No association between an intronic presenilin-1 gene polymorphism and schizophrenia in a Chinese population

被引:2
|
作者
Chiu, HJ
Tsai, SJ
Chen, JY
Lin, CY
Bai, YM
Song, HL
Lai, HC
Hong, CJ
机构
[1] Vet Gen Hosp, Dept Psychiat, Taipei, Taiwan
[2] Yu Li Vet Hosp, Sect Psychiat, Taipei, Taiwan
[3] Natl Yang Ming Univ, Sch Med, Div Psychiat, Taipei 112, Taiwan
关键词
association study; polymorphism; genotype; presenilin; schizophrenia;
D O I
10.1016/S0165-1781(99)00066-9
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
We investigated the association between schizophrenic psychosis and an intronic polymorphism of the presenilin-1 (PS1) gene in a Chinese population. Schizophrenic and control groups had similar PS1 genotype distributions and allele frequencies, indicating that this polymorphism may not be involved in the development of schizophrenia. (C) 1999 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:245 / 248
页数:4
相关论文
共 50 条
  • [1] No association between an intronic polymorphism in the presenilin-1 gene and Alzheimer disease in a Tunisian population
    Afef Achouri Rassas
    Sondess Hadj Fredj
    Hela Mrabet Khiari
    Safa Sahnoun
    Amina Bibi
    Hajer Siala
    Amel Mrabet
    Taieb Messaoud
    Journal of Neural Transmission, 2013, 120 : 1355 - 1358
  • [2] No association between an intronic polymorphism in the presenilin-1 gene and Alzheimer disease in a Tunisian population
    Rassas, Afef Achouri
    Fredj, Sondess Hadj
    Khiari, Hela Mrabet
    Sahnoun, Safa
    Bibi, Amina
    Siala, Hajer
    Mrabet, Amel
    Messaoud, Taieb
    JOURNAL OF NEURAL TRANSMISSION, 2013, 120 (09) : 1355 - 1358
  • [3] No association between an intronic polymorphism in the presenilin-1 gene and Alzheimer disease in a German population
    Bagli, M
    Papassotiropoulos, A
    Schwab, SG
    Jessen, F
    Rao, ML
    Maier, W
    Heun, R
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 1999, 167 (01) : 34 - 36
  • [4] Genetic association between an intronic polymorphism in presenilin-1 gene and sporadic dementia
    Wu, DB
    Ye, L
    Wang, L
    Liu, JW
    Wang, LN
    NEUROBIOLOGY OF AGING, 2002, 23 (01) : S339 - S340
  • [5] No association between an intronic polymorphism in the presenilin-1 gene and Alzheimer's disease
    Singleton, AB
    Lamb, H
    Leake, A
    McKeith, IG
    Perry, RH
    Morris, CM
    NEUROSCIENCE LETTERS, 1997, 234 (01) : 19 - 22
  • [6] No association between the intronic presenilin 1 polymorphism and Alzheimer's disease in the Chinese population
    Wu, XD
    Jiang, SD
    Lin, SC
    Tang, GM
    Feng, GY
    Qian, YP
    Wang, DX
    Ren, DM
    Gul, NF
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1999, 88 (01): : 1 - 3
  • [7] No association between the intronic Presenilin-1 polymorphism and Alzheimer's disease in clinic and population-based samples
    Cai, XG
    Stanton, J
    Fallin, D
    Hoyne, J
    Duara, R
    Gold, M
    Sevush, S
    Scibelli, P
    Crawford, F
    Mullan, M
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1997, 74 (02): : 202 - 203
  • [8] Genetic association between intronic polymorphism in presenilin-1 gene and late-onset Alzheimer's disease
    Wragg, M
    Hutton, M
    Talbot, C
    Busfield, F
    Han, SW
    Lendon, C
    Clark, RF
    Morris, JC
    Edwards, D
    Goate, A
    Pfeiffer, E
    Crook, R
    Prihar, G
    Phillips, H
    Baker, M
    Hardy, J
    Rossor, M
    Houlden, H
    Karran, E
    Roberts, G
    Craddock, N
    LANCET, 1996, 347 (9000): : 509 - 512
  • [9] No association of Presenilin-1 intronic polymorphism and Alzheimer's disease in Australia
    Taddei, K
    Yang, D
    Fisher, C
    Clarnette, R
    Hallmayer, J
    Barnetson, R
    Maller, R
    Brooks, WS
    Whyte, S
    Nicholson, GA
    Masters, CL
    Broe, GA
    Gandy, SE
    Martins, RN
    NEUROSCIENCE LETTERS, 1998, 246 (03) : 178 - 180
  • [10] Association of apolipoprotein E genotype and intronic polymorphism of the presenilin-1 gene with Alzheimer's disease in elderly Taiwan Chinese
    Hu, CJ
    Sung, SM
    Liu, HC
    Chang, JG
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 1998, 157 (02) : 158 - 161