About: Michiel Albertus Basson

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About: Michiel Albertus Basson Goto Sponge NotDistinct Permalink

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) forsker (nb) ikertzailea (eu) researcher (en) 연구원 (ko) 研究者 (ja) дослідник (uk) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) Brits onderzoeker (nl)
rdfs:label	M. Albert Basson (es) M. Albert Basson (nl) M. Albert Basson (sl) M. Albert Basson (ast) Michiel Albertus Basson (ca) Michiel Albertus Basson (en) Michiel Albertus Basson (nb)
skos:prefLabel	M. Albert Basson (es) M. Albert Basson (nl) M. Albert Basson (sl) M. Albert Basson (ast) Michiel Albertus Basson (ca) Michiel Albertus Basson (en) Michiel Albertus Basson (nb)
name	M. Albert Basson (es) M. Albert Basson (nl) M. Albert Basson (sl) M. Albert Basson (ast) Michiel Albertus Basson (ca) Michiel Albertus Basson (en) Michiel Albertus Basson (nb)
Scopus author ID	wds:Q55283770-A9FABD2B-7ABB-4180-A1CF-A87727765215
Scopus author ID	7006201864
given name	wds:Q55283770-488BA7B9-382D-4017-804B-77AAD3565D5A
given name	M.
instance of	wds:Q55283770-0A1C3D10-6C72-43F0-856C-70E0DE004215
instance of	Homo sapiens
skos:altLabel	M. Albert Basson (en)
occupation	wds:Q55283770-20662673-D148-4BE7-9BB3-0F6FF2926666
employer	wds:Q55283770-0425E25F-07FB-40B2-9B85-A26730DD75B5 wds:Q55283770-49FA2C1B-D938-4DA9-82F4-6424F6E9A97F wds:Q55283770-93AD082E-6209-4A05-8C3F-A9D3F0642C66 wds:Q55283770-F7E00739-E6E3-4394-AAA0-EB2A2ED84EC3
languages spoken, written or signed	wds:Q55283770-D3B6EA07-F80F-41FE-980E-893F4ECC2380
country of citizenship	wds:Q55283770-51EC2C0F-F7D0-41A1-82B6-6E91EEBBE6AB
educated at	wds:Q55283770-67200532-BA06-4C30-AB97-CD8002E4EE2F wds:Q55283770-ACB92D19-C031-4466-8951-D8CD6A6D40FC wds:Q55283770-C9A107B8-B5C0-4DCA-82FA-F1015FDC3412 wds:Q55283770-EBAFADEA-674F-4A94-8E00-CE16CEA211B4 wds:Q55283770-F50E6802-15E2-42A7-8B39-BD110F729E1E
family name	wds:Q55283770-2F7B02B9-D4A4-4D8B-B24F-B3E56508DA18
official website	wds:Q55283770-50F8A972-3FF2-4A93-8483-1B576691A427
occupation	researcher
employer	Francis Crick Institute University of California, San Francisco University of Exeter King's College London
languages spoken, written or signed	English
country of citizenship	United Kingdom
educated at	John Ffowcs Williams King's College London University of Pretoria
family name	Basson
official website	https://kclpure.kcl.ac.uk/portal/en/persons/albert-basson(13147099-a415-4a85-bca2-78aff08a6761).html
ORCID iD	wds:Q55283770-83195E69-5A99-42B0-8FD6-95DBED2DD596
ORCID iD	https://orcid.org/0000-0001-9834-7528
ORCID iD	0000-0001-9834-7528
Gateway to Research person ID	wds:Q55283770-B31018DA-2243-43DE-AB73-DA515F0BB809
Gateway to Research person ID	2EF172A2-5A4A-4B80-B8EA-B568B42790AF
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q55283770
is author of	MicroRNA-21 contributes to myocardial disease by stimulating MAP kinase signalling in fibroblasts Sprouty genes prevent excessive FGF signalling in multiple cell types throughout development of the cerebellum. Gli3 controls corpus callosum formation by positioning midline guideposts during telencephalic patterning. The influence of the src-family kinases, Lck and Fyn, on T cell differentiation, survival and activation The aged niche disrupts muscle stem cell quiescence. Sprouty is a negative regulator of transforming growth factor β-induced epithelial-to-mesenchymal transition and cataract. Sprouty proteins: multifaceted negative-feedback regulators of receptor tyrosine kinase signaling. Functional Insights into Chromatin Remodelling from Studies on CHARGE Syndrome A bi-modal function of Wnt signalling directs an FGF activity gradient to spatially regulate neuronal differentiation in the midbrain Specific regions within the embryonic midbrain and cerebellum require different levels of FGF signaling during development. Loss of Sprouty1 rescues renal agenesis caused by Ret mutation. Characterization of a Dchs1 mutant mouse reveals requirements for Dchs1-Fat4 signaling during mammalian development Periodic stripe formation by a Turing mechanism operating at growth zones in the mammalian palate. Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice Tbx1 controls cardiac neural crest cell migration during arch artery development by regulating Gbx2 expression in the pharyngeal ectoderm Sprouty1 haploinsufficiency prevents renal agenesis in a model of Fraser syndrome. Insights into T-Cell Development from Studies Using Transgenic and Knockout Mice Synergistic activity of Sef and Sprouty proteins in regulating the expression of Gbx2 in the mid-hindbrain region. Itch-/- alphabeta and gammadelta T cells independently contribute to autoimmunity in Itchy mice Localised inhibition of FGF signalling in the third pharyngeal pouch is required for normal thymus and parathyroid organogenesis Coordinated activity of Spry1 and Spry2 is required for normal development of the external genitalia. Advanced paternal age effects in neurodevelopmental disorders-review of potential underlying mechanisms CHD7 maintains neural stem cell quiescence and prevents premature stem cell depletion in the adult hippocampus. Heparan sulfotransferases Hs6st1 and Hs2st keep Erk in check for mouse corpus callosum development Congenital hypoplasia of the cerebellum: developmental causes and behavioral consequences Epistatic interactions between Chd7 and Fgf8 during cerebellar development: Implications for CHARGE syndrome. Sprouty proteins inhibit receptor-mediated activation of phosphatidylinositol-specific phospholipase C.

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