About: Tatu Pantsar

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

Finnish pharmacologist

Attributes	Values
rdf:type	wdno:P227 Item
description	wetenschapper (nl) дослідник (uk) farmacólogo finlandés (es) finnischer Pharmakologe (de) عالم صيدلية فنلندي (ar) Finnish pharmacologist (en)
rdfs:label	Tatu Pantsar (de) Tatu Pantsar (en) Tatu Pantsar (es) Tatu Pantsar (fr) Tatu Pantsar (nl) Tatu Pantsar (sq) Tatu Pantsar (ast)
skos:prefLabel	Tatu Pantsar (de) Tatu Pantsar (en) Tatu Pantsar (es) Tatu Pantsar (fr) Tatu Pantsar (nl) Tatu Pantsar (sq) Tatu Pantsar (ast)
name	Tatu Pantsar (de) Tatu Pantsar (en) Tatu Pantsar (es) Tatu Pantsar (fr) Tatu Pantsar (nl) Tatu Pantsar (sq) Tatu Pantsar (ast)
Scopus author ID	wds:Q59676477-B09F6A94-4C79-45AE-8B13-05940ECA230F
Scopus author ID	55633036000
instance of	wds:Q59676477-AFFEE7CC-B208-427C-AA64-DC3434B71373
instance of	Homo sapiens
occupation	wds:Q59676477-BB440DAC-900D-456B-AA3C-C7FE39915413
employer	wds:Q59676477-BF79A04B-D16A-4ACB-B427-A5BBC9E540E0
sex or gender	wds:Q59676477-8f59c787-42e6-829b-91c7-ece223256365
ISNI	wds:Q59676477-71338a96-4500-72e0-bc90-a2402184b271
GND ID	wds:Q59676477-bb1b259f-4fce-bf68-76ab-1788cf562b60
educated at	wds:Q59676477-301fee9f-4d03-f06d-b77a-4e977fdeb00e
occupation	pharmacologist
employer	University of Tübingen
sex or gender	male
ISNI	0000000484330671
educated at	University of Eastern Finland
ORCID iD	wds:Q59676477-5BD3CE77-99D9-4CF7-9846-4CDFCA78E941
ORCID iD	https://orcid.org/0000-0002-0369-2909
ORCID iD	0000-0002-0369-2909
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q59676477
is author of	Mutation of Cys242 of human monoacylglycerol lipase disrupts balanced hydrolysis of 1- and 2-monoacylglycerols and selectively impairs inhibitor potency A MYC-aurora kinase A protein complex represents an actionable drug target in p53-altered liver cancer. The use of molecular descriptors in the development of co-amorphous formulations. Robust Hydrolysis of Prostaglandin Glycerol Esters by Human Monoacylglycerol Lipase (MAGL) Binding Affinity via Docking: Fact and Fiction. Assessment of mutation probabilities of KRAS G12 missense mutants and their long-timescale dynamics by atomistic molecular simulations and Markov state modeling Pyridinylimidazoles as GSK3β Inhibitors: The Impact of Tautomerism on Compound Activity via Water Networks Pyridinylimidazoles as dual glycogen synthase kinase 3β/p38α mitogen-activated protein kinase inhibitors Design, synthesis, and biological evaluation of 2,4-dihydropyrano[2,3-c]pyrazole derivatives as autotaxin inhibitors. Decisive role of water and protein dynamics in residence time of p38α MAP kinase inhibitors Design, Synthesis and Biological Evaluation of 7-Chloro-9H-pyrimido[4,5-b]indole-based Glycogen Synthase Kinase-3β Inhibitors
is author of	wds:Q48225584-6CEC653A-64C3-4DFF-83F2-4BFA9074A560 wds:Q52591642-1063EE28-BE77-4EA4-AEC7-4C9B4344B839 wds:Q39039894-52EC1D80-6A06-496B-A804-58AE7EC5FC51 wds:Q58753858-C4E1B5E1-5F57-42D0-9AE1-C487861407C9 wds:Q90757373-0C7F1CC1-4879-43E4-8103-9CEF13724B38 wds:Q48728168-6D3382F0-45F6-454E-9D56-371EA26E21C2 wds:Q64966935-AD632735-C5D1-4F96-B263-2446767665B5 wds:Q61442375-E45A341D-DE14-4636-ACFD-1DD33205D8D5 wds:Q92079181-5FEAB98C-2E99-4D0D-8304-D33C7A2B71C1 wds:Q111322486-5C8F6F71-E6E6-460C-BC39-70EE92944CED wds:Q93048379-E6B2B537-7983-4997-987A-5666793BFFAD

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