About: Anne Blangy

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

Attributes	Values
rdf:type	Item
description	forskare (sv) ikertzailea (eu) researcher (en) 연구원 (ko) গবেষক (bn) 研究者 (ja) wetenschapper (nl) дослідниця (uk) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtuese (sq) ricercatrice (it)
rdfs:label	Anne Blangy (en) Anne Blangy (es) Anne Blangy (nl) Anne Blangy (ast)
skos:prefLabel	Anne Blangy (en) Anne Blangy (es) Anne Blangy (nl) Anne Blangy (ast)
name	Anne Blangy (en) Anne Blangy (es) Anne Blangy (nl) Anne Blangy (ast)
Scopus author ID	wds:Q42875386-5D25CA26-9AAE-431C-AF7D-4EF84D12208A wds:Q42875386-A75EBFD8-E87B-49AE-B5BF-29ED582D4D49
Scopus author ID	57203263664 6701643730
given name	wds:Q42875386-3D233FE0-9E70-47AD-8887-2A0EB9BCDE30
given name	Anne
instance of	wds:Q42875386-3AE31F37-C0ED-45FF-8178-567A7C38EC30
instance of	Homo sapiens
doctoral advisor	wds:Q42875386-11B6F792-B4F4-44DE-B23B-E8EEF0368D37
doctoral advisor	François Cuzin
occupation	wds:Q42875386-3C2C6BF4-11D0-44C0-B8A3-C22A2E98E9CE
employer	wds:Q42875386-6AC571E9-B94D-480C-A829-63D4174CECEE wds:Q42875386-DA30AA38-5989-49BF-937E-CFB2AC84D195
sex or gender	wds:Q42875386-36C1BBD9-21FD-4DE1-9583-84E10044557D
ISNI	wds:Q42875386-24314599-E202-4F0D-B64A-10737F2B3AAF
VIAF ID	wds:Q42875386-369CC1F3-49A2-4E9E-AB8C-E1D1B8EA274D
IdRef ID	wds:Q42875386-2A0BF14F-CCBF-4297-8A09-21760F8E9E13
WorldCat Identities ID (superseded)	wds:Q42875386-4BA11A0A-ED99-48E9-9628-A67BBA9304BB
official website	wds:Q42875386-89793A78-6CFE-46F3-AADF-660029D28344
VIAF ID	http://viaf.org/viaf/192790773
IdRef ID	http://www.idref.fr/079097650/id
occupation	researcher
employer	Institute of Human Genetics Délégation Languedoc Roussillon
sex or gender	female organism
ISNI	0000000431119004
VIAF ID	192790773
IdRef ID	079097650
WorldCat Identities ID (superseded)	lccn-n2017184899
official website	http://www.crbm.cnrs.fr/en/team/blangy/
ORCID iD	wds:Q42875386-C810DEE5-EA23-451C-928F-81FD13B6599C
ORCID iD	https://orcid.org/0000-0001-7043-0784
ORCID iD	0000-0001-7043-0784
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q42875386
is author of	Dynamic changes in nuclear architecture during mitosis: on the role of protein phosphorylation in spindle assembly and chromosome segregation. The Rac1 exchange factor Dock5 is essential for bone resorption by osteoclasts Promyelocytic leukemia zinc-finger induction signs mesenchymal stem cell commitment: identification of a key marker for stemness maintenance? Induction of lamellipodia by Kalirin does not require its guanine nucleotide exchange factor activity Characterization of TCL, a new GTPase of the rho family related to TC10 andCcdc42 Identification of TRIO-GEFD1 chemical inhibitors using the yeast exchange assay Rho GTPases in osteoclasts: orchestrators of podosome arrangement The Rho GTPase Wrch1 regulates osteoclast precursor adhesion and migration The atypical Rac activator Dock180 (Dock1) regulates myoblast fusion in vivo Phosphorylation by p34cdc2 regulates spindle association of human Eg5, a kinesin-related motor essential for bipolar spindle formation in vivo The Human Rho-GEF trio and its target GTPase RhoG are involved in the NGF pathway, leading to neurite outgrowth Phosphorylation by p34cdc2 protein kinase regulates binding of the kinesin-related motor HsEg5 to the dynactin subunit p150 N-cadherin-dependent cell-cell contact regulates Rho GTPases and beta-catenin localization in mouse C2C12 myoblasts A cell active chemical GEF inhibitor selectively targets the Trio/RhoG/Rac1 signaling pathway Rigor-type mutation in the kinesin-related protein HsEg5 changes its subcellular localization and induces microtubule bundling. The DH-PH region of the giant protein UNC-89 activates RHO-1 GTPase in Caenorhabditis elegans body wall muscle RhoA GTPase regulates M-cadherin activity and myoblast fusion The GTP/GDP cycling of rho GTPase TCL is an essential regulator of the early endocytic pathway Phagocytosis of apoptotic cells is regulated by a UNC-73/TRIO-MIG-2/RhoG signaling module and armadillo repeats of CED-12/ELMO Kinectin is a key effector of RhoG microtubule-dependent cellular activity Interaction of the mitotic inhibitor monastrol with human kinesin Eg5. Interaction of ezrin with the novel guanine nucleotide exchange factor PLEKHG6 promotes RhoG-dependent apical cytoskeleton rearrangements in epithelial cells Cofilin activation during podosome belt formation in osteoclasts Identification of a bipartite focal adhesion localization signal in RhoU/Wrch-1, a Rho family GTPase that regulates cell adhesion and migration Interferon-alpha and -beta differentially regulate osteoclastogenesis: role of differential induction of chemokine CXCL11 expression. Expression profile of RhoGTPases and RhoGEFs during RANKL-stimulated osteoclastogenesis: identification of essential genes in osteoclasts The RhoE/ROCK/ARHGAP25 signaling pathway controls cell invasion by inhibition of Rac activity RhoE controls myoblast alignment prior fusion through RhoA and ROCK. Modulation of osteoclast differentiation and bone resorption by Rho GTPases Biogenesis of N-cadherin-dependent cell-cell contacts in living fibroblasts is a microtubule-dependent kinesin-driven mechanism Recognition of the CDEl motif GTCACATG by mouse nuclear proteins and interference with the early development of the mouse embryo Dock-family exchange factors in cell migration and disease Tensins are versatile regulators of Rho GTPase signalling and cell adhesion The gene for a new brain specific RhoA exchange factor maps to the highly unstable chromosomal region 1p36.2-1p36.3. Tensin 3 is a new partner of Dock5 that controls osteoclast podosome organization and activity. Pharmacological inhibition of Dock5 prevents osteolysis by affecting osteoclast podosome organization while preserving bone formation The mineral dissolution function of osteoclasts is dispensable for hypertrophic cartilage degradation during long bone development and growth. Using a Modified Yeast Two-Hybrid System to Screen for Chemical GEF Inhibitors Signalling pathways controlled by the GTPase RhoG Podosomes are dispensable for osteoclast differentiation and migration

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