-
1
-
-
0032536016
-
Identification of a novel mutation (Leu282Arg) of the human presenilin 1 gene in Alzheimer's disease
-
Aldudo J, Bullido MJ, Arbizu T, Oliva R, Valdivieso F. 1998a. Identification of a novel mutation (Leu282Arg) of the human presenilin 1 gene in Alzheimer's disease. Neurosci Lett 240:174-176.
-
(1998)
Neurosci Lett
, vol.240
, pp. 174-176
-
-
Aldudo, J.1
Bullido, M.J.2
Arbizu, T.3
Oliva, R.4
Valdivieso, F.5
-
2
-
-
0031768676
-
Missense mutation E318G of the presenilin-1 gene appears to be a nonpathogenic polymorphism
-
Aldudo J, Bullido MJ, Frank A, Valdivieso F. 1998b. Missense mutation E318G of the presenilin-1 gene appears to be a nonpathogenic polymorphism. Ann Neurol 44:985-986.
-
(1998)
Ann Neurol
, vol.44
, pp. 985-986
-
-
Aldudo, J.1
Bullido, M.J.2
Frank, A.3
Valdivieso, F.4
-
3
-
-
0029115555
-
The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD families
-
Alzheimer's Disease Collaborative Group. 1995. The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD families. Nat Genet 11:219-222.
-
(1995)
Nat Genet
, vol.11
, pp. 219-222
-
-
-
4
-
-
0025730640
-
A rapid micropreparation technique for extraction of DNA-binding proteins from limiting numbers of mammalian cells
-
Andrews NC, Faller DV. 1991. A rapid micropreparation technique for extraction of DNA-binding proteins from limiting numbers of mammalian cells. Nucleic Acids Res 19:2499.
-
(1991)
Nucleic Acids Res
, vol.19
, pp. 2499
-
-
Andrews, N.C.1
Faller, D.V.2
-
5
-
-
7844229878
-
Risk for Alzheimer's disease correlates with transcriptional activity of the APOE gene
-
Artiga MJ, Bullido MJ, Frank A, Sastre I, Recuero M, Garcia MA, Lendon CL, Han SW, Morris JC, Vazquez J, Goate A, Valdivieso F. 1998a. Risk for Alzheimer's disease correlates with transcriptional activity of the APOE gene. Hum Mol Genet 12:1887-1892.
-
(1998)
Hum Mol Genet
, vol.12
, pp. 1887-1892
-
-
Artiga, M.J.1
Bullido, M.J.2
Frank, A.3
Sastre, I.4
Recuero, M.5
Garcia, M.A.6
Lendon, C.L.7
Han, S.W.8
Morris, J.C.9
Vazquez, J.10
Goate, A.11
Valdivieso, F.12
-
6
-
-
0032498118
-
Allelic polymorphisms in the transcriptional regulatory region of apolipoprotein E gene
-
Artiga MJ, Bullido MJ, Sastre I, Recuero M, Garcia MA, Aldudo J, Vázquez J, Valdivieso F. 1998b. Allelic polymorphisms in the transcriptional regulatory region of apolipoprotein E gene. FEBS Lett 421:105-108.
-
(1998)
FEBS Lett
, vol.421
, pp. 105-108
-
-
Artiga, M.J.1
Bullido, M.J.2
Sastre, I.3
Recuero, M.4
Garcia, M.A.5
Aldudo, J.6
Vázquez, J.7
Valdivieso, F.8
-
7
-
-
16144367382
-
Presenilin-1 polymorphism and Alzheimer's disease
-
Bouras C, Giannakopoulos P, Schioi J, Tezapsidis J, Robakis NK. 1996. Presenilin-1 polymorphism and Alzheimer's disease. Lancet 347:1185-1186.
-
(1996)
Lancet
, vol.347
, pp. 1185-1186
-
-
Bouras, C.1
Giannakopoulos, P.2
Schioi, J.3
Tezapsidis, J.4
Robakis, N.K.5
-
8
-
-
17344374322
-
A polymorphism in the transcriptional regulatory region of apolipoprotein E associated with risk for dementia of the Alzheimer type
-
Bullido MJ, Artiga MJ, Recuero M, Sastre I, Garcia MA, Aldudo J, Lendon C, Han SW, Morris JC, Frank A, Vázquez J, Goate A, Valdivieso F. 1998. A polymorphism in the transcriptional regulatory region of apolipoprotein E associated with risk for dementia of the Alzheimer type. Nat Genet 18:69-71.
