About: HERP1 is a cell type-specific primary target of Notch

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scientific journal article

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rdf:type	Item
description	artículu científicu espublizáu en 2002 (ast) vědecký článek publikovaný v roce 2002 (cs) наукова стаття, опублікована в лютому 2002 (uk) vedecký článok (publikovaný 2002/02/22) (sk) 2002 թվականի փետրվարին հրատարակված գիտական հոդված (hy) 2002 թուականի Փետրուարին հրատարակուած գիտական յօդուած (hyw) wetenschappelijk artikel (gepubliceerd op 2002/02/22) (nl) مقالة علمية (نشرت في 22-2-2002) (ar) article publié dans la revue scientifique Journal of Biological Chemistry (fr) im Februar 2002 veröffentlichter wissenschaftlicher Artikel (de) scientific journal article (en)
publication date	wds:Q28512071-A0F3DC1A-FCAB-48A2-9BCD-3A5E9DEAB61C
publication date	2002-02-22 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q28512071-92DF13ED-137C-46BB-AD32-DC0BDF5BCD85
language of work or name	English
author name string	wds:Q28512071-2E5A9B1B-9F86-49B2-AD73-8320273BB1C1 wds:Q28512071-886E6F1F-F603-453C-A18B-0FD538BFFFBD wds:Q28512071-ECD3FD65-CE41-4491-A608-9CBB0E42D412 wds:Q28512071-F81166BC-58C8-4B3B-B5CF-2BCD6D68E3AA
OpenCitations bibliographic resource ID	wds:Q28512071-134CCA9B-8B8E-4368-8AB6-D0E8E886DCC3
OpenCitations bibliographic resource ID	https://w3id.org/oc/corpus/br/4839441
author name string	Larry Kedes Tatsuya Iso Yasuo Hamamori Gene Chung
OpenCitations bibliographic resource ID	4839441
rdfs:label	HERP1 is a cell type-specific primary target of Notch (en) HERP1 is a cell type-specific primary target of Notch (nl) HERP1 is a cell type-specific primary target of Notch (ast)
skos:prefLabel	HERP1 is a cell type-specific primary target of Notch (en) HERP1 is a cell type-specific primary target of Notch (nl) HERP1 is a cell type-specific primary target of Notch (ast)
name	HERP1 is a cell type-specific primary target of Notch (en) HERP1 is a cell type-specific primary target of Notch (nl) HERP1 is a cell type-specific primary target of Notch (ast)
title	wds:Q28512071-24AD7AF6-7289-4B88-A6E9-226819F7FAE1
title	HERP1 is a cell type-specific primary target of Notch (en)
page(s)	wds:Q28512071-FC068780-E465-4170-8861-3D9692A4879B
page(s)	6598–6607
instance of	wds:Q28512071-00368A5C-745C-4161-B904-5BDB1E527A76
instance of	scholarly article
main subject	wds:Q28512071-F9EB7AC5-6900-4329-9D14-79DFBC86B751
main subject	wd:Q21990370
PubMed ID	wds:Q28512071-80C5DF29-DF26-423C-B5D0-221F4849FF16
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/11741889
PubMed ID	11741889
published in	wds:Q28512071-5750FAD0-1EC1-4FC5-BFA1-F4CD1182540E
published in	Journal of Biological Chemistry
issue	wds:Q28512071-A4F63A57-122D-45CA-90C7-50F72A124419
volume	wds:Q28512071-E2BF9404-DBD8-4DD2-9B37-720B267E9DC0
issue	8
volume	277
DOI	wds:Q28512071-6EC3F42B-0C48-4AE7-A48E-AF36D721C8C5
DOI	http://dx.doi.org/10.1074/JBC.M110495200
DOI	10.1074/JBC.M110495200
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q28512071
is cites work of	CADASIL-associated Notch3 mutations have differential effects both on ligand binding and ligand-induced Notch3 receptor signaling through RBP-Jk Jagged1-selective notch signaling induces smooth muscle differentiation via a RBP-Jkappa-dependent pathway KSHV manipulates Notch signaling by DLL4 and JAG1 to alter cell cycle genes in lymphatic endothelia Hes1 is expressed in the second heart field and is required for outflow tract development HeyL promotes neuronal differentiation of neural progenitor cells Hey1, a mediator of notch signaling, is an androgen receptor corepressor Helt, a novel basic-helix-loop-helix transcriptional repressor expressed in the