A presenilin-1 truncating mutation causing Alzheimer's disease

被引：0
|
作者：
De Jonghe, C [1 ]
Tysoe, C [1 ]
Cruts, M [1 ]
Vanderhoeven, I [1 ]
Vanderstichele, H [1 ]
Vanmechelen, E [1 ]
Van Broeckhoven, C [1 ]
Rubinsztein, DC [1 ]
Hendriks, L [1 ]
机构：
[1] Univ Instelling Antwerp, Dept Biochem, Neurogenet Lab, B-2610 Wilrijk, Belgium
来源：
ALZHEIMER'S DISEASE AND RELATED DISORDERS: ETIOLOGY, PATHOGENESIS AND THERAPEUTICS | 1999年
关键词：
D O I：
暂无
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
引用
收藏
页码：81 / 86
页数：6
相关论文
共 50 条
  • [31] A presenilin-1 mutation in a Japanese family with Alzheimer's disease and distinctive abnormalities on cranial MRI
    Aoki, M
    Abe, K
    Oda, N
    Ikeda, M
    Tsuda, T
    Kanai, M
    Shoji, M
    StGeorgeHyslop, PH
    Itoyama, Y
    NEUROLOGY, 1997, 48 (04) : 1118 - 1120
  • [32] A presenilin-1 mutation causes Alzheimer disease without affecting Notch signaling
    Zhang, Shuting
    Cai, Fang
    Wu, Yili
    Bozorgmehr, Tahereh
    Wang, Zhe
    Zhang, Si
    Huang, Daochao
    Guo, Jifeng
    Shen, Lu
    Rankin, Catharine
    Tang, Beisha
    Song, Weihong
    MOLECULAR PSYCHIATRY, 2020, 25 (03) : 603 - 613
  • [33] Alzheimer's disease-causing presenilin-1 mutations have deleterious effects on mitochondrial function
    Han, Jihoon
    Park, Heejin
    Maharana, Chinmoyee
    Gwon, A-Ryeong
    Park, Jinsu
    Baek, Seung Hyun
    Bae, Han-Gyu
    Cho, Yoonsuk
    Kim, Hark Kyun
    Sul, Jae Hoon
    Lee, Jeongmi
    Kim, Eunae
    Kim, Junsik
    Cho, Yongeun
    Park, Sunyoung
    Palomera, Leon F.
    Arumugam, Thiruma, V
    Mattson, Mark P.
    Jo, Dong-Gyu
    THERANOSTICS, 2021, 11 (18): : 8855 - 8873
  • [34] Multimodal Imaging in a Patient With Alzheimer Disease and Parkinsonism Because of a Presenilin-1 Mutation
    Lu, Jia-Ying
    Sun, Yi-Min
    Yen, Tzu-Chen
    Zuo, Chuan-Tao
    Wang, Jian
    CLINICAL NUCLEAR MEDICINE, 2021, 46 (09) : E483 - E484
  • [35] A presenilin-1 mutation causes Alzheimer disease without affecting Notch signaling
    Shuting Zhang
    Fang Cai
    Yili Wu
    Tahereh Bozorgmehr
    Zhe Wang
    Si Zhang
    Daochao Huang
    Jifeng Guo
    Lu Shen
    Catharine Rankin
    Beisha Tang
    Weihong Song
    Molecular Psychiatry, 2020, 25 : 603 - 613
  • [36] Cytoskeletal alterations differentiate presenilin-1 and sporadic Alzheimer’s disease
    Adele Woodhouse
    Claire E. Shepherd
    Anna Sokolova
    Victoria L. Carroll
    Anna E. King
    Glenda M. Halliday
    Tracey C. Dickson
    James C. Vickers
    Acta Neuropathologica, 2009, 117
  • [37] CSF Studies Facilitate DNA Diagnosis in Familial Alzheimer's Disease Due to a Presenilin-1 Mutation
    de Bot, Susanne T.
    Kremer, H. P. H.
    Dooijes, Dennis
    Verbeek, Marcel M.
    JOURNAL OF ALZHEIMERS DISEASE, 2009, 17 (01) : 53 - 57
  • [38] Are presenilin-1 and β-catenin interactions relevant to the pathogenesis of Alzheimer's disease
    Bursaux, E
    M S-MEDECINE SCIENCES, 1999, 15 (01): : 119 - 120
  • [39] Monogenic determinants of familial Alzheimer's disease: Presenilin-1 mutations
    Kovacs, DM
    Tanzi, RE
    CELLULAR AND MOLECULAR LIFE SCIENCES, 1998, 54 (09) : 902 - 909
  • [40] Presenilin-1 may mediate Taupathy in Sporadic Alzheimer's disease
    Zhu, C. Q.
    JOURNAL OF ALZHEIMERS DISEASE, 2002, 4 (01) : 54 - 55
12345