 로고
    • Migraine with persistent visual aura: response to furosemide
    • de Almeida R.F., et al. Migraine with persistent visual aura: response to furosemide. Clinics 2009, 64(4):375-376.
    • (2009) Clinics , vol.64 , Issue.4 , pp. 375-376
    • de Almeida, R.F.1
  • 14
    • 70350068690 scopus 로고    scopus 로고
    • DNA methylation and cancer diagnosis: new methods and applications
    • Dehan P., et al. DNA methylation and cancer diagnosis: new methods and applications. Expert Review of Molecular Diagnostics 2009, 9(7):651-657.
    • (2009) Expert Review of Molecular Diagnostics , vol.9 , Issue.7 , pp. 651-657
    • Dehan, P.1
  • 15
    • 0021798888 scopus 로고
    • Mitochondrial myopathies
    • DiMauro S., et al. Mitochondrial myopathies. Annals of Neurology 1985, 17(6):521-538.
    • (1985) Annals of Neurology , vol.17 , Issue.6 , pp. 521-538
    • DiMauro, S.1
  • 16
    • 0030811838 scopus 로고    scopus 로고
    • Association of the mitochondrial tRNA(A4336G) mutation with Alzheimer's and Parkinson's diseases
    • Egensperger R., et al. Association of the mitochondrial tRNA(A4336G) mutation with Alzheimer's and Parkinson's diseases. Neuropathology and Applied Neurobiology 1997, 23(4):315-321.
    • (1997) Neuropathology and Applied Neurobiology , vol.23 , Issue.4 , pp. 315-321
    • Egensperger, R.1
  • 17
    • 2642531973 scopus 로고    scopus 로고
    • Epigenetics in human disease and prospects for epigenetic therapy
    • Egger G., et al. Epigenetics in human disease and prospects for epigenetic therapy. Nature 2004, 429(6990):457-463.
    • (2004) Nature , vol.429 , Issue.6990 , pp. 457-463
    • Egger, G.1
  • 18
    • 84873171845 scopus 로고    scopus 로고
    • Epigenetic mechanisms in migraine: a promising avenue?
    • Eising E., et al. Epigenetic mechanisms in migraine: a promising avenue?. BMC Medicine 2013, 11:26.
    • (2013) BMC Medicine , vol.11 , pp. 26
    • Eising, E.1
  • 19
    • 33846625058 scopus 로고    scopus 로고
    • Associating mitochondrial DNA variation with complex traits
    • (author reply 382-3)
    • Elson J.L., et al. Associating mitochondrial DNA variation with complex traits. American Journal of Human Genetics 2007, 80(2):378-382. (author reply 382-3).
    • (2007) American Journal of Human Genetics , vol.80 , Issue.2 , pp. 378-382
    • Elson, J.L.1
  • 20
    • 4644343975 scopus 로고    scopus 로고
    • New international classification of migraine with aura (ICHD-2) applied to 362 migraine patients
    • Eriksen M.K., Thomsen L.L., Olesen J. New international classification of migraine with aura (ICHD-2) applied to 362 migraine patients. European Journal of Neurology 2004, 11(9):583-591.
    • (2004) European Journal of Neurology , vol.11 , Issue.9 , pp. 583-591
    • Eriksen, M.K.1    Thomsen, L.L.2    Olesen, J.3
  • 21
    • 84899655437 scopus 로고    scopus 로고
    • Mitochondrial DNA and inherited diseases a comprehensive review
    • Geetha R.V.A.R. Mitochondrial DNA and inherited diseases a comprehensive review. Drug Invention Today 2011, 3(9).
    • (2011) Drug Invention Today , vol.3 , Issue.9
    • Geetha, R.V.A.R.1
  • 22
    • 84856261341 scopus 로고    scopus 로고
    • The trigeminovascular system does not require a peripheral sensory input to be activated - migraine is a central disorder focus on 'effect of cortical spreading depression on basal and evoked traffic in the trigeminovascular sensory system'
    • Goadsby P.J., Akerman S. The trigeminovascular system does not require a peripheral sensory input to be activated - migraine is a central disorder focus on 'effect of cortical spreading depression on basal and evoked traffic in the trigeminovascular sensory system'. Cephalalgia: an international journal of headache 2012, 32(1):3-5.
