-
1
-
-
0033616590
-
Unusual phenotypic alteration of beta amyloid precursor protein (betaAPP) maturation by a new Val-715 -- Met betaAPP-770 mutation responsible for probable early-onset Alzheimer's disease
-
Ancolio K., Dumanchin C., Barelli H., Warter J.M., Brice A., Campion D., Frebourg T., Checler F. Unusual phenotypic alteration of beta amyloid precursor protein (betaAPP) maturation by a new Val-715 -- Met betaAPP-770 mutation responsible for probable early-onset Alzheimer's disease. Proc. Natl. Acad. Sci. U.S.A 1999, 96:4119-4124.
-
(1999)
Proc. Natl. Acad. Sci. U.S.A
, vol.96
, pp. 4119-4124
-
-
Ancolio, K.1
Dumanchin, C.2
Barelli, H.3
Warter, J.M.4
Brice, A.5
Campion, D.6
Frebourg, T.7
Checler, F.8
-
2
-
-
79952747862
-
Alzheimer's disease
-
Ballard C., Gauthier S., Corbett A., Brayne C., Aarsland D., Jones E. Alzheimer's disease. Lancet 2011, 377:1019-1031.
-
(2011)
Lancet
, vol.377
, pp. 1019-1031
-
-
Ballard, C.1
Gauthier, S.2
Corbett, A.3
Brayne, C.4
Aarsland, D.5
Jones, E.6
-
3
-
-
0030293676
-
Familial Alzheimer's disease-linked presenilin 1 variants elevate Abeta1-42/1-40 ratio invitro and invivo
-
Borchelt D.R., Thinakaran G., Eckman C.B., Lee M.K., Davenport F., Ratovitsky T., Prada C.M., Kim G., Seekins S., Yager D., Slunt H.H., Wang R., Seeger M., Levey A.I., Gandy S.E., Copeland N.G., Jenkins N.A., Price D.L., Younkin S.G., Sisodia S.S. Familial Alzheimer's disease-linked presenilin 1 variants elevate Abeta1-42/1-40 ratio invitro and invivo. Neuron 1996, 17:1005-1013.
-
(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..
-
4
-
-
0025863618
-
Neuropathological stageing of Alzheimer-related changes
-
Braak H., Braak E. Neuropathological stageing of Alzheimer-related changes. Acta Neuropathol. 1991, 82:239-259.
-
(1991)
Acta Neuropathol.
, vol.82
, pp. 239-259
-
-
Braak, H.1
Braak, E.2
-
5
-
-
84878660799
-
Epidemiology of Alzheimer's disease and other forms of dementia in China, 1990-2010: a systematic review and analysis
-
Chan K.Y., Wang W., Wu J.J., Liu L., Theodoratou E., Car J., Middleton L., Russ T.C., Deary I.J., Campbell H., Rudan I. Epidemiology of Alzheimer's disease and other forms of dementia in China, 1990-2010: a systematic review and analysis. Lancet 2013, 381:2016-2023.
-
(2013)
Lancet
, vol.381
, pp. 2016-2023
-
-
Chan, K.Y.1
Wang, W.2
Wu, J.J.3
Liu, L.4
Theodoratou, E.5
Car, J.6
Middleton, L.7
Russ, T.C.8
Deary, I.J.9
Campbell, H.10
Rudan, I.11
-
6
-
-
43249124446
-
APOE epsilon 4 allele predicts faster cognitive decline in mild Alzheimer disease
-
Cosentino S., Scarmeas N., Helzner E., Glymour M.M., Brandt J., Albert M., Blacker D., Stern Y. APOE epsilon 4 allele predicts faster cognitive decline in mild Alzheimer disease. Neurology 2008, 70:1842-1849.
