About: Martina Živná

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

Czech biochemist

Attributes	Values
rdf:type	Item
field of work	wds:Q114797271-66F82A71-BEDF-4591-8411-3096A83E09C7 wds:Q114797271-ECFCAB00-9D9F-47C4-92C2-1536069F906C wds:Q114797271-FFDA2C35-F4D5-444E-824C-B696BB6A642A
field of work	biochemistry cell biology molecular biology
description	wetenschapper (nl) дослідниця (uk) Czech biochemist (en) česká biochemička (cs)
rdfs:label	Martina Živná (cs) Martina Živná (en) Martina Živná (es) Martina Živná (fr) Martina Živná (sk) Martina Živná (ast)
skos:prefLabel	Martina Živná (cs) Martina Živná (en) Martina Živná (es) Martina Živná (fr) Martina Živná (sk) Martina Živná (ast)
name	Martina Živná (cs) Martina Živná (en) Martina Živná (es) Martina Živná (fr) Martina Živná (sk) Martina Živná (ast)
given name	wds:q114797271-52da87ab-4fcd-01e8-4e7d-58b38e52b738
given name	Martina
instance of	wds:Q114797271-0CB08764-16C9-4570-BB9C-122D2A1CCF24
NL CR AUT ID	wds:Q114797271-9d41468b-4f1e-ebe7-9e97-30a69cc69dbe
instance of	Homo sapiens
NL CR AUT ID	xx0208846
award received	wds:Q114797271-9321E1BA-37B6-4161-81A4-EE2E30F7BA27
award received	Neuron Prize for young promising scientists
ResearchGate profile ID	wds:Q114797271-7eb5e75a-4ede-5ed1-4993-d56530873baa
ResearchGate profile ID	Martina-Zivna
vedidk ID	wds:Q114797271-761ce442-4c27-faab-17c7-10f97cc25378
vedidk ID	5016681
skos:altLabel	Mgr. Martina Živná, Ph.D. (cs)
occupation	wds:Q114797271-5596bcae-4f3c-3642-fe17-fec80fb28803 wds:Q114797271-dd96e3a7-41d8-ec41-b8a3-111c7b74ef59 wds:Q114797271-f460f628-1433-4e33-91da-3789a1baaa8f
employer	wds:Q114797271-69ec5524-4fe0-592f-6d90-bbb8a51b5991
languages spoken, written or signed	wds:Q114797271-1efb47ac-4bd9-4bc5-a6f7-e15509039a25 wds:Q114797271-9a3a9af0-1c71-4af1-bb35-52abe57eb347
sex or gender	wds:Q114797271-E038F28F-1BFA-42E5-A348-49E7081AE529
VIAF ID	wds:Q114797271-ff85d724-4587-8829-9ff4-0c17bee572ab
country of citizenship	wds:Q114797271-12152A16-370B-4CC2-9AEF-854E2405947C
VIAF ID	http://viaf.org/viaf/4148389504110712813
occupation	researcher biologist biochemist
employer	First Faculty of Medicine, Charles University
languages spoken, written or signed	English Czech
sex or gender	female organism
VIAF ID	4148389504110712813
country of citizenship	Czech Republic
ORCID iD	wds:Q114797271-3b8a1050-4450-192a-eab9-642d7612c9fb
ORCID iD	https://orcid.org/0000-0003-1968-824X
ORCID iD	0000-0003-1968-824X
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q114797271
is author of	Uromodulin-associated kidney disease Variable clinical presentation of an MUC1 mutation causing medullary cystic kidney disease type 1 Autosomal Dominant Tubulointerstitial Kidney Disease Acadian variant of Fanconi syndrome is caused by mitochondrial respiratory chain complex I deficiency due to a non-coding mutation in complex I assembly factor NDUFAF6. Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic kidney failure Heterozygous Loss-of-Function SEC61A1 Mutations Cause Autosomal-Dominant Tubulo-Interstitial and Glomerulocystic Kidney Disease with Anemia Autosomal Dominant Tubulointerstitial Kidney Disease Due to MUC1 Mutation. Noninvasive Immunohistochemical Diagnosis and Novel Mutations Causing Autosomal Dominant Tubulointerstitial Kidney Disease Autosomal dominant tubulointerstitial kidney disease-UMOD is the most frequent non polycystic genetic kidney disease Small Molecule Targets TMED9 and Promotes Lysosomal Degradation to Reverse Proteinopathy An International Cohort Study of Autosomal Dominant Tubulointerstitial Kidney Disease due to REN Mutations Identifies Distinct Clinical Subtypes Clinical manifestations and molecular aspects of phosphoribosylpyrophosphate synthetase superactivity in females. Quality of life in patients with autosomal dominant tubulointerstitial kidney disease Renal transplant outcomes in patients with autosomal dominant tubulointerstitial kidney disease Chronic tubulointerstitial kidney disease in untreated adenine phosphoribosyl transferase (APRT) deficiency: A case report Outcomes of patient self-referral for the diagnosis of several rare inherited kidney diseases Genetic and Clinical Predictors of Age of ESKD in Individuals With Autosomal Dominant Tubulointerstitial Kidney Disease Due to UMOD Mutations
is author of	wds:Q39174016-A0841A23-DC7A-4C98-95A7-F059F4B01F67 wds:Q57164422-8514DD62-E0E4-4793-B006-B9BCC433A6D9 wds:Q49881851-CB64503A-0227-4D87-8BBC-ADDC8DA46ED0 wds:Q28118506-A1A8D40A-9EA9-45D4-BD3B-C99D190AAF4D wds:Q34996277-1FDA322D-E30F-4A28-A4B4-B1B6F3134205 wds:Q95578536-220E2AC0-1469-43EB-8856-49975E4322AA wds:Q92770867-3DC32850-985E-4203-A9F0-416222DB077D wds:Q58093377-A6A9BF21-9689-43B5-A169-6DE08C4C0719 wds:Q95596371-5192D1E1-44C4-4087-8EB2-AF5B31ED712A wds:Q92134887-F00BE2D2-FA2F-4DFF-8EC0-9C1D6C07C779 wds:Q37621551-460B93A7-0A3F-484D-B210-7C5054F0E625 wds:Q64992581-CC9BFF62-9438-48B1-A89F-94B85F890F54 wds:Q82433246-B0F918EC-D23F-4801-9AED-A31F1C89B8C4 wds:Q98200287-37830AF6-E5D7-4F78-9D3E-10335D464679 wds:Q92204301-CA7279D2-DF4E-4E26-87FD-2B7DA9B82EF1 wds:Q99584611-E05DC73E-86CC-47CB-AD50-B8B676590365 wds:Q50023529-D468BEE1-A7D7-4C5F-96B4-FC0F30A621DD

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