R01-AG11762/AG/NIA NIH HHS/United States[Grant Number] - Search Results

Year	Number of Results
1995	2
1996	3
1998	2
2000	3
2001	1
2002	1
2003	1
2005	1
2006	1
2024	0

1

Genetic dissection of Alzheimer disease, a heterogeneous disorder.

Schellenberg GD. Schellenberg GD. Proc Natl Acad Sci U S A. 1995 Sep 12;92(19):8552-9. doi: 10.1073/pnas.92.19.8552. Proc Natl Acad Sci U S A. 1995. PMID: 7567974 Free PMC article. Review.

2

Recent advances in the genetics of Alzheimer's disease.

Levy-Lahad E, Tsuang D, Bird TD. Levy-Lahad E, et al. J Geriatr Psychiatry Neurol. 1998 Summer;11(2):42-54. doi: 10.1177/089198879801100202. J Geriatr Psychiatry Neurol. 1998. PMID: 9877525 Review.

3

Genetic factors in Alzheimer's disease: a review of recent advances.

Levy-Lahad E, Bird TD. Levy-Lahad E, et al. Ann Neurol. 1996 Dec;40(6):829-40. doi: 10.1002/ana.410400604. Ann Neurol. 1996. PMID: 9007087 Review. No abstract available.

4

The genetics of Alzheimer's disease.

Schellenberg GD, D'Souza I, Poorkaj P. Schellenberg GD, et al. Curr Psychiatry Rep. 2000 Apr;2(2):158-64. doi: 10.1007/s11920-000-0061-z. Curr Psychiatry Rep. 2000. PMID: 11122949 Review.

5

An expression map from human chromosome 14q24.3.

Sharma V, Poorkaj P, Hisama F, Bonnycastle L, Yu CE, Massa H, Trask B, Clancy KP, Patterson D, Weissman SM, Schellenberg GD. Sharma V, et al. Genomics. 1998 Jan 15;47(2):314-8. doi: 10.1006/geno.1997.5106. Genomics. 1998. PMID: 9479506 Free article.

6

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 CE, Jondro PD, Schmidt SD, Wang K, et al. Levy-Lahad E, et al. Science. 1995 Aug 18;269(5226):973-7. doi: 10.1126/science.7638622. Science. 1995. PMID: 7638622

7

A genomic sequence analysis of the mouse and human microtubule-associated protein tau.

Poorkaj P, Kas A, D'Souza I, Zhou Y, Pham Q, Stone M, Olson MV, Schellenberg GD. Poorkaj P, et al. Mamm Genome. 2001 Sep;12(9):700-12. doi: 10.1007/s00335-001-2044-8. Mamm Genome. 2001. PMID: 11641718

8

The clinical phenotype of two missense mutations in the presenilin I gene in Japanese patients.

Ikeda M, Sharma V, Sumi SM, Rogaeva EA, Poorkaj P, Sherrington R, Nee L, Tsuda T, Oda N, Watanabe M, Aoki M, Shoji M, Abe K, Itoyama Y, Hirai S, Schellenberg GD, Bird TD, St George-Hyslop PH. Ikeda M, et al. Ann Neurol. 1996 Dec;40(6):912-7. doi: 10.1002/ana.410400614. Ann Neurol. 1996. PMID: 9007097

9

tau Exon 10 expression involves a bipartite intron 10 regulatory sequence and weak 5' and 3' splice sites.

D'Souza I, Schellenberg GD. D'Souza I, et al. J Biol Chem. 2002 Jul 19;277(29):26587-99. doi: 10.1074/jbc.M203794200. Epub 2002 May 8. J Biol Chem. 2002. PMID: 12000767 Free article.

10

A novel mutation at position +12 in the intron following exon 10 of the tau gene in familial frontotemporal dementia (FTD-Kumamoto).

Yasuda M, Takamatsu J, D'Souza I, Crowther RA, Kawamata T, Hasegawa M, Hasegawa H, Spillantini MG, Tanimukai S, Poorkaj P, Varani L, Varani G, Iwatsubo T, Goedert M, Schellenberg DG, Tanaka C. Yasuda M, et al. Ann Neurol. 2000 Apr;47(4):422-9. Ann Neurol. 2000. PMID: 10762152

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