-
(2008)
Neurology
, vol.70
, pp. 1842-1849
-
-
Cosentino, S.1
Scarmeas, N.2
Helzner, E.3
Glymour, M.M.4
Brandt, J.5
Albert, M.6
Blacker, D.7
Stern, Y.8
-
7
-
-
6844255860
-
Estimation of the genetic contribution of presenilin-1 and -2 mutations in a population-based study of presenile Alzheimer disease
-
Cruts M., van Duijn C.M., Backhovens H., Van den Broeck M., Wehnert A., Serneels S., Sherrington R., Hutton M., Hardy J., St George-Hyslop P.H., Hofman A., Van Broeckhoven C. Estimation of the genetic contribution of presenilin-1 and -2 mutations in a population-based study of presenile Alzheimer disease. Hum. Mol. Genet. 1998, 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
Hofman, A.11
Van Broeckhoven, C.12
-
8
-
-
0035421638
-
Pathogenic APP mutations near the gamma-secretase cleavage site differentially affect Abeta secretion and APP C-terminal fragment stability
-
De Jonghe C., Esselens C., Kumar-Singh S., Craessaerts K., Serneels S., Checler F., Annaert W., Van Broeckhoven C., De Strooper B. Pathogenic APP mutations near the gamma-secretase cleavage site differentially affect Abeta secretion and APP C-terminal fragment stability. Hum. Mol. Genet. 2001, 10:1665-1671.
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 1665-1671
-
-
De Jonghe, C.1
Esselens, C.2
Kumar-Singh, S.3
Craessaerts, K.4
Serneels, S.5
Checler, F.6
Annaert, W.7
Van Broeckhoven, C.8
De Strooper, B.9
-
9
-
-
9844261165
-
Anew pathogenic mutation in the APP gene (I716V) increases the relative proportion of A beta 42(43)
-
Eckman C.B., Mehta N.D., Crook R., Perez-tur J., Prihar G., Pfeiffer E., Graff-Radford N., Hinder P., Yager D., Zenk B., Refolo L.M., Prada C.M., Younkin S.G., Hutton M., Hardy J. Anew pathogenic mutation in the APP gene (I716V) increases the relative proportion of A beta 42(43). Hum. Mol. Genet. 1997, 6:2087-2089.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 2087-2089
-
-
Eckman, C.B.1
Mehta, N.D.2
Crook, R.3
Perez-tur, J.4
Prihar, G.5
Pfeiffer, E.6
Graff-Radford, N.7
Hinder, P.8
Yager, D.9
Zenk, B.10
Refolo, L.M.11
Prada, C.M.12
Younkin, S.G.13
Hutton, M.14
Hardy, J.15
-
10
-
-
34247481473
-
The effect of two newly Chinese presenilin-1 mutations on the sensitivity to trophic factor withdrawal in human neuroblastoma cells
-
Fang B.Y., Jia J.P. The effect of two newly Chinese presenilin-1 mutations on the sensitivity to trophic factor withdrawal in human neuroblastoma cells. Zhonghua Yi Xue Za Zhi 2007, 87:336-340.
-
(2007)
Zhonghua Yi Xue Za Zhi
, vol.87
, pp. 336-340
-
-
Fang, B.Y.1
Jia, J.P.2
-
11
-
-
33748084379
-
Chinese presenilin-1 V97L mutation enhanced Abeta42 levels in SH-SY5Y neuroblastoma cells
-
Fang B.Y., Jia L.F., Jia J.P. Chinese presenilin-1 V97L mutation enhanced Abeta42 levels in SH-SY5Y neuroblastoma cells. Neurosci. Lett. 2006, 406:33-37.
-
(2006)
Neurosci. Lett.
, vol.406
, pp. 33-37
-
-
Fang, B.Y.1
Jia, L.F.2
Jia, J.P.3
-
12
-
-
0016823810
-
"Mini-mental state". A practical method for grading the cognitive state of patients for the clinician
-
Folstein M.F., Folstein S.E., McHugh P.R. "Mini-mental state". A practical method for grading the cognitive state of patients for the clinician. J.Psychiatr. Res. 1975, 12:189-198.
