Results 1 to 10 of about 22,028 (227)

FUNCIÓN PULMONAR EN FIBROSIS QUÍSTICA

Neumología Pediátrica, 2022
La fibrosis quística (FQ) es una enfermedad hereditaria autosómica recesiva, causada por la mutación del gen que codifica la proteína CFTR (cystic fibrosis transmembrane conductance regulator), afecta varios órganos, pero la enfermedad pulmonar es la ...
Hortensia Barrientos
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Mitochondrial proteomics reveals reductive metabolism dependent on glutamine in fibroblasts of idiopathic pulmonary fibrosis under hypoxia [PDF]

Scientific Reports
Pulmonary fibrosis, particularly idiopathic pulmonary fibrosis (IPF), is a chronic disease characterized not only by a transcriptionally active signature associated with hypoxia but also by feedback loops that may underlie disease progression.
Yair Romero, Manuel Castillejos-López, Erika Rubí Luis-Garcia, Adriana Becerra-Cervera, Diana I. Aparicio-Bautista, Iliana Herrera, Víctor Ruiz, Emmanuel Ríos-Castro, Carina Becerril, Nayeli Torres-Ramírez, Rosario Ortiz-Hernández, Jose Cisneros, Ana Karen Torres-Soria, Joaquin Zuñiga, Edgar Flores-Soto, Yalbi Itzel Balderas-Martinez, Ángeles Carlos-Reyes, Luz María Torres-Espíndola, Rafael Velázquez-Cruz, Arnoldo Aquino-Gálvez   +19 more
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Eosinophilic cytokines and small airway dysfunction in women with COPD: correlation with exposure to biomass smoke versus tobacco smoking [PDF]

IJTLD Open
BACKGROUND: Chronic obstructive pulmonary disease (COPD) is a chronic inflammatory disease characterised by progressive airflow obstruction. Tobacco smoking is the leading cause of COPD (COPD-TS); however, chronic exposure to biomass smoke (COPD-BS) is ...
R. Robles-Hernández, R. Pérez-Padilla, A. Ramírez-Venegas, Y. Velasco-Torres, M. Montaño, C. Ramos, A.S. Ramírez-GarciaLuna, O. Pérez-Bautista   +7 more
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Absence of HDAC3 by Matrix Stiffness Promotes Chromatin Remodeling and Fibroblast Activation in Idiopathic Pulmonary Fibrosis

Cells, 2023
Idiopathic pulmonary fibrosis (IPF) is a chronic and fatal disease characterized by progressive and irreversible lung scarring associated with persistent activation of fibroblasts.
Fernanda Toscano-Marquez, Yair Romero, Marco Espina-Ordoñez, José Cisneros   +3 more
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Short-Term Exposure to Wood Smoke Increases the Expression of Pro-Inflammatory Cytokines, Gelatinases, and TIMPs in Guinea Pigs

Toxics, 2021
Exposure to air pollutants in wildfire smoke and indoor pollution causes lung diseases. Short-term exposure to wood smoke (WS) is partially known to alter the expression of human matrix metalloproteinases (MMPs), inflammatory cytokines, and tissue ...
Carlos Ramos, Rebeca Cañedo-Mondragón, Carina Becerril, Georgina González-Ávila, Ana Laura Esquivel, Ana Lilia Torres-Machorro, Martha Montaño   +6 more
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Síndrome combinado de fibrosis pulmonar y enfisema: albores del tratamiento antifibrótico en el Paraguay

Memorias del Instituto de Investigaciones en Ciencias de la Salud, 2022
La concomitancia de fibrosis pulmonar en regiones inferiores del pulmón y enfisema en lóbulos superiores caracterizan a una entidad poco frecuente denominada síndrome combinado de fibrosis pulmonar y enfisema, que usualmente se asocia a alta carga de ...
Domingo Pérez-Bejarano
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Pharmacokinetic evaluation of two pirfenidone formulations in patients with idiopathic pulmonary fibrosis and chronic hypersensitivity pneumonitis

Heliyon, 2020
Idiopathic pulmonary fibrosis (IPF) is a progressive and fatal disease characterized by an abnormal activation of lung epithelium and fibroblasts, as well as an excessive accumulation of extracellular matrix.
Lina Marcela Barranco-Garduño, Ivette Buendía-Roldan, Juan Jose Rodriguez, Rodrigo González-Ramírez, Ariadna N. Cervantes-Nevárez, Juan Carlos Neri-Salvador, Miriam del Carmen Carrasco-Portugal, Gilberto Castañeda-Hernández, Karen Martinez-Espinosa, Moisés Selman, Francisco Javier Flores-Murrieta   +10 more
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Effect of Hypoxia in the Transcriptomic Profile of Lung Fibroblasts from Idiopathic Pulmonary Fibrosis

Cells, 2022
Idiopathic pulmonary fibrosis (IPF) is an aging-associated disease characterized by exacerbated extracellular matrix deposition that disrupts oxygen exchange.
Yair Romero, Yalbi Itzel Balderas-Martínez, Miguel Angel Vargas-Morales, Manuel Castillejos-López, Joel Armando Vázquez-Pérez, Jazmín Calyeca, Luz María Torres-Espíndola, Nelly Patiño, Angel Camarena, Ángeles Carlos-Reyes, Edgar Flores-Soto, Guadalupe León-Reyes, Martha Patricia Sierra-Vargas, Iliana Herrera, Erika Rubí Luis-García, Víctor Ruiz, Rafael Velázquez-Cruz, Arnoldo Aquino-Gálvez   +17 more
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Toxicidad pulmonar secundaria a bleomicina. Reporte de caso

Respirar, 2023
La toxicidad pulmonar por antineoplásicos es muy variable dependiente del grupo farmacológico; la bleomicina es uno de los medicamentos en los que se ha reportado este evento.
Luis Eduardo Ramirez Bejarano, Karen Yuliana Ramírez Iriarte, Luisa Alejandra Maya Caicedo, Wilmer Orlando Aponte Barrios   +3 more
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Fibrosis quística: patogenia bacteriana y moduladores del CFTR (regulador de conductancia transmembranal de la fibrosis quística)

Boletín Médico del Hospital Infantil de México, 2022
La fibrosis quística es una enfermedad hereditaria autosómica recesiva que se origina por mutaciones en el gen regulador de conductancia transmembranal de la fibrosis quística (CFTR, cystic fibrosis transmembrane conductance regulator).
Silvia Y. Vargas-Roldán, José L. Lezana-Fernández, Jorge F. Cerna-Cortés, Santiago Partida-Sánchez, José I. Santos-Preciado, Roberto Rosales-Reyes   +5 more
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