Polimorfismos genéticos do fator de crescimento do endotélio vascular na pré-eclâmpsia Genetic polymorphisms of vascular endothelial growth factor in pre-eclampsia

Autor: Valquiria Maria de Paula Cunha, Roseane Lopes da Silva Grecco, Marina Carvalho Paschoini, Sueli Riul da Silva, Mariângela Torreglosa Ruiz, Marly Aparecida Spadotto Balarin

Publikováno v: Revista Brasileira de Ginecologia e Obstetrícia, Vol 33, Iss 7, Pp 158-163 (2011)

OBJETIVO: Identificar polimorfismos genéticos do fator de crescimento do endotélio vascular (VEGF), posições +936C/T e -2578C/A, em mulheres com pré-eclâmpsia. MÉTODOS:Trata-se de um estudo transversal,constituído por 80 mulheres distribuída

Externí odkaz: https://doaj.org/article/27043e80243a486e81665282781d36bd

Prevalence of Y-chromosome sequences and gonadoblastoma in Turner syndrome

Autor: Alessandra Bernadete Trovó de Marqui, Roseane Lopes da Silva-Grecco, Marly Aparecida Spadotto Balarin

Publikováno v: Revista Paulista de Pediatria, Vol 34, Iss 1, Pp 114-121 (2016)

Abstract Objective: To assess the prevalence of Y-chromosome sequences and gonadoblastoma in patients with Turner syndrome (TS) using molecular techniques. Data source: A literature search was performed in Pubmed, limiting the period of time to the y

Externí odkaz: https://doaj.org/article/ce11081116aa4f778c50d3ebb02c06af

Contribution of rs1799998 polymorphism in CYP11B2 gene in susceptibility to preeclampsia

Autor: Vanessa Resende Souza Silva, Sarah Cristina Sato Vaz Tanaka, Roseane Lopes da Silva Grecco, Fernanda Caroline Soardi, Kaio Raffael Valotta Bezerra, Marina Carvalho Paschoinni, Marly Aparecida Spadotto Balarin

Publikováno v: Revista Brasileira de Saúde Materno Infantil, Volume: 20, Issue: 2, Pages: 467-471, Published: 05 AUG 2020
Revista Brasileira de Saúde Materno Infantil
Revista Brasileira de Saúde Materno Infantil v.20 n.2 2020
Instituto de Medicina Integral Prof. Fernando Figueira (IMIPFF)
instacron:IMIPFF

Objectives: the present study aimed to evaluate the association between the rs1799998 polymorphism of the CYP11B2 gene and the susceptibility to preeclampsia (PE) in a Brazilian population. Methods: the study group comprised 61 women who were diagnos

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d31f968bb3f2b2f4cae1a1bab1443bd
https://doi.org/10.1590/1806-93042020000200008

Relation of TGF-β1 gene with the prognosis of patients with Covid-19

Autor: Christiane Ruffato Carminati, Anna Cecília Dias Maciel Carneiro, Andrezza Cristina Cancian Hortolani da Cunha, Loren Queli Pereira, Fernanda Bernadelli De Vito, Marcos Vinicíus da Silva, Virmondes Rodrigues Júnior, Mariângela Torreglosa Ruiz Cintra, Roseane Lopes da Silva Grecco, Sarah Cristina Sato Vaz Tanaka, Helio Moraes de Sousa

Publikováno v: Research, Society and Development. 11:e03111536658

This study aimed to investigate the role of the TGF-β1 gene in SARS-CoV-2 infection. A total of 178 individuals diagnosed with Covid-19 participated and, they were divided in two groups related to the outcome (discharge or death). Genotyping of rs18

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4e2c7cd4ce744eea0e02cf488c4822d8
https://doi.org/10.33448/rsd-v11i15.36658

A de novo mutation in CYP21A2 gene in a case of in vitro fertilization

Autor: Débora de Paula Michelatto, Heloísa Marcelina da Cunha, Pamela Pontes Henrique, Maricilda Palandi-de-Mello, Roseane Lopes da Silva-Grecco, Carolina Rodrigues Lincoln-de-Carvalho

Publikováno v: Molecular Genetics and Metabolism Reports, Vol 5, Iss C, Pp 98-102 (2015)

Congenital adrenal hyperplasia, one of the most frequent autosome recessive disorders, is caused by defects in steroidogenic enzymes involved in the cortisol biosynthesis. Approximately 95% of the cases are caused by abnormal function of the 21-hydro

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84a30e3784336a06f892f2fe515e6efd
https://doi.org/10.1016/j.ymgmr.2015.10.011