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Volumn 31, Issue 3, 2011, Pages 264-270

Association of a Notch 3 gene polymorphism with migraine susceptibility

Author keywords

CADASIL; Migraine; Notch 3

Indexed keywords

ARTICLE; AUSTRALIA; CONTROLLED STUDY; EXON; FEMALE; FOLLOW UP; GENE; GENE FREQUENCY; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; MIGRAINE; MIGRAINE WITH AURA; NOTCH 3 GENE; NUCLEOTIDE SEQUENCE; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 79953201568     PISSN: 03331024     EISSN: 14682982     Source Type: Journal    
DOI: 10.1177/0333102410381143     Document Type: Article
Times cited : (21)

References (27)
  • 2
    • 3042536354 scopus 로고    scopus 로고
    • The estrogen receptor 1 G594A polymorphism is associated with migraine susceptibility in two independent case/control groups
    • DOI 10.1007/s10048-004-0181-4
    • Colson NJ, Lea RA, Quinlan S., MacMillan J. and Griffiths LR The estrogen receptor 1 G594A polymorphism is associated with migraine susceptibility in two independent case/control groups. Neurogenetics 2004 ; 5 (2). 129-133. (Pubitemid 38828673)
    • (2004) Neurogenetics , vol.5 , Issue.2 , pp. 129-133
    • Colson, N.J.1    Lea, R.A.2    Quinlan, S.3    MacMillan, J.4    Griffiths, L.R.5
  • 3
    • 4243070837 scopus 로고    scopus 로고
    • The methylenetetrahydrofolate reductase gene variant C677 T influences susceptibility to migraine with aura
    • Lea RA, Ovcaric M., Sundholm J., MacMillan J. and Griffiths LR The methylenetetrahydrofolate reductase gene variant C677 T influences susceptibility to migraine with aura. BMC Med 2004 ; 2: 3.
    • (2004) BMC Med , vol.2 , pp. 3
    • Lea, R.A.1    Ovcaric, M.2    Sundholm, J.3    MacMillan, J.4    Griffiths, L.R.5
  • 4
    • 0033785342 scopus 로고    scopus 로고
    • Description of a simple test for CADASIL disease and determination of mutation frequencies in sporadic ischaemic stroke and dementia patients
    • Wang T., Sharma SD, Fox N., Rossor M., Brown MJ and Sharma P. Description of a simple test for CADASIL disease and determination of mutation frequencies in sporadic ischaemic stroke and dementia patients. J Neurol Neurosurg Psychiatry 2000 ; 69 (5). 652-654.
    • (2000) J Neurol Neurosurg Psychiatry , vol.69 , Issue.5 , pp. 652-654
    • Wang, T.1    Sharma, S.D.2    Fox, N.3    Rossor, M.4    Brown, M.J.5    Sharma, P.6
  • 5
    • 22144484846 scopus 로고    scopus 로고
    • The spectrum of mutations for CADASIL diagnosis
    • DOI 10.1007/s10072-005-0444-3
    • Federico A., Bianchi S. and Dotti MT The spectrum of mutations for CADASIL diagnosis. Neurol Sci 2005 ; 26 (2). 117-124. (Pubitemid 40975512)
    • (2005) Neurological Sciences , vol.26 , Issue.2 , pp. 117-124
    • Federico, A.1    Bianchi, S.2    Dotti, M.T.3
  • 9
    • 0034279414 scopus 로고    scopus 로고
    • Evidence for allelic association of the dopamine beta-hydroxylase gene (DBH) with susceptibility to typical migraine
    • Lea RA, Dohy A., Jordan K., Quinlan S., Brimage PJ and Griffiths LR Evidence for allelic association of the dopamine beta-hydroxylase gene (DBH) with susceptibility to typical migraine. Neurogenetics 2000 ; 3 (1). 35-40.
    • (2000) Neurogenetics , vol.3 , Issue.1 , pp. 35-40
    • Lea, R.A.1    Dohy, A.2    Jordan, K.3    Quinlan, S.4    Brimage, P.J.5    Griffiths, L.R.6
