-
1
-
-
0021256895
-
Alzheimer's disease: Initial report of the purification and characterization of a novel cerebrovascular amyloid protein
-
Glenner GG, Wong CW. Alzheimer's disease: initial report of the purification and characterization of a novel cerebrovascular amyloid protein. Biochem Biophys Res Commun. 1984;120(3): 885-890. (Pubitemid 14104991)
-
(1984)
Biochemical and Biophysical Research Communications
, vol.120
, Issue.3
, pp. 885-890
-
-
Glenner, G.G.1
Wong, C.W.2
-
2
-
-
0032105394
-
The role of Aβ42 in Alzheimer's disease
-
Younkin SG. The role of Aβ42 in Alzheimer's disease. J Physiol Paris. 1998;92(3-4):289-292.
-
(1998)
J Physiol Paris.
, vol.92
, Issue.3-4
, pp. 289-292
-
-
Younkin, S.G.1
-
4
-
-
70349558522
-
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease
-
Harold D, Abraham R, Hollingworth P, et al. Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease. Nat Genet. 2009;41(10):1088-1093.
-
(2009)
Nat Genet.
, vol.41
, Issue.10
, pp. 1088-1093
-
-
Harold, D.1
Abraham, R.2
Hollingworth, P.3
-
5
-
-
78549264026
-
Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease
-
European Alzheimer's Disease Initiative Investigators.
-
Lambert JC, Heath S, Even G, et al; European Alzheimer's Disease Initiative Investigators. Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease. Nat Genet. 2009;41(10):1094- 1099.
-
(2009)
Nat Genet.
, vol.41
, Issue.10
, pp. 1094-1099
-
-
Lambert, J.C.1
Heath, S.2
Even, G.3
-
6
-
-
77955463899
-
Replication of CLU CR1 and PICALM associations with Alzheimer disease
-
Carrasquillo MM, Belbin O, Hunter TA, et al. Replication of CLU, CR1, and PICALM associations with Alzheimer disease. Arch Neurol. 2010;67(8):961-964.
-
(2010)
Arch Neurol.
, vol.67
, Issue.8
, pp. 961-964
-
-
Carrasquillo, M.M.1
Belbin, O.2
Hunter, T.A.3
-
7
-
-
79955464911
-
Common variantsat MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease
-
Naj AC, Jun G, Beecham GW, et al. Common variantsat MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease. Nat Genet. 2011;43(5):436-441.
-
(2011)
Nat Genet.
, vol.43
, Issue.5
, pp. 436-441
-
-
Naj, A.C.1
Jun, G.2
Beecham, G.W.3
-
8
-
-
79955484414
-
Common variantsat ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease
-
Alzheimer's Disease Neuroimaging Initiative; CHARGE Consortium; EADI1 Consortium.
-
Hollingworth P, Harold D, Sims R, et al; Alzheimer's Disease Neuroimaging Initiative; CHARGE Consortium; EADI1 Consortium. Common variantsat ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease. Nat Genet. 2011;43(5):429-435.
-
(2011)
Nat Genet.
, vol.43
, Issue.5
, pp. 429-435
-
-
Hollingworth, P.1
Harold, D.2
Sims, R.3
-
9
-
-
84866745289
-
Genetic association of CR1 with Alzheimer's disease: A tentative disease mechanism
-
doi:10.1016/j.neurobiolaging.2012.07.001
-
Hazrati LN, Van Cauwenberghe C, Brooks PL, et al. Genetic association of CR1 with Alzheimer's disease: a tentative disease mechanism. Neurobiol Aging. 2012;33(12):2949.e5-2949.e12. doi:10.1016/j.neurobiolaging.2012.07.001.
-
(2012)
Neurobiol Aging.
, vol.33
, Issue.12
-
-
Hazrati, L.N.1
Van Cauwenberghe, C.2
Brooks, P.L.3
-
10
-
-
33846613222
-
The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease
-
DOI 10.1038/ng1943, PII NG1943
-
Rogaeva E, Meng Y, Lee JH, et al. The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease. Nat Genet. 2007;39(2):168-177. (Pubitemid 46184347)
-
(2007)
Nature Genetics
, vol.39
, Issue.2
, pp. 168-177
-
-
Rogaeva, E.1
Meng, Y.2
Lee, J.H.3
Gu, Y.4
Kawarai, T.5
Zou, F.6
Katayama, T.7
Baldwin, C.T.8
Cheng, R.9
Hasegawa, H.10
Chen, F.11
Shibata, N.12
Lunetta, K.L.13
Pardossi-Piquard, R.14
Bohm, C.15
Wakutani, Y.16
Cupples, L.A.17
Cuenco, K.T.18
Green, R.C.19
Pinessi, L.20
Rainero, I.21
Sorbi, S.22
Bruni, A.23
Duara, R.24
Friedland, R.P.25
Inzelberg, R.26
Hampe, W.27
Bujo, H.28
Song, Y.-Q.29
Andersen, O.M.30
Willnow, T.E.31
Graff-Radford, N.32
Petersen, R.C.33
Dickson, D.34
Der, S.D.35
Fraser, P.E.36
Schmitt-Ulms, G.37
Younkin, S.38
Mayeux, R.39
Farrer, L.A.40
St. George-Hyslop, P.41
more..