-
(1975)
J.Psychiatr. Res.
, vol.12
, pp. 189-198
-
-
Folstein, M.F.1
Folstein, S.E.2
McHugh, P.R.3
-
13
-
-
0026088977
-
Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease
-
Goate A., Chartier-Harlin M.C., 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. Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease. Nature 1991, 349:704-706.
-
(1991)
Nature
, vol.349
, pp. 704-706
-
-
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..
-
14
-
-
0030050286
-
Clinical and pathological correlates of apolipoprotein E epsilon 4 in Alzheimer's disease
-
Gomez-Isla T., West H.L., Rebeck G.W., Harr S.D., Growdon J.H., Locascio J.J., Perls T.T., Lipsitz L.A., Hyman B.T. Clinical and pathological correlates of apolipoprotein E epsilon 4 in Alzheimer's disease. Ann. Neurol. 1996, 39:62-70.
-
(1996)
Ann. Neurol.
, vol.39
, pp. 62-70
-
-
Gomez-Isla, T.1
West, H.L.2
Rebeck, G.W.3
Harr, S.D.4
Growdon, J.H.5
Locascio, J.J.6
Perls, T.T.7
Lipsitz, L.A.8
Hyman, B.T.9
-
15
-
-
77950529014
-
Genetic screening of Alzheimer's disease genes in Iberian and African samples yields novel mutations in presenilins and APP
-
Guerreiro R.J., Baquero M., Blesa R., Boada M., Bras J.M., Bullido M.J., Calado A., Crook R., Ferreira C., Frank A., Gomez-Isla T., Hernandez I., Lleo A., Machado A., Martinez-Lage P., Masdeu J., Molina-Porcel L., Molinuevo J.L., Pastor P., Perez-Tur J., Relvas R., Oliveira C.R., Ribeiro M.H., Rogaeva E., Sa A., Samaranch L., Sanchez-Valle R., Santana I., Tarraga L., Valdivieso F., Singleton A., Hardy J., Clarimon J. Genetic screening of Alzheimer's disease genes in Iberian and African samples yields novel mutations in presenilins and APP. Neurobiol. Aging 2010, 31:725-731.
-
(2010)
Neurobiol. Aging
, vol.31
, pp. 725-731
-
-
Guerreiro, R.J.1
Baquero, M.2
Blesa, R.3
Boada, M.4
Bras, J.M.5
Bullido, M.J.6
Calado, A.7
Crook, R.8
Ferreira, C.9
Frank, A.10
Gomez-Isla, T.11
Hernandez, I.12
Lleo, A.13
Machado, A.14
Martinez-Lage, P.15
Masdeu, J.16
Molina-Porcel, L.17
Molinuevo, J.L.18
Pastor, P.19
Perez-Tur, J.20
Relvas, R.21
Oliveira, C.R.22
Ribeiro, M.H.23
Rogaeva, E.24
Sa, A.25
Samaranch, L.26
Sanchez-Valle, R.27
Santana, I.28
Tarraga, L.29
Valdivieso, F.30
Singleton, A.31
Hardy, J.32
Clarimon, J.33
more..
-
16
-
-
70449518439
-
Anovel presenilin 1 mutation (Ser169del) in a Chinese family with early-onset Alzheimer's disease
-
Guo J.F., Wei J.H., Liao S.S., Wang L., Jiang H., Tang B.S. Anovel presenilin 1 mutation (Ser169del) in a Chinese family with early-onset Alzheimer's disease. Neurosci. Lett. 2010, 468:34-37.
-
(2010)
Neurosci. Lett.
, vol.468
, pp. 34-37
-
-
Guo, J.F.1
Wei, J.H.2
Liao, S.S.3
Wang, L.4
Jiang, H.5
Tang, B.S.6
-
17
-
-
77956453910
-
Progress in the development of therapeutic antibodies targeting prion proteins and beta-amyloid peptides
-
He J., Zhang Y., Hong T. Progress in the development of therapeutic antibodies targeting prion proteins and beta-amyloid peptides. Sci. China Life Sci. 2010, 53:959-963.