    • (2012) Cephalalgia: an international journal of headache , vol.32 , Issue.1 , pp. 3-5
    • Goadsby, P.J.1    Akerman, S.2
  • 24
    • 80053496448 scopus 로고    scopus 로고
    • Cost of disorders of the brain in Europe 2010
    • Gustavsson A., et al. Cost of disorders of the brain in Europe 2010. European Neuropsychopharmacology 2011, 21(10):718-779.
    • (2011) European Neuropsychopharmacology , vol.21 , Issue.10 , pp. 718-779
    • Gustavsson, A.1
  • 25
    • 0027288377 scopus 로고
    • The mitochondrial-DNA transfer RNA(Lys) a→G(8344) mutation and the syndrome of myoclonic epilepsy with ragged-red fibers (MERRF) - relationship of clinical phenotype to proportion of mutant mitochondrial-DNA
    • Hammans S.R., et al. The mitochondrial-DNA transfer RNA(Lys) a→G(8344) mutation and the syndrome of myoclonic epilepsy with ragged-red fibers (MERRF) - relationship of clinical phenotype to proportion of mutant mitochondrial-DNA. Brain: A Journal of Neurology 1993, 116:617-632.
    • (1993) Brain: A Journal of Neurology , vol.116 , pp. 617-632
    • Hammans, S.R.1
  • 26
    • 0031727452 scopus 로고    scopus 로고
    • MELAS: a new disease associated mitochondrial DNA mutation and evidence for further genetic heterogeneity
    • Hanna M.G., et al. MELAS: a new disease associated mitochondrial DNA mutation and evidence for further genetic heterogeneity. Journal of Neurology, Neurosurgery, and Psychiatry 1998, 65(4):512-517.
    • (1998) Journal of Neurology, Neurosurgery, and Psychiatry , vol.65 , Issue.4 , pp. 512-517
    • Hanna, M.G.1
  • 27
    • 0030027561 scopus 로고    scopus 로고
    • Functional and molecular mitochondrial abnormalities associated with a C→T transition at position 3256 of the human mitochondrial genome - the effects of a pathogenic mitochondrial tRNA point mutation in organelle translation and RNA processing
    • Hao H.L., Moraes C.T. Functional and molecular mitochondrial abnormalities associated with a C→T transition at position 3256 of the human mitochondrial genome - the effects of a pathogenic mitochondrial tRNA point mutation in organelle translation and RNA processing. Journal of Biological Chemistry 1996, 271(4):2347-2352.
    • (1996) Journal of Biological Chemistry , vol.271 , Issue.4 , pp. 2347-2352
    • Hao, H.L.1    Moraes, C.T.2
  • 28
    • 0027767774 scopus 로고
    • Accumulation of mtDNA with a mutation at position-3271 in transfer RNA(Leu)(UUR) gene introduced from a MELAS patient to HeLa-cells lacking mtDNA results in progressive inhibition of mitochondrial respiratory-function
    • Hayashi J.I., et al. Accumulation of mtDNA with a mutation at position-3271 in transfer RNA(Leu)(UUR) gene introduced from a MELAS patient to HeLa-cells lacking mtDNA results in progressive inhibition of mitochondrial respiratory-function. Biochemical and Biophysical Research Communications 1993, 197(3):1049-1055.
    • (1993) Biochemical and Biophysical Research Communications , vol.197 , Issue.3 , pp. 1049-1055
    • Hayashi, J.I.1
  • 29
    • 4644245702 scopus 로고    scopus 로고
    • Introduction to quantitative genetics
    • Hill W.G., Mackay T.F., Falconer D.S. Introduction to quantitative genetics. Genetics 2004, 167(4):1529-1536.
