rs63750590
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We found the mutations, G384A, E280A in two FAD and H163R in one sporadic AD patient, and no N1411 or M239V mutation in PS-2 gene, and no mutation in exons 16 and 17 in amyloid precursor protein (APP) gene.
|
8945747 |
1996 |
rs63750391
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Here we describe a new substitution of methionine 146 for isoleucine that co-segregates with Alzheimer's disease with age of the onset in the early forties.
|
9007311 |
1996 |
rs765670175
|
|
|
0.060 |
GeneticVariation |
BEFREE |
We describe a new mutation causing Alzheimer's disease (AD) in presenilin-1 (N135D) that is at the homologous site to the presenilin 2 mutation (N141I) in Volga German kindreds.
|
9225696 |
1997 |
rs63750353
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We describe a new mutation causing Alzheimer's disease (AD) in presenilin-1 (N135D) that is at the homologous site to the presenilin 2 mutation (N141I) in Volga German kindreds.
|
9225696 |
1997 |
rs63750231
|
|
|
0.100 |
GeneticVariation |
BEFREE |
E280A PS-1 mutation causes Alzheimer's disease but age of onset is not modified by ApoE alleles.
|
9298817 |
1997 |
rs765670175
|
|
|
0.060 |
GeneticVariation |
BEFREE |
Increased apoptosis arising from increased expression of the Alzheimer's disease-associated presenilin-2 mutation (N141I).
|
9334350 |
1997 |
rs63751163
|
|
|
0.020 |
GeneticVariation |
BEFREE |
PS1 L250S familial Alzheimer's disease is an early onset form of Alzheimer's disease with clinical features similar to other reported familial Alzheimer's disease pedigrees, except that seizures were absent.
|
9436726 |
1998 |
rs63750050
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Identification of a novel mutation (Leu282Arg) of the human presenilin 1 gene in Alzheimer's disease.
|
9502232 |
1998 |
rs63749885
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The large range in age at onset in this family with a uniform genetic basis for the disease, a His163Tyr mutation in PS1, supports the existence of other unknown genetic or environmental factors of importance for the expression of the AD phenotype.
|
9605727 |
1998 |
rs63749805
|
|
|
0.020 |
GeneticVariation |
BEFREE |
The presenilin-1 (PS1) gene mutation (Pro117Leu), recently identified in a Polish family is characterized by the earliest reported onset (from 24-31 years) of Alzheimer disease (AD) and a very short duration of disease (4-6 years).
|
9737546 |
1998 |
rs17125721
|
|
|
0.090 |
GeneticVariation |
BEFREE |
The Glu318Gly mutation of the presenilin-1 gene does not necessarily cause Alzheimer's disease.
|
9851443 |
1998 |
rs765670175
|
|
|
0.060 |
GeneticVariation |
BEFREE |
BrdU labeling was decreased in cells expressing presenilin-1 (PS1), presenilin-2 (PS2), an Alzheimer's disease-associated missense mutation PS2(N141I), and the carboxyl-terminally deleted PS2 construct PS2(166aa), compared with mock and neurofilament-light (NF-L) transfected cells.
|
10393846 |
1999 |
rs63750004
|
|
|
0.030 |
GeneticVariation |
BEFREE |
Both families segregate a different missense mutation in PSEN1 located in different parts of the protein: I143T in family AD/A and G384A in family AD/B.
|
10448055 |
1999 |
rs63750646
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Both families segregate a different missense mutation in PSEN1 located in different parts of the protein: I143T in family AD/A and G384A in family AD/B.
|
10448055 |
1999 |
rs63750004
|
|
|
0.030 |
GeneticVariation |
BEFREE |
Presenilin-1 (PSEN1) mutations I143T and G384A give rise to severe early onset Alzheimers's disease in two extensively studied Belgian families, AD/A and AD/B.
|
10548420 |
1999 |
rs63750646
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Presenilin-1 (PSEN1) mutations I143T and G384A give rise to severe early onset Alzheimers's disease in two extensively studied Belgian families, AD/A and AD/B.
|
10548420 |
1999 |
rs17125721
|
|
|
0.090 |
GeneticVariation |
BEFREE |
Is the presenilin-1 E318G missense mutation a risk factor for Alzheimer's disease?
|
10643802 |
2000 |
rs63750311
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Postmortem examination of one patient with N405S showed limited cerebral amyloid angiopathy, whereas postmortem examination of another Japanese patient with Alzheimer's disease with the E184D mutation disclosed severe cerebral amyloid angiopathy.
|
10644793 |
2000 |
rs63751254
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The N405S mutation of PS1 is a major determinant of cortical Abeta deposition but not cerebral amyloid angiopathy in Alzheimer's disease.
|
10644793 |
2000 |
rs63751163
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Alzheimer's disease presenilin-1 exon 9 deletion and L250S mutations sensitize SH-SY5Y neuroblastoma cells to hyperosmotic stress-induced apoptosis.
|
10658639 |
2000 |
rs63751141
|
|
|
0.010 |
GeneticVariation |
BEFREE |
This analysis revealed that PS1 C92S increased Abeta42 levels in a similar fashion to other pathogenic Alzheimer's disease (AD) PS1 mutations.
|
11027672 |
2000 |
rs63750526
|
|
|
0.070 |
GeneticVariation |
BEFREE |
To test whether oxidative stress is an inherent property of AD tissues, the ability of cultured fibroblasts bearing the AD Presenilin-1 246 Ala-->Glu mutation to handle reactive oxygen species (ROS) was compared to controls.
|
11068175 |
2000 |
rs63750306
|
|
|
0.100 |
GeneticVariation |
BEFREE |
To elucidate the role of presenilin-1 in the Alzheimer's disease pathology, we tested two such mutations (P117L and M146L) for their effect in stably transfected mouse neuroblastoma cell lines.
|
11311782 |
2001 |
rs63750306
|
|
|
0.100 |
GeneticVariation |
BEFREE |
We examined the brains of 12-month-old singly and doubly transgenic mice overexpressing mutant amyloid precursor protein (APP(swe)) and/or presenilin-1 (PS1(M146L)) to investigate the effects of these AD-related genes on plaque and tangle pathology, astrocytic expression, and the CBF projection system.
|
11476589 |
2001 |
rs63750082
|
|
|
0.030 |
GeneticVariation |
BEFREE |
The Gly206Ala mutation was found in 8 of 19 unrelated Caribbean Hispanic families with early-onset familial AD.
|
11710891 |
2001 |