About: Mariano Sentí

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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) ricercatore (it) গবেষক (bn) 研究者 (ja) ഗവേഷകൻ (ml) дослідник (uk) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq) onderzoeker (nl)
rdfs:label	Mariano Sentí (en) Mariano Sentí (es) Mariano Sentí (nl) Mariano Sentí (sl) Mariano Sentí (ast)
skos:prefLabel	Mariano Sentí (en) Mariano Sentí (es) Mariano Sentí (nl) Mariano Sentí (sl) Mariano Sentí (ast)
name	Mariano Sentí (en) Mariano Sentí (es) Mariano Sentí (nl) Mariano Sentí (sl) Mariano Sentí (ast)
Scopus author ID	wds:Q46809380-900DA112-EE83-41C9-8F11-9F40EC4604D0
Scopus author ID	7005170996
given name	wds:Q46809380-BE11B35D-8E45-47B8-A292-025CAEEFFFE1
given name	Mariano
instance of	wds:Q46809380-BF058DD5-0662-48BE-A287-3CA5347DDA17
instance of	Homo sapiens
Google Scholar author ID	wds:Q46809380-AA19AF94-EF35-4B45-9D87-B9BD1ACE5E6C
Google Scholar author ID	RpqUUxsAAAAJ
skos:altLabel	Senti-Clapés M Sentí M (en)
occupation	wds:Q46809380-C1B6520C-2504-4902-B946-EC8E635AC360
University of Barcelona authority ID	wds:Q46809380-C533F508-1624-4E3C-B049-FF65B9512A32
University of Barc...D (former scheme)	wds:Q46809380-1784CB1B-3049-4DC9-9687-15B68B99DA08
sex or gender	wds:Q46809380-99B7AB90-5832-40C3-AD97-7BF66455ED49
ISNI	wds:Q46809380-B48B1A8A-750B-4F1D-97D3-BFE608083532
VIAF ID	wds:Q46809380-91C77E22-D41E-42AB-B218-AC4BAFE36057
WorldCat Identities ID (superseded)	wds:Q46809380-B0F4970A-F057-49F8-B1F8-7DDC69BF24D7
National Library of Spain ID	wds:Q46809380-F1163DB6-260C-4A08-9C39-809389BA832F
CANTIC ID	wds:Q46809380-6FFB565D-7309-48BE-8D48-97E907788F5F
VIAF ID	http://viaf.org/viaf/169679232
National Library of Spain ID	http://datos.bne.es/resource/XX1514629
occupation	researcher
University of Barcelona authority ID	981058514086706706
University of Barc...D (former scheme)	a1061497
sex or gender	male
ISNI	0000000118530825
VIAF ID	169679232
WorldCat Identities ID (superseded)	viaf-169679232
National Library of Spain ID	XX1514629
CANTIC ID	981058514086706706
ORCID iD	wds:Q46809380-80656B32-9B0B-4D81-A84C-E2ACC5F270A3
ORCID iD	https://orcid.org/0000-0002-6983-3831
ORCID iD	0000-0002-6983-3831
ResearcherID	wds:Q46809380-AC57CEE1-FC49-405A-9946-2A5A754D359A
ResearcherID	D-4309-2014
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q46809380
is author of	Protective effect of the KCNMB1 E65K genetic polymorphism against diastolic hypertension in aging women and its relevance to cardiovascular risk. Gain-of-function mutation in the KCNMB1 potassium channel subunit is associated with low prevalence of diastolic hypertension Platelet glycoprotein IIb/IIIa genetic polymorphism is associated with plasma fibrinogen levels in myocardial infarction patients. The REGICOR Investigators. Risk of myocardial infarction associated with Gln/Arg 192 polymorphism in the human paraoxonase gene and diabetes mellitus Antioxidant paraoxonase 1 activity in the metabolic syndrome A gain-of-function SNP in TRPC4 cation channel protects against myocardial infarction Interaction between the Gln-Arg 192 variants of the paraoxonase gene and oleic acid intake as a determinant of high-density lipoprotein cholesterol and paraoxonase activity. Variables associated with fibrinogen in a population-based study: interaction between smoking and age on fibrinogen concentration Assessment of the value of a genetic risk score in improving the estimation of coronary risk Relationship of classical and non-classical risk factors with genetic variants relevant to coronary heart disease Physical activity modulates the combined effect of a common variant of the lipoprotein lipase gene and smoking on serum triglyceride levels and high-density lipoprotein cholesterol in men. Genetic variation in the KCNMA1 potassium channel α subunit as risk factor for severe essential hypertension and myocardial infarction Asociación de los polimorfismos de la paraoxonasa 1 y la paraoxonasa 2 con el riesgo de infarto agudo de miocardio Association between ESR2 Genetic Variants and Risk of Myocardial Infarction Paraoxonase1-192 polymorphism modulates the effects of regular and acute exercise on paraoxonase1 activity. High oxidative stress in patients with stable coronary heart disease Effect of cyclosporine on serum lipoprotein(a) levels in renal transplant recipients Hypothesis-based analysis of gene-gene interactions and risk of myocardial infarction Effect of physical activity on lipid levels in a population-based sample of men with and without the Arg192 variant of the human paraoxonase gene Post-genomic update on a classical candidate gene for coronary artery disease: ESR1 Qualitative assessment of previous evidence and an updated meta-analysis confirms lack of association between the ESR1 rs2234693 (PvuII) variant and coronary heart disease in men and women Interaction of family history of atherosclerosis with atherogenic lipid traits in men with non-coronary atherosclerosis.
is author of	wds:Q36968652-43947D01-6485-45E0-9C09-94ECD16C96F2 wds:Q57235888-CEFFEE1F-147A-406E-A70A-DF0E60D8E22B wds:Q57235917-9CEB9433-E8A4-4FBE-84DE-0D1F88B1B37C wds:Q28195855-1BC5C2A1-CCED-438E-AFD6-6C800F85E9B0 wds:Q43640208-D45E86CE-4055-42F7-AC8B-9B3CC888D3F0 wds:Q57235893-B837B7CB-3D67-43E6-883E-4A5DE0A61D12 wds:Q37553425-EE9F102A-BB49-44B3-A694-404614B95ACF wds:Q44645579-4E483690-9D44-40AA-99D3-CCEFD44767AF wds:Q46809291-0B8AACE4-2AF8-4F97-954F-0B0F5C94B588 wds:Q43969257-2E844D31-865A-46C6-A1CE-8B7806186B6A wds:Q73625302-1BD786CD-7C83-4FE2-8956-2557E085FEF2 wds:Q46373181-6776BDC6-859F-4AEA-888E-2E49B1DF331D wds:Q52228135-E0546990-C0EB-4199-B962-2756DD1BF0FB

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