Results 201 to 210 of about 24,368 (229)
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Cloning of the cDNA encoding rat Presenilin-1

Gene, 1997
We isolated rat presenilin-1 (PS-1; also called S182 previously) cDNA from total brain RNA by using a reverse transcription-polymerase chain reaction (RT-PCR) technique with primers homologous to the conserved sequences of human and mouse PS-1. Rat PS-1 cDNA encoded 468 amino acids (aa) and the deduced aa sequence was highly homologous to those of the ...
T, Taniguchi   +10 more
openaire   +2 more sources

Characterization and expression of presenilin 1 in mouse brain

NeuroReport, 1996
The expression pattern of presenilin 1 (PS-1) in adult mouse brain was investigated using antibodies to specific peptides of PS-1. One antibody, Alz14A, specifically detected a 53 kDa protein in retinoic acid-treated P19 cells and mouse brain protein extracts consistent with the predicted PS-1 molecular weight.
D P, Huynh, V V, Ho, S M, Pulst
openaire   +2 more sources

Role of Presenilin‐1 in Murine Neural Development

Annals of the New York Academy of Sciences, 2000
Abstract: Our previous studies showed that presenilin‐1 (PS1) is required for murine neural and skeletal development. Here we report that the reduction in the neural progenitor cells observed in the PS1−/− mouse brain is due to premature differentiation of progenitor cells, rather than to increased apoptotic cell death or decreased cell proliferation.
X, Yang, M, Handler, J, Shen
openaire   +2 more sources

[Biochemistry of presenilin 1].

Rinsho shinkeigaku = Clinical neurology, 1998
The majority of cases of early-onset familial Alzheimer disease are caused by mutations in the recently identified presenilin 1 (PS 1) gene, located on chromosome 14. PS1, a 467 amino acid protein, is predicted to be an integral membrane protein containing seven putative transmembrane domains and a large hydrophilic loop between the sixth and seventh ...
openaire   +1 more source

Inhibition of AMPA responses by mutated presenilin 1

Journal of Neuroscience Research, 1999
The inheritance of Alzheimer's disease in some families, as well as ablation/rescue genetics in mice, suggest that point mutations in the presenilin-1 (PS1) gene can cause disease through an unknown gain-of-function. While mutations associated with familial Alzheimer's can alter apoptotic rates and beta-amyloid precursor processing, it is possible that
A M, Moerman, S W, Barger
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Localization of presenilin-1 mRNA in rat brain

NeuroReport, 1996
We examined the regional and cellular distribution of presenilin-1 gene expression in the rat brain by in situ hybridization. Microscopic analysis demonstrated that presenilin-1 mRNA is predominantly expressed in areas such as the occipital cortex, the pyramidal layer of the hippocampus, thalamic nuclei and the cerebellar granular layer. The expression
D, Quarteronet   +6 more
openaire   +2 more sources

Molecular consequences of presenilin-1 mutation

Nature, 2001
C. RUSSO   +9 more
openaire   +2 more sources

Identification and characterization of presenilin I-467, I-463 and I-374

FEBS Letters, 1996
Naruhiko Sahara   +2 more
exaly  

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