About: Grzegorz Kurzawski

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

researcher ORCID ID = 0000-0002-2414-9868

Attributes	Values
rdf:type	Item
description	ikertzailea (eu) araştırmacı (tr) wetenschapper (nl) дослідник (uk) изилдөөчү (ky) polski biochemik, genetyk molekularny (pl) researcher ORCID ID = 0000-0002-2414-9868 (en)
rdfs:label	Grzegorz Kurzawski (en) Grzegorz Kurzawski (es) Grzegorz Kurzawski (it) Grzegorz Kurzawski (nl) Grzegorz Kurzawski (pl) Grzegorz Kurzawski (ast)
skos:prefLabel	Grzegorz Kurzawski (en) Grzegorz Kurzawski (es) Grzegorz Kurzawski (it) Grzegorz Kurzawski (nl) Grzegorz Kurzawski (pl) Grzegorz Kurzawski (ast)
name	Grzegorz Kurzawski (en) Grzegorz Kurzawski (es) Grzegorz Kurzawski (it) Grzegorz Kurzawski (nl) Grzegorz Kurzawski (pl) Grzegorz Kurzawski (ast)
Polish scientist ID (deprecated)	wds:Q59543960-02421D51-EEAC-49AA-B282-2170A3D886E5
Polish scientist ID (deprecated)	73166
Scopus author ID	wds:Q59543960-856DABE4-15FA-4821-BA55-37A69DAC0C94
Scopus author ID	7003996695
given name	wds:Q59543960-06DD1F9F-0648-42A2-BA17-309729C2CCC3 wds:Q59543960-C35AB5A1-23D1-4328-B82D-E6A29446E846
given name	Włodzimierz Grzegorz
instance of	wds:Q59543960-72373D9F-D28E-4C32-B4AC-B1720F12B70C
instance of	Homo sapiens
doctoral student	wds:Q59543960-98173CDF-3113-4FB6-8CB3-ED2581743F51
doctoral student	Dagmara Dymerska
skos:altLabel	Grzegorz Włodzimierz Kurzawski (pl)
occupation	wds:Q59543960-DD651A60-FFD1-42E6-9E59-399BFE2273EE
employer	wds:Q59543960-43F88ABF-3E53-4FA6-9713-18BFC2D4F8CC
sex or gender	wds:Q59543960-2408b405-433f-ddbf-95c2-81864717b7a4
VIAF ID	wds:Q59543960-CE1AC100-4A88-4576-8512-8074B48BB9B2
academic degree	wds:Q59543960-613643F3-8420-4180-A98A-B6A11449A6D9 wds:Q59543960-B22DDF5A-B610-48A1-97DD-950A65E32A35
PLWABN ID	wds:Q59543960-67D88E1A-F04B-471C-8D2A-69C41CB84497
family name	wds:Q59543960-DC49CB3F-BC1C-4355-BC84-97E0B258D828
WorldCat Identities ID (superseded)	wds:Q59543960-0E3DF81B-7117-43C8-849B-EAB9F8DEFFDF
VIAF ID	http://viaf.org/viaf/161903059
occupation	researcher
employer	Pomeranian Medical University
sex or gender	male
VIAF ID	161903059
academic degree	habilitation scientific professorship degree
PLWABN ID	9810590112005606
family name	Kurzawski
WorldCat Identities ID (superseded)	viaf-161903059
ORCID iD	wds:Q59543960-B017B011-CE3E-4BBF-B3B7-622071E4B8E9
Dimensions author ID	wds:Q59543960-6D29E4FB-D3E6-4E88-ADA8-B1849EB70C87
ORCID iD	https://orcid.org/0000-0002-2414-9868
ORCID iD	0000-0002-2414-9868
Dimensions author ID	01001117662.21
ResearcherID	wds:Q59543960-E6F8A52C-2D11-497E-84C4-8F87013C7561
ResearcherID	T-9225-2018
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q59543960
is author of	The 3020insC allele of NOD2 predisposes to early-onset breast cancer Leptin receptor isoforms expressed in human adipose tissue The NOD2 3020insC mutation and the risk of colorectal cancer. CHEK2 is a multiorgan cancer susceptibility gene Frequency and nature of germline Rb-1 gene mutations in a series of patients with sporadic unilateral retinoblastoma CDKN2A common variants and their association with melanoma risk: a population-based study. IGF1 is a modifier of disease risk in hereditary non-polyposis colorectal cancer MC1R common variants, CDKN2A and their association with melanoma and breast cancer risk Germline mutation and large deletion analysis of the CDKN2A and ARF genes in families with multiple melanoma or an aggregation of malignant melanoma and breast cancer. Rarity of germline 1100delC mutation in CHK2 in patients with malignant melanoma of the skin. Germline 657del5 mutation in the NBS1 gene in patients with malignant melanoma of the skin. Increased risk of breast cancer in relatives of malignant melanoma patients from families with strong cancer familial aggregation Inflammatory response gene polymorphisms and their relationship with colorectal cancer risk Polymorphism in the P-glycoprotein drug transporter MDR1 gene in colon cancer patients. Germline MSH2 and MLH1 mutational spectrum in HNPCC families from Poland and the Baltic States DNA repair gene polymorphisms and risk of early onset colorectal cancer in Lynch syndrome Analysis of gamma delta+ T cells in peripheral blood of children with perinatal human immunodeficiency virus (HIV) infection Germline CHEK2 mutations and colorectal cancer risk: different effects of a missense and truncating mutations? A novel founder CHEK2 mutation is associated with increased prostate cancer risk. AMPD1 gene mutations are associated with obesity and diabetes in Polish patients with cardiovascular diseases Mutation analysis of MLH1 and MSH2 genes performed by denaturing high-performance liquid chromatography Mechanism of the inhibitory effect of curdlan sulfate on HIV-1 infection in vitro. Colorectal cancer susceptibility loci on chromosome 8q23.3 and 11q23.1 as modifiers for disease expression in Lynch syndrome. BRCA1 mutations and colorectal cancer in Poland. Molecular basis of inherited predispositions for tumors. Value of pedigree/clinical data, immunohistochemistry and microsatellite instability analyses in reducing the cost of determining hMLH1 and hMSH2 gene mutations in patients with colorectal cancer Haemochromatosis HFE gene polymorphisms as potential modifiers of hereditary nonpolyposis colorectal cancer risk and onset age. Aurora-A and Cyclin D1 polymorphisms and the age of onset of colorectal cancer in hereditary nonpolyposis colorectal cancer. Genetic Polymorphisms in Xenobiotic Clearance Genes and Their Influence on Disease Expression in Hereditary Nonpolyposis Colorectal Cancer Patients Germline MSH2 and MLH1 mutational spectrum including large rearrangements in HNPCC families from Poland (update study) MTHFR 677 C>T and 1298 A>C polymorphisms and the age of onset of colorectal cancer in hereditary nonpolyposis colorectal cancer Losses at 3p common deletion sites in subtypes of kidney tumours: histopathological correlations Is plasma soluble CD36 associated with cardiovascular risk factors in early onset coronary artery disease patients? Novel germline mutations in the adenomatous polyposis coli gene in Polish families with familial adenomatous polyposis

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