-
11
-
-
84872057940
-
TREM2 variants in Alzheimer's disease
-
Alzheimer Genetic Analysis Group
-
Guerreiro R, Wojtas A, Bras J, et al; Alzheimer Genetic Analysis Group. TREM2 variants in Alzheimer's disease. N Engl J Med. 2013;368(2):117-127.
-
(2013)
N Engl J Med.
, vol.368
, Issue.2
, pp. 117-127
-
-
Guerreiro, R.1
Wojtas, A.2
Bras, J.3
-
12
-
-
84856132922
-
Repeat expansion in C9ORF72 in Alzheimer's disease
-
Majounie E, Abramzon Y, Renton AE, et al. Repeat expansion in C9ORF72 in Alzheimer's disease. N Engl J Med. 2012;366(3):283-284.
-
(2012)
N Engl J Med.
, vol.366
, Issue.3
, pp. 283-284
-
-
Majounie, E.1
Abramzon, Y.2
Renton, A.E.3
-
13
-
-
84875267247
-
C9orf72 G4C2 repeat expansions in Alzheimer's disease and mild cognitive impairment
-
doi:10.1016/j.neurobiolaging.2012.12.019
-
Cacace R, Van Cauwenberghe C, Bettens K, et al. C9orf72 G 4C2 repeat expansions in Alzheimer's disease and mild cognitive impairment. Neurobiol Aging. 2013;34(6):1712.e1-1712.e7. doi:10.1016/j.neurobiolaging.2012.12.019.
-
(2013)
Neurobiol Aging.
, vol.34
, Issue.6
-
-
Cacace, R.1
Van Cauwenberghe, C.2
Bettens, K.3
-
14
-
-
84871243649
-
Investigation of c9orf72 in 4 neurodegenerative disorders
-
Xi Z, Zinman L, Grinberg Y, et al. Investigation of c9orf72 in 4 neurodegenerative disorders. Arch Neurol. 2012;69(12):1583-1590.
-
(2012)
Arch Neurol.
, vol.69
, Issue.12
, pp. 1583-1590
-
-
Xi, Z.1
Zinman, L.2
Grinberg, Y.3
-
15
-
-
84855585694
-
Autosomal recessive causes likely in early-onset Alzheimer disease
-
Wingo TS, Lah JJ, Levey AI, Cutler DJ. Autosomal recessive causes likely in early-onset Alzheimer disease. Arch Neurol. 2012;69(1):59-64.
-
(2012)
Arch Neurol.
, vol.69
, Issue.1
, pp. 59-64
-
-
Wingo, T.S.1
Lah, J.J.2
Levey, A.I.3
Cutler, D.J.4
-
16
-
-
62449330486
-
A recessive mutation in the APP gene with dominant-negative effect on amyloidogenesis
-
Di Fede G, Catania M, Morbin M, et al. A recessive mutation in the APP gene with dominant-negative effect on amyloidogenesis. Science. 2009;323(5920):1473-1477.
-
(2009)
Science.
, vol.323
, Issue.5920
, pp. 1473-1477
-
-
Di Fede, G.1
Catania, M.2
Morbin, M.3
-
17
-
-
80052857468
-
Exome sequencing identifies a novel missense variant in RRM2B associated with autosomal recessive progressive external ophthalmoplegia
-
doi:10.1186/gb-2011-12-9-r92
-
Takata A, Kato M, Nakamura M, et al. Exome sequencing identifies a novel missense variant in RRM2B associated with autosomal recessive progressive external ophthalmoplegia. Genome Biol. 2011;12(9):R92. doi:10.1186/gb-2011-12-9- r92.
-
(2011)
Genome Biol.
, vol.12
, Issue.9
-
-
Takata, A.1
Kato, M.2
Nakamura, M.3
-
18
-
-
84867854926
-
Re-assigned diagnosis of D4ST1-deficient Ehlers-Danlos syndrome (adducted thumb-clubfoot syndrome) after initial diagnosis of Marden-Walker syndrome
-
Winters KA, Jiang Z, Xu W, et al. Re-assigned diagnosis of D4ST1-deficient Ehlers-Danlos syndrome (adducted thumb-clubfoot syndrome) after initial diagnosis of Marden-Walker syndrome. Am J Med Genet A. 2012;158A(11):2935-2940.