-
(2010)
Sci. China Life Sci.
, vol.53
, pp. 959-963
-
-
He, J.1
Zhang, Y.2
Hong, T.3
-
18
-
-
17844375091
-
One novel presenilin-1 gene mutation in a Chinese pedigree of familial Alzheimer's disease
-
discussion 173-80
-
Jia J.P., Xu E., Shao Y.K., Sun Y.X., Li D. One novel presenilin-1 gene mutation in a Chinese pedigree of familial Alzheimer's disease. J.Alzheimers Dis. 2005, 7:119-124. discussion 173-80.
-
(2005)
J.Alzheimers Dis.
, vol.7
, pp. 119-124
-
-
Jia, J.P.1
Xu, E.2
Shao, Y.K.3
Sun, Y.X.4
Li, D.5
-
19
-
-
84899983353
-
Mutational analysis in early-onset familial Alzheimer's disease in MainlandChina
-
e1-1957.e6
-
Jiao B., Tang B.S., Liu X.Y., Xu J., Wang Y.J., Zhou L., Zhang F.F., Yan X.X., Zhou Y.F., Shen L. Mutational analysis in early-onset familial Alzheimer's disease in MainlandChina. Neurobiol. Aging 2014, 35:1957.e1-1957.e6.
-
(2014)
Neurobiol. Aging
, vol.35
, pp. 1957
-
-
Jiao, B.1
Tang, B.S.2
Liu, X.Y.3
Xu, J.4
Wang, Y.J.5
Zhou, L.6
Zhang, F.F.7
Yan, X.X.8
Zhou, Y.F.9
Shen, L.10
-
20
-
-
84864471159
-
Amutation in APP protects against Alzheimer's disease and age-related cognitive decline
-
Jonsson T., Atwal J.K., Steinberg S., Snaedal J., Jonsson P.V., Bjornsson S., Stefansson H., Sulem P., Gudbjartsson D., Maloney J., Hoyte K., Gustafson A., Liu Y.C., Lu Y.M., Bhangale T., Graham R.R., Huttenlocher J., Bjornsdottir G., Andreassen O.A., Jonsson E.G., Palotie A., Behrens T.W., Magnusson O.T., Kong A., Thorsteinsdottir U., Watts R.J., Stefansson K. Amutation in APP protects against Alzheimer's disease and age-related cognitive decline. Nature 2012, 488:96-99.
-
(2012)
Nature
, vol.488
, pp. 96-99
-
-
Jonsson, T.1
Atwal, J.K.2
Steinberg, S.3
Snaedal, J.4
Jonsson, P.V.5
Bjornsson, S.6
Stefansson, H.7
Sulem, P.8
Gudbjartsson, D.9
Maloney, J.10
Hoyte, K.11
Gustafson, A.12
Liu, Y.C.13
Lu, Y.M.14
Bhangale, T.15
Graham, R.R.16
Huttenlocher, J.17
Bjornsdottir, G.18
Andreassen, O.A.19
Jonsson, E.G.20
Palotie, A.21
Behrens, T.W.22
Magnusson, O.T.23
Kong, A.24
Thorsteinsdottir, U.25
Watts, R.J.26
Stefansson, K.27
more..
-
21
-
-
84863472459
-
Novel APP/Abeta mutation K16N produces highly toxic heteromeric Abeta oligomers
-
Kaden D., Harmeier A., Weise C., Munter L.M., Althoff V., Rost B.R., Hildebrand P.W., Schmitz D., Schaefer M., Lurz R., Skodda S., Yamamoto R., Arlt S., Finckh U., Multhaup G. Novel APP/Abeta mutation K16N produces highly toxic heteromeric Abeta oligomers. EMBO Mol. Med. 2012, 4:647-659.
-
(2012)
EMBO Mol. Med.