    • (2004) Genetics , vol.167 , Issue.4 , pp. 1529-1536
    • Hill, W.G.1    Mackay, T.F.2    Falconer, D.S.3
  • 30
    • 77957922955 scopus 로고    scopus 로고
    • CGRP and its receptors provide new insights into migraine pathophysiology
    • Ho T.W., Edvinsson L., Goadsby P.J. CGRP and its receptors provide new insights into migraine pathophysiology. Nature Reviews. Neurology 2010, 6(10):573-582.
    • (2010) Nature Reviews. Neurology , vol.6 , Issue.10 , pp. 573-582
    • Ho, T.W.1    Edvinsson, L.2    Goadsby, P.J.3
  • 31
    • 0028905597 scopus 로고
    • Migraine and concomitant symptoms among 8167 adult twin-pairs
    • Honkasalo M.L., et al. Migraine and concomitant symptoms among 8167 adult twin-pairs. Headache 1995, 35(2):70-78.
    • (1995) Headache , vol.35 , Issue.2 , pp. 70-78
    • Honkasalo, M.L.1
  • 32
    • 84882847104 scopus 로고    scopus 로고
    • Mitochondrial DNA methylation as a next-generation biomarker and diagnostic tool
    • Iacobazzi V., et al. Mitochondrial DNA methylation as a next-generation biomarker and diagnostic tool. Molecular Genetics and Metabolism 2013, 110(1-2):25-34.
    • (2013) Molecular Genetics and Metabolism , vol.110 , Issue.1-2 , pp. 25-34
    • Iacobazzi, V.1
  • 33
    • 79851512298 scopus 로고    scopus 로고
    • Impairment of methyl cycle affects mitochondrial methyl availability and glutathione level in Down's syndrome
    • Infantino V., et al. Impairment of methyl cycle affects mitochondrial methyl availability and glutathione level in Down's syndrome. Molecular Genetics and Metabolism 2011, 102(3):378-382.
    • (2011) Molecular Genetics and Metabolism , vol.102 , Issue.3 , pp. 378-382
    • Infantino, V.1
  • 34
    • 0025957444 scopus 로고
    • Mitochondrial leucine tRNA mutation in a mitochondrial encephalomyopathy
    • Ino H., et al. Mitochondrial leucine tRNA mutation in a mitochondrial encephalomyopathy. Lancet 1991, 337(8735):234-235.
    • (1991) Lancet , vol.337 , Issue.8735 , pp. 234-235
    • Ino, H.1
  • 35
    • 10744233452 scopus 로고    scopus 로고
    • Phase 1 study of low-dose prolonged exposure schedules of the hypomethylating agent 5-aza-2'-deoxycytidine (decitabine) in hematopoietic malignancies
    • Issa J.P., et al. Phase 1 study of low-dose prolonged exposure schedules of the hypomethylating agent 5-aza-2'-deoxycytidine (decitabine) in hematopoietic malignancies. Blood 2004, 103(5):1635-1640.
    • (2004) Blood , vol.103 , Issue.5 , pp. 1635-1640
    • Issa, J.P.1
  • 36
    • 0012487405 scopus 로고    scopus 로고
    • Screening for mitochondrial, DNA heteroplasmy in children at risk for mitochondrial disease
    • Ito M., et al. Screening for mitochondrial, DNA heteroplasmy in children at risk for mitochondrial disease. Mitochondrion 2001, 1(3):269-278.
    • (2001) Mitochondrion , vol.1 , Issue.3 , pp. 269-278
    • Ito, M.1
  • 37
    • 0018860957 scopus 로고
    • Cellular differentiation, cytidine analogs and DNA methylation
    • Jones P.A., Taylor S.M. Cellular differentiation, cytidine analogs and DNA methylation. Cell 1980, 20(1):85-93.
    • (1980) Cell , vol.20 , Issue.1 , pp. 85-93
    • Jones, P.A.1    Taylor, S.M.2
  • 38
    • 15044356152 scopus 로고    scopus 로고
    • Epigenetics: surveillance team against cancer
    • Klein G. Epigenetics: surveillance team against cancer. Nature 2005, 434(7030):150.