-
(1998)
Nat Genet
, vol.18
, pp. 69-71
-
-
Bullido, M.J.1
Artiga, M.J.2
Recuero, M.3
Sastre, I.4
Garcia, M.A.5
Aldudo, J.6
Lendon, C.7
Han, S.W.8
Morris, J.C.9
Frank, A.10
Vázquez, J.11
Goate, A.12
Valdivieso, F.13
-
9
-
-
0031938304
-
Presenilin mutations in Alzheimer's disease
-
Cruts M, Van Broeckhoven C. 1998. Presenilin mutations in Alzheimer's disease. Hum Mutat 11:183-190.
-
(1998)
Hum Mutat
, vol.11
, pp. 183-190
-
-
Cruts, M.1
Van Broeckhoven, C.2
-
10
-
-
6844255860
-
Estimation of the genetic contribution of presenilin-1 and -2 mutations in a population-based study of presenilin Alzheimer disease
-
Cruts M, Van Duijn CM, Backhovens H, Van den Broeck M, Wehnert A, Serneels S, Sherrington R, Hutton M, Hardy J, St George-Hyslop PH, Van Broeckhoven C. 1998. Estimation of the genetic contribution of presenilin-1 and -2 mutations in a population-based study of presenilin Alzheimer disease. Hum Mol Genet 7:43-51.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 43-51
-
-
Cruts, M.1
Van Duijn, C.M.2
Backhovens, H.3
Van Den Broeck, M.4
Wehnert, A.5
Serneels, S.6
Sherrington, R.7
Hutton, M.8
Hardy, J.9
St George-Hyslop, P.H.10
Van Broeckhoven, C.11
-
11
-
-
0033366606
-
The Glu318Gly substitution in presenilin 1 is not causally related to Alzheimer disease
-
Dermaut B, Cruts M, Slooter AJ, Van Gestel S, De Jonghe C, Vanderstichele H, Vanmechelen E, Breteler MM, Hofman A, van Duijn CM, Van Broeckhoven C. 1999. The Glu318Gly substitution in presenilin 1 is not causally related to Alzheimer disease. Am J Hum Genet 64:290-292.
-
(1999)
Am J Hum Genet
, vol.64
, pp. 290-292
-
-
Dermaut, B.1
Cruts, M.2
Slooter, A.J.3
Van Gestel, S.4
De Jonghe, C.5
Vanderstichele, H.6
Vanmechelen, E.7
Breteler, M.M.8
Hofman, A.9
Van Duijn, C.M.10
Van Broeckhoven, C.11
-
12
-
-
17344363967
-
De novo presenilin 1 mutations are rare in clinically sporadic, early onset Alzheimer's disease cases
-
Dumanchin C, Brice A, Campion D, Hannequin D, Martin C, Moreau V, Agid Y, Martinez M, Clerget-Darpoux F, Frebourg T. 1998. De novo presenilin 1 mutations are rare in clinically sporadic, early onset Alzheimer's disease cases. J Med Genet 35:672-673.
-
(1998)
J Med Genet
, vol.35
, pp. 672-673
-
-
Dumanchin, C.1
Brice, A.2
Campion, D.3
Hannequin, D.4
Martin, C.5
Moreau, V.6
Agid, Y.7
Martinez, M.8
Clerget-Darpoux, F.9
Frebourg, T.10
-
13
-
-
0029969180
-
Transcriptional factor AP-2 regulates human apolipoprotein E gene expression in astrocytoma cells
-
García MA, Vázquez J, Giménez C, Valdivieso F, Zafra F. 1996. Transcriptional factor AP-2 regulates human apolipoprotein E gene expression in astrocytoma cells. J Neurosci 16:7550-7556.
-
(1996)
J Neurosci
, vol.16
, pp. 7550-7556
-
-
García, M.A.1
Vázquez, J.2
Giménez, C.3
Valdivieso, F.4
Zafra, F.5
-
14
-
-
0031017150
-
Presenilin-1 immunoreactive neurons are preserved in late-onset Alzheimer's disease
-
Giannakopoulos P, Bouras C, Kovari E, Schioi J, Tezapsidis N, Hof PR, Robakis NK. 1997. Presenilin-1 immunoreactive neurons are preserved in late-onset Alzheimer's disease. Am J Pathol 150:429-436.
