Zobrazeno 1 - 10
of 92
pro vyhledávání: '"Humberto, Arboleda"'
Autor:
Johanna Forero-Rodríguez, Johannes Zimmermann, Jan Taubenheim, Natalia Arias-Rodríguez, Juan David Caicedo-Narvaez, Lena Best, Cindy V. Mendieta, Julieth López-Castiblanco, Laura Alejandra Gómez-Muñoz, Janneth Gonzalez-Santos, Humberto Arboleda, William Fernandez, Christoph Kaleta, Andrés Pinzón
Publikováno v:
Microorganisms, Vol 12, Iss 2, p 325 (2024)
Parkinson’s disease (PD) is a chronic and progressive neurodegenerative disease with the major symptoms comprising loss of movement coordination (motor dysfunction) and non-motor dysfunction, including gastrointestinal symptoms. Alterations in the
Externí odkaz:
https://doaj.org/article/88e13a73b56a4b7cb80e93dc11a7cd9a
Autor:
Erika Yolanda Hernandez Sandoval, Karim-Martina Alvis-Gómez, Humberto Arboleda Granados, Ana-Gabriela Concha-Mera
Publikováno v:
Revista de Investigación e Innovación en Ciencias de la Salud, Vol 5, Iss 1 (2023)
Introducción: El trastorno del espectro autista (TEA) es un trastorno del neurodesarrollo que provoca déficits en áreas cognitivas y motoras y es causado por varios mecanismos, entre ellos la regulación epigenética. Los procesos epigenéticos pu
Externí odkaz:
https://doaj.org/article/7785e22d46054bfdb32ffe69f974fac0
Autor:
Ana Cecília Guimarães Alves, Natalie Mary Sukow, Gabriel Adelman Cipolla, Marla Mendes, Thiago P. Leal, Maria Luiza Petzl-Erler, Ricardo Lehtonen Rodrigues Souza, Ilíada Rainha de Souza, Cesar Sanchez, Meddly Santolalla, Douglas Loesch, Michael Dean, Moara Machado, Jee-Young Moon, Robert Kaplan, Kari E. North, Scott Weiss, Mauricio L. Barreto, M. Fernanda Lima-Costa, Heinner Guio, Omar Cáceres, Carlos Padilla, Eduardo Tarazona-Santos, Ignacio F. Mata, Elena Dieguez, Víctor Raggio, Andres Lescano, Vitor Tumas, Vanderci Borges, Henrique B. Ferraz, Carlos R. Rieder, Artur Schumacher-Schuh, Bruno L. Santos-Lobato, Pedro Chana-Cuevas, William Fernandez, Gonzalo Arboleda, Humberto Arboleda, Carlos E. Arboleda-Bustos, Timothy D. O’Connor, Marcia Holsbach Beltrame, Victor Borda
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
In adulthood, the ability to digest lactose, the main sugar present in milk of mammals, is a phenotype (lactase persistence) observed in historically herder populations, mainly Northern Europeans, Eastern Africans, and Middle Eastern nomads. As the
Externí odkaz:
https://doaj.org/article/83fade9eedf24b7d99f1452beb4bd4e7
Autor:
Juan David Caicedo, Alejandro Cáceres, Carlos E. Arboleda-Bustos, María Fernanda Mahecha, Jenny Ortega, Gonzalo Arboleda, Humberto Arboleda
Publikováno v:
Biomédica: revista del Instituto Nacional de Salud, Vol 39, Iss 3, Pp 595-600 (2019)
Introducción. Los proyectos del mapa de haplotipos (HapMap) y de los 1.000 genomas han sido fundamentales para la compresión del componente genético de las enfermedades comunes y los fenotipos normales. Sin embargo, la variabilidad genética colom
Externí odkaz:
https://doaj.org/article/f72fd7699dd24ddea735fa0eb8b3a046
Autor:
Thiago P Leal, Jennifer N French-Kwawu, Mateus H Gouveia, Victor Borda, Miguel Inca-Martinez, Emily A Mason, Andrea RVR Horimoto, Douglas P Loesch, Elif I Sarihan, Mario R Cornejo-Olivas, Luis E Torres, Pilar E Mazzetti-Soler, Carlos Cosentino, Elison H Sarapura-Castro, Andrea Rivera-Valdivia, Angel C Medina, Elena M Dieguez, Víctor E Raggio, Andrés Lescano, Vitor Tumas, Vanderci Borges, Henrique B Ferraz, Carlos R Rieder, Artur Schumacher-Schuh, Bruno L Santos-Lobato, Carlos Velez-Pardo, Marlene Jimenez-Del-Rio, Francisco Lopera, Sonia Moreno, Pedro Chana-Cuevas, William Fernandez, Gonzalo Arboleda, Humberto Arboleda, Carlos E Arboleda Bustos, Dora Yearout, Maria F Lima-Costa, Eduardo Tarazona, Cyrus Zabetian, Timothy A Thornton, Timothy D O’Connor, Ignacio F Mata
Publikováno v:
medRxiv
Sex differences in Parkinson Disease (PD) risk are well-known. However, it is still unclear the role of sex chromosomes in the development and progression of PD. We performed the first X-chromosome Wide Association Study (XWAS) for PD risk in Latin A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::611448199f677e7660d221b8a0d775d6
https://europepmc.org/articles/PMC9915833/
https://europepmc.org/articles/PMC9915833/
Autor:
Belfran Carbonell M, Francy Bayona R, Zayra V Garavito-Aguilar, Carolina Parada B, Humberto Arboleda G, Clementina Infante-Contreras C
Publikováno v:
Revista MVZ Cordoba, Vol 23, Iss 3 (2018)
Objetivo. El presente estudio tuvo como objetivo describir detalladamente los patrones de expresión del gen Hey1, un efector de la vía Notch durante el desarrollo de arcos branquiales y prominencias faciales. Materiales y métodos. Se incubaron hue
Externí odkaz:
https://doaj.org/article/4f509466d7dd4368b170a4d94043b0f5
Autor:
Kelly Estrada-Orozco, Kely Bonilla-Vargas, Francy Cruz, Oscar Mancera, Miguel Ruiz, Laura Alvarez, Rodrigo Pardo, Humberto Arboleda
Publikováno v:
International Journal of Alzheimer's Disease, Vol 2018 (2018)
Introduction. Cognitive disorders are a clinical and research challenge; in particular, the mild cognitive disorder (MiCD) requires diagnostic suspicion and tools with adequate performance for its detection. The objective of this study was the valida
Externí odkaz:
https://doaj.org/article/18a50b320e0c49e1893bb50fb86597ee
Autor:
F. Mahecha María, Jenny Ortega-Rojas, Rodrigo Pardo, Humberto Arboleda, O. Mancera, V. Celeita, Kely Bonilla-Vargas, E. Guerrero, K. Estrada, E. Vega, A. Romero, F. Cruz-Sanabria, Patricia Montañés
Publikováno v:
Neurología. 36:681-691
Resumen Introduccion Los polimorfismos de riesgo para el desarrollo de enfermedad de Alzheimer (se han estudiado en pacientes con demencia, pero aun no se han explorado en trastorno neurocognitivo leve (TNL) en nuestra poblacion, ni se han considerad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::97d6c228cab9dde2caecfdb31bb22982
https://doi.org/10.1016/j.nrl.2018.07.002
https://doi.org/10.1016/j.nrl.2018.07.002
Publikováno v:
BioTechniques, Vol 55, Iss 4, Pp 181-197 (2013)
Comprehensive analysis of DNA methylation patterns is critical for understanding the molecular basis of many human diseases. While hundreds of PCR-based DNA methylation studies are published every year, the selection and implementation of appropriate
Externí odkaz:
https://doaj.org/article/526cca54346740b2a58966e89e64b312
Publikováno v:
Acta Biológica Colombiana, Vol 12, Iss 2, Pp 135-141 (2007)
This essay explores the role of folate in disruption of neural cell integrity. Here, it is discussed recent evidence which shows DNA reparation as a process related to neuronal apoptosis induced by folate depletion.
Externí odkaz:
https://doaj.org/article/eefe585263594854aa6c4008346fa107