-
(2012)
Am J Med Genet A.
, vol.158 A
, Issue.11
, pp. 2935-2940
-
-
Winters, K.A.1
Jiang, Z.2
Xu, W.3
-
19
-
-
82355181594
-
Diagnostic implications of excessive homozygosity detected by SNP-based microarrays: Consanguinity, uniparental disomy, and recessive single-gene mutations
-
ix
-
Kearney HM, Kearney JB, Conlin LK. Diagnostic implications of excessive homozygosity detected by SNP-based microarrays: consanguinity, uniparental disomy, and recessive single-gene mutations. Clin Lab Med. 2011;31(4):595-613; ix.
-
(2011)
Clin Lab Med.
, vol.31
, Issue.4
, pp. 595-613
-
-
Kearney, H.M.1
Kearney, J.B.2
Conlin, L.K.3
-
20
-
-
79953321196
-
UPD detection using homozygosity profiling with a SNP genotyping microarray
-
Papenhausen P, Schwartz S, Risheg H, et al. UPD detection using homozygosity profiling with a SNP genotyping microarray. Am J Med Genet A. 2011;155A(4):757-768.
-
(2011)
Am J Med Genet A.
, vol.155 A
, Issue.4
, pp. 757-768
-
-
Papenhausen, P.1
Schwartz, S.2
Risheg, H.3
-
21
-
-
84860009658
-
A genome-wide homozygosity association study identifies runs of homozygosity associated with rheumatoid arthritis in the human major histocompatibility complex
-
doi:10.1371/journal.pone.0034840
-
Yang HC, Chang LC, Liang YJ, Lin CH, Wang PL. A genome-wide homozygosity association study identifies runs of homozygosity associated with rheumatoid arthritis in the human major histocompatibility complex. PLoS One. 2012;7(4):e34840. doi:10.1371/journal.pone.0034840.
-
(2012)
PLoS One.
, vol.7
, Issue.4
-
-
Yang, H.C.1
Chang, L.C.2
Liang, Y.J.3
Lin, C.H.4
Wang, P.L.5
-
22
-
-
84860879137
-
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
-
Casey JP, Magalhaes T, Conroy JM, et al. A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. Hum Genet. 2012;131(4):565-579.
-
(2012)
Hum Genet.
, vol.131
, Issue.4
, pp. 565-579
-
-
Casey, J.P.1
Magalhaes, T.2
Conroy, J.M.3
-
23
-
-
33750911214
-
Long contiguous stretches of homozygosity in the human genome
-
Li LH, Ho SF, Chen CH, et al. Long contiguous stretches of homozygosity in the human genome. Hum Mutat. 2006;27(11):1115-1121.
-
(2006)
Hum Mutat.
, vol.27
, Issue.11
, pp. 1115-1121
-
-
Li, L.H.1
Ho, S.F.2
Chen, C.H.3
-
24
-
-
33144460067
-
Extended tracts of homozygosity in outbred human populations
-
DOI 10.1093/hmg/ddi493
-
Gibson J, Morton NE, Collins A. Extended tracts of homozygosity in outbred human populations. Hum Mol Genet. 2006;15(5):789-795. (Pubitemid 43264703)
-
(2006)
Human Molecular Genetics
, vol.15
, Issue.5
, pp. 789-795
-
-
Gibson, J.1
Morton, N.E.2
Collins, A.3
-
25
-
-
78649730822
-
Genomic runs of homozygosity record population history and consanguinity
-
doi:10.1371/journal.pone.0013996
-
Kirin M, McQuillan R, Franklin CS, Campbell H, McKeigue PM, Wilson JF. Genomic runs of homozygosity record population history and consanguinity. PLoS One. 2010;5(11):e13996. doi:10.1371/journal.pone.0013996.
-
(2010)
PLoS One.
, vol.5
, Issue.11
-
-
Kirin, M.1
McQuillan, R.2
Franklin, C.S.3
Campbell, H.4
McKeigue, P.M.5
Wilson, J.F.6
-
26
-
-
38949169544
-
Study of regions of extended homozygosity provides a powerful method to explore haplotype structure of human populations
-
DOI 10.1111/j.1469-1809.2007.00411.x
-
Curtis D, Vine AE, Knight J. Study of regions of extended homozygosity provides a powerful method to explore haplotype structure of human populations. Ann Hum Genet. 2008;72(pt 2):261-278. (Pubitemid 351228465)
-
(2008)
Annals of Human Genetics
, vol.72
, Issue.2
, pp. 261-278
-
-
Curtis, D.1
Vine, A.E.2
Knight, J.3
-
27
-
-
70249085939
-
Extended tracts of homozygosity identify novel candidate genes associated with late-onset Alzheimer's disease
-
Nalls MA, Guerreiro RJ, Simon-Sanchez J, et al. Extended tracts of homozygosity identify novel candidate genes associated with late-onset Alzheimer's disease. Neurogenetics. 2009;10(3):183-190.