    • (2005) Nature , vol.434 , Issue.7030 , pp. 150
    • Klein, G.1
  • 39
    • 0026764974 scopus 로고
    • The mutant mitochondrial genes in mitochondrial myopathy, encephalopathy, lactic-acidosis and stroke-like episodes (MELAS) were selectively amplified through generations
    • Kobayashi Y., et al. The mutant mitochondrial genes in mitochondrial myopathy, encephalopathy, lactic-acidosis and stroke-like episodes (MELAS) were selectively amplified through generations. Journal of Inherited Metabolic Disease 1992, 15(5):803-808.
    • (1992) Journal of Inherited Metabolic Disease , vol.15 , Issue.5 , pp. 803-808
    • Kobayashi, Y.1
  • 40
    • 0038576158 scopus 로고    scopus 로고
    • The power and the promise of DNA methylation markers
    • Laird P.W. The power and the promise of DNA methylation markers. Nature Reviews. Cancer 2003, 3(4):253-266.
    • (2003) Nature Reviews. Cancer , vol.3 , Issue.4 , pp. 253-266
    • Laird, P.W.1
  • 41
    • 80054712491 scopus 로고    scopus 로고
    • Effect of cortical spreading depression on basal and evoked traffic in the trigeminovascular sensory system
    • Lambert G.A., Truong L., Zagami A.S. Effect of cortical spreading depression on basal and evoked traffic in the trigeminovascular sensory system. Cephalalgia: An International Journal of Headache 2011, 31(14):1439-1451.
    • (2011) Cephalalgia: An International Journal of Headache , vol.31 , Issue.14 , pp. 1439-1451
    • Lambert, G.A.1    Truong, L.2    Zagami, A.S.3
  • 42
    • 30544454938 scopus 로고    scopus 로고
    • The global burden of migraine: measuring disability in headache disorders with WHO's Classification of Functioning, Disability and Health (ICF)
    • Leonardi M., et al. The global burden of migraine: measuring disability in headache disorders with WHO's Classification of Functioning, Disability and Health (ICF). Journal of Headache and Pain 2005, 6(6):429-440.
    • (2005) Journal of Headache and Pain , vol.6 , Issue.6 , pp. 429-440
    • Leonardi, M.1
  • 43
    • 0023877476 scopus 로고
    • Kearns-Sayre syndrome with muscle mitochondrial DNA deletion
    • Lestienne P., Ponsot G. Kearns-Sayre syndrome with muscle mitochondrial DNA deletion. Lancet 1988, 1(8590):885.
    • (1988) Lancet , vol.1 , Issue.8590 , pp. 885
    • Lestienne, P.1    Ponsot, G.2
  • 44
    • 33750544922 scopus 로고    scopus 로고
    • Bias, precision and heritability of self-reported and clinically measured height in Australian twins
    • Macgregor S., et al. Bias, precision and heritability of self-reported and clinically measured height in Australian twins. Human Genetics 2006, 120(4):571-580.
    • (2006) Human Genetics , vol.120 , Issue.4 , pp. 571-580
    • Macgregor, S.1
  • 46
    • 1042302757 scopus 로고    scopus 로고
    • Revelation of a new mitochondrial DNA mutation (G12147A) in a MELAS/MERFF phenotype
    • Melone M.A.B., et al. Revelation of a new mitochondrial DNA mutation (G12147A) in a MELAS/MERFF phenotype. Archives of Neurology 2004, 61(2):269-272.
    • (2004) Archives of Neurology , vol.61 , Issue.2 , pp. 269-272
    • Melone, M.A.B.1
  • 48
    • 79953692105 scopus 로고    scopus 로고
    • (-)-Epigallocatechin-3-gallate reactivates silenced tumor suppressor genes, Cip1/p21 and p16INK4a, by reducing DNA methylation and increasing histones acetylation in human skin cancer cells
    • Nandakumar V., Vaid M., Katiyar S.K. (-)-Epigallocatechin-3-gallate reactivates silenced tumor suppressor genes, Cip1/p21 and p16INK4a, by reducing DNA methylation and increasing histones acetylation in human skin cancer cells. Carcinogenesis 2011, 32(4):537-544.
