-
1
-
-
0029004341
-
Cloning of a gene bearing missense mutations in early-onset familial AD
-
Sherrington R, Rogaev EI, Liang Y, Rogaeva EA, Levesque G, Ikeda M et al. Cloning of a gene bearing missense mutations in early-onset familial AD. Nature (London) 1995; 375: 754-760.
-
(1995)
Nature (London)
, 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
-
2
-
-
0029101491
-
Familial AD in kindreds with missense mutations in a gene on chromosome 1 related to the AD type 3 gene
-
Rogaev EI, Sherrington R, Rogaeva EA, Levesque G, Ikeda M, Liang Y et al. Familial AD in kindreds with missense mutations in a gene on chromosome 1 related to the AD type 3 gene. Nature (London) 1995; 376: 775-778.
-
(1995)
Nature (London)
, 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
-
3
-
-
85006235997
-
A familial AD locus on chromosome 1
-
Levi-Lahad E, Wasko W, Poorkaj P, Romano D, Oshima J, Pettingell W et al. A familial AD locus on chromosome 1. Science 1995; 269: 970-973.
-
(1995)
Science
, vol.269
, pp. 970-973
-
-
Levi-Lahad, E.1
Wasko, W.2
Poorkaj, P.3
Romano, D.4
Oshima, J.5
Pettingell, W.6
-
4
-
-
6844255860
-
Estimation of the genetic contribution of presenilin-1 and -2 mutations in a population-based study of presenile AD
-
Cruts M, van Dujin C, Backhoven H, Van den B, Wehnert A, Serneels S et al. Estimation of the genetic contribution of presenilin-1 and -2 mutations in a population-based study of presenile AD. Human Molec Genet 1998; 7: 43-51.
-
(1998)
Human Molec Genet
, vol.7
, pp. 43-51
-
-
Cruts, M.1
Van Dujin, C.2
Backhoven, H.3
Van den, B.4
Wehnert, A.5
Serneels, S.6
-
5
-
-
8944241774
-
AD associated with mutations in presenilin 2 is rare and variably penetrant
-
Sherrington R, Floerich S, Sorbi S, Campion D, Chi H, Rogaeva E et al. AD associated with mutations in presenilin 2 is rare and variably penetrant. Human Molec Genet 1996; 5: 985-988.
-
(1996)
Human Molec Genet
, vol.5
, pp. 985-988
-
-
Sherrington, R.1
Floerich, S.2
Sorbi, S.3
Campion, D.4
Chi, H.5
Rogaeva, E.6
-
6
-
-
0035964209
-
Screening for PS1 mutations in a referral-based series of AD cases: 21 Novel mutations
-
Rogaeva EA, Fafel K, Song Y, Medeiros H, Sato C, Liang Y et al. Screening for PS1 mutations in a referral-based series of AD cases: 21 novel mutations. Neurology 2001; 57: 621-625.
-
(2001)
Neurology
, vol.57
, pp. 621-625
-
-
Rogaeva, E.A.1
Fafel, K.2
Song, Y.3
Medeiros, H.4
Sato, C.5
Liang, Y.6
-
7
-
-
0029115555
-
The structure of the presenilin 1 (S182) gene and the identification of six novel mutations in early onset AD pedigrees
-
The AD Collaborative group. The structure of the presenilin 1 (S182) gene and the identification of six novel mutations in early onset AD pedigrees. Nat Genet 1995; 11: 219-222.
-
(1995)
Nat Genet
, vol.11
, pp. 219-222
-
-
-
8
-
-
85006235995
-
-
AD forum: www.alzforum.org
-
-
-
-
9
-
-
0031569390
-
Analysis of the 5′ sequence, genomic structure and alternative splicing of the presenilin 1 gene associated with early-onset AD
-
Rogaev EI, Sherrington R, Rogaeva E, Ikeda M, Levesque G, Lin C et al. Analysis of the 5′ sequence, genomic structure and alternative splicing of the presenilin 1 gene associated with early-onset AD. Genomics 1997; 40: 415-424.
-
(1997)
Genomics
, vol.40
, pp. 415-424
-
-
Rogaev, E.I.1
Sherrington, R.2
Rogaeva, E.3
Ikeda, M.4
Levesque, G.5
Lin, C.6
-
10
-
-
0033214675
-
Presenilins: Molecular switches between protelysis and signal transduction
-
Annaert W, Strooper B. Presenilins: molecular switches between protelysis and signal transduction. Trends Neurosci 1999; 22: 439-442.
