Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Vanessa S. Mattevi"'
Autor:
Vanessa Feistauer, Márcia R. Vitolo, Paula D.B. Campagnolo, Vanessa S. Mattevi, Silvana Almeida
Publikováno v:
Genetics and Molecular Biology, Vol 41, Iss 3, Pp 562-569 (2018)
Abstract The reward sensation after food intake may be different between individuals and variants in genes related to the dopaminergic system may indicate a different response in people exposed to the same environmental factors. This study investigat
Externí odkaz:
https://doaj.org/article/09ab3e8c8f4c4be5a6149edaa4d49e8b
Autor:
Silvia V. Melo, Grasiela Agnes, Márcia R. Vitolo, Vanessa S. Mattevi, Paula D.B. Campagnolo, Silvana Almeida
Publikováno v:
Genetics and Molecular Biology, Vol 40, Iss 2, Pp 415-420 (2017)
Abstract Taste perception plays a key role in determining individual food preferences and dietary habits and may influence nutritional status. This study aimed to investigate the association of TAS1R2 (Ile191Val - rs35874116) and TAS1R3 (-1266 C/T -
Externí odkaz:
https://doaj.org/article/b61e79238373402da5270cecb5aaa638
Autor:
Bruno Toson, Rafael T. Michita, Maria C. T. Matte, Robson Soares, Gabriela K. S. Lawisch, Vanessa S. Mattevi, José A. B. Chies
Publikováno v:
Journal of Human Genetics. 67:475-479
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::534a11281bb0a4a368c3867d0f6db77a
https://doi.org/10.1038/s10038-022-01029-w
https://doi.org/10.1038/s10038-022-01029-w
Autor:
Deise C. Friedrich, Fabiana M de Andrade, Marilu Fiegenbaum, Silvana de Almeida, Vanessa S. Mattevi, Sidia M. Callegari-Jacques, Mara H. Hutz
Publikováno v:
Genetics and Molecular Biology, Vol 37, Iss 4, Pp 611-615 (2014)
The Metabolic Syndrome (MetS) is defined as a pattern of metabolic disturbances, which include central obesity, insulin resistance and hyperglycemia, dyslipidemia, and hypertension. Milk has been promoted as a healthy beverage that can improve the ma
Externí odkaz:
https://doaj.org/article/8fab1b028a3b4abcb35e59a7fd097869
Autor:
Aline Simas Gasparotto, Diego Olschowsky Borges, Marília Remuzzi Zandoná, Mauricio Jacques Ramos, Nelson Guardiola Meihnardt, Vanessa S. Mattevi
Publikováno v:
Genetics and Molecular Biology, Iss 0 (2017)
Abstract Our aim was to investigate if single nucleotide polymorphisms (SNPs) located in the 5′ regions of leptin (LEP, -2548 G > A, rs7799039), resistin (RETN, -420 C > G, rs1862513) and adiponectin (ADIPOQ, -11391 G > A, rs17300539 and -11377 C >
Externí odkaz:
https://doaj.org/article/7f658c1feafd491db28cd723fbf799a1
Autor:
Bruno, Toson, Rafael T, Michita, Maria C T, Matte, Robson, Soares, Gabriela K S, Lawisch, Vanessa S, Mattevi, José A B, Chies
Publikováno v:
Journal of human genetics. 67(8)
Human Immunodeficiency Virus (HIV) infection dynamics is strongly influenced by the host genetic background. NKG2C is an activating receptor expressed mainly on Natural Killer (NK) cells, and a polymorphism of copy number variation in the gene coding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::befc47697db637a2a02fd21f9b186631
https://pubmed.ncbi.nlm.nih.gov/35314764
https://pubmed.ncbi.nlm.nih.gov/35314764
Autor:
Rosmeri K. Lazzaretti, Aline S. Gasparotto, Marina G. de M. Sassi, Carísi A. Polanczyk, Regina Kuhmmer, Jussara M. Silveira, Rossana P. Basso, Cezar A. T. Pinheiro, Mariângela F. Silveira, Eduardo Sprinz, Vanessa S. Mattevi
Publikováno v:
The Scientific World Journal, Vol 2013 (2013)
This study evaluated the impact of 9 single nucleotide polymorphisms (SNPs) in 6 candidate genes (APOB, APOA5, APOE, APOC3, SCAP, and LDLR) over dyslipidemia in HIV-infected patients on stable antiretroviral therapy (ART) with undetectable viral load
Externí odkaz:
https://doaj.org/article/6d5fc963e88e4fb89b8fb0d5168228ba
Autor:
Vanessa S Mattevi, Pedro Kern Menna Barreto, Roberta Kern Menna Barreto, Manuel Vilela, Juliana Mf Sallum
Publikováno v:
International Medical Case Reports Journal
Objective To describe, in a multimodal way, a new RHO gene mutation with lysine-for-asparagine substitution in autosomal dominant retinitis pigmentosa. Methods Case report. Retrospective data analysis. Results The mutation is located within codon 15
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8dd51358830d120e18e0c84d9f2a5ea
https://doi.org/10.2147/imcrj.s179105
https://doi.org/10.2147/imcrj.s179105
Autor:
Nadine, Glesse, Odirlei A, Monticielo, Vanessa S, Mattevi, Joao C T, Brenol, Ricardo M, Xavier, Gabriela K, da Silva, Bruno P, Dos Santos, Guilherme G, Rucatti, José A B, Chies
Publikováno v:
Clinical and experimental rheumatology. 29(6)
This study investigates the role of mannose-binding lectin (MBL) in susceptibility and clinical expression of systemic lupus erythematosus (SLE), through the analysis of promoter region and exon 1 polymorphisms of the MBL2 gene.We analysed 325 SLE pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dac5ff18bb2626124107fa281bb546b1
https://pubmed.ncbi.nlm.nih.gov/22206649
https://pubmed.ncbi.nlm.nih.gov/22206649
Publikováno v:
American Journal of Human Biology; Mar2006, Vol. 18 Issue 2, p182-186, 5p