  • 10
    • 0345671971 scopus 로고    scopus 로고
    • International classification of headache disorders
    • Headache Classification Committee Of The International Headache Society 2nd ed.
    • Headache Classification Committee of the International Headache Society. International classification of headache disorders. 2nd ed. Cephalalgia 2004 ; 24 (Suppl 1): 1-160.
    • (2004) Cephalalgia , vol.24 , pp. 1-160
  • 11
    • 70249118588 scopus 로고    scopus 로고
    • Association between migraine and a functional polymorphism at the dopamine beta-hydroxylase locus
    • Fernandez F., Colson N., Quinlan S., MacMillan J., Lea RA and Griffiths LR Association between migraine and a functional polymorphism at the dopamine beta-hydroxylase locus. Neurogenetics 2009 ; 10 (3). 199-208.
    • (2009) Neurogenetics , vol.10 , Issue.3 , pp. 199-208
    • Fernandez, F.1    Colson, N.2    Quinlan, S.3    MacMillan, J.4    Lea, R.A.5    Griffiths, L.R.6
  • 12
    • 19044375834 scopus 로고    scopus 로고
    • Genetic variants of angiotensin converting enzyme and methylenetetrahydrofolate reductase may act in combination to increase migraine susceptibility
    • DOI 10.1016/j.molbrainres.2005.01.006, PII S0169328X05000276
    • Lea RA, Ovcaric M., Sundholm J., Solyom L., Macmillan J. and Griffiths LR Genetic variants of angiotensin converting enzyme and methylenetetrahydrofolate reductase may act in combination to increase migraine susceptibility. Brain Res Mol Brain Res 2005 ; 136 (1-2). 112-117. (Pubitemid 40711189)
    • (2005) Molecular Brain Research , vol.136 , Issue.1-2 , pp. 112-117
    • Lea, R.A.1    Ovcaric, M.2    Sundholm, J.3    Solyom, L.4    MacMillan, J.5    Griffiths, L.R.6
  • 13
    • 15444369324 scopus 로고    scopus 로고
    • Investigation of hormone receptor genes in migraine
    • DOI 10.1007/s10048-004-0205-0
    • Colson NJ, Lea RA, Quinlan S., MacMillan J. and Griffiths LR Investigation of hormone receptor genes in migraine. Neurogenetics 2005 ; 6 (1). 17-23. (Pubitemid 40394826)
    • (2005) Neurogenetics , vol.6 , Issue.1 , pp. 17-23
    • Colson, N.J.1    Lea, R.A.2    Quinlan, S.3    MacMillan, J.4    Griffiths, L.R.5
  • 14
    • 0024284028 scopus 로고
    • A simple salting out procedure for extracting DNA from human nucleated cells
    • Miller SA, Dykes DD and Polesky HF A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 1988 ; 16 (3). 1215.
    • (1988) Nucleic Acids Res , vol.16 , Issue.3 , pp. 1215
    • Miller, S.A.1    Dykes, D.D.2    Polesky, H.F.3
  • 15
    • 84959801619 scopus 로고
    • Statistical aspects of the analysis of data from retrospective studies of disease
    • Mantel N. and Haenszel W. Statistical aspects of the analysis of data from retrospective studies of disease. J Natl Cancer Inst 1959 ; 22 (4). 719-748.
    • (1959) J Natl Cancer Inst , vol.22 , Issue.4 , pp. 719-748
    • Mantel, N.1    Haenszel, W.2
  • 16
    • 13444269543 scopus 로고    scopus 로고
    • Haploview: Analysis and visualization of LD and haplotype maps
    • DOI 10.1093/bioinformatics/bth457
    • Barrett JC, Fry B., Maller J. and Daly MJ Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics 2005 ; 21 (2). 263-265. (Pubitemid 40202029)
    • (2005) Bioinformatics , vol.21 , Issue.2 , pp. 263-265