-
(1997)
Am J Pathol
, vol.150
, pp. 429-436
-
-
Giannakopoulos, P.1
Bouras, C.2
Kovari, E.3
Schioi, J.4
Tezapsidis, N.5
Hof, P.R.6
Robakis, N.K.7
-
15
-
-
0026088977
-
Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease
-
Goate A, Chartier-Harlin MC, Mullan M, Brown J, Crawford F, Fidani L, Giuffra L, Haynes A, Irving N, James L, Mant R, Newton P, Rooke K, Roques P, Talbot C, Pericak-Vance M, Roses A, Williamson R, Rossor M, Owen M, Hardy J. 1991. Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease. Nature 349:704-709.
-
(1991)
Nature
, vol.349
, pp. 704-709
-
-
Goate, A.1
Chartier-Harlin, M.C.2
Mullan, M.3
Brown, J.4
Crawford, F.5
Fidani, L.6
Giuffra, L.7
Haynes, A.8
Irving, N.9
James, L.10
Mant, R.11
Newton, P.12
Rooke, K.13
Roques, P.14
Talbot, C.15
Pericak-Vance, M.16
Roses, A.17
Williamson, R.18
Rossor, M.19
Owen, M.20
Hardy, J.21
more..
-
16
-
-
8244260610
-
Two novel (M233T and R278T) presenilin-1 mutations in early-onset Alzheimer's disease pedigrees and preliminary evidence for association of presenilin-1 mutations with a novel phenotype
-
Kwok JB, Taddei K, Hallupp M, Fisher C, Brooks WS, Broe GA, Hardy J, Fulham MJ, Nicholson GA, Stell R, St George Hyslop PH, Fraser PE, Kakulas B, Clarnett R, Relkin N, Gandy SE, Schofield PR, Martins RN. 1997. Two novel (M233T and R278T) presenilin-1 mutations in early-onset Alzheimer's disease pedigrees and preliminary evidence for association of presenilin-1 mutations with a novel phenotype. Neuroreport 8:1537-1542.
-
(1997)
Neuroreport
, vol.8
, pp. 1537-1542
-
-
Kwok, J.B.1
Taddei, K.2
Hallupp, M.3
Fisher, C.4
Brooks, W.S.5
Broe, G.A.6
Hardy, J.7
Fulham, M.J.8
Nicholson, G.A.9
Stell, R.10
St George Hyslop, P.H.11
Fraser, P.E.12
Kakulas, B.13
Clarnett, R.14
Relkin, N.15
Gandy, S.E.16
Schofield, P.R.17
Martins, R.N.18
-
17
-
-
0031911596
-
A new polymorphism in the APOE promoter associated with risk of developing Alzheimer's dementia
-
Lambert JC, Pasquier F, Cottel D, Frigard B, Amouyel P, Chartier-Harlin MC. 1998. A new polymorphism in the APOE promoter associated with risk of developing Alzheimer's dementia. Hum Mol Gen 7:533-540.
-
(1998)
Hum Mol Gen
, vol.7
, pp. 533-540
-
-
Lambert, J.C.1
Pasquier, F.2
Cottel, D.3
Frigard, B.4
Amouyel, P.5
Chartier-Harlin, M.C.6
-
18
-
-
0023476284
-
Computational simulation of DNA melting and its application to denaturing gradient gel electrophoresis
-
Lerman LS, Silverstein K. 1987. Computational simulation of DNA melting and its application to denaturing gradient gel electrophoresis. Methods Enzymol 155:482-501.
-
(1987)
Methods Enzymol
, vol.155
, pp. 482-501
-
-
Lerman, L.S.1
Silverstein, K.2
-
19
-
-
0029087026
-
Candidate gene for the chromosome 1 familial Alzheimer's disease locus
-
Levy-Lahad E, Wasco W, Poorkaj P, Romano DM, Oshima J, Pettingell WH, Yu C, Jondro PD, Schmidt SD, Wang K, Crowley AC, Fu Y, Guenette SY, Galas D, Wijsman EM, Bird TD, Schelenberg GD, Tanzi RE. 1995. Candidate gene for the chromosome 1 familial Alzheimer's disease locus. Science 269:973-977.