-
(2009)
Neurogenetics.
, vol.10
, Issue.3
, pp. 183-190
-
-
Nalls, M.A.1
Guerreiro, R.J.2
Simon-Sanchez, J.3
-
28
-
-
80052428106
-
No evidence that extended tracts of homozygosity are associated with Alzheimer's disease
-
Sims R, Dwyer S, Harold D, et al. No evidence that extended tracts of homozygosity are associated with Alzheimer's disease. Am J Med Genet B Neuropsychiatr Genet. 2011;156B(7): 764-771.
-
(2011)
Am J Med Genet B Neuropsychiatr Genet.
, vol.156 B
, Issue.7
, pp. 764-771
-
-
Sims, R.1
Dwyer, S.2
Harold, D.3
-
29
-
-
63449093255
-
Genome-wide autozygosity mapping in human populations
-
Wang S, Haynes C, Barany F, Ott J. Genome-wide autozygosity mapping in human populations. Genet Epidemiol. 2009;33(2):172-180.
-
(2009)
Genet Epidemiol.
, vol.33
, Issue.2
, pp. 172-180
-
-
Wang, S.1
Haynes, C.2
Barany, F.3
Ott, J.4
-
30
-
-
79957827090
-
Identification of novel schizophrenia loci by homozygosity mapping using DNA microarray analysis
-
doi:10.1371/journal.pone.0020589
-
Kurotaki N, Tasaki S, Mishima H, et al. Identification of novel schizophrenia loci by homozygosity mapping using DNA microarray analysis. PLoS One. 2011;6(5):e20589. doi:10.1371/journal.pone.0020589.
-
(2011)
PLoS One.
, vol.6
, Issue.5
-
-
Kurotaki, N.1
Tasaki, S.2
Mishima, H.3
-
31
-
-
79951572644
-
Identification of novel candidate genes for Alzheimer's disease by autozygosity mapping using genome wide SNP data
-
Sherva R, Baldwin CT, Inzelberg R, et al. Identification of novel candidate genes for Alzheimer's disease by autozygosity mapping using genome wide SNP data. J Alzheimers Dis. 2011;23(2):349-359.
-
(2011)
J Alzheimers Dis.
, vol.23
, Issue.2
, pp. 349-359
-
-
Sherva, R.1
Baldwin, C.T.2
Inzelberg, R.3
-
32
-
-
70349998614
-
Whole genome analysis in a consanguineous family with early onset Alzheimer's disease
-
Clarimón J, Djaldetti R, Lleó A, et al. Whole genome analysis in a consanguineous family with early onset Alzheimer's disease. Neurobiol Aging. 2009;30(12):1986-1991.
-
(2009)
Neurobiol Aging.
, vol.30
, Issue.12
, pp. 1986-1991
-
-
Clarimón, J.1
Djaldetti, R.2
Lleó, A.3
-
33
-
-
79952592605
-
Identification of novel loci for Alzheimer disease and replication of CLU PICALM and BIN1 in Caribbean Hispanic individuals
-
Lee JH, Cheng R, Barral S, et al. Identification of novel loci for Alzheimer disease and replication of CLU, PICALM, and BIN1 in Caribbean Hispanic individuals. Arch Neurol. 2011;68(3):320-328.
-
(2011)
Arch Neurol.
, vol.68
, Issue.3
, pp. 320-328
-
-
Lee, J.H.1
Cheng, R.2
Barral, S.3
-
34
-
-
84866771520
-
Genome-wide survey of large rare copy number variants in Alzheimer's disease among Caribbean Hispanics
-
Ghani M, Pinto D, Lee JH, et al. Genome-wide survey of large rare copy number variants in Alzheimer's disease among Caribbean Hispanics. G3 (Bethesda). 2012;2(1):71-78.
-
(2012)
G3 (Bethesda).