    • Barrett, J.C.1    Fry, B.2    Maller, J.3    Daly, M.J.4
  • 17
    • 65949110572 scopus 로고    scopus 로고
    • CADASIL: Extended polymorphisms and mutational analysis of the NOTCH3 gene
    • Ungaro C., Mazzei R., Conforti FL, et al. CADASIL: extended polymorphisms and mutational analysis of the NOTCH3 gene. J Neurosci Res 2009 ; 87 (5). 1162-1167.
    • (2009) J Neurosci Res , vol.87 , Issue.5 , pp. 1162-1167
    • Ungaro, C.1    Mazzei, R.2    Conforti, F.L.3
  • 18
    • 0028785253 scopus 로고
    • Familial hemiplegic migraine and autosomal dominant arteriopathy with leukoencephalopathy (CADASIL)
    • Hutchinson M., O'Riordan J., Javed M., et al. Familial hemiplegic migraine and autosomal dominant arteriopathy with leukoencephalopathy (CADASIL). Ann Neurol 1995 ; 38 (5). 817-824.
    • (1995) Ann Neurol , vol.38 , Issue.5 , pp. 817-824
    • Hutchinson, M.1    O'Riordan, J.2    Javed, M.3
  • 19
    • 0028858163 scopus 로고
    • New phenotype of the cerebral autosomal dominant arteriopathy mapped to chromosome 19: Migraine as the prominent clinical feature
    • Vérin M., Rolland Y., Landgraf F., et al. New phenotype of the cerebral autosomal dominant arteriopathy mapped to chromosome 19: migraine as the prominent clinical feature. J Neurol Neurosurg Psychiatry 1995 ; 59 (6). 579-585.
    • (1995) J Neurol Neurosurg Psychiatry , vol.59 , Issue.6 , pp. 579-585
    • Vérin, M.1    Rolland, Y.2    Landgraf, F.3
  • 21
    • 24344486827 scopus 로고    scopus 로고
    • Infarcts in the posterior circulation territory in migraine. The population-based MRI CAMERA study
    • DOI 10.1093/brain/awh542
    • Kruit MC, Launer LJ, Ferrari MD and van Buchem MA Infarcts in the posterior circulation territory in migraine. The population-based MRI CAMERA study. Brain 2005 ; 128 (Pt 9). 2068-2077. (Pubitemid 41253274)
    • (2005) Brain , vol.128 , Issue.9 , pp. 2068-2077
    • Kruit, M.C.1    Launer, L.J.2    Ferrari, M.D.3    Van Buchem, M.A.4
  • 24
    • 67349256414 scopus 로고    scopus 로고
    • Association of three-gene interaction among MTHFR, ALOX5AP and NOTCH3 with thrombotic stroke: A multicenter case-control study
    • Liu J., Sun K., Bai Y., et al. Association of three-gene interaction among MTHFR, ALOX5AP and NOTCH3 with thrombotic stroke: a multicenter case-control study. Hum Genet 2009 ; 125 (5-6). 649-656.
    • (2009) Hum Genet , vol.125 , Issue.5-6 , pp. 649-656
    • Liu, J.1    Sun, K.2    Bai, Y.3
  • 26
    • 33645093960 scopus 로고    scopus 로고
    • Investigating the association between Notch3 polymorphism and migraine
    • Borroni B., Brambilla C., Liberini P., et al. Investigating the association between Notch3 polymorphism and migraine. Headache 2006 ; 46 (2). 317-321.
    • (2006) Headache , vol.46 , Issue.2 , pp. 317-321
    • Borroni, B.1    Brambilla, C.2    Liberini, P.3
  • 27
    • 1942467065 scopus 로고    scopus 로고
    • Genomic variants in exons and introns: Identifying the splicing spoilers
    • DOI 10.1038/nrg1327
    • Pagani F. and Baralle FE Genomic variants in exons and introns: identifying the splicing spoilers. Nat Rev Genet 2004 ; 5 (5). 389-396. (Pubitemid 38529410)
    • (2004) Nature Reviews Genetics , vol.5 , Issue.5 , pp. 389-396
    • Pagani, F.1    Baralle, F.E.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.