-
(1995)
Science
, vol.269
, pp. 973-977
-
-
Levy-Lahad, E.1
Wasco, W.2
Poorkaj, P.3
Romano, D.M.4
Oshima, J.5
Pettingell, W.H.6
Yu, C.7
Jondro, P.D.8
Schmidt, S.D.9
Wang, K.10
Crowley, A.C.11
Fu, Y.12
Guenette, S.Y.13
Galas, D.14
Wijsman, E.M.15
Bird, T.D.16
Schelenberg, G.D.17
Tanzi, R.E.18
-
20
-
-
17944404642
-
The Glu318Gly mutation of the presenilin-1 gene does not necessarily cause Alzheimer's disease
-
Mattila KM, Forsell C, Pirttila T, Rinne JO, Lehtimaki T, Roytta M, Lilius L, Eerola A, St George-Hyslop PH, Frey H, Lannfelt L. 1998. The Glu318Gly mutation of the presenilin-1 gene does not necessarily cause Alzheimer's disease. Ann Neurol 44:965-967.
-
(1998)
Ann Neurol
, vol.44
, pp. 965-967
-
-
Mattila, K.M.1
Forsell, C.2
Pirttila, T.3
Rinne, J.O.4
Lehtimaki, T.5
Roytta, M.6
Lilius, L.7
Eerola, A.8
St George-Hyslop, P.H.9
Frey, H.10
Lannfelt, L.11
-
21
-
-
0030054380
-
A newly identified polymorphism in the apolipoprotein E enhancer gene region is associated with Alzheimer's disease and strongly with the e4 allele
-
Mui S, Briggs M, Chung H, Wallace RB, Gomez-Isla T, Rebeck GW, Hyman BT 1996. A newly identified polymorphism in the apolipoprotein E enhancer gene region is associated with Alzheimer's disease and strongly with the e4 allele. Neurology 47:196-201.
-
(1996)
Neurology
, vol.47
, pp. 196-201
-
-
Mui, S.1
Briggs, M.2
Chung, H.3
Wallace, R.B.4
Gomez-Isla, T.5
Rebeck, G.W.6
Hyman, B.T.7
-
22
-
-
0023476285
-
Detection and localization of single base changes by denaturing gradient gel electrophoresis
-
Myers RM, Maniatis T, Lerman LS. 1987. Detection and localization of single base changes by denaturing gradient gel electrophoresis. Methods Enzymol 155:501-527.
-
(1987)
Methods Enzymol
, vol.155
, pp. 501-527
-
-
Myers, R.M.1
Maniatis, T.2
Lerman, L.S.3
-
23
-
-
0007696315
-
Detection of single base changes in DNA; ribonuclease cleavage and denaturing gradient gel electrophoresis
-
Davies KE, editor Oxford: IRL Press
-
Myers RM, Sheffield VC, Cox DR. 1988. Detection of single base changes in DNA; ribonuclease cleavage and denaturing gradient gel electrophoresis. In: Davies KE, editor. Genome analysis - a practical approach. Oxford: IRL Press. p 94-139.
-
(1988)
Genome Analysis - a Practical Approach
, pp. 94-139
-
-
Myers, R.M.1
Sheffield, V.C.2
Cox, D.R.3
-
24
-
-
6844258883
-
Missense mutations in the chromosome 14 familial Alzheimer's disease presenilin 1 gene
-
Poorkaj P, Sharma V, Anderson L, Nemens E, Alonso ME, Orr H, White J, Heston L, Bird TD, Schellenberg GD. 1998. Missense mutations in the chromosome 14 familial Alzheimer's disease presenilin 1 gene. Hum Mutat 11:216-221.
-
(1998)
Hum Mutat
, vol.11
, pp. 216-221
-
-
Poorkaj, P.1
Sharma, V.2
Anderson, L.3
Nemens, E.4
Alonso, M.E.5
Orr, H.6
White, J.7
Heston, L.8
Bird, T.D.9
Schellenberg, G.D.10
-
25
-
-
0031790549
-
A novel Leu171Pro mutation in presenilin-1 gene in a mexican family with early onset Alzheimer disease
-
Ramirez-Dueñas MG, Rogaeva EA, Leal CA, Lin C, Ramirez-Casillas GA, Hernandez-Romo JA, St George-Hyslop PH, Cantu JM. 1998. A novel Leu171Pro mutation in presenilin-1 gene in a Mexican family with early onset Alzheimer disease. Ann Genet 41:149-153.