, vol.4
, pp. 647-659
-
-
Kaden, D.1
Harmeier, A.2
Weise, C.3
Munter, L.M.4
Althoff, V.5
Rost, B.R.6
Hildebrand, P.W.7
Schmitz, D.8
Schaefer, M.9
Lurz, R.10
Skodda, S.11
Yamamoto, R.12
Arlt, S.13
Finckh, U.14
Multhaup, G.15
-
22
-
-
0030743251
-
Rapid and efficient site-directed mutagenesis by single-tube 'megaprimer' PCR method
-
Ke S.H., Madison E.L. Rapid and efficient site-directed mutagenesis by single-tube 'megaprimer' PCR method. Nucleic Acids Res. 1997, 25:3371-3372.
-
(1997)
Nucleic Acids Res.
, vol.25
, pp. 3371-3372
-
-
Ke, S.H.1
Madison, E.L.2
-
23
-
-
0033966705
-
Novel Leu723Pro amyloid precursor protein mutation increases amyloid beta42(43) peptide levels and induces apoptosis
-
Kwok J.B., Li Q.X., Hallupp M., Whyte S., Ames D., Beyreuther K., Masters C.L., Schofield P.R. Novel Leu723Pro amyloid precursor protein mutation increases amyloid beta42(43) peptide levels and induces apoptosis. Ann. Neurol. 2000, 47:249-253.
-
(2000)
Ann. Neurol.
, vol.47
, pp. 249-253
-
-
Kwok, J.B.1
Li, Q.X.2
Hallupp, M.3
Whyte, S.4
Ames, D.5
Beyreuther, K.6
Masters, C.L.7
Schofield, P.R.8
-
24
-
-
3943092621
-
Pathways towards and away from Alzheimer's disease
-
Mattson M.P. Pathways towards and away from Alzheimer's disease. Nature 2004, 430:631-639.
-
(2004)
Nature
, vol.430
, pp. 631-639
-
-
Mattson, M.P.1
-
25
-
-
0026907151
-
Apathogenic mutation for probable Alzheimer's disease in the APP gene at the N-terminus of beta-amyloid
-
Mullan M., Crawford F., Axelman K., Houlden H., Lilius L., Winblad B., Lannfelt L. Apathogenic mutation for probable Alzheimer's disease in the APP gene at the N-terminus of beta-amyloid. Nat. Genet. 1992, 1:345-347.
-
(1992)
Nat. Genet.
, vol.1
, pp. 345-347
-
-
Mullan, M.1
Crawford, F.2
Axelman, K.3
Houlden, H.4
Lilius, L.5
Winblad, B.6
Lannfelt, L.7
-
26
-
-
0037188380
-
An Iranian family with Alzheimer's disease caused by a novel APP mutation (Thr714Ala)
-
Pasalar P., Najmabadi H., Noorian A.R., Moghimi B., Jannati A., Soltanzadeh A., Krefft T., Crook R., Hardy J. An Iranian family with Alzheimer's disease caused by a novel APP mutation (Thr714Ala). Neurology 2002, 58:1574-1575.
-
(2002)
Neurology
, vol.58
, pp. 1574-1575
-
-
Pasalar, P.1
Najmabadi, H.2
Noorian, A.R.3
Moghimi, B.4
Jannati, A.5
Soltanzadeh, A.6
Krefft, T.7
Crook, R.8
Hardy, J.9
-
27
-
-
0020490536
-
Human apolipoprotein E: the complete amino acid sequence
-
Rall S.C., Weisgraber K.H., Mahley R.W. Human apolipoprotein E: the complete amino acid sequence. J.Biol. Chem. 1982, 257:4171-4178.
-
(1982)
J.Biol. Chem.