, vol.2
, Issue.1
, pp. 71-78
-
-
Ghani, M.1
Pinto, D.2
Lee, J.H.3
-
35
-
-
0035860986
-
A founder mutation in presenilin 1 causing early-onset Alzheimer disease in unrelated Caribbean Hispanic families
-
Athan ES, Williamson J, Ciappa A, et al. A founder mutation in presenilin 1 causing early-onset Alzheimer disease in unrelated Caribbean Hispanic families. JAMA. 2001;286(18):2257-2263. (Pubitemid 33063148)
-
(2001)
Journal of the American Medical Association
, vol.286
, Issue.18
, pp. 2257-2263
-
-
Athan, E.S.1
Williamson, J.2
Ciappa, A.3
Santana, V.4
Romas, S.N.5
Lee, J.H.6
Rondon, H.7
Lantigua, R.A.8
Medrano, M.9
Torres, M.10
Arawaka, S.11
Rogaeva, E.12
Song, Y.-Q.13
Sato, C.14
Kawarai, T.15
Fafel, K.C.16
Boss, M.A.17
Seltzer, W.K.18
Stern, Y.19
St George-Hyslop, P.20
Tycko, B.21
Mayeux, R.22
more..
-
36
-
-
34548210938
-
Recent genetic selection in the ancestral admixture of Puerto Ricans
-
DOI 10.1086/520769
-
Tang H, Choudhry S, Mei R, et al. Recent genetic selection in the ancestral admixture of Puerto Ricans. Am J Hum Genet. 2007;81(3): 626-633. (Pubitemid 47330221)
-
(2007)
American Journal of Human Genetics
, vol.81
, Issue.3
, pp. 626-633
-
-
Tang, H.1
Choudhry, S.2
Mei, R.3
Morgan, M.4
Rodriguez-Cintron, W.5
Burchard, E.G.6
Risch, N.J.7
-
37
-
-
84885805565
-
-
Accessed May 2013
-
Demographics of Puerto Rico. http://en.wikipedia.org/wiki/Demographics- of-Puerto-Rico. Accessed May 2013.
-
Demographics of Puerto Rico
-
-
-
39
-
-
0035830436
-
Incidence of AD in African-Americans, Caribbean Hispanics, and Caucasians in northern Manhattan
-
Tang MX, Cross P, Andrews H, et al. Incidence of AD in African-Americans, Caribbean Hispanics, and Caucasians in northern Manhattan. Neurology. 2001;56(1):49-56. (Pubitemid 32059651)
-
(2001)
Neurology
, vol.56
, Issue.1
, pp. 49-56
-
-
Tang, M.-X.1
Cross, P.2
Andrews, H.3
Jacobs, D.M.4
Small, S.5
Bell, K.6
Merchant, C.7
Lantigua, R.8
Costa, R.9
Stern, Y.10
Mayeux, R.11
-
41
-
-
13444269543
-
Haploview: Analysis and visualization of LD and haplotype maps
-
DOI 10.1093/bioinformatics/bth457
-
Barrett JC, Fry B, Maller J, Daly MJ. Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics. 2005;21(2):263-265. (Pubitemid 40202029)
-
(2005)
Bioinformatics
, vol.21
, Issue.2
, pp. 263-265
-
-
Barrett, J.C.1
Fry, B.2
Maller, J.3
Daly, M.J.4
-
42
-
-
78650856517
-
GCTA: A tool for genome-wide complex trait analysis
-
Yang J, Lee SH, Goddard ME, Visscher PM. GCTA: a tool for genome-wide complex trait analysis. Am J Hum Genet. 2011;88(1):76-82.
-
(2011)
Am J Hum Genet.
, vol.88
, Issue.1
, pp. 76-82
-
-
Yang, J.1
Lee, S.H.2
Goddard, M.E.3
Visscher, P.M.4
-
43
-
-
77954140531
-
Common SNPs explain a large proportion of the heritability for human height
-
Yang J, Benyamin B, McEvoy BP, et al. Common SNPs explain a large proportion of the heritability for human height. Nat Genet. 2010;42(7):565-569.
-
(2010)
Nat Genet.
, vol.42
, Issue.7
, pp. 565-569
-
-
Yang, J.1
Benyamin, B.2
McEvoy, B.P.3
-
44
-
-
84860559560
-
Runs of homozygosity implicate autozygosity as a schizophrenia risk factor
-
Schizophrenia Psychiatric Genome-Wide Association Study Consortium doi:10.1371/journal.pgen.1002656
-
Keller MC, Simonson MA, Ripke S, et al; Schizophrenia Psychiatric Genome-Wide Association Study Consortium. Runs of homozygosity implicate autozygosity as a schizophrenia risk factor. PLoS Genet. 2012;8(4):e1002656. doi:10.1371/journal.pgen.1002656.
-
(2012)
PLoS Genet.
