About: Gábor Czirják

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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) researcher (en) 연구원 (ko) গবেষক (bn) 研究者 (ja) дослідник (uk) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq) taighdeoir (ga) Hongaars onderzoeker (nl) (1973–) magyar kutatóorvos (hu)
rdfs:label	Czirják Gábor (hu) Gabor Czirjak (sq) Gábor Czirják (en) Gábor Czirják (es) Gábor Czirják (ga) Gábor Czirják (nl) Gábor Czirják (sl) Gábor Czirják (tr) Gábor Czirják (ast)
skos:prefLabel	Czirják Gábor (hu) Gabor Czirjak (sq) Gábor Czirják (en) Gábor Czirják (es) Gábor Czirják (ga) Gábor Czirják (nl) Gábor Czirják (sl) Gábor Czirják (tr) Gábor Czirják (ast)
name	Czirják Gábor (hu) Gabor Czirjak (sq) Gábor Czirják (en) Gábor Czirják (es) Gábor Czirják (ga) Gábor Czirják (nl) Gábor Czirják (sl) Gábor Czirják (tr) Gábor Czirják (ast)
PIM authority ID	wds:Q48787000-581AB473-C1CC-4144-B27A-5D35469EB754
PIM authority ID	PIM387999
given name	wds:Q48787000-43803CF4-6471-4D6F-9FF6-8D93ECCDDB3B
given name	Gábor
instance of	wds:Q48787000-AF51FA8E-69D1-424E-8A05-F2BF91876828
instance of	Homo sapiens
skos:altLabel	Gabor Czirjak (tr) Gábor Czirják (sq)
occupation	wds:Q48787000-31a11147-4224-7076-7b4b-6f4812a96553 wds:Q48787000-9E087F38-AABF-49D8-9112-96A33761A90B
employer	wds:Q48787000-635C9C3F-B655-498A-8CC9-81F2F51CB697
place of birth	wds:Q48787000-4d910f6d-45fc-8207-f915-6eac9b3eec9f
sex or gender	wds:Q48787000-1178862F-A918-43E0-89CC-11CC37A90091
country of citizenship	wds:Q48787000-b9b9134a-4bd4-1d9b-1f67-013af401bf79
date of birth	wds:Q48787000-04669AAD-8AD7-4C93-BDF6-116820989B2F
occupation	physician researcher
employer	Semmelweis University
place of birth	Budapest
sex or gender	male
country of citizenship	Hungary
date of birth	1973-01-01 00:00:00Z (xsd:dateTime)
ORCID iD	wds:Q48787000-9D6D5C77-41A4-461E-AF17-15A2A950BF03
ORCID iD	https://orcid.org/0000-0002-5485-2327
ORCID iD	0000-0002-5485-2327
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q48787000
is author of	The antibacterial activity of human neutrophils and eosinophils requires proton channels but not BK channels Molecular background of leak K+ currents: two-pore domain potassium channels Neonatal severe hyperparathyroidism associated with a novel de novo heterozygous R551K inactivating mutation and a heterozygous A986S polymorphism of the calcium-sensing receptor gene. TRESK background K(+) channel is inhibited by phosphorylation via two distinct pathways. TASK-3 dominates the background potassium conductance in rat adrenal glomerulosa cells. Formation of functional heterodimers between the TASK-1 and TASK-3 two-pore domain potassium channel subunits. TASK (TWIK-related acid-sensitive K+ channel) is expressed in glomerulosa cells of rat adrenal cortex and inhibited by angiotensin II. PIP2 hydrolysis underlies agonist-induced inhibition and regulates voltage gating of two-pore domain K+ channels. TRESK background K(+) channel is inhibited by PAR-1/MARK microtubule affinity-regulating kinases in Xenopus oocytes The LQLP calcineurin docking site is a major determinant of the calcium-dependent activation of human TRESK background K+ channel Tubulin binds to the cytoplasmic loop of TRESK background K⁺ channel in vitro Targeting of calcineurin to an NFAT-like docking site is required for the calcium-dependent activation of the background K+ channel, TRESK. Phosphorylation-dependent binding of 14-3-3 proteins controls TRESK regulation Characterization of the heteromeric potassium channel formed by kv2.1 and the retinal subunit kv8.2 in Xenopus oocytes. Properties, regulation, pharmacology, and functions of the K₂p channel, TRESK. Ruthenium red inhibits TASK-3 potassium channel by interconnecting glutamate 70 of the two subunits. Immune response of hibernating European bats to a fungal challenge Chemically Modified Derivatives of the Activator Compound Cloxyquin Exert Inhibitory Effect on TRESK (K2P18.1) Background Potassium Channel Differential sensitivity of TREK-1, TREK-2 and TRAAK background potassium channels to the polycationic dye ruthenium red. Selective and state-dependent activation of TRESK (K2P 18.1) background potassium channel by cloxyquin. [Effects and significance of estradiol in men] [Significance of biochemical markers in the diagnosis of neuroendocrine tumours and for the follow-up of patients] PrinCCes: Continuity-based geometric decomposition and systematic visualization of the void repertoire of proteins. TRESK (K2P18.1) Background Potassium Channel Is Activated by Novel-Type Protein Kinase C via Dephosphorylation TRESK background potassium channel is not gated at the helix bundle crossing near the cytoplasmic end of the pore.
is author of	wds:Q34396710-C6BADC1B-230C-4064-9993-4509F9B81109 wds:Q90928729-E184EB71-CE6D-4517-ACA1-13B0BE6441A0 wds:Q93064955-011F41AF-973D-4B44-B9C4-67C85781CDDE wds:Q35168933-89E01324-4797-47A6-875C-46D17C19D10A wds:Q35223927-FF2B40B6-4C6F-4BA4-956D-3F9D7D77661D wds:Q48888879-90E501B9-0A9A-405C-9F16-7F97A3E2CE01 wds:Q50651251-B28EA70F-539C-41A5-9269-E07D37816A0D

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