, vol.257
, pp. 4171-4178
-
-
Rall, S.C.1
Weisgraber, K.H.2
Mahley, R.W.3
-
29
-
-
4644348172
-
Afamily with Alzheimer disease and strokesassociated with A713T mutation of the APP gene
-
Rossi G., Giaccone G., Maletta R., Morbin M., Capobianco R., Mangieri M., Giovagnoli A.R., Bizzi A., Tomaino C., Perri M., Di Natale M., Tagliavini F., Bugiani O., Bruni A.C. Afamily with Alzheimer disease and strokesassociated with A713T mutation of the APP gene. Neurology 2004, 63:910-912.
-
(2004)
Neurology
, vol.63
, pp. 910-912
-
-
Rossi, G.1
Giaccone, G.2
Maletta, R.3
Morbin, M.4
Capobianco, R.5
Mangieri, M.6
Giovagnoli, A.R.7
Bizzi, A.8
Tomaino, C.9
Perri, M.10
Di Natale, M.11
Tagliavini, F.12
Bugiani, O.13
Bruni, A.C.14
-
30
-
-
16044373524
-
Secreted amyloid beta-protein similar to that in thesenileplaques of Alzheimer's disease is increased invivo by the presenilin 1 and 2 and APP mutations linked to familial Alzheimer's disease
-
Scheuner D., Eckman C., Jensen M., Song X., Citron M., Suzuki N., Bird T.D., Hardy J., Hutton M., Kukull W., Larson E., Levy-Lahad E., Viitanen M., Peskind E., Poorkaj P., Schellenberg G., Tanzi R., Wasco W., Lannfelt L., Selkoe D., Younkin S. Secreted amyloid beta-protein similar to that in thesenileplaques of Alzheimer's disease is increased invivo by the presenilin 1 and 2 and APP mutations linked to familial Alzheimer's disease. Nat. Med. 1996, 2:864-870.
-
(1996)
Nat. Med.
, vol.2
, pp. 864-870
-
-
Scheuner, D.1
Eckman, C.2
Jensen, M.3
Song, X.4
Citron, M.5
Suzuki, N.6
Bird, T.D.7
Hardy, J.8
Hutton, M.9
Kukull, W.10
Larson, E.11
Levy-Lahad, E.12
Viitanen, M.13
Peskind, E.14
Poorkaj, P.15
Schellenberg, G.16
Tanzi, R.17
Wasco, W.18
Lannfelt, L.19
Selkoe, D.20
Younkin, S.21
more..
-
31
-
-
0035066332
-
Alzheimer's disease: genes, proteins, and therapy
-
Selkoe D.J. Alzheimer's disease: genes, proteins, and therapy. Physiol. Rev. 2001, 81:741-766.
-
(2001)
Physiol. Rev.
, vol.81
, pp. 741-766
-
-
Selkoe, D.J.1
-
32
-
-
57649174625
-
Intramembrane proteolysis by gamma-secretase
-
Steiner H., Fluhrer R., Haass C. Intramembrane proteolysis by gamma-secretase. J.Biol. Chem. 2008, 283:29627-29631.
-
(2008)
J.Biol. Chem.
, vol.283
, pp. 29627-29631
-
-
Steiner, H.1
Fluhrer, R.2
Haass, C.3
-
33
-
-
33748368729
-
Alzheimer dementia caused by a novel mutation located in the APP C-terminal intracytosolic fragment
-
Theuns J., Marjaux E., Vandenbulcke M., Van Laere K., Kumar-Singh S., Bormans G., Brouwers N., Van den Broeck M., Vennekens K., Corsmit E., Cruts M., De Strooper B., Van Broeckhoven C., Vandenberghe R. Alzheimer dementia caused by a novel mutation located in the APP C-terminal intracytosolic fragment. Hum. Mutat. 2006, 27:888-896.
-
(2006)
Hum. Mutat.