, vol.8
, Issue.4
-
-
Keller, M.C.1
Simonson, M.A.2
Ripke, S.3
-
45
-
-
0037431329
-
The exocyst complex is required for targeting of Glut4 to the plasma membrane by insulin
-
DOI 10.1038/nature01533
-
Inoue M, Chang L, Hwang J, Chiang SH, Saltiel AR. The exocyst complex is required for targeting of Glut4 to the plasma membrane by insulin. Nature. 2003;422(6932):629-633. (Pubitemid 36460418)
-
(2003)
Nature
, vol.422
, Issue.6932
, pp. 629-633
-
-
Inoue, M.1
Chang, L.2
Hwang, J.3
Chiang, S.-H.4
Saltiel, A.R.5
-
46
-
-
78149233413
-
Opening ahead: Early steps in lumen formation revealed
-
Apodaca G. Opening ahead: early steps in lumen formation revealed. Nat Cell Biol. 2010;12(11):1026-1028.
-
(2010)
Nat Cell Biol.
, vol.12
, Issue.11
, pp. 1026-1028
-
-
Apodaca, G.1
-
47
-
-
0038713372
-
NMDA receptor trafficking through an interaction between PDZ proteins and the exocyst complex
-
DOI 10.1038/ncb990
-
Sans N, Prybylowski K, Petralia RS, et al. NMDA receptor trafficking through an interaction between PDZ proteins and the exocyst complex. Nat Cell Biol. 2003;5(6):520-530. (Pubitemid 36781085)
-
(2003)
Nature Cell Biology
, vol.5
, Issue.6
, pp. 520-530
-
-
Sans, N.1
Prybylowski, K.2
Petralia, R.S.3
Chang, K.4
Wang, Y.-X.5
Racca, C.6
Vicini, S.7
Wenthold, R.J.8
-
48
-
-
0035911161
-
Where Notch and Wnt signaling meet: The presenilin hub
-
De Strooper B, Annaert W. Where Notch and Wnt signaling meet: the presenilin hub. J Cell Biol. 2001;152(4):F17-F20.
-
(2001)
J Cell Biol.
, vol.152
, Issue.4
-
-
De Strooper, B.1
Annaert, W.2
-
49
-
-
58149204047
-
Gamma-secretase-dependent and-independent effects of presenilin1 on β-catenin·Tcf-4 transcriptional activity
-
doi:10.1371/journal.pone.0004080
-
Raurell I, Codina M, Casagolda D, et al. Gamma-secretase-dependent and-independent effects of presenilin1 on β-catenin·Tcf-4 transcriptional activity. PLoS One. 2008;3(12):e4080. doi:10.1371/journal.pone. 0004080.
-
(2008)
PLoS One.
, vol.3
, Issue.12
-
-
Raurell, I.1
Codina, M.2
Casagolda, D.3
-
50
-
-
58449113266
-
Accumulation of phosphorylated β-catenin enhances ROS-induced cell death in presenilin-deficient cells
-
doi:10.1371/journal.pone.0004172
-
Boo JH, Song H, Kim JE, Kang DE, Mook-Jung I. Accumulation of phosphorylated β-catenin enhances ROS-induced cell death in presenilin-deficient cells. PLoS One. 2009;4(1):e4172. doi:10.1371/journal.pone. 0004172.
-
(2009)
PLoS One.
, vol.4
, Issue.1
-
-
Boo, J.H.1
Song, H.2
Kim, J.E.3
Kang, D.E.4
Mook-Jung, I.5
-
51
-
-
0033401526
-
Presenilin-1 forms complexes with the cadherin/catenin cell-cell adhesion system and is recruited to intercellular and synaptic contacts
-
Georgakopoulos A, Marambaud P, Efthimiopoulos S, et al. Presenilin-1 forms complexes with the cadherin/catenin cell-cell adhesion system and is recruited to intercellular and synaptic contacts. Mol Cell. 1999;4(6): 893-902. (Pubitemid 30054896)
-
(1999)
Molecular Cell
, vol.4
, Issue.6
, pp. 893-902
-
-
Georgakopoulos, A.1
Marambaud, P.2
Efthimiopoulos, S.3
Shioi, J.4
Cui, W.5
Li, H.-C.6
Schutte, M.7
Gordon, R.8
Holstein, G.R.9
Martinelli, G.10
Mehta, P.11
Friedrich Jr., V.L.12
Robakis, N.K.13
-
52
-
-
18344380083
-
A presenilin-1/γ-secretase cleavage releases the E-cadherin intracellular domain and regulates disassembly of adherens junctions
-
DOI 10.1093/emboj/21.8.1948
-
Marambaud P, Shioi J, Serban G, et al. A presenilin-1/γ-secretase cleavage releases the E-cadherin intracellular domain and regulates disassembly of adherens junctions. EMBO J. 2002;21(8):1948-1956. (Pubitemid 34437192)
-
(2002)
EMBO Journal
, vol.21
, Issue.8
, pp. 1948-1956
-
-
Marambaud, P.1
Shioi, J.2
Serban, G.3
Georgakopoulos, A.4
Sarner, S.5
Nagy, V.6
Baki, L.7
Wen, P.8
Efthimiopoulos, S.9
Shao, Z.10
Wisniewski, T.11
Robakis, N.K.12
-
53
-
-
0034704197
-
Susceptibility locus for Alzheimer's disease on chromosome 10
-
DOI 10.1126/science.290.5500.2304
-
Myers A, Holmans P, Marshall H, et al. Susceptibility locus for Alzheimer's disease on chromosome 10. Science. 2000;290(5500):2304-2305. (Pubitemid 32041572)
-
(2000)
Science
, vol.290
, Issue.5500
, pp. 2304-2305
-
-
Myers, A.1
Holmans, P.2
Marshall, H.3
Kwon, J.4
Meyer, D.5
Ramic, D.6
Shears, S.7
Booth, J.8
DeVrieze, F.W.9
Crook, R.10
Hamshere, M.11
Abraham, R.12
Tunstall, N.13
Rice, F.14
Carty, S.15
Lillystone, S.16
Kehoe, P.17
Rudrasingham, V.18
Jones, L.19
Lovestone, S.20
Perez-Tur, J.21
Williams, J.22
Owen, M.J.23
Hardy, J.24
Goate, A.M.25
more..
