Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Juan Alvaro López"'
Autor:
Gabriel de Jesús Bedoya, Juan Alvaro López Quintero, Fabian Alberto Jaimes, Susana Pamela Mejía de Los Ríos, Julian Camilo Arango, Pablo Javier Patiño Grajales, Laura Yaneth Gámez Díaz
Publikováno v:
Iatreia, Vol 23, Iss 2, Pp 127-136 (2010)
Sepsis, a syndrome of systemic response to infection is a major public health problem, because it is associated with high morbidity and mortality. Among the genes shown to be associated with this syndrome, there is one which encodes for caspase-12 (c
Externí odkaz:
https://doaj.org/article/65392b5fb7004b18ba80cd6ca006c848
Autor:
Carlos Julio Montoya, Juan Alvaro López, Paula Andrea Velilla, Claudia Rugeles, Pablo Javier Patiño, Diana María García de Olarte
Publikováno v:
Biomédica: revista del Instituto Nacional de Salud, Vol 23, Iss 1, Pp 60-76 (2003)
El síndrome de hiper-IgE con infecciones recurrentes (SHIEIR) se caracteriza por infecciones de la piel y el aparato respiratorio causadas especialmente por Staphylococcus aureus y algunos hongos, infecciones que se asocian frecuentemente con daño
Externí odkaz:
https://doaj.org/article/2c2d90fefc4040b893b70f32cf220697
Autor:
Juan Alvaro López, María Teresa Rugeles López, Pablo Javier Patiño Grajales, Andrés Augusto Arias Sierra
Publikováno v:
Iatreia, Vol 13, Iss 2 (2000)
Los neutrófilos responden a diferentes estímulos con un fenómeno conocido como “explosión respiratoria” la cual depende del sistema NADPH oxidasa. La importancia de este sistema para la actividad microbicida de las células fagocíticas es ev
Externí odkaz:
https://doaj.org/article/448e2e0c694440f88725ac79ee1ab5ba
Autor:
Piedad Agudelo-Flórez, Antonio Condino-Neto, Sara T. Olalla-Saad, Juan Alvaro López, Jussara Redher, Beatriz Tavares Costa-Carvalho, Peter E. Newburger
Publikováno v:
American Journal of Hematology. 75:151-156
Patients with severe leukocyte G6PD deficiency may present with impairment of NADPH oxidase activity and a history of recurrent infections, mimicking the phenotype of chronic granulomatous disease. We report herein a child with recurrent infections w
Autor:
Maria Aparecida de Souza Paiva, Piedad Agudelo-Flórez, Carolina Prando-Andrade, Antonio Condino-Neto, Juan Alvaro López, Beatriz Tavares Costa-Carvalho
Publikováno v:
Jornal de Pediatria. 80:425-428
OBJETIVO: Relatar dois casos de irmaos com doenca granulomatosa cronica. A doenca granulomatosa cronica e uma imunodeficiencia primaria caracterizada por atividade microbicida deficiente. Mutacoes no gene que codifica a proteina p47-phox (NCF-1) esta
Autor:
Alexa Schuettenberg, Alejandra Piña, Morgan Metrailer, Ronald Guillermo Peláez-Sánchez, Piedad Agudelo-Flórez, Juan Álvaro Lopez, Luke Ryle, Fernando P. Monroy, John A. Altin, Jason T. Ladner
Publikováno v:
Microbiology Spectrum, Vol 10, Iss 5 (2022)
ABSTRACT Emerging infectious diseases represent a serious and ongoing threat to humans. Most emerging viruses are maintained in stable relationships with other species of animals, and their emergence within the human population results from cross-spe
Externí odkaz:
https://doaj.org/article/ac54d2fb6c8b4c66a91d8e119f50d3ae
Autor:
Piedad, Agudelo-Flórez, Sara, Navarro, Pamela, Luttges, Juan Alvaro, López, Ximena, Norambuena, Carmen Luz, Navarrete S, Arnoldo, Quezada, Michael, Spencer, Antonio, Condino-Neto, Mónica, Cornejo de
Publikováno v:
Revista medica de Chile. 134(8)
The X-linked form of chronic granulomatous disease (CGD) is a primary immunodeficiency that affects phagocytes of the innate immune system and is characterized by an increased susceptibility to severe bacterial and fungal infections. It is caused by
Autor:
Sara Navarro V, Arnoldo Quezada L, Antonio Condino-Neto, Piedad Agudelo-Flórez, Pamela Luttges D, Mónica Cornejo De L, Carmen Luz Navarrete S, Michael Spencer Y, Ximena Norambuena R, Juan Alvaro López
Publikováno v:
Revista médica de Chile v.134 n.8 2006
SciELO Chile
CONICYT Chile
instacron:CONICYT
SciELO Chile
CONICYT Chile
instacron:CONICYT
Background: The X-linked form of chronic granulomatous disease (CGD) is a primary immunodeficiency that affects phagocytes of the innate immune system and is characterized by an increased susceptibility to severe bacterial and fungal infections. It i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97245958642c83a27a4fa5a9a9e41671
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872006000800004
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872006000800004
Autor:
Antonio Condino-Neto, Cristina Miuki Abe Jacob, Pérsio Roxo, Juan Alvaro López, Piedad Agudelo-Flórez, Anete Sevciovic Grumach, Carolina Prando-Andrade, Magda Maria Salles Carneiro-Sampaio, Maria Aparecida de Souza Paiva, Arnoldo Quezada, Francisco Jose Espinosa, Peter E. Newburger, Beatriz Tavares Costa-Carvalho
Publikováno v:
Pediatric bloodcancer. 46(2)
Chronic granulomatous disease (CGD) is a primary immunodeficiency characterized by early onset of recurrent and severe infections. The molecular defects causing CGD are heterogeneous and lead to absence, low expression, or malfunctioning of one of th
Publikováno v:
Journal of interferoncytokine research : the official journal of the International Society for Interferon and Cytokine Research. 23(12)
The aim of this study was to investigate the effect of interferon-gamma (IFN-gamma) and tumor necrosis factor-alpha (TNF-alpha) on NADPH oxidase activity and gp91-phox gene expression in HL-60 clone 15 cells as they differentiate along the eosinophil