, vol.27
, pp. 888-896
-
-
Theuns, J.1
Marjaux, E.2
Vandenbulcke, M.3
Van Laere, K.4
Kumar-Singh, S.5
Bormans, G.6
Brouwers, N.7
Van den Broeck, M.8
Vennekens, K.9
Corsmit, E.10
Cruts, M.11
De Strooper, B.12
Van Broeckhoven, C.13
Vandenberghe, R.14
-
34
-
-
84858720343
-
Molecular consequences of amyloid precursor protein and presenilin mutations causing autosomal-dominant Alzheimer's disease
-
Weggen S., Beher D. Molecular consequences of amyloid precursor protein and presenilin mutations causing autosomal-dominant Alzheimer's disease. Alzheimers Res. Ther. 2012, 4:9.
-
(2012)
Alzheimers Res. Ther.
, vol.4
, pp. 9
-
-
Weggen, S.1
Beher, D.2
-
35
-
-
0019783892
-
Human E apoprotein heterogeneity: cysteine-arginine interchanges in the amino acid sequence of the apo-E isoforms
-
Weisgraber K.H., Rall S.C., Mahley R.W. Human E apoprotein heterogeneity: cysteine-arginine interchanges in the amino acid sequence of the apo-E isoforms. J.Biol. Chem. 1981, 256:9077-9083.
-
(1981)
J.Biol. Chem.
, vol.256
, pp. 9077-9083
-
-
Weisgraber, K.H.1
Rall, S.C.2
Mahley, R.W.3
-
36
-
-
60349113111
-
Gamma-secretase catalyzes sequential cleavages of the AbetaPP transmembrane domain
-
Xu X.M. Gamma-secretase catalyzes sequential cleavages of the AbetaPP transmembrane domain. J.Alzheimers Dis. 2009, 16:211-224.
-
(2009)
J.Alzheimers Dis.
, vol.16
, pp. 211-224
-
-
Xu, X.M.1
-
37
-
-
70350438262
-
Preparation and characterization of a monoclonal antibody with high affinity for soluble Abeta oligomers
-
Zhang Y., Wang X., He J.S., Bao F.X., Sun W.M., Dai X.X., Wang X.B., Li Y.Q., Zheng X.X., Hu H.G., Peng X.L., Zheng Y.P., Hou L.L., Hong T. Preparation and characterization of a monoclonal antibody with high affinity for soluble Abeta oligomers. Hybridoma (Larchmt) 2009, 28:349-354.
-
(2009)
Hybridoma (Larchmt)
, vol.28
, pp. 349-354
-
-
Zhang, Y.1
Wang, X.2
He, J.S.3
Bao, F.X.4
Sun, W.M.5
Dai, X.X.6
Wang, X.B.7
Li, Y.Q.8
Zheng, X.X.9
Hu, H.G.10
Peng, X.L.11
Zheng, Y.P.12
Hou, L.L.13
Hong, T.14
-
38
-
-
79951931432
-
Administration of amyloid-beta42 oligomer-specific monoclonal antibody improved memory performance in SAMP8 mice
-
Zhang Y., He J.S., Wang X., Wang J., Bao F.X., Pang S.Y., Yin F., Hu H.G., Peng X.L., Sun W.M., Zheng Y.P., Hou L.L., Hong T. Administration of amyloid-beta42 oligomer-specific monoclonal antibody improved memory performance in SAMP8 mice. J.Alzheimers Dis. 2011, 23:551-561.
-
(2011)
J.Alzheimers Dis.
, vol.23
, pp. 551-561
-
-
Zhang, Y.1
He, J.S.2
Wang, X.3
Wang, J.4
Bao, F.X.5
Pang, S.Y.6
Yin, F.7
Hu, H.G.8
Peng, X.L.9
Sun, W.M.10
Zheng, Y.P.11
Hou, L.L.12
Hong, T.13
-
39
-
-
78650944520
-
APP processing in Alzheimer's disease
-
Zhang Y.W., Thompson R., Zhang H., Xu H.X. APP processing in Alzheimer's disease. Mol. Brain 2011, 4:3.
-
(2011)
Mol. Brain
, vol.4
, pp. 3
-
-
Zhang, Y.W.1
Thompson, R.2
Zhang, H.3
Xu, H.X.4
|