Zobrazeno 1 - 10
of 379
pro vyhledávání: '"Moisés, Selman"'
Autor:
Ana Lilia Torres-Machorro, Carina Becerril, Everardo Hernández-Plata, Erika Rubí Luis-García, Mariel Maldonado, Iliana Herrera, Miguel Negreros, Fernando Hernández-Sánchez, Criselda Mendoza-Milla, Miguel Gaxiola, Remedios Ramírez, Annie Pardo, Ivette Buendía-Roldán, Moisés Selman, José Cisneros
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-14 (2024)
Abstract Hypersensitivity pneumonitis (HP) is an immune-mediated inflammatory interstitial lung disease that may evolve to pulmonary fibrosis, a progressive disorder with a poor prognosis characterized by fibroblast activation and extracellular matri
Externí odkaz:
https://doaj.org/article/7289dbc72dcb4c04af56d49223beee3f
Autor:
Marco Espina-Ordoñez, Yalbi Itzel Balderas-Martínez, Ana Lilia Torres-Machorro, Iliana Herrera, Mariel Maldonado, Yair Romero, Fernanda Toscano-Marquez, Annie Pardo, Moisés Selman, José Cisneros
Publikováno v:
Non-coding RNA Research, Vol 9, Iss 3, Pp 865-875 (2024)
Background: Hypersensitivity pneumonitis (HP) is an inflammatory disorder affecting lung parenchyma and often evolves into fibrosis (fHP). The altered regulation of genes involved in the pathogenesis of the disease is not well comprehended, while the
Externí odkaz:
https://doaj.org/article/1a2e784eab4346b7b7d23a5bcb15cf5d
Autor:
Toby M. Maher, R. Gisli Jenkins, Vincent Cottin, Yasuhiko Nishioka, Imre Noth, Moisés Selman, Jin Woo Song, Carina Ittrich, Claudia Diefenbach, Susanne Stowasser, Eric S. White
Publikováno v:
ERJ Open Research, Vol 10, Iss 4 (2024)
Background We used data from the INMARK trial to investigate associations between circulating biomarkers of extracellular matrix (ECM) turnover, inflammation and epithelial dysfunction and disease progression in subjects with idiopathic pulmonary fib
Externí odkaz:
https://doaj.org/article/ce61e17c82d743fd983423633afe417a
Autor:
Ivette Buendia‐Roldan, Karen Martínez‐Espinosa, Maria‐Jose Aguirre, Hiram Aguilar‐Duran, Alexia Palma‐Lopez, Yadira Palacios, Andy Ruiz, Lucero A. Ramón‐Luing, Ranferi Ocaña‐Guzmán, Gloria Pérez‐Rubio, Ramcés Falfán‐Valencia, Moisés Selman, Leslie Chavez‐Galan
Publikováno v:
Immunity, Inflammation and Disease, Vol 12, Iss 7, Pp n/a-n/a (2024)
Abstract Background Persistent respiratory symptoms and lung abnormalities post‐COVID‐19 are public health problems. This study evaluated biomarkers to stratify high‐risk patients to the development or persistence of post‐COVID‐19 interstit
Externí odkaz:
https://doaj.org/article/c31221dfb90f4bafa8e953dd73c67f3e
Autor:
Leslie Chavez-Galan, Carina Becerril, Andy Ruiz, Lucero A. Ramon-Luing, José Cisneros, Martha Montaño, Alfonso Salgado, Carlos Ramos, Ivette Buendía-Roldán, Annie Pardo, Moisés Selman
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Idiopathic pulmonary fibrosis (IPF) is a progressive and irreversible lung disease of unknown etiology. Myofibroblasts are organized in peculiar subepithelial fibroblasts foci (FF), where they abnormally persist and exclude lymphocytes by unclear mec
Externí odkaz:
https://doaj.org/article/0c05597472494e479090bf82e392d5eb
Autor:
Juan Urista, Mariel Maldonado, Fernanda Toscano-Marquez, Remedios Ramírez, Yalbi Itzel Balderas-Martínez, Carina Becerril, Yair Romero, Moisés Selman, Annie Pardo
Publikováno v:
Cells, Vol 11, Iss 18, p 2848 (2022)
Idiopathic pulmonary fibrosis (IPF) is characterized by aberrant activation of the alveolar epithelium, the expansion of the fibroblast population, and the accumulation of extracellular matrix. Global gene expression of human lung fibroblasts stimula
Externí odkaz:
https://doaj.org/article/2b098519bc494ecfae4438b6c55a6570
Publikováno v:
The Lancet Respiratory Medicine. 11:188-196
Autor:
Chintan K. Gandhi, Chixiang Chen, Shaili Amatya, Lili Yang, Chenqi Fu, Shouhao Zhou, Rongling Wu, Ivette Buendía-Roldan, Moisés Selman, Annie Pardo, Joanna Floros
Publikováno v:
Frontiers in Medicine, Vol 7 (2021)
Background: Hypersensitivity pneumonitis (HP) is an interstitial lung disease caused by inhalation of common environmental organic particles. Surfactant proteins (SPs) play a role in innate immunity and surfactant function. We hypothesized that singl
Externí odkaz:
https://doaj.org/article/18b746747606460eb2fce7733159d703
Autor:
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
Publikováno v:
Heliyon, Vol 6, Iss 10, Pp e05279- (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. Pirfenidone was introduced as a therapeut
Externí odkaz:
https://doaj.org/article/ef3d41efaf1b44298bdcd6406e562753
Autor:
Erika Rubí Luis-García, Carina Becerril, Alfonso Salgado-Aguayo, Omar Emiliano Aparicio-Trejo, Yair Romero, Edgar Flores-Soto, Criselda Mendoza-Milla, Martha Montaño, Victoria Chagoya, José Pedraza-Chaverri, Mohammed El Hafidi, Marisol Orozco-Ibarra, Annie Pardo, Moisés Selman
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 15, p 7870 (2021)
Idiopathic pulmonary fibrosis (IPF) is a devastating disease characterized by increased activation of fibroblasts/myofibroblasts. Previous reports have shown that IPF fibroblasts are resistant to apoptosis, