About: Stefano Duga

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

full professor of molecular biology

Attributes	Values
rdf:type	Item
description	연구원 (ko) 研究者 (ja) araştırmacı (tr) wetenschapper (nl) дослідник (uk) 研究者 (zh) հետազոտող (hy) hulumtues (sq) chercheur dans le domaine des maladies héréditaires humaines (fr) full professor of molecular biology (en) professore ordinario di biologia molecolare (it)
rdfs:label	Stefano Duga (en) Stefano Duga (es) Stefano Duga (fr) Stefano Duga (it) Stefano Duga (nl) Stefano Duga (sl) Stefano Duga (ast)
skos:prefLabel	Stefano Duga (en) Stefano Duga (es) Stefano Duga (fr) Stefano Duga (it) Stefano Duga (nl) Stefano Duga (sl) Stefano Duga (ast)
name	Stefano Duga (en) Stefano Duga (es) Stefano Duga (fr) Stefano Duga (it) Stefano Duga (nl) Stefano Duga (sl) Stefano Duga (ast)
Scopus author ID	wds:Q42371122-7E1E4E5B-E2C4-411E-BF8D-8109211DD8D7
Scopus author ID	6701674825
given name	wds:Q42371122-1E70DA87-2419-4B2D-9768-B346C2206BFB
given name	Stefano
instance of	wds:Q42371122-0D9A5208-8EC3-48CA-BDAF-2D7029A14807
instance of	Homo sapiens
Loop ID	wds:Q42371122-9D4E3FB7-89F3-4A40-B1A8-0EEE33732FF6
Loop ID	474636
occupation	wds:Q42371122-f75b794a-4b3a-54b2-572d-9ea50154f162
employer	wds:Q42371122-6433484D-7B55-404A-B668-C261C117BDCA wds:Q42371122-81A6B007-A1C8-4C20-9982-FC63269FCB3E wds:Q42371122-A48658FE-895E-4461-9FC5-9CBE0953CCFB
sex or gender	wds:Q42371122-7D307264-7BAA-4CD2-B4F1-FDBEBD0B75F7
on focus list of Wikimedia project	wds:Q42371122-9DDDBD62-AFEE-4654-9391-61278A023136
educated at	wds:Q42371122-95F3DE08-4E0B-41BB-83CC-E5B90684146C wds:Q42371122-CA5F2089-EBE1-41F5-B452-82B668A4EE2C
family name	wds:Q42371122-F2164BAE-A556-4F98-A551-2E6606107CDC
occupation	university teacher
employer	Humanitas University Department of Mathematics "Federigo Enriques"
sex or gender	male
on focus list of Wikimedia project	WikiProject COVID-19
educated at	University of Milan
family name	Duga
ORCID iD	wds:Q42371122-0F851D0B-5FE1-4C86-B3E8-EFFE6BED1F3D
ORCID iD	https://orcid.org/0000-0003-3457-1410
ORCID iD	0000-0003-3457-1410
IRIS UNIMI author ID	wds:Q42371122-932DB9AF-C28C-4EA3-B7E7-0111BBBD0565
IRIS UNIMI author ID	10130
ResearcherID	wds:Q42371122-C0C0224F-4101-4138-A2E2-42095C5733F9
Publons author ID	wds:Q42371122-481320ec-2ee9-4b36-b752-f289fc400f90
ResearcherID	F-8173-2014
Publons author ID	2528606
Bicocca Open Archive author ID	wds:Q42371122-A88C5AB2-233C-44CE-9074-E94F024990E8
Bicocca Open Archive author ID	11074
IRIS UNIFE author ID	wds:Q42371122-1295FD65-7FB4-42C7-B735-0DAAE5713C98
IRIS UNIFE author ID	15160
OPENBS author ID	wds:Q42371122-50B93A9B-8F71-4C56-ACDC-508AF3FBFFCB
OPENBS author ID	56486
IRIS HUNIMED author ID	wds:Q42371122-9F3784D1-31AD-4BBD-B73F-FDA86C8E18DF
IRIS HUNIMED author ID	00757
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q42371122
is author of	Molecular characterization of in-frame and out-of-frame alternative splicings in coagulation factor XI pre-mRNA. Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants Systematic cell-based phenotyping of missense alleles empowers rare variant association studies: a case for LDLR and myocardial infarction Inherited defects of coagulation factor V: the hemorrhagic side. cDNA cloning of turtle prion protein Loss-of-function mutations in APOC3, triglycerides, and coronary disease Recessively inherited coagulation disorders. Mutational screening and zebrafish functional analysis of GIGYF2 as a Parkinson-disease gene SER252PHE and 776INS3 mutations in the CHRNA4 gene are rare in the Italian ADNFLE population. Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks Inactivating mutations in NPC1L1 and protection from coronary heart disease Exclusion of linkage of nine neuronal nicotinic acetylcholine receptor subunit genes expressed in brain in autosomal dominant nocturnal frontal lobe epilepsy in four unrelated families Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS. TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutations. A novel mutation within the MIR96 gene causes non-syndromic inherited hearing loss in an Italian family by altering pre-miRNA processing Genetic diagnosis of haemophilia and other inherited bleeding disorders. Congenital factor XI deficiency: an update. Premature termination codon mutations in the von Willebrand factor gene are associated with allele-specific and position-dependent mRNA decay Alterations of mRNA processing and stability as a pathogenic mechanism in von Willebrand factor quantitative deficiencies A type II mutation (Glu117stop), induction of allele-specific mRNA degradation and factor XI deficiency. A novel two base pair deletion in the factor V gene associated with severe factor V deficiency Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies In vivo RNA-RNA duplexes from human alpha3 and alpha5 nicotinic receptor subunit mRNAs Simultaneous genotyping of coagulation factor XI type II and type III mutations by multiplex real-time polymerase chain reaction to determine their prevalence in healthy and factor XI-deficient Italians

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