    • (2011) Carcinogenesis , vol.32 , Issue.4 , pp. 537-544
    • Nandakumar, V.1    Vaid, M.2    Katiyar, S.K.3
  • 49
    • 0030969942 scopus 로고    scopus 로고
    • Protein import into mitochondria
    • Neupert W. Protein import into mitochondria. Annual Review of Biochemistry 1997, 66(1):863-917.
    • (1997) Annual Review of Biochemistry , vol.66 , Issue.1 , pp. 863-917
    • Neupert, W.1
  • 50
    • 77949912763 scopus 로고    scopus 로고
    • Extensive screening system using suspension array technology to detect mitochondrial DNA point mutations
    • Nishigaki Y., et al. Extensive screening system using suspension array technology to detect mitochondrial DNA point mutations. Mitochondrion 2010, 10(3):300-308.
    • (2010) Mitochondrion , vol.10 , Issue.3 , pp. 300-308
    • Nishigaki, Y.1
  • 51
    • 0031912334 scopus 로고    scopus 로고
    • Evidence for an X-linked genetic component in familial typical migraine
    • Nyholt D.R., et al. Evidence for an X-linked genetic component in familial typical migraine. Human Molecular Genetics 1998, 7(3):459-463.
    • (1998) Human Molecular Genetics , vol.7 , Issue.3 , pp. 459-463
    • Nyholt, D.R.1
  • 52
    • 0028454493 scopus 로고
    • Migraine classification and diagnosis. International Headache Society criteria
    • Olesen J., Lipton R.B. Migraine classification and diagnosis. International Headache Society criteria. Neurology 1994, 44(6 Suppl. 4):S6-S10.
    • (1994) Neurology , vol.44 , Issue.6 SUPPL. 4
    • Olesen, J.1    Lipton, R.B.2
  • 53
    • 33646920316 scopus 로고    scopus 로고
    • Neurochemistry of trigeminal activation in an animal model of migraine
    • Oshinsky M.L., Luo J. Neurochemistry of trigeminal activation in an animal model of migraine. Headache 2006, 46(Suppl. 1):S39-S44.
    • (2006) Headache , vol.46 , Issue.SUPPL. 1
    • Oshinsky, M.L.1    Luo, J.2
  • 54
    • 0031026069 scopus 로고    scopus 로고
    • Myoclonus epilepsy associated with ragged-red fibers: a G-to-A mutation at nucleotide pair 8363 in mitochondrial tRNA(Lys) in two families
    • Ozawa M., et al. Myoclonus epilepsy associated with ragged-red fibers: a G-to-A mutation at nucleotide pair 8363 in mitochondrial tRNA(Lys) in two families. Muscle & Nerve 1997, 20(3):271-278.
    • (1997) Muscle & Nerve , vol.20 , Issue.3 , pp. 271-278
    • Ozawa, M.1
  • 55
    • 79953739378 scopus 로고    scopus 로고
    • Fetal-specific DNA methylation ratio permits noninvasive prenatal diagnosis of trisomy 21
    • Papageorgiou E.A., et al. Fetal-specific DNA methylation ratio permits noninvasive prenatal diagnosis of trisomy 21. Nature Medicine 2011, 17(4):510-513.
    • (2011) Nature Medicine , vol.17 , Issue.4 , pp. 510-513
    • Papageorgiou, E.A.1
  • 56
    • 77950858804 scopus 로고    scopus 로고
    • Epigenetic chromatin modifications in the cortical spreading depression
    • Passaro D., et al. Epigenetic chromatin modifications in the cortical spreading depression. Brain Research 2010, 1329:1-9.
    • (2010) Brain Research , vol.1329 , pp. 1-9
    • Passaro, D.1
  • 57
    • 77952887283 scopus 로고    scopus 로고
    • Epigenetic mechanisms underlying human epileptic disorders and the process of epileptogenesis
    • Qureshi I.A., Mehler M.F. Epigenetic mechanisms underlying human epileptic disorders and the process of epileptogenesis. Neurobiology of Disease 2010, 39(1):53-60.