-
(1999)
Trends Neurosci
, vol.22
, pp. 439-442
-
-
Annaert, W.1
Strooper, B.2
-
11
-
-
0033966452
-
Notch and presenilins in vertebrates and inverebrates: Implications for neuronal development and degeneration
-
Selkoe DJ. Notch and presenilins in vertebrates and inverebrates: implications for neuronal development and degeneration. Curr Opin Neurobiol 2000; 10: 50-57.
-
(2000)
Curr Opin Neurobiol
, vol.10
, pp. 50-57
-
-
Selkoe, D.J.1
-
12
-
-
0033371315
-
Molecular genetics of AD
-
St George-Hyslop P. Molecular genetics of AD. Seminal Neurol 1999; 19: 371-383.
-
(1999)
Seminal Neurol
, vol.19
, pp. 371-383
-
-
St George-Hyslop, P.1
-
13
-
-
0034618715
-
Nicastrin modulates presenilin-mediated notch/glp-1 signal transduction and betaAPP processing
-
Yu G, Nishimura M, Arawaka S, Levitan D, Zhang L, Tandon A et al. Nicastrin modulates presenilin-mediated notch/glp-1 signal transduction and betaAPP processing. Nature 2000; 407: 48-54.
-
(2000)
Nature
, vol.407
, pp. 48-54
-
-
Yu, G.1
Nishimura, M.2
Arawaka, S.3
Levitan, D.4
Zhang, L.5
Tandon, A.6
-
14
-
-
0032364393
-
Presenilins: Discovery and characterization of genes for AD
-
Rogaev EI. Presenilins: discovery and characterization of genes for AD. Molec Biol 1998; 32: 58-69.
-
(1998)
Molec Biol
, vol.32
, pp. 58-69
-
-
Rogaev, E.I.1
-
16
-
-
0034302872
-
Neuroinflammatory signaling upregulation in Alzheimer's disease
-
Lukiw WJ, Bazan NG. Neuroinflammatory signaling upregulation in Alzheimer's disease. Neurochem Res 2000; 25: 1173-1184.
-
(2000)
Neurochem Res
, vol.25
, pp. 1173-1184
-
-
Lukiw, W.J.1
Bazan, N.G.2
-
17
-
-
0033555896
-
Contrasting role of presenilin-1 and presenilin-2 in neuronal differentiation in vitro
-
Hong CS, Caromile L, Nomata Y et al. Contrasting role of presenilin-1 and presenilin-2 in neuronal differentiation in vitro. J Neurosci 1999; 19: 637-643.
-
(1999)
J Neurosci
, vol.19
, pp. 637-643
-
-
Hong, C.S.1
Caromile, L.2
Nomata, Y.3
-
18
-
-
0035931493
-
Presenilin-2 (PSEN2) expression upregulation in a model of retinopathy of prematurity and pathoangiogenesis
-
Lukiw WJ, Gordon WC, Rogaev EI, Thompson H, Bazan N. Presenilin-2 (PSEN2) expression upregulation in a model of retinopathy of prematurity and pathoangiogenesis. NeuroReport 2001; 12: 53-57.
-
(2001)
NeuroReport
, vol.12
, pp. 53-57
-
-
Lukiw, W.J.1
Gordon, W.C.2
Rogaev, E.I.3
Thompson, H.4
Bazan, N.5
-
19
-
-
0034945475
-
Platelet-activating factor and endotoxin activate CCAAT/enhancer binding protein in rat small intestine
-
Wang H, Qu X, De Plaen IG, Hsueh W. Platelet-activating factor and endotoxin activate CCAAT/enhancer binding protein in rat small intestine. Br J Pharmacol 2001; 133: 713-721.
-
(2001)
Br J Pharmacol
, vol.133
, pp. 713-721
-
-
Wang, H.1
Qu, X.2
De Plaen, I.G.3
Hsueh, W.4
-
20
-
-
0032742952
-
Genetic association of the presenilin 1 regulatory region with early-onset AD in a population-based sample
-
van Duijin C, Cruts M, Theuns J, Van Gassen G, Bachoven H, van den Broeck M et al. Genetic association of the presenilin 1 regulatory region with early-onset AD in a population-based sample. Eur J Hum Genet 1999; 7: 801-806.
