Zobrazeno 1 - 10
of 32
pro vyhledávání: '"HERNÁN CABELLO A."'
Autor:
Ana Carolina Proença da Fonseca, Izadora Sthephanie da Silva Assis, Kaio Cezar Rodrigues Salum, Lohanna Palhinha, Gabriella de Medeiros Abreu, Verônica Marques Zembrzuski, Mario Campos Junior, José Firmino Nogueira-Neto, Amanda Cambraia, Mauro Lucio Ferreira Souza Junior, Clarissa Menezes Maya-Monteiro, Pedro Hernán Cabello, Patrícia Torres Bozza, João Regis Ivar Carneiro
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
IntroductionObesity is a multifactorial disease associated with the development of many comorbidities. This disease is associated with several metabolic alterations; however, it has been shown that some individuals with obesity do not exhibit metabol
Externí odkaz:
https://doaj.org/article/ef0f3ba97c0946f49a666c8bbd0bfd90
Autor:
María Trinidad González, Raimundo Santolaya, Miguel Antúnez, Hernán Cabello, José Ignacio Ortega, Manfred Zink, Delia Muñoz, Pablo Pérez
Publikováno v:
Revista Panamericana de Salud Pública, Vol 46, Iss 97, Pp 1-2 (2022)
Externí odkaz:
https://doaj.org/article/950ad5b1afee4b1a925e4fda897f37be
Autor:
Proença da Fonseca, Ana Carolina, Sthephanie da SilvaAssis, Izadora, Rodrigues Salum, Kaio Cezar, Palhinha, Lohanna, de Medeiros Abreu, Gabriella, Marques Zembrzuski, Verônica, Campos Junior, Mario, Firmino Nogueira-Neto, José, Cambraia, Amanda, Ferreira Souza Junior, Mauro Lucio, Menezes Maya-Monteiro, Clarissa, Hernán Cabello, Pedro, Torres Bozza, Patrícia, Ivar Carneiro, João Regis
Publikováno v:
Frontiers in Genetics; 2024, p1-16, 16p
Autor:
Kaio Cezar Rodrigues Salum, Guilherme Orofino de Souza, Gabriella de Medeiros Abreu, Mário Campos Junior, Fabiana Barzotto Kohlrausch, João Regis Ivar Carneiro, José Firmino Nogueira Neto, Fernanda Cristina C. Mattos Magno, Eliane Lopes Rosado, Lohanna Palhinha, Clarissa Menezes Maya-Monteiro, Giselda Maria Kalil de Cabello, Pedro Hernán Cabello, Patrícia Torres Bozza, Verônica Marques Zembrzuski, Ana Carolina Proença da Fonseca
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
BackgroundThe melanocortinergic pathway orchestrates the energy homeostasis and impairments in this system often lead to an increase in body weight. Rare variants in the melanocortin 4 receptor (MC4R) gene resulting in partial or complete loss of fun
Externí odkaz:
https://doaj.org/article/2761b05651344a41966f54f212cb79cd
Autor:
Ana Carolina Proença da Fonseca, Bruna Marchesini, Verônica Marques Zembrzuski, Danielle Dutra Voigt, Vivianne Galante Ramos, João Regis Ivar Carneiro, José Firmino Nogueira Neto, Giselda Maria Kalil de Cabello, Pedro Hernán Cabello
Publikováno v:
Genetics and Molecular Biology, Vol 43, Iss 1 (2020)
Abstract Obesity is a major public health problem worldwide. It has a complex etiology, influenced by environmental and genetic factors. FTO has been recognized as an important genetic factor for obesity development. This study evaluated the contribu
Externí odkaz:
https://doaj.org/article/bf117b037b7040589a15ffa15a0d8989
Akademický článek
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Autor:
Tamara, Silva, Caroliny Pinto, Gomes, Danielle Dutra, Voigt, Ritiele Bastos, de Souza, Karoline, Medeiros, Nicole Lima, Cosentino, Ana Carolina Proença, Fonseca, Tatiana Martins, Tilli, Enrique Antonio Covarrubias, Loayza, Vivianne Galante, Ramos, Pedro Hernán Cabello, Acero
Publikováno v:
Disease markers. 2022
By the year 2050, the world's elderly population may increase exponentially, raising the rate of disease characteristic of this group, such as prostate cancer (PCa) and benign prostatic hyperplasia (BPH). Prostate disorders have a multifactorial etio
Autor:
Tamara Silva, Caroliny Pinto Gomes, Danielle Dutra Voigt, Ritiele Bastos de Souza, Karoline Medeiros, Nicole Lima Cosentino, Ana Carolina Proença Fonseca, Tatiana Martins Tilli, Enrique Antonio Covarrubias Loayza, Vivianne Galante Ramos, Pedro Hernán Cabello Acero
Publikováno v:
Disease Markers.
By the year 2050, the world’s elderly population may increase exponentially, raising the rate of disease characteristic of this group, such as prostate cancer (PCa) and benign prostatic hyperplasia (BPH). Prostate disorders have a multifactorial et
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 63, Iss 1, Pp 145-149 (2005)
OBJETIVO: Descrever o perfil clínico e laboratorial de pacientes com atrofia muscular espinhal (AME) com deleção no gene da proteína sobrevivência do neurônio motor (SMN). MÉTODO: Estudo descritivo de uma série de casos confirmados pela prese
Externí odkaz:
https://doaj.org/article/1485854dfb5c4c9cb20eb0c4da070476