    • (2010) Neurobiology of Disease , vol.39 , Issue.1 , pp. 53-60
    • Qureshi, I.A.1    Mehler, M.F.2
  • 58
    • 0016692220 scopus 로고
    • X inactivation, differentiation, and DNA methylation
    • Riggs A.D. X inactivation, differentiation, and DNA methylation. Cytogenetics and Cell Genetics 1975, 14(1):9-25.
    • (1975) Cytogenetics and Cell Genetics , vol.14 , Issue.1 , pp. 9-25
    • Riggs, A.D.1
  • 59
    • 0344530960 scopus 로고    scopus 로고
    • X chromosome inactivation, differentiation, and DNA methylation revisited, with a tribute to Susumu Ohno
    • Riggs A.D. X chromosome inactivation, differentiation, and DNA methylation revisited, with a tribute to Susumu Ohno. Cytogenetic and Genome Research 2002, 99(1-4):17-24.
    • (2002) Cytogenetic and Genome Research , vol.99 , Issue.1-4 , pp. 17-24
    • Riggs, A.D.1
  • 60
    • 33646895827 scopus 로고    scopus 로고
    • NARP-MILS syndrome caused by 8993 T>G mitochondrial DNA mutation: a clinical, genetic and neuropathological study
    • Rojo A., et al. NARP-MILS syndrome caused by 8993 T>G mitochondrial DNA mutation: a clinical, genetic and neuropathological study. Acta Neuropathologica 2006, 111(6):610-616.
    • (2006) Acta Neuropathologica , vol.111 , Issue.6 , pp. 610-616
    • Rojo, A.1
  • 61
    • 0029962873 scopus 로고    scopus 로고
    • Maternally inherited cardiomyopathy and hearing loss associated with a novel mutation in the mitochondrial tRNA(Lys) gene (G8363A)
    • Santorelli F.M., et al. Maternally inherited cardiomyopathy and hearing loss associated with a novel mutation in the mitochondrial tRNA(Lys) gene (G8363A). American Journal of Human Genetics 1996, 58(5):933-939.
    • (1996) American Journal of Human Genetics , vol.58 , Issue.5 , pp. 933-939
    • Santorelli, F.M.1
  • 62
    • 79953746628 scopus 로고    scopus 로고
    • Impairment of mitochondrial tRNA(Ile) processing by a novel mutation associated with chronic progressive external ophthalmoplegia
    • Schaller A., et al. Impairment of mitochondrial tRNA(Ile) processing by a novel mutation associated with chronic progressive external ophthalmoplegia. Mitochondrion 2011, 11(3):488-496.
    • (2011) Mitochondrion , vol.11 , Issue.3 , pp. 488-496
    • Schaller, A.1
  • 63
    • 2642570305 scopus 로고    scopus 로고
    • The histone modification pattern of active genes revealed through genome-wide chromatin analysis of a higher eukaryote
    • Schubeler D., et al. The histone modification pattern of active genes revealed through genome-wide chromatin analysis of a higher eukaryote. Genes & Development 2004, 18(11):1263-1271.
    • (2004) Genes & Development , vol.18 , Issue.11 , pp. 1263-1271
    • Schubeler, D.1
  • 64
    • 67849084562 scopus 로고    scopus 로고
    • The cost and impact of health conditions on presenteeism to employers: a review of the literature
    • Schultz A.B., Chen C.Y., Edington D.W. The cost and impact of health conditions on presenteeism to employers: a review of the literature. PharmacoEconomics 2009, 27(5):365-378.
    • (2009) PharmacoEconomics , vol.27 , Issue.5 , pp. 365-378
    • Schultz, A.B.1    Chen, C.Y.2    Edington, D.W.3
  • 65
    • 0034521771 scopus 로고    scopus 로고
    • G8363A mutation in the mitochondrial DNA transfer ribonucleic acid(Lys) gene: another cause of Leigh syndrome
    • Shtilbans A., et al. G8363A mutation in the mitochondrial DNA transfer ribonucleic acid(Lys) gene: another cause of Leigh syndrome. Journal of Child Neurology 2000, 15(11):759-761.