-
(1999)
Eur J Hum Genet
, vol.7
, pp. 801-806
-
-
Van Duijin, C.1
Cruts, M.2
Theuns, J.3
Van Gassen, G.4
Bachoven, H.5
Van den Broeck, M.6
-
21
-
-
0034639656
-
Genetic variability in the regulatory region of presenilin 1 associated with risk for Alzheimer's disease and variable expression
-
Theuns J, Del-Favero J, Dermut B, van Dujin C, Backhovens H, Van den Broeck M et al. Genetic variability in the regulatory region of presenilin 1 associated with risk for Alzheimer's disease and variable expression. Human Molec Genetics 2001; 9: 325-331.
-
(2001)
Human Molec Genetics
, vol.9
, pp. 325-331
-
-
Theuns, J.1
Del-Favero, J.2
Dermut, B.3
Van Dujin, C.4
Backhovens, H.5
Van den Broeck, M.6
-
22
-
-
0034984156
-
The -48 C/T polymorphism in the presenilin 1 promoter is associated with an increased risk of developing AD and an increased Abeta load in brain
-
Lambert J-C, Mann DM, Harris J, Chartier-Harlin M-C, Cumming A, Coates J et al. The -48 C/T polymorphism in the presenilin 1 promoter is associated with an increased risk of developing AD and an increased Abeta load in brain. J Med Genet 2001; 38: 353-355.
-
(2001)
J Med Genet
, vol.38
, pp. 353-355
-
-
Lambert, J.-C.1
Mann, D.M.2
Harris, J.3
Chartier-Harlin, M.-C.4
Cumming, A.5
Coates, J.6
-
23
-
-
0027360792
-
Identification of the genetic locus for Keratosis Palmaris and Plantaris on chromosome 17 near the RARA and Keratin type 1 genes
-
Rogaev E, Rogaeva E, Ginter E, Korovaitseva G, Farrer L, Shlensky A et al. Identification of the genetic locus for Keratosis Palmaris and Plantaris on chromosome 17 near the RARA and Keratin type 1 genes. Nature Genet 1993; 5: 158-162.
-
(1993)
Nature Genet
, vol.5
, pp. 158-162
-
-
Rogaev, E.1
Rogaeva, E.2
Ginter, E.3
Korovaitseva, G.4
Farrer, L.5
Shlensky, A.6
-
24
-
-
0027363954
-
Analysis of the c-Fos gene on chromosome 14 and its relationships to the 5′-promoter of the amyloid precursor protein (APP) gene on chr 21 in familial AD
-
Rogaev E, Lukiw W, Vaula G, Haines J, Rogaeva E, Tsuda T et al. Analysis of the c-Fos gene on chromosome 14 and its relationships to the 5′-promoter of the amyloid precursor protein (APP) gene on chr 21 in familial AD. Neurology 1993; 43: 2275-2279.
-
(1993)
Neurology
, vol.43
, pp. 2275-2279
-
-
Rogaev, E.1
Lukiw, W.2
Vaula, G.3
Haines, J.4
Rogaeva, E.5
Tsuda, T.6
-
25
-
-
0029984784
-
Genomic structure and expression of STR2, the chromosome 1 familial AD gene
-
Levy-Lahad E, Poorkaj P, Wang K, Fu Y, Oshima J, Milligan J, Schellenberg G. Genomic structure and expression of STR2, the chromosome 1 familial AD gene. Genomics 1996; 34: 198-204.
-
(1996)
Genomics
, vol.34
, pp. 198-204
-
-
Levy-Lahad, E.1
Poorkaj, P.2
Wang, K.3
Fu, Y.4
Oshima, J.5
Milligan, J.6
Schellenberg, G.7
-
27
-
-
0021271971
-
Clinical diagnosis of AD: Report of the NINCDS-ADRDA work group under the auspices of the Department of Health and Human Services Task Force on Alzheimer's Disease
-
McKhann G, Drachman D, Folstein M, Katzman R, Price D, Stadlan E. Clinical diagnosis of AD: report of the NINCDS-ADRDA work group under the auspices of the Department of Health and Human Services Task Force on Alzheimer's Disease. Neurology 1984; 34: 939-945.
-
(1984)
Neurology
, vol.34
, pp. 939-945
-
-
McKhann, G.1
Drachman, D.2
Folstein, M.3
Katzman, R.4
Price, D.5
Stadlan, E.6
-
28
-
-
12944310975
-
Association between angiotensin-converting enzyme and AD
-
Farrer L, Sherbatich T, Keryanov S, Korovaitseva G, Rogaeva E, Petruk S et al. Association between angiotensin-converting enzyme and AD. Arch Neurol 2000; 57: 210-214.
