-
2
-
-
0030293676
-
Familial Alzheimer's disease-linked presenilin 1 variants elevate Abeta1-42/1-40 ratio in vitro and in vivo
-
(1996)
Neuron
, vol.17
, pp. 1005-1013
-
-
Borchelt, D.R.1
Thinakaran, G.2
Eckman, C.B.3
Lee, M.K.4
Davenport, F.5
Ratovitsky, T.6
Prada, C.M.7
Kim, G.8
Seekins, S.9
Yager, D.10
Slunt, H.H.11
Wang, R.12
Seeger, M.13
Levey, A.I.14
Gandy, S.E.15
Copeland, N.G.16
Jenkins, N.A.17
Price, D.L.18
Younkin, S.G.19
Sisodia, S.S.20
more..
-
3
-
-
0032488995
-
The proteolytic fragments of the Alzheimer's disease-associated presenilin-1 form heterodimers and occur as a 100-150-kDa molecular mass complex
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 3205-3211
-
-
Capell, A.1
Grunberg, J.2
Pesold, B.3
Diehlmann, A.4
Citron, M.5
Nixon, R.6
Beyreuther, K.7
Selkoe, D.J.8
Haass, C.9
-
4
-
-
0032854745
-
Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimer's disease by increased Abeta42 secretion
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 1529-1540
-
-
De Jonghe, C.1
Cruts, M.2
Rogaeva, E.A.3
Tysoe, C.4
Singleton, A.5
Vanderstichele, H.6
Meschino, W.7
Dermaut, B.8
Vanderhoeven, I.9
Backhovens, H.10
Vanmechelen, E.11
Morris, C.M.12
Hardy, J.13
Rubinsztein, D.C.14
St. George-Hyslop, P.H.15
Van Broeckhoven, C.16
-
5
-
-
0033586810
-
Apoptosis. Dead end for neurodegeneration?
-
(1999)
Nature
, vol.399
, pp. 204-205
-
-
Haass, C.1
-
6
-
-
0033258544
-
Presenilin-1 mutations downregulate the signalling pathway of the unfolded-protein response
-
(1999)
Nat. Cell Biol.
, vol.1
, pp. 479-485
-
-
Katayama, T.1
Imaizumi, K.2
Sato, N.3
Miyoshi, K.4
Kudo, T.5
Hitomi, J.6
Morihara, T.7
Yoneda, T.8
Gomi, F.9
Mori, Y.10
Nakano, Y.11
Takeda, J.12
Tsuda, T.13
Itoyama, Y.14
Murayama, O.15
Takashima, A.16
St. George-Hyslop, P.17
Takeda, M.18
Tohyama, M.19
-
7
-
-
0032032013
-
Aberrant RNA processing in a neurodegenerative disease: The cause for absent EAAT2, a glutamate transporter, in amyotrophic lateral sclerosis
-
(1998)
Neuron
, vol.20
, pp. 589-602
-
-
Lin, C.L.1
Bristol, L.A.2
Jin, L.3
Dykes-Hoberg, M.4
Crawford, T.5
Clawson, L.6
Rothstein, J.D.7
-
8
-
-
10144264560
-
Structure and alternative splicing of the presenilin-2 gene
-
(1996)
Neuroreport
, vol.7
, pp. 1680-1684
-
-
Prihar, G.1
Fuldner, R.A.2
Perez-Tur, J.3
Lincoln, S.4
Duff, K.5
Crook, R.6
Hardy, J.7
Philips, C.A.8
Venter, C.9
Talbot, C.10
Clark, R.F.11
Goate, A.12
Li, J.13
Potter, H.14
Karran, E.15
Roberts, G.W.16
Hutton, M.17
Adams, M.D.18
-
9
-
-
0029101491
-
Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene
-
(1995)
Nature
, vol.376
, pp. 775-778
-
-
Rogaev, E.I.1
Sherrington, R.2
Rogaeva, E.A.3
Levesque, G.4
Ikeda, M.5
Liang, Y.6
Chi, H.7
Lin, C.8
Holman, K.9
Tsuda, T.10
-
10
-
-
0031569390
-
Analysis of the 5′ sequence, genomic structure, and alternative splicing of the presenilin-1 gene (PSEN1) associated with early onset Alzheimer disease
-
(1997)
Genomics
, vol.40
, pp. 415-424
-
-
Rogaev, E.I.1
Sherrington, R.2
Wu, C.3
Levesque, G.4
Liang, Y.5
Rogaeva, E.A.6
Ikeda, M.7
Holman, K.8
Lin, C.9
Lukiw, W.J.10
De Jong, P.J.11
Fraser, P.E.12
Rommens, J.M.13
St. George-Hyslop, P.14
-
11
-
-
0030048505
-
Identification and characterization of presenilin I-467, I-463 and I-374
-
(1996)
FEBS Lett.
, vol.381
, pp. 7-11
-
-
Sahara, N.1
Yahagi, Y.2
Takagi, H.3
Kondo, T.4
Okochi, M.5
Usami, M.6
Shirasawa, T.7
Mori, H.8
-
12
-
-
0032973469
-
A novel presenilin-2 splice variant in human Alzheimer's disease brain tissu
-
(1999)
J. Neurochem.
, vol.72
, pp. 2498-2505
-
-
Sato, N.1
Hori, O.2
Yamaguchi, A.3
Lambert, J.C.4
Chartier-Harlin, M.C.5
Robinson, P.A.6
Delacourte, A.7
Schmidt, A.M.8
Furuyama, T.9
Imaizumi, K.10
Tohyama, M.11
Takagi, T.12
-
13
-
-
0029004341
-
Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease
-
(1995)
Nature
, vol.375
, pp. 754-760
-
-
Sherrington, R.1
Rogaev, E.I.2
Liang, Y.3
Rogaeva, E.A.4
Levesque, G.5
Ikeda, M.6
Chi, H.7
Lin, C.8
Li, G.9
Holman, K.10
-
14
-
-
0033583047
-
The biological and pathological function of the presenilin-1 Deltaexon 9 mutation is independent of its defect to undergo proteolytic processing
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 7615-7618
-
-
Steiner, H.1
Romig, H.2
Grim, M.G.3
Philipp, U.4
Pesold, B.5
Citron, M.6
Baumeister, R.7
Haass, C.8
-
15
-
-
0033517844
-
Amyloidogenic function of the Alzheimer's disease-associated presenilin 1 in the absence of endoproteolysis
-
(1999)
Biochemistry
, vol.38
, pp. 14600-14605
-
-
Steiner, H.1
Romig, H.2
Pesold, B.3
Philipp, U.4
Baader, M.5
Citron, M.6
Loetscher, H.7
Jacobsen, H.8
Haass, C.9
-
16
-
-
15844425969
-
Endoproteolysis of presenilin 1 and accumulation of processed derivatives in vivo
-
(1996)
Neuron
, vol.17
, pp. 181-190
-
-
Thinakaran, G.1
Borchelt, D.R.2
Lee, M.K.3
Slunt, H.H.4
Spitzer, L.5
Kim, G.6
Ratovitsky, T.7
Davenport, F.8
Nordstedt, C.9
Seeger, M.10
Hardy, J.11
Levey, A.I.12
Gandy, S.E.13
Jenkins, N.A.14
Copeland, N.G.15
Price, D.L.16
Sisodia, S.S.17
|