(Q52189082)

26 April 2018

title

An Alzheimer's Disease-Linked PS1 Variant Rescues the Developmental Abnormalities of PS1-Deficient Embryos (English)

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

16 December 2024

main subject

cell surface receptor

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:9539132

16 December 2024

author name string

J. A. Davis

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:9539132

16 December 2024

S. Naruse

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:9539132

16 December 2024

H. Chen

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:9539132

16 December 2024

C. Eckman

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:9539132

16 December 2024

S. Younkin

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:9539132

16 December 2024

D. L. Price

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:9539132

16 December 2024

D. R. Borchelt

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:9539132

16 December 2024

S. S. Sisodia

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:9539132

16 December 2024

P. C. Wong

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:9539132

16 December 2024

language of work or name

English

0 references

publication date

1 March 1998

1 reference

26 April 2018

March 1998

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=9539132

full work available at URL

16 December 2024

http://www.cell.com/article/S0896627300809988/pdf

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:9539132

https://api.elsevier.com/content/article/PII:S0896627300809988?httpAccept=text/xml

16 December 2024

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

https://api.elsevier.com/content/article/PII:S0896627300809988?httpAccept=text/plain

16 December 2024

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

16 December 2024

1 reference

26 April 2018

volume

20

1 reference

26 April 2018

issue

3

1 reference

26 April 2018

page(s)

603-609

1 reference

26 April 2018

The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD families

cites work

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

7 January 2021

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

1 reference

7 January 2021

Human presenilin‐1, but not familial Alzheimer’s disease (FAD) mutants, facilitate Caenorhabditis elegans Notch signalling independently of proteolytic processing

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

7 January 2021

Familial Alzheimer's disease-linked presenilin 1 variants elevate Abeta1-42/1-40 ratio in vitro and in vivo

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

7 January 2021

Accelerated amyloid deposition in the brains of transgenic mice coexpressing mutant presenilin 1 and amyloid precursor proteins

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

7 January 2021

Mutations of the presenilin I gene in families with early-onset Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

7 January 2021

Familial Alzheimer's disease associated with S182 codon 286 mutation

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

7 January 2021

Early-onset Alzheimer's disease caused by mutations at codon 717 of the beta-amyloid precursor protein gene

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

7 January 2021

Mutant presenilins of Alzheimer's disease increase production of 42-residue amyloid beta-protein in both transfected cells and transgenic mice

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

7 January 2021

The presenilin genes: a new gene family involved in Alzheimer disease pathology

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

7 January 2021

Role of Olf-1 and Pax-6 transcription factors in neurodevelopment

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

7 January 2021

Increased amyloid-beta42(43) in brains of mice expressing mutant presenilin 1

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

7 January 2021

Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

7 January 2021

Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the beta-amyloid precursor protein gene.

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

7 January 2021

Maintenance of somite borders in mice requires the Delta homologue DII1.

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

7 January 2021

Light and electron microscopic localization of presenilin-1 in primate brain.

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

7 January 2021

Hyperaccumulation of FAD-linked presenilin 1 variants in vivo

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

7 January 2021

Facilitation of lin-12-mediated signalling by sel-12, a Caenorhabditis elegans S182 Alzheimer's disease gene

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

7 January 2021

Assessment of normal and mutant human presenilin function in Caenorhabditis elegans

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

7 January 2021

Candidate gene for the chromosome 1 familial Alzheimer's disease locus

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

7 January 2021

Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

7 January 2021

A pathogenic mutation for probable Alzheimer's disease in the APP gene at the N-terminus of beta-amyloid

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

7 January 2021

Mis-sense mutation Val&rarr;Ile in exon 17 of amyloid precursor protein gene in Japanese familial Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

7 January 2021

Mutations in the human Jagged1 gene are responsible for Alagille syndrome

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

7 January 2021

Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

7 January 2021

Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

7 January 2021

Secreted amyloid beta-protein similar to that in the senile plaques of Alzheimer's disease is increased in vivo by the presenilin 1 and 2 and APP mutations linked to familial Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

7 January 2021

Skeletal and CNS defects in Presenilin-1-deficient mice

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

7 January 2021

Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

7 January 2021

Genetic evidence for a novel familial Alzheimer's disease locus on chromosome 14.

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

7 January 2021

An increased percentage of long amyloid beta protein secreted by familial amyloid beta protein precursor (beta APP717) mutants.

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

7 January 2021

Notch1 is essential for postimplantation development in mice.

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

7 January 2021

Endoproteolysis of presenilin 1 and accumulation of processed derivatives in vivo

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

7 January 2021

Evidence That Levels of Presenilins (PS1 and PS2) Are Coordinately Regulated by Competition for Limiting Cellular Factors

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

7 January 2021

Familial Alzheimer's chromosome 14 mutations

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

7 January 2021

Presenilin 1 is required for Notch1 and DII1 expression in the paraxial mesoderm

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

7 January 2021

An early marker of axial pattern in the chick embryo and its respecification by retinoic acid

34

1 reference

https://api.crossref.org/works/10.1016/S0896-6273(00)80998-8

16 December 2024

Identifiers

1 reference

26 April 2018

1 reference

26 April 2018