-
(2000)
Arch Neurol
, vol.57
, pp. 210-214
-
-
Farrer, L.1
Sherbatich, T.2
Keryanov, S.3
Korovaitseva, G.4
Rogaeva, E.5
Petruk, S.6
-
30
-
-
0032584205
-
Budesonide epimer R or dexamethasone selectively inhibit platelet-activating factor-induced or interleukin 1 beta-induced DNA binding activity of cis-acting transcription factors and cyclooxygenase-2 gene expression in human epidermal keratinocytes
-
Lukiw WJ, Pelaez RP, Martinez J, Bazan NG. Budesonide epimer R or dexamethasone selectively inhibit platelet-activating factor-induced or interleukin 1 beta-induced DNA binding activity of cis-acting transcription factors and cyclooxygenase-2 gene expression in human epidermal keratinocytes. Proc Natl Acad Sci USA 1998; 95: 3914-3919.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 3914-3919
-
-
Lukiw, W.J.1
Pelaez, R.P.2
Martinez, J.3
Bazan, N.G.4
-
31
-
-
0027250364
-
Recognition DNA sequences of interferon regulatory factor 1 (IRF-1) and IRF-2, regulators of cell growth and the interferon system
-
Tanaka N, Kawakami T, Taniguchi T Recognition DNA sequences of interferon regulatory factor 1 (IRF-1) and IRF-2, regulators of cell growth and the interferon system. Mol Cell Biol 1993; 13: 4531-4538.
-
(1993)
Mol Cell Biol
, vol.13
, pp. 4531-4538
-
-
Tanaka, N.1
Kawakami, T.2
Taniguchi, T.3
-
32
-
-
0031003233
-
The Alzheimer's family of diseases: Many etiologies, one pathogenesis?
-
Hardy J. The Alzheimer's family of diseases: many etiologies, one pathogenesis? Proc Natl Acad Sci USA 1997; 94: 2095-2097.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 2095-2097
-
-
Hardy, J.1
-
33
-
-
0030028429
-
Genetic association between intronic polymorphism in presenilin-1 gene and late-onset AD
-
AD Collaborative Group
-
Wrag M, Hutton M, Talbot C et al. Genetic association between intronic polymorphism in presenilin-1 gene and late-onset AD. AD Collaborative Group. Lancet 1996; 347: 509-512.
-
(1996)
Lancet
, vol.347
, pp. 509-512
-
-
Wrag, M.1
Hutton, M.2
Talbot, C.3
-
34
-
-
0030910513
-
No association or linkage between an intronic polymorphism of presenilin 1 and sporadic and late-onset familial AD
-
Scott WK, Yamaoka L, Locke P et al. No association or linkage between an intronic polymorphism of presenilin 1 and sporadic and late-onset familial AD. Genet Epidemiol 1997; 14: 307-315.
-
(1997)
Genet Epidemiol
, vol.14
, pp. 307-315
-
-
Scott, W.K.1
Yamaoka, L.2
Locke, P.3
-
35
-
-
0033535508
-
Presenilin is required for activity and nuclear access of notch in drosophila
-
Struhl G, Greenwald I. Presenilin is required for activity and nuclear access of notch in drosophila. Nature 1999; 398: 522-525.
-
(1999)
Nature
, vol.398
, pp. 522-525
-
-
Struhl, G.1
Greenwald, I.2
-
36
-
-
0035816661
-
A transcriptively active complex of APP with Fe65 and Histone Acetyltransferase Tip60
-
Cao X, Sudhov TC. A transcriptively active complex of APP with Fe65 and Histone Acetyltransferase Tip60. Science 2001; 293: 115-120.
-
(2001)
Science
, vol.293
, pp. 115-120
-
-
Cao, X.1
Sudhov, T.C.2
-
37
-
-
4243578821
-
Antisense reduction of presenilin 1 significantly increases Aβ42(43) secreted by human embrionic kidney cells
-
Refolo L, Eckman C, Parada CM, Yager D, Younkin S. Antisense reduction of presenilin 1 significantly increases Aβ42(43) secreted by human embrionic kidney cells. Neurobiol Aging 1998; 19: S63.
-
(1998)
Neurobiol Aging
, vol.19
, pp. S63
-
-
Refolo, L.1
Eckman, C.2
Parada, C.M.3
Yager, D.4
Younkin, S.5
|