    • (2000) Journal of Child Neurology , vol.15 , Issue.11 , pp. 759-761
    • Shtilbans, A.1
  • 66
    • 0026688649 scopus 로고
    • A new mtDNA mutation in the trans RNALys gene associated with myoclonic epilepsy and ragged-red fibers (MERRF)
    • Silvestri G., et al. A new mtDNA mutation in the trans RNALys gene associated with myoclonic epilepsy and ragged-red fibers (MERRF). American Journal of Human Genetics 1992, 51(6):1213-1217.
    • (1992) American Journal of Human Genetics , vol.51 , Issue.6 , pp. 1213-1217
    • Silvestri, G.1
  • 67
    • 0013773866 scopus 로고
    • 5-Azacytidine, a new, highly effective cancerostatic
    • Sorm F., et al. 5-Azacytidine, a new, highly effective cancerostatic. Experientia 1964, 20(4):202-203.
    • (1964) Experientia , vol.20 , Issue.4 , pp. 202-203
    • Sorm, F.1
  • 68
    • 33645123748 scopus 로고    scopus 로고
    • Mitochondrial dysfunction and migraine: evidence and hypotheses
    • Sparaco M., et al. Mitochondrial dysfunction and migraine: evidence and hypotheses. Cephalalgia 2006, 26(4):361-372.
    • (2006) Cephalalgia , vol.26 , Issue.4 , pp. 361-372
    • Sparaco, M.1
  • 69
    • 0035019225 scopus 로고    scopus 로고
    • Mitochondrial DNA transfer RNA gene sequence variations in patients with mitochondrial disorders
    • Sternberg D., et al. Mitochondrial DNA transfer RNA gene sequence variations in patients with mitochondrial disorders. Brain: A Journal of Neurology 2001, 124:984-994.
    • (2001) Brain: A Journal of Neurology , vol.124 , pp. 984-994
    • Sternberg, D.1
  • 70
    • 84870424207 scopus 로고    scopus 로고
    • A possible role for mitochondrial dysfunction in migraine
    • Stuart S., Griffiths L.R. A possible role for mitochondrial dysfunction in migraine. Molecular Genetics and Genomics 2012, 287(11-12):837-844.
    • (2012) Molecular Genetics and Genomics , vol.287 , Issue.11-12 , pp. 837-844
    • Stuart, S.1    Griffiths, L.R.2
  • 71
    • 84869096094 scopus 로고    scopus 로고
    • Epigenetics of the depressed brain: role of histone acetylation and methylation
    • Sun H., Kennedy P.J., Nestler E.J. Epigenetics of the depressed brain: role of histone acetylation and methylation. Neuropsychopharmacology 2013, 38(1):124-137.
    • (2013) Neuropsychopharmacology , vol.38 , Issue.1 , pp. 124-137
    • Sun, H.1    Kennedy, P.J.2    Nestler, E.J.3
  • 73
    • 0035782896 scopus 로고    scopus 로고
    • Neuropathological features of mitochondrial disorders
    • Tanji K., et al. Neuropathological features of mitochondrial disorders. Seminars in Cell & Developmental Biology 2001, 12(6):429-439.
    • (2001) Seminars in Cell & Developmental Biology , vol.12 , Issue.6 , pp. 429-439
    • Tanji, K.1
  • 74
    • 0032481279 scopus 로고    scopus 로고
    • A novel mitochondrial DNA point mutation in the tRNA(Ile) gene: studies in a patient presenting with chronic progressive external ophthalmoplegia and multiple sclerosis
    • Taylor R.W., et al. A novel mitochondrial DNA point mutation in the tRNA(Ile) gene: studies in a patient presenting with chronic progressive external ophthalmoplegia and multiple sclerosis. Biochemical and Biophysical Research Communications 1998, 243(1):47-51.