-
(1998)
Ann Genet
, vol.41
, pp. 149-153
-
-
Ramirez-Dueñas, M.G.1
Rogaeva, E.A.2
Leal, C.A.3
Lin, C.4
Ramirez-Casillas, G.A.5
Hernandez-Romo, J.A.6
St George-Hyslop, P.H.7
Cantu, J.M.8
-
26
-
-
13144250191
-
Germline mutational analysis of presenilin 1 and APP genes in Jewish-Israeli individuals with familial or early-onset Alzheimer disease using denaturing gradient gel electrophoresis (DGGE)
-
Reznik-Wolf H, Treves TA, Shabtai H, Aharon-Peretz J, Chapman J, Davidson M, Barkai G, Hyslop PH, Goldman B, Korczyn AD, Friedman E. 1998. Germline mutational analysis of presenilin 1 and APP genes in Jewish-Israeli individuals with familial or early-onset Alzheimer disease using denaturing gradient gel electrophoresis (DGGE). Eur J Hum Genet 6:176-180.
-
(1998)
Eur J Hum Genet
, vol.6
, pp. 176-180
-
-
Reznik-Wolf, H.1
Treves, T.A.2
Shabtai, H.3
Aharon-Peretz, J.4
Chapman, J.5
Davidson, M.6
Barkai, G.7
Hyslop, P.H.8
Goldman, B.9
Korczyn, A.D.10
Friedman, E.11
-
27
-
-
0029101491
-
Familial Alzheimer's disease in kindreds with missense in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene
-
Rogaev EI, Sherrington R, Rogaeva EA, Levesque G, Ikeda M, Liang Y, Chi H, Lin C, Holman K, Tsuda T, Mar L, Sorbi S, Nacmias B, Piacentini S, Amaducci L, Chumakov I, Cohen D, Lannfelt L, Fraser PE, Rommens JM, St George-Hyslop PH. 1995. Familial Alzheimer's disease in kindreds with missense in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene. Nature 376:775-778.
-
(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
Mar, L.11
Sorbi, S.12
Nacmias, B.13
Piacentini, S.14
Amaducci, L.15
Chumakov, I.16
Cohen, D.17
Lannfelt, L.18
Fraser, P.E.19
Rommens, J.M.20
St George-Hyslop, P.H.21
more..
-
28
-
-
0031569390
-
Analysis of the 5′ sequence, genomic structure, and alternative splicing of the presenilin-1 gene (PSEN1) associated with early onset Alzheimer disease
-
Rogaev EI, Sherrington R, Wu C, Levesque G, Liang Y, Rogaeva EA, Ikeda M, Holman K, Lin C, Lukiw WJ, de Jong PJ, Fraser PE, Rommens JM, St George-Hyslop P. 1997. Analysis of the 5′ sequence, genomic structure, and alternative splicing of the presenilin-1 gene (PSEN1) associated with early onset Alzheimer disease. Genomics 40:415-424.
-
(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
-
29
-
-
0029790382
-
Missense mutations of the PS-1/S182 gene in German early-onset Alzheimer's disease patients
-
Sandbrink R, Zhang D, Schaeffer S, Masters CL, Bauer J, Forstl H, Beyreuther K. 1996. Missense mutations of the PS-1/S182 gene in German early-onset Alzheimer's disease patients. Ann Neurol 40:265-266.
-
(1996)
Ann Neurol
, vol.40
, pp. 265-266
-
-
Sandbrink, R.1
Zhang, D.2
Schaeffer, S.3
Masters, C.L.4
Bauer, J.5
Forstl, H.6
Beyreuther, K.7
-
30
-
-
0029004341
-
Cloning a gene bearing missense mutations in early-onset familial Alzheimer's disease
-
Sherrington R, Rogaev E, Liang Y, Rogaeva EA, Levesque G, Ikeda M, Chi H, Lin C, Holman K, Tsuda T, Mar L, Foncin JF, Bruni AC, Montesi MP, Sorbi S, Rainero Y, Pinessi L, Nee L, Chumakov Y, Pollen D, Brookes A, Sanseau P, Polinsky J, Wasco W, Da Silva HAR, Haines JL, Pericak-Vance MA, Tanzi RE, Roses AD, Fraser PE, Rommens JM, St George-Hyslop PH. 1995. Cloning a gene bearing missense mutations in early-onset familial Alzheimer's disease. Nature 375:754-760.
-
(1995)
Nature
, vol.375
, pp. 754-760
-
-
Sherrington, R.1
Rogaev, E.2
Liang, Y.3
Rogaeva, E.A.4
Levesque, G.5
Ikeda, M.6
Chi, H.7
Lin, C.8
Holman, K.9
Tsuda, T.10
Mar, L.11
Foncin, J.F.12
Bruni, A.C.13
Montesi, M.P.14
Sorbi, S.15
Rainero, Y.16
Pinessi, L.17
Nee, L.18
Chumakov, Y.19
Pollen, D.20
Brookes, A.21
Sanseau, P.22
Polinsky, J.23
Wasco, W.24
Da Silva, H.A.R.25
Haines, J.L.26
Pericak-Vance, M.A.27
Tanzi, R.E.28
Roses, A.D.29
Fraser, P.E.30
Rommens, J.M.31
St George-Hyslop, P.H.32
more..
-
31
-
-
7844246535
-
Two novel presenilin-1 mutations (Ser169Leu and Pro436Gln) associated with very early onset Alzheimer's disease
-
Taddei K, Kwok JB, Kril JJ, Halliday GM, Creasey H, Hallupp M, Fisher C, Brooks WS, Chung C, Andrews C, Masters CL, Schofield PR, Martins RN. 1998. Two novel presenilin-1 mutations (Ser169Leu and Pro436Gln) associated with very early onset Alzheimer's disease. Neuroreport 9:3335-3339.
-
(1998)
Neuroreport
, vol.9
, pp. 3335-3339
-
-
Taddei, K.1
Kwok, J.B.2
Kril, J.J.3
Halliday, G.M.4
Creasey, H.5
Hallupp, M.6
Fisher, C.7
Brooks, W.S.8
Chung, C.9
Andrews, C.10
Masters, C.L.11
Schofield, P.R.12
Martins, R.N.13
-
32
-
-
0031044834
-
Expression of presenilin-1 and -2 mRNAs in rat and Alzheimer's disease brains
-
Takami K, Terai K, Matsuo A, Walker DG, McGeer PL. 1997. Expression of presenilin-1 and -2 mRNAs in rat and Alzheimer's disease brains. Brain Res 748:122-130.
-
(1997)
Brain Res
, vol.748
, pp. 122-130
-
-
Takami, K.1
Terai, K.2
Matsuo, A.3
Walker, D.G.4
McGeer, P.L.5
-
33
-
-
0030297259
-
Sequence analysis of presenilin-1 gene mutations in Japanese Alzheimer's disease patients
-
Tanahashi H, Kawakatsu S, Kaneko M, Yamanaka H, Takahashi K, Tabira T. 1996. Sequence analysis of presenilin-1 gene mutations in Japanese Alzheimer's disease patients. Neurosci Lett 218:139-141.
-
(1996)
Neurosci Lett
, vol.218
, pp. 139-141
-
-
Tanahashi, H.1
Kawakatsu, S.2
Kaneko, M.3
Yamanaka, H.4
Takahashi, K.5
Tabira, T.6
-
34
-
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0031893609
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A presenilin-1 truncating mutation is present in two cases with autopsy-confirmed early-onset Alzheimer disease
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Tysoe C, Whittaker J, Xuereb J, Cairns NJ, Cruts M, Van Broeckhoven C, Wilcock G, Rubinsztein DC. 1998. A presenilin-1 truncating mutation is present in two cases with autopsy-confirmed early-onset Alzheimer disease. Am J Hum Genet 62:70-76.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 70-76
-
-
Tysoe, C.1
Whittaker, J.2
Xuereb, J.3
Cairns, N.J.4
Cruts, M.5
Van Broeckhoven, C.6
Wilcock, G.7
Rubinsztein, D.C.8
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35
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6844240203
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A novel Polish presenilin-1 mutation (P117L) is associated with familial Alzheimer's disease and leads to death as early as the age of 23 years
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Wisniewski T, Dowjat WK, Buxbaum JD, Khorkova O, Efthimiopoulos S, Kulczycki J, Lojkowska W, Wegiel J, Wisniewski HM, Frangione B. 1998. A novel Polish presenilin-1 mutation (P117L) is associated with familial Alzheimer's disease and leads to death as early as the age of 23 years. Neuroreport 9:217-221.
-
(1998)
Neuroreport
, vol.9
, pp. 217-221
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Wisniewski, T.1
Dowjat, W.K.2
Buxbaum, J.D.3
Khorkova, O.4
Efthimiopoulos, S.5
Kulczycki, J.6
Lojkowska, W.7
Wegiel, J.8
Wisniewski, H.M.9
Frangione, B.10
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