-
54
-
-
0034703979
-
Linkage of plasma Aβ42 to a quantitative locus on chromosome 10 in late-onset Alzheimer's disease pedigrees
-
DOI 10.1126/science.290.5500.2303
-
Ertekin-Taner N, Graff-Radford N, Younkin LH, et al. Linkage of plasma Aβ42 to a quantitative locus on chromosome 10 in late-onset Alzheimer's disease pedigrees. Science. 2000;290(5500): 2303-2304. (Pubitemid 32041571)
-
(2000)
Science
, vol.290
, Issue.5500
, pp. 2303-2304
-
-
Ertekin-Taner, N.1
Graff-Radford, N.2
Younkin, L.H.3
Eckman, C.4
Baker, M.5
Adamson, J.6
Ronald, J.7
Blangero, J.8
Hutton, M.9
Younkin, S.G.10
-
55
-
-
33846897499
-
Is α-T catenin (VR22) an Alzheimer's disease risk gene?
-
doi:10.1136/jmg.2005.039263
-
Bertram L, Mullin K, Parkinson M, et al. Is α-T catenin (VR22) an Alzheimer's disease risk gene? J Med Genet. 2007;44(1):e63. doi:10.1136/jmg. 2005.039263.
-
(2007)
J Med Genet.
, vol.44
, Issue.1
-
-
Bertram, L.1
Mullin, K.2
Parkinson, M.3
-
56
-
-
35748957469
-
Genetic association of CTNNA3 with late-onset Alzheimer's disease in females
-
DOI 10.1093/hmg/ddm244
-
Miyashita A, Arai H, Asada T, et al; Japanese Genetic Study Consortium for Alzheimer's Disease. Genetic association of CTNNA3 with late-onset Alzheimer's disease in females. Hum Mol Genet. 2007;16(23):2854-2869. (Pubitemid 350048384)
-
(2007)
Human Molecular Genetics
, vol.16
, Issue.23
, pp. 2854-2869
-
-
Miyashita, A.1
Arai, H.2
Asada, T.3
Imagawa, M.4
Matsubara, E.5
Shoji, M.6
Higuchi, S.7
Urakami, K.8
Kakita, A.9
Takahashi, H.10
Toyabe, S.11
Akazawa, K.12
Kanazawa, I.13
Ihara, Y.14
Kuwano, R.15
-
57
-
-
26944473203
-
Interaction between the α-T catenin gene (VR22) and APOE in Alzheimer's disease
-
DOI 10.1136/jmg.2004.029553
-
Martin ER, Bronson PG, Li YJ, et al. Interaction between the α-T catenin gene (VR22) and APOE in Alzheimer's disease. J Med Genet. 2005;42(10):787-792. (Pubitemid 41475256)
-
(2005)
Journal of Medical Genetics
, vol.42
, Issue.10
, pp. 787-792
-
-
Martin, E.R.1
Bronson, P.G.2
Li, Y.-J.3
Wall, N.4
Chung, R.-H.5
Schmechel, D.E.6
Small, G.7
Xu, P.-T.8
Bartlett, J.9
Schnetz-Boutaud, N.10
Haines, J.L.11
Gilbert, J.R.12
Pericak-Vance, M.A.13
-
58
-
-
0344668728
-
Fine mapping of the α-T catenin gene to a quantitative trait locus on chromosome 10 in late-onset Alzheimer's disease pedigrees
-
DOI 10.1093/hmg/ddg343
-
Ertekin-Taner N, Ronald J, Asahara H, et al. Fine mapping of the α-T catenin gene to a quantitative trait locus on chromosome 10 in late-onset Alzheimer's disease pedigrees. Hum Mol Genet. 2003;12(23):3133-3143. (Pubitemid 37508884)
-
(2003)
Human Molecular Genetics
, vol.12
, Issue.23
, pp. 3133-3143
-
-
Ertekin-Taner, N.1
Ronald, J.2
Asahara, H.3
Younkin, L.4
Hella, M.5
Jain, S.6
Gnida, E.7
Younkin, S.8
Fadale, D.9
Ohyagi, Y.10
Singleton, A.11
Scanlin, L.12
De Andrade, M.13
Petersen, R.14
Graff-Radford, N.15
Hutton, M.16
Younkin, S.17
-
59
-
-
84863810310
-
Effect of genetic variation in LRRTM3 on risk of Alzheimer disease
-
Reitz C, Conrad C, Roszkowski K, Rogers RS, Mayeux R. Effect of genetic variation in LRRTM3 on risk of Alzheimer disease. Arch Neurol. 2012;69(7):894-900.