developing central nervous system Gene regulatory factors in pancreatic development Tetralogy of fallot and other congenital heart defects in Hey2 mutant mice Mouse hesr1 and hesr2 genes are redundantly required to mediate Notch signaling in the developing cardiovascular system The Notch target genes Hey1 and Hey2 are required for embryonic vascular development Notch mediates TGF alpha-induced changes in epithelial differentiation during pancreatic tumorigenesis Delta-Notch--and then? Protein interactions and proposed modes of repression by Hes and Hey bHLH factors Gamma secretase inhibitor blocks Notch activation and induces apoptosis in Kaposi's sarcoma tumor cells The multifaceted role of Notch in cardiac development and disease Reciprocal regulation of Notch and nuclear factor of activated T-cells (NFAT) c1 transactivation in osteoblasts Nuclear factor of activated T-cells (NFAT)C2 inhibits Notch receptor signaling in osteoblasts Synergy and antagonism between Notch and BMP receptor signaling pathways in endothelial cells. Chemical suppression of a genetic mutation in a zebrafish model of aortic coarctation. Zebrafish genetics and formation of embryonic vasculature The Ku antigen-recombination signal-binding protein Jkappa complex binds to the nuclear factor-kappaB p50 promoter and acts as a positive regulator of p50 expression in human gastric cancer cells Co-ordinating Notch, BMP, and TGF-β signaling during heart valve development gamma-secretase inhibitor induces adipogenesis of adipose-derived stem cells by regulation of Notch and PPAR-gamma. Jagged-1-mediated activation of notch signalling induces adipogenesis of adipose-derived stem cells Hajdu Cheney Mouse Mutants Exhibit Osteopenia, Increased Osteoclastogenesis, and Bone Resorption HEY2, a target of miR-137, indicates poor outcomes and promotes cell proliferation and migration in hepatocellular carcinoma The Notch effector Hey1 associates with myogenic target genes to repress myogenesis. The Notch pathway attenuates interleukin 1β (IL1β)-mediated induction of adenylyl cyclase 8 (AC8) expression during vascular smooth muscle cell (VSMC) trans-differentiation. A TAG on to the neurogenic functions of APP Cre-conditional expression of constitutively active Notch1 in transgenic mice. Evidence of Notch pathway activation in the ectatic ducts of chronic pancreatitis MiR-34c represses muscle development by forming a regulatory loop with Notch1 Osteogenesis of Adipose-Derived Stem Cells Neural stem cell quiescence and stemness are molecularly distinct outputs of the Notch3 signaling cascade in the vertebrate adult brain. Protein kinase C activates human lipocalin-type prostaglandin D synthase gene expression through de-repression of notch-HES signaling and enhancement of AP-2 beta function in brain-derived TE671 cells. Notch suppresses nuclear factor of activated T cells (NFAT) transactivation and Nfatc1 expression in chondrocytes Notch signaling regulates Hey2 expression in a spatiotemporal dependent manner during cardiac morphogenesis and trabecular specification. Phenotypic variability in Hey2 -/- mice and absence of HEY2 mutations in patients with congenital heart defects or Alagille syndrome Expression of Hey2 transcription factor in the early embryonic ventricles is controlled through a distal enhancer by Tbx20 and Gata transcription factors The NOTCH1-HEY1 pathway regulates self-renewal and epithelial-mesenchymal transition of salivary adenoid cystic carcinoma cells Notch3 signalling and vascular remodelling in pulmonary arterial hypertension
is cites work of	wds:Q28507429-5CE4463B-1A81-46DF-B394-EF6357A052CE wds:Q33823680-549F392E-DB1F-4B5D-BADB-2B3FCBBEEB7D

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