About: Milada Kohoutova

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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) ikertzailea (eu) researcher (en) 연구원 (ko) 研究者 (ja) wetenschapper (nl) дослідниця (uk) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtuese (sq) ricercatrice (it) genetička, biochemička (cs)
rdfs:label	Milada Kohoutova (en) Milada Kohoutova (es) Milada Kohoutova (nl) Milada Kohoutova (sl) Milada Kohoutova (sq) Milada Kohoutova (ast) Milada Kohoutová (cs)
skos:prefLabel	Milada Kohoutova (en) Milada Kohoutova (es) Milada Kohoutova (nl) Milada Kohoutova (sl) Milada Kohoutova (sq) Milada Kohoutova (ast) Milada Kohoutová (cs)
name	Milada Kohoutova (en) Milada Kohoutova (es) Milada Kohoutova (nl) Milada Kohoutova (sl) Milada Kohoutova (sq) Milada Kohoutova (ast) Milada Kohoutová (cs)
Scopus author ID	wds:Q55755844-BE9E20CD-1492-4B09-81EB-00EE2B757BC5
Scopus author ID	12770643000
given name	wds:Q55755844-ffb90e73-4013-16e5-8b6c-39276611bd89
given name	Milada
described by source	wds:Q55755844-6537DB44-3463-4859-A3DE-4847A6D3BBAD
instance of	wds:Q55755844-2B2CDD7D-FA41-4217-B953-D3709CF67416
NL CR AUT ID	wds:Q55755844-5bbb2dde-45c2-0ad5-8437-5da1d7364281
described by source	Medvik
instance of	Homo sapiens
NL CR AUT ID	nlk19990073383
occupation	wds:Q55755844-75378D39-3818-48F8-A0F5-A9EAF5345210 wds:Q55755844-786EAA0C-3FA7-4B66-9703-BEB65778C6B1 wds:Q55755844-BC1DFBE4-1A57-42BA-A82D-9D150A9BDF48
employer	wds:Q55755844-B2F20162-568F-4CD2-9612-F7A989465E3A wds:Q55755844-D11B5E1F-018A-4701-86E2-04C595325037
place of birth	wds:Q55755844-619DCF77-0A16-442C-BA08-19BCA64C90CE
sex or gender	wds:Q55755844-B7DD062F-7533-4191-88AA-B4C4FEE71832
VIAF ID	wds:Q55755844-127D6891-A88D-498B-AA2B-A7248434A515
date of birth	wds:Q55755844-DB94BEBB-1015-48F6-A445-DB8DF22B8DD0
WorldCat Identities ID (superseded)	wds:Q55755844-592160A9-EF91-4349-97D9-593A9B6BD82F
VIAF ID	http://viaf.org/viaf/84786302
occupation	researcher geneticist biochemist
employer	First Faculty of Medicine, Charles University Second Faculty of Medicine – Charles University
place of birth	Prag
sex or gender	female organism
VIAF ID	84786302
date of birth	1948-05-16 00:00:00Z (xsd:dateTime)
WorldCat Identities ID (superseded)	viaf-84786302
ORCID iD	wds:Q55755844-0E60D077-5785-477B-A4F3-1905FC6D8660
Dimensions author ID	wds:Q55755844-1426D4EB-0B04-4BE3-943D-0469526B9680
ORCID iD	https://orcid.org/0000-0001-6563-6059
ORCID iD	0000-0001-6563-6059
Dimensions author ID	01136266207.53
ResearcherID	wds:Q55755844-5F21C1CB-5AC5-4BF3-88B5-25D0627B7AD9
ResearcherID	H-6277-2017
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q55755844
is translator of	wd:Q122071252
is translator of	wds:Q122071252-D3C664FB-3FE8-48A6-9F00-210177792729
is author of	New mutations in the PKD1 gene in Czech population with autosomal dominant polycystic kidney disease Evaluation of Cell-Free Urine microRNAs Expression for the Use in Diagnosis of Ovarian and Endometrial Cancers. A Pilot Study Autosomal dominant polycystic kidney disease in a family with mosaicism and hypomorphic allele. Molecular analysis of the APC and MYH genes in Czech families affected by FAP or multiple adenomas: 13 novel mutations. Mutation analysis of the MYH gene in unrelated Czech APC mutation-negative polyposis patients. Novel APC mutations in Czech and Slovak FAP families: clinical and genetic aspects Cell-Free Urinary MicroRNAs Expression in Small-Scale Experiments. Heterochromatin variants in human karyotypes: a possible association with reproductive failure Novel mutations of PKD genes in the Czech population with autosomal dominant polycystic kidney disease. The influence of G-protein beta3-subunit gene and endothelial nitric oxide synthase gene in exon 7 polymorphisms on progression of autosomal dominant polycystic kidney disease. Major histocompatibility complex in the rat and blood pressure regulation. New perspectives in diagnosis of gynaecological cancers: Emerging role of circulating microRNAs as novel biomarkers. Novel mutations of the APC gene and genetic consequences of splicing mutations in the Czech FAP families. wd:Q121952756 Inhibition of acute graft-versus-host disease in (LEW.1W x LEW.1A)F1 rats using 9-(2-phosphonomethoxyethyl)-2,6-diaminopurine
is author of	wds:Q33494204-CD725E03-5EA8-41FC-951A-633D3E1F003D wds:Q88077462-CBF735D2-0B19-4FE8-A90F-8F841A748F5D wds:Q121952756-5490D150-21CC-463D-A66F-34FE2E8604AE wds:Q33281301-AFBF1BE7-64D4-4DE1-B122-53F3D7227864 wds:Q35138042-B4926D5A-E74E-43BF-A5DD-C40B6F053EAE wds:Q54327637-F3817062-6362-45A8-8BA3-F15C04E0A518 wds:Q40492229-3C41F7A3-5265-4102-AC07-BB0E5A523A5C wds:Q38495914-3C90E091-4C71-49E4-AB8E-776FF908387A wds:Q57557750-E51FBA28-4CEE-4909-82E6-51B909B7CEA3

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