-
(2012)
Arch Neurol.
, vol.69
, Issue.7
, pp. 894-900
-
-
Reitz, C.1
Conrad, C.2
Roszkowski, K.3
Rogers, R.S.4
Mayeux, R.5
-
60
-
-
33646184680
-
ARF proteins: Roles in membrane traffic and beyond
-
D'Souza-Schorey C, Chavrier P. ARF proteins: roles in membrane traffic and beyond. Nat Rev Mol Cell Biol. 2006;7(5):347-358.
-
(2006)
Nat Rev Mol Cell Biol.
, vol.7
, Issue.5
, pp. 347-358
-
-
D'Souza-Schorey, C.1
Chavrier, P.2
-
61
-
-
33744966028
-
Role of the Arf6 GDP/GTP cycle and Arf6 GTPase-activating proteins in actin remodeling and intracellular transport
-
DOI 10.1074/jbc.M601021200
-
Klein S, Franco M, Chardin P, Luton F. Role of the Arf6 GDP/GTP cycle and Arf6 GTPase-activating proteins in actin remodeling and intracellular transport. J Biol Chem. 2006;281(18):12352-12361. (Pubitemid 43855320)
-
(2006)
Journal of Biological Chemistry
, vol.281
, Issue.18
, pp. 12352-12361
-
-
Klein, S.1
Franco, M.2
Chardin, P.3
Luton, F.4
-
62
-
-
79960189859
-
The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease
-
doi:10.1186/gm249
-
Antunez C, Boada M, Gonzalez-Perez A, et al. The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease. Genome Med. 2011;3(5):33. doi:10.1186/gm249.
-
(2011)
Genome Med.
, vol.3
, Issue.5
, pp. 33
-
-
Antunez, C.1
Boada, M.2
Gonzalez-Perez, A.3
-
63
-
-
83455211863
-
A comprehensive genetic association study of Alzheimer disease in African Americans
-
Multi-institutional Research on Alzheimer Genetic Epidemiology (MIRAGE) Study Group.
-
Logue MW, Schu M, Vardarajan BN, et al; Multi-institutional Research on Alzheimer Genetic Epidemiology (MIRAGE) Study Group. A comprehensive genetic association study of Alzheimer disease in African Americans. Arch Neurol. 2011;68(12):1569-1579.
-
(2011)
Arch Neurol.
, vol.68
, Issue.12
, pp. 1569-1579
-
-
Logue, M.W.1
Schu, M.2
Vardarajan, B.N.3
-
64
-
-
84870053102
-
Genome-wide association analysis of age-at-onset in Alzheimer's disease
-
Kamboh MI, Barmada MM, Demirci FY, et al. Genome-wide association analysis of age-at-onset in Alzheimer's disease. Mol Psychiatry. 2012;17(12):1340-1346.
-
(2012)
Mol Psychiatry.
, vol.17
, Issue.12
, pp. 1340-1346
-
-
Kamboh, M.I.1
Barmada, M.M.2
Demirci, F.Y.3
-
65
-
-
77957597251
-
Genome-wide association reveals genetic effects on human Aβ42 and τ protein levels in cerebrospinal fluids: A case control study
-
Alzheimer's Disease Neuroimaging Initiative. October doi:10.1186/1471- 2377-10-90
-
Han MR, Schellenberg GD, Wang LS; Alzheimer's Disease Neuroimaging Initiative. Genome-wide association reveals genetic effects on human Aβ42 and τ protein levels in cerebrospinal fluids: a case control study. BMC Neurol. October 2010;10:90. doi:10.1186/1471-2377-10-90.
-
(2010)
BMC Neurol
, vol.10
, pp. 90
-
-
Han, M.R.1
Schellenberg, G.D.2
Wang, L.S.3
|