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Human Presenilin 1 ELISA Kit for Sandwich ELISA - ABIN1110865
Ankarcrona, Hultenby: Presenilin-1 is located in rat mitochondria. in Biochemical and biophysical research communications 2002
Human Presenilin 1 ELISA Kit for Sandwich ELISA - ABIN417919
Paulasir, Kaoutzanis, Welch, Vandewarker, Krapohl, Lampman, Franz, Cleary: Nonsteroidal Anti-inflammatory Drugs: Do They Increase the Risk of Anastomotic Leaks Following Colorectal Operations? in Diseases of the colon and rectum 2015
Using an antisense morpholino oligonucleotide, study blocked induction of PS1IV isoform that normally occurs under hypoxia,identified gene regulatory networks that are modulated by PS1IV: observed changes in expression of genes controlling inflammation, vascular development, the UPR, protein synthesis, calcium homeostasis, catecholamine biosynthesis, TOR signaling, and cell proliferation
We identified psen1 as a regulator of the development of histaminergic neurons in zebrafish
These results suggest that Psen2 (show PSEN2 ELISA Kits) plays a more prominent role in Notch (show NOTCH1 ELISA Kits) signalling and embryo development in zebrafish than in mammals, and that the effect of reduced Psen2 (show PSEN2 ELISA Kits) can be ameliorated by Psen1 loss.
Cultured hippocampal neurons expressing mutant PS1 had attenuated CCE that was associated with destabilized dendritic spines, which were rescued by either gamma-secretase inhibition or overexpression of STIM1 (show STIM1 ELISA Kits).
PSEN1 mutations responsible for early-onset Alzheimer's disease with extrapyramidal phenotype.
A novel mutation in exon 7 of presenilin 1 (Leu232Pro) was discovered in a Korean patient with early-onset Alzheimer's disease.
PSEN1 pathogenic mutation M84V is found in autosomal dominant Alzheimer's disease.
The authors demonstrate that pathological PS1 loss-of-function impinges on neurite formation through a selective APP (show APP ELISA Kits) gain-of-function that could impact on axodendritic connectivity and contribute to aberrant axonal sprouting observed in Alzheimer's disease patients.
early-onset Alzheimer's disease is caused by a novel N135Y mutation in PSEN1.
PSEN1 rare variants collectively show a significant association with the brain atrophy in regions preferentially affected by late-onset Alzheimer's disease
Tspan3 (show TSPAN3 ELISA Kits) is a central endocytic membrane component regulating the expression of ADAM10 (show ADAM10 ELISA Kits), presenilin and the amyloid precursor protein (show APP ELISA Kits).
Familial Alzheimer's disease-associated PS1 mutations induce disease pathogenesis by increasing Abeta42/Abeta40 ratio.
a novel mutation PSEN1 c.1156T>A, p.F386I was detected in a Chinese family with FAD (show BRCA2 ELISA Kits). The mutation cosegregates with affected family members suggesting a mutagenic and probably pathogenic effect.
Conditionally targeted deletion of PSEN1 leads to diastolic heart dysfunction and ultrastructural cardiomyocyte abnormalities.
findings indicate that impaired processing or localization of apoER2 (show LRP8 ELISA Kits) may contribute to the pathogenic effects of familial Alzheimer's disease mutations in PS1
Study shows that the binding of HSF-1 (show HSF1 ELISA Kits), Cdx1 (show CDX1 ELISA Kits), Ets-1 (show ETS1 ELISA Kits) and Sp1 (show SP1 ELISA Kits) to Presenilin 1 promoter and that of Nkx2.2 (show Nkx2-2 ELISA Kits), HFH-2 (show FOXD3 ELISA Kits), Cdx1 (show CDX1 ELISA Kits) and NF-kappaB (show NFKB1 ELISA Kits) to Presenilin 2 (show PSEN2 ELISA Kits) promoter regulate their differential expression during brain development.
conclusion that the PSEN1 mutations are extreme examples of the previously proposed ''dysfunction'' of gamma-secretase that characterizes familial Alzheimer's disease
PS1 expression is triggered by glutamate (show GRIN1 ELISA Kits) through p38alpha (show MAPK14 ELISA Kits), contributing to the excitotoxic stimulus of EW
amino acid sensing of mechanistic target of rapamycin (show FRAP1 ELISA Kits) complex 1 (mTORC1) is dysregulated in cells deficient in presenilin.
the G206D mutation reduced presenilin-1-presenilin enhancer 2 (show PSENEN ELISA Kits) interaction, but did not abolish gamma-secretase formation and presenilin-1 endoproteolysis
This study deals with the effect of attenuated endoproteolysis of PS1 on store-operated calcium (SOC (show UBXN11 ELISA Kits)) entry in neuronal cells and mouse fibroblasts with double knockouts of PS1 and PS2 (show PDCD6 ELISA Kits)
maternal dietary betaine supplementation during gestation inhibits hepatic cell proliferation in neonatal piglets, at least partly, through epigenetic regulation of hepatic CCND2 (show CCND2 ELISA Kits) and PSEN1 genes via a STAT3 (show STAT3 ELISA Kits)-dependent pathway
gamma-Secretase and presenilin mediate cleavage and phosphorylation of vascular endothelial growth factor receptor-1 (show FLT1 ELISA Kits)
Alzheimer's disease (AD) patients with an inherited form of the disease carry mutations in the presenilin proteins (PSEN1\; PSEN2) or in the amyloid precursor protein (APP). These disease-linked mutations result in increased production of the longer form of amyloid-beta (main component of amyloid deposits found in AD brains). Presenilins are postulated to regulate APP processing through their effects on gamma-secretase, an enzyme that cleaves APP. Also, it is thought that the presenilins are involved in the cleavage of the Notch receptor, such that they either directly regulate gamma-secretase activity or themselves are protease enzymes. Several alternatively spliced transcript variants encoding different isoforms have been identified for this gene, the full-length nature of only some have been determined.
, presenilin 1 (Alzheimer disease 3)
, presenilin-1 isoform I-463
, presenilin-1 isoform I-467
, presenilin 1
, presenilin alpha