    • (1998) Biochemical and Biophysical Research Communications , vol.243 , Issue.1 , pp. 47-51
    • Taylor, R.W.1
  • 75
    • 0037336905 scopus 로고    scopus 로고
    • Characterization of the human heart mitochondrial proteome
    • Taylor S.W., et al. Characterization of the human heart mitochondrial proteome. Nature Biotechnology 2003, 21(3):281-286.
    • (2003) Nature Biotechnology , vol.21 , Issue.3 , pp. 281-286
    • Taylor, S.W.1
  • 76
    • 0038587683 scopus 로고    scopus 로고
    • Leigh syndrome with cytochrome-c oxidase deficiency and a single T insertion nt 5537 in the mitochondrial tRNA(Trp) gene
    • Tulinius M., et al. Leigh syndrome with cytochrome-c oxidase deficiency and a single T insertion nt 5537 in the mitochondrial tRNA(Trp) gene. Neuropediatrics 2003, 34(2):87-91.
    • (2003) Neuropediatrics , vol.34 , Issue.2 , pp. 87-91
    • Tulinius, M.1
  • 77
    • 0033022635 scopus 로고    scopus 로고
    • The inheritance of migraine with aura estimated by means of structural equation modelling
    • Ulrich V., et al. The inheritance of migraine with aura estimated by means of structural equation modelling. Journal of Medical Genetics 1999, 36(3):225-227.
    • (1999) Journal of Medical Genetics , vol.36 , Issue.3 , pp. 225-227
    • Ulrich, V.1
  • 78
    • 0034256023 scopus 로고    scopus 로고
    • Neuromuscular syndrome associated with the 3291T→C mutation of mitochondrial DNA: a second case
    • Uziel G., et al. Neuromuscular syndrome associated with the 3291T→C mutation of mitochondrial DNA: a second case. Neuromuscular Disorders 2000, 10(6):415-418.
    • (2000) Neuromuscular Disorders , vol.10 , Issue.6 , pp. 415-418
    • Uziel, G.1
  • 79
    • 33645760679 scopus 로고    scopus 로고
    • Assumption-free estimation of heritability from genome-wide identity-by-descent sharing between full siblings
    • Visscher P.M., et al. Assumption-free estimation of heritability from genome-wide identity-by-descent sharing between full siblings. PLoS Genetics 2006, 2(3):316-325.
    • (2006) PLoS Genetics , vol.2 , Issue.3 , pp. 316-325
    • Visscher, P.M.1
  • 80
    • 0042328332 scopus 로고    scopus 로고
    • Genotype-phenotype correlation in the 5703G>A mutation in the tRNA(Asn) gene of mitochondrial DNA
    • Vives-Bauza C., et al. Genotype-phenotype correlation in the 5703G>A mutation in the tRNA(Asn) gene of mitochondrial DNA. Journal of Inherited Metabolic Disease 2003, 26(5):507-508.
    • (2003) Journal of Inherited Metabolic Disease , vol.26 , Issue.5 , pp. 507-508
    • Vives-Bauza, C.1
  • 81
    • 34248371229 scopus 로고    scopus 로고
    • Migraine: a complex genetic disorder
    • Wessman M., et al. Migraine: a complex genetic disorder. Lancet Neurology 2007, 6(6):521-532.
    • (2007) Lancet Neurology , vol.6 , Issue.6 , pp. 521-532
    • Wessman, M.1
  • 82
    • 33745286231 scopus 로고    scopus 로고
    • TUF love for "junk" DNA
    • Willingham A.T., Gingeras T.R. TUF love for "junk" DNA. Cell 2006, 125(7):1215-1220.
    • (2006) Cell , vol.125 , Issue.7 , pp. 1215-1220
    • Willingham, A.T.1    Gingeras, T.R.2
  • 84
    • 0347003512 scopus 로고    scopus 로고
    • Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family
    • Zhao H., et al. Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family. American Journal of Human Genetics 2004, 74(1):139-152.
    • (2004) American Journal of Human Genetics , vol.74 , Issue.1 , pp. 139-152
    • Zhao, H.1


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