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Notch signaling and bone remodeling
scientific article published on June 2013
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
3645324
retrieved
28 August 2017
title
Notch signaling and bone remodeling
(English)
1 reference
stated in
Europe PubMed Central
PMCID
3645324
retrieved
28 August 2017
author name string
Jenna Regan
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
3645324
retrieved
28 August 2017
Fanxin Long
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
3645324
retrieved
28 August 2017
language of work or name
English
1 reference
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inferred from title
publication date
1 June 2013
1 reference
stated in
Europe PubMed Central
PMCID
3645324
retrieved
28 August 2017
published in
Current osteoporosis reports
1 reference
stated in
Europe PubMed Central
PMCID
3645324
retrieved
28 August 2017
volume
11
1 reference
stated in
Europe PubMed Central
PMCID
3645324
retrieved
28 August 2017
issue
2
1 reference
stated in
Europe PubMed Central
PMCID
3645324
retrieved
28 August 2017
page(s)
126-129
1 reference
stated in
Europe PubMed Central
PMCID
3645324
retrieved
28 August 2017
exact match
https://scigraph.springernature.com/pub.10.1007/s11914-013-0145-4
0 references
cites work
Osteoblast lineage-specific effects of notch activation in the skeleton
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=3645324
retrieved
6 September 2017
Physiological notch signaling maintains bone homeostasis via RBPjk and Hey upstream of NFATc1
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=3645324
retrieved
6 September 2017
Differential regulation of osteoclastogenesis by Notch2/Delta-like 1 and Notch1/Jagged1 axes
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=3645324
retrieved
6 September 2017
Alagille syndrome: pathogenesis, diagnosis and management
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=3645324
retrieved
6 September 2017
Notch signaling: simplicity in design, versatility in function
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=3645324
retrieved
6 September 2017
Serpentine fibula polycystic kidney syndrome is part of the phenotypic spectrum of Hajdu-Cheney 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=3645324
retrieved
6 September 2017
Mutations in NOTCH2 in families with Hajdu-Cheney 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=3645324
retrieved
6 September 2017
Truncating mutations in the last exon of NOTCH2 cause a rare skeletal disorder with osteoporosis
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=3645324
retrieved
6 September 2017
Mutations in NOTCH2 cause Hajdu-Cheney syndrome, a disorder of severe and progressive bone loss
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=3645324
retrieved
6 September 2017
Osteosclerosis owing to Notch gain of function is solely Rbpj-dependent
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=3645324
retrieved
6 September 2017
Pathologic lower extremity fractures in children with 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=3645324
retrieved
6 September 2017
Association of JAG1 with bone mineral density and osteoporotic fractures: a genome-wide association study and follow-up replication studies.
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=3645324
retrieved
6 September 2017
Notch signaling: the core pathway and its posttranslational regulation
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=3645324
retrieved
6 September 2017
The canonical Notch signaling pathway: unfolding the activation mechanism
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=3645324
retrieved
6 September 2017
The association of Notch2 and NF-kappaB accelerates RANKL-induced osteoclastogenesis
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=3645324
retrieved
6 September 2017
Notch signaling in osteoblasts
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=3645324
retrieved
6 September 2017
Notch inhibits osteoblast differentiation and causes osteopenia
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=3645324
retrieved
6 September 2017
Dimorphic effects of Notch signaling in bone homeostasis.
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=3645324
retrieved
6 September 2017
Notch signaling maintains bone marrow mesenchymal progenitors by suppressing osteoblast differentiation
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=3645324
retrieved
6 September 2017
The osteoclast: friend or foe?
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=3645324
retrieved
6 September 2017
NOTCH2 mutations cause Alagille syndrome, a heterogeneous disorder of the notch signaling pathway
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=3645324
retrieved
6 September 2017
Critical regulation of bone morphogenetic protein-induced osteoblastic differentiation by Delta1/Jagged1-activated Notch1 signaling
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=3645324
retrieved
6 September 2017
Activating mutations of NOTCH1 in human T cell acute lymphoblastic leukemia
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=3645324
retrieved
6 September 2017
Notch signaling controls multiple steps of pancreatic differentiation
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=3645324
retrieved
6 September 2017
Regulation of osteoclast development by Notch signaling directed to osteoclast precursors and through stromal cells
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=3645324
retrieved
6 September 2017
Axial skeletal defects caused by mutation in the spondylocostal dysplasia/pudgy gene Dll3 are associated with disruption of the segmentation clock within the presomitic mesoderm
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=3645324
retrieved
6 September 2017
Hajdu--Cheney syndrome: evolution of phenotype and clinical problems
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=3645324
retrieved
6 September 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=3645324
retrieved
6 September 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=3645324
retrieved
6 September 2017
Skeletal and CNS defects in Presenilin-1-deficient 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=3645324
retrieved
6 September 2017
Presenilin 1 is required for Notch1 and DII1 expression in the paraxial mesoderm
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=3645324
retrieved
6 September 2017
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=3645324
retrieved
6 September 2017
Notch 1 overexpression inhibits osteoblastogenesis by suppressing Wnt/beta-catenin but not bone morphogenetic protein signaling
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=3645324
retrieved
14 September 2017
Syndrome of Alagille: radiological and sonographic findings. A review of 37 cases
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=3645324
retrieved
28 September 2017
Notch 1 impairs osteoblastic cell differentiation
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=3645324
retrieved
23 June 2018
Ubiquitous overexpression of Hey1 transcription factor leads to osteopenia and chondrocyte hypertrophy in bone
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=3645324
retrieved
31 August 2018
NOTCH1 regulates osteoclastogenesis directly in osteoclast precursors and indirectly via osteoblast lineage cells.
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=3645324
retrieved
31 August 2018
Outcome of syndromic paucity of interlobular bile ducts (Alagille syndrome) with onset of cholestasis in infancy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1007%2FS11914-013-0145-4
retrieved
21 January 2018
Vertebral anomalies in children with Alagille syndrome: an analysis of 50 consecutive patients
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/23519781
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Serpentine fibula-polycystic kidney syndrome caused by truncating mutations in NOTCH2
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/23519781
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Stimulation of osteoblastic cell differentiation by Notch
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/23519781
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1007/S11914-013-0145-4
1 reference
stated in
Europe PubMed Central
PMCID
3645324
retrieved
28 August 2017
Dimensions Publication ID
1002571827
0 references
PMCID
3645324
1 reference
stated in
Europe PubMed Central
PMCID
3645324
retrieved
28 August 2017
PubMed ID
23519781
1 reference
stated in
Europe PubMed Central
PMCID
3645324
retrieved
28 August 2017
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