About: Andre J van Wijnen

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

researcher ORCID ID = 0000-0002-4458-0946

Attributes	Values
rdf:type	Item
field of work	wds:Q60974897-2A027277-A881-43BB-8AED-1B0095E2C074 wds:Q60974897-6BF477FA-70B0-4992-95E1-AFDC853CE45D wds:Q60974897-9E65325C-4CD9-4ABD-BBD5-CB1AAD25044C wds:Q60974897-B6F4158F-E278-4FAB-8C40-870DF6AF00C7 wds:Q60974897-EA446D2B-930E-453E-AB86-11A064BD2687
field of work	osteoporosis biochemistry stem cell molecular biology orthopedics
description	ikertzailea (eu) 연구원 (ko) araştırmacı (tr) باحت (ary) изилдөөчү (ky) 研究者 (zh) onderzoeker (nl) researcher ORCID ID = 0000-0002-4458-0946 (en) Odborník v oblasti ortopedické chirurgie, biochemie a molekulární biologie, specializuje se na osteoporózu, kmenové buňky, buněčné signály a proteiny RUNX. Publikace v oboru. (cs)
rdfs:label	Andre J van Wijnen (en) Andre J van Wijnen (nl) Andre J van Wijnen (ast) Andre J. Van Wijnen (cs)
skos:prefLabel	Andre J van Wijnen (en) Andre J van Wijnen (nl) Andre J van Wijnen (ast) Andre J. Van Wijnen (cs)
name	Andre J van Wijnen (en) Andre J van Wijnen (nl) Andre J van Wijnen (ast) Andre J. Van Wijnen (cs)
given name	wds:Q60974897-1df71f4e-41fa-10e7-4135-b236a5b3405f
given name	Andre
instance of	wds:Q60974897-AF7CE4C6-D9F3-4B3F-AAE7-565015BEB941
NL CR AUT ID	wds:Q60974897-389A20F4-F49C-4E57-BCF1-A21AE0CF96FF
instance of	Homo sapiens
NL CR AUT ID	ntk20211112232
occupation	wds:Q60974897-28C2EDC9-46EE-4D26-8799-E32BF35972AB wds:Q60974897-8984133a-1df0-4870-9b97-f4ce1db22dc4
employer	wds:Q60974897-0D440FBE-6BFD-462E-8305-FD3170C24C03 wds:Q60974897-48651310-96EB-4BEA-9490-0BC436F030C4 wds:Q60974897-AAA44DED-4ABE-4272-BF0B-E4FFC404829E wds:Q60974897-B939B14E-39E5-45D5-85D4-15A2734DC30F
languages spoken, written or signed	wds:Q60974897-B111656D-8434-435F-BA34-CF08E2162770
sex or gender	wds:Q60974897-eafdf113-4c7e-55a3-f6e5-3533e6a8fbbc
ISNI	wds:Q60974897-324580ed-4433-4d6e-84a1-8ae76712b87c
VIAF ID	wds:Q60974897-C4D40E62-F8D7-4721-AF22-2A98C3F2E068
IdRef ID	wds:Q60974897-40aecae8-6823-4a4a-9045-940b25b99269
educated at	wds:Q60974897-81035C1A-8AF0-46D0-923A-6E9C3EDC6453
family name	wds:Q60974897-43c0683e-42e5-41ed-0ada-0266de275beb
VIAF ID	http://viaf.org/viaf/311475055
IdRef ID	http://www.idref.fr/182481719/id
occupation	scientist researcher
employer	Worcester Foundation for Biomedical Research Mayo Clinic University of Vermont University of Massachusetts Medical School
languages spoken, written or signed	English
sex or gender	male
ISNI	0000000440127006
VIAF ID	311475055
IdRef ID	182481719
educated at	University of Massachusetts Medical School
family name	van Wijnen
ORCID iD	wds:Q60974897-F8AA5A08-95A2-4C2A-8512-760D59C2DC08
ORCID iD	https://orcid.org/0000-0002-4458-0946
ORCID iD	0000-0002-4458-0946
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q60974897
is author of	The HiNF-P/p220NPAT cell cycle signaling pathway controls nonhistone target genes SWI/SNF chromatin remodeling complex is obligatory for BMP2-induced, Runx2-dependent skeletal gene expression that controls osteoblast differentiation Mitotic control of RUNX2 phosphorylation by both CDK1/cyclin B kinase and PP1/PP2A phosphatase in osteoblastic cells Bookmarking target genes in mitosis: a shared epigenetic trait of phenotypic transcription factors and oncogenes? The interactome of the histone gene regulatory factor HiNF-P suggests novel cell cycle related roles in transcriptional control and RNA processing MicroRNAs 221 and 222 bypass quiescence and compromise cell survival A program of microRNAs controls osteogenic lineage progression by targeting transcription factor Runx2 A network connecting Runx2, SATB2, and the miR-23a~27a~24-2 cluster regulates the osteoblast differentiation program Bookmarking the genome: maintenance of epigenetic information. Control of mesenchymal lineage progression by microRNAs targeting skeletal gene regulators Trps1 and Runx2. miR-218 directs a Wnt signaling circuit to promote differentiation of osteoblasts and osteomimicry of metastatic cancer cells Biological functions of miR-29b contribute to positive regulation of osteoblast differentiation Smad function and intranuclear targeting share a Runx2 motif required for osteogenic lineage induction and BMP2 responsive transcription. Canonical WNT Signaling Promotes Osteogenesis by Directly StimulatingRunx2Gene Expression The leukemogenic t(8;21) fusion protein AML1-ETO controls rRNA genes and associates with nucleolar-organizing regions at mitotic chromosomes. A RUNX2-HDAC1 co-repressor complex regulates rRNA gene expression by modulating UBF acetylation The rat intervertebral disk degeneration pain model: relationships between biological and structural alterations and pain Phenotype discovery by gene expression profiling: mapping of biological processes linked to BMP-2-mediated osteoblast differentiation Inhibiting DNA-PKCS radiosensitizes human osteosarcoma cells Basic fibroblast growth factor activates the MAPK and NFkappaB pathways that converge on Elk-1 to control production of matrix metalloproteinase-13 by human adult articular chondrocytes. Runx2 protein expression utilizes the Runx2 P1 promoter to establish osteoprogenitor cell number for normal bone formation p68 (Ddx5) interacts with Runx2 and regulates osteoblast differentiation Expression of Runx2 transcription factor in non-skeletal tissues, sperm and brain Dicer inactivation in osteoprogenitor cells compromises fetal survival and bone formation, while excision in differentiated osteoblasts increases bone mass in the adult mouse Runx2 protein represses Axin2 expression in osteoblasts and is required for craniosynostosis in Axin2-deficient mice The dynamic organization of gene-regulatory machinery in nuclear microenvironments Nuclear microenvironments support physiological control of gene expression Functional architecture of the nucleus: organizing the regulatory machinery for gene expression, replication and repair. Lymphocyte enhancer-binding factor 1 (Lef1) inhibits terminal differentiation of osteoblasts. A microRNA signature for a BMP2-induced osteoblast lineage commitment program

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