Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Julliane Tamara Araújo de Melo Campos"'
Autor:
Monique Alvares da Silva, Reivla Marques Vasconcelos Soares, Antônio Fernandes de Oliveira Filho, Leonardo René Santos Campos, Josivan Gomes de Lima, Julliane Tamara Araújo de Melo Campos
Publikováno v:
Diabetology & Metabolic Syndrome, Vol 16, Iss 1, Pp 1-13 (2024)
Abstract Introduction and aim Type 3 Familial Partial Lipodystrophy (FPLD3) is a rare metabolic disease related to pathogenic PPARG gene variants. FPLD3 is characterized by a loss of fatty tissue in the upper and lower limbs, hips, and face. FPLD3 pa
Externí odkaz:
https://doaj.org/article/8a727031b4af4dc882bf1766c726572c
Autor:
Reivla Marques Vasconcelos Soares, Monique Alvares da Silva, Julliane Tamara Araújo de Melo Campos, Josivan Gomes Lima
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
The PPARG gene encodes a member of a nuclear receptor superfamily known as peroxisome proliferator-activated gamma (PPARγ). PPARγ plays an essential role in adipogenesis, stimulating the differentiation of preadipocytes into adipocytes. Loss-of-fun
Externí odkaz:
https://doaj.org/article/1810e2508dc94577a1426ea809cee9d3
Autor:
Jorge Luiz Dantas de Medeiros, Bruno Carneiro Bezerra, Helen Rainara Araújo Cruz, Katarina Azevedo de Medeiros, Maria Eduarda Cardoso de Melo, Aquiles Sales Craveiro Sarmento, Marcela Abbott Galvão Ururahy, Lucymara Fassarella Agnez Lima, Alcebíades José dos Santos Neto, Josivan Gomes Lima, Vanessa Resqueti, Lucien Peroni Gualdi, Guilherme Fregonezi, Julliane Tamara Araújo de Melo Campos
Publikováno v:
BMC Cardiovascular Disorders, Vol 22, Iss 1, Pp 1-14 (2022)
Abstract Background Congenital Generalized Lipodystrophy (CGL) is an ultra-rare disease characterized by metabolic disorders. However, the evaluation of functional exercise capacity, cardiovascular (CV) response to exercise, and peripheral arterial d
Externí odkaz:
https://doaj.org/article/d159033567974215a1d75ed58a0b351c
Autor:
Julliane Tamara Araújo de Melo Campos, Matheus Sena de Oliveira, Luisa Pessoa Soares, Katarina Azevedo de Medeiros, Leonardo René dos Santos Campos, Josivan Gomes Lima
Publikováno v:
Genetics and Molecular Biology, Vol 45, Iss 3 suppl 1 (2022)
Abstract Classical and progeroid congenital lipodystrophies are a collection of rare diseases displaying a large genetic heterogeneity. They occur due to pathogenic variants in genes associated with adipogenesis, DNA repair pathways, and genome stabi
Externí odkaz:
https://doaj.org/article/6ec31597d1d24563b1c980e0e7e68e37
Autor:
Jorge Luiz Dantas de Medeiros, Bruno Carneiro Bezerra, Thiago Anderson Brito de Araújo, Aquiles Sales Craveiro Sarmento, Lázaro Batista de Azevedo Medeiros, Lucien Peroni Gualdi, Maria do Socorro Luna Cruz, Thaiza Teixeira Xavier Nobre, Josivan Gomes Lima, Julliane Tamara Araújo de Melo Campos
Publikováno v:
Respiratory Research, Vol 19, Iss 1, Pp 1-11 (2018)
Abstract Background Berardinelli-Seip Congenital Generalized Lipodystrophy (BSCL) is an ultra-rare metabolic disease characterized by hypertriglyceridemia, hyperinsulinemia, hyperglycemia, hypoleptinemia, and diabetes mellitus. Although cardiovascula
Externí odkaz:
https://doaj.org/article/f2d814d5ef1d44e7880b225b27c456e7
Autor:
Lázaro Batista de Azevedo Medeiros, Verônica Kristina Cândido Dantas, Aquiles Sales Craveiro Sarmento, Lucymara Fassarella Agnez-Lima, Adriana Lúcia Meireles, Thaiza Teixeira Xavier Nobre, Josivan Gomes de Lima, Julliane Tamara Araújo de Melo Campos
Publikováno v:
Diabetology & Metabolic Syndrome, Vol 9, Iss 1, Pp 1-6 (2017)
Abstract Background Berardinelli-Seip Congenital Lipodystrophy (BSCL) is a rare disease characterized by the almost complete absence of adipose tissue. Although a large number of BSCL cases was previously identified in Rio Grande do Norte (RN), a sta
Externí odkaz:
https://doaj.org/article/bd469e6262c245ff8cc9f66b09ca263b
Autor:
Josivan Gomes Lima, Lucia Helena C Nobrega, Natalia Nobrega Lima, Marcel Catão Ferreira Dos Santos, Pedro Henrique Dantas Silva, Maria de Fatima P Baracho, Debora Nobrega Lima, Julliane Tamara Araújo de Melo Campos, Leonardo Capistrano Ferreira, Francisco Paulo Freire Neto, Carolina de O Mendes-Aguiar, Selma Maria B Jeronimo
Publikováno v:
PLoS ONE, Vol 13, Iss 6, p e0199052 (2018)
INTRODUCTION:Berardinelli-Seip Congenital Lipodystrophy (BSCL) is a rare autosomal recessive disease that affects the development of adipocytes and leads to an inability to store fat in adipocytes. This study aimed to evaluate the life expectancy and
Externí odkaz:
https://doaj.org/article/da5a39f0203b42bb91c33c448106898e
Autor:
Verônica Kristina Cândido Dantas, Joice da Silva Soares, Lázaro Batista de Azevedo Medeiros, Aquiles Sales Craveiro Sarmento, Thaiza Teixeira Xavier Nobre, Fábia Barbosa de Andrade, Josivan Gomes de Lima, Julliane Tamara Araújo de Melo Campos
Publikováno v:
PLoS ONE, Vol 13, Iss 6, p e0197784 (2018)
Berardinelli-Seip Congenital Lipodystrophy (BSCL) is a rare autosomal recessive disease characterized by the almost complete absence of adipose tissue. Due to a strong founder effect that resulted in a higher prevalence of BSCL in Rio Grande do Norte
Externí odkaz:
https://doaj.org/article/969b9eee78494548a3f7c0021a75dac2
Autor:
Aquiles Sales Craveiro Sarmento, Lázaro Batista de Azevedo Medeiros, Lucymara Fassarella Agnez-Lima, Josivan Gomes Lima, Julliane Tamara Araújo de Melo Campos
Publikováno v:
International Journal of Cell Biology, Vol 2018 (2018)
Seipin is a nonenzymatic protein encoded by the BSCL2 gene. It is involved in lipodystrophy and seipinopathy diseases. Named in 2001, all seipin functions are still far from being understood. Therefore, we reviewed much of the research, trying to fin
Externí odkaz:
https://doaj.org/article/d2a440ecee854ee8b36efd6a0a56b2f2
Autor:
João Vitor Silva, Bruno Henrique E Silva Bezerra, Rayssa Maria Do Nascimento, Jocellem Alves de Medeiros, Virgínia Thalita Da Silva, Lázaro Batista De Azevedo Medeiros, Aquiles Sales Craveiro Sarmento, Jane Carla De Souza, Julliane Tamara Araújo de Melo Campos
Publikováno v:
Revista Extensão em Ação. 23:70-79
Os Cursos de Férias de Morfofisiologia Humana têm sido realizados desde 2012 para estudantes do ensino médio das escolas públicas do Trairi, no estado do Rio Grande do Norte. O presente trabalho objetivou demonstrar os seus resultados positivos n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9c93ebe57c4246c1ec4aed0fee857939
https://doi.org/10.32356/exta.v23.n1.41683
https://doi.org/10.32356/exta.v23.n1.41683