Literature DB >> 7475576

Familial Alzheimer's disease associated with S182 codon 286 mutation.

J Chapman, A Asherov, N Wang, T A Treves, A D Korczyn, L G Goldfarb.   

Abstract

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Year:  1995        PMID： 7475576     DOI： 10.1016/s0140-6736(95)91723-3

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  3 in total

1.  Expression of presenilin 1 and 2 (PS1 and PS2) in human and murine tissues.

Authors:  M K Lee; H H Slunt; L J Martin; G Thinakaran; G Kim; S E Gandy; M Seeger; E Koo; D L Price; S S Sisodia
Journal:  J Neurosci       Date:  1996-12-01       Impact factor: 6.167

Review 2.  Clinical phenotypic heterogeneity of Alzheimer's disease associated with mutations of the presenilin-1 gene.

Authors:  A J Larner; M Doran
Journal:  J Neurol       Date:  2005-11-04       Impact factor: 6.682

3.  Increased apoptosis arising from increased expression of the Alzheimer's disease-associated presenilin-2 mutation (N141I).

Authors:  S Janicki; M J Monteiro
Journal:  J Cell Biol       Date:  1997-10-20       Impact factor: 10.539
  3 in total

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