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CADASIL: Notch signaling defect or protein accumulation problem?
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title
CADASIL: Notch signaling defect or protein accumulation problem?
(English)
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author name string
N B Spinner
series ordinal
1
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language of work or name
English
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publication date
March 2000
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published in
Journal of Clinical Investigation
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volume
105
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issue
5
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page(s)
561-2
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cites work
The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patients
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=292459
retrieved
7 April 2017
Spectrum and frequency of jagged1 (JAG1) mutations in Alagille syndrome patients and their families
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=292459
retrieved
7 April 2017
Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=292459
retrieved
7 April 2017
Mutations in the human Jagged1 gene are responsible for Alagille syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=292459
retrieved
7 April 2017
TAN-1, the human homolog of the Drosophila Notch gene, is broken by chromosomal translocations in T lymphoblastic neoplasms
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=292459
retrieved
7 April 2017
Notch signaling: cell fate control and signal integration in development
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=292459
retrieved
7 April 2017
Mutation in the alpha-synuclein gene identified in families with Parkinson's disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=292459
retrieved
7 April 2017
Mutations in JAGGED1 gene are predominantly sporadic in Alagille syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=292459
retrieved
7 April 2017
Notch-1 signalling requires ligand-induced proteolytic release of intracellular domain
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=292459
retrieved
7 April 2017
Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=292459
retrieved
7 April 2017
Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=292459
retrieved
7 April 2017
Embryonic lethality and vascular defects in mice lacking the Notch ligand Jagged1
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=292459
retrieved
7 April 2017
Defects in limb, craniofacial, and thymic development in Jagged2 mutant mice
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=292459
retrieved
7 April 2017
Alzheimer's disease: Initial report of the purification and characterization of a novel cerebrovascular amyloid protein
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=292459
retrieved
7 April 2017
Self-assembly of polyglutamine-containing huntingtin fragments into amyloid-like fibrils: implications for Huntington's disease pathology
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=292459
retrieved
27 September 2017
The mouse pudgy mutation disrupts Delta homologue Dll3 and initiation of early somite boundaries.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=292459
retrieved
30 May 2018
Requirement for dynamin during Notch signaling in Drosophila neurogenesis.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=292459
retrieved
30 May 2018
α-synuclein—a link between Parkinson and Alzheimer diseases?
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=292459
retrieved
28 November 2018
Epidermal growth factor-like modules
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1172%2FJCI9511
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1172/JCI9511
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PMCID
292459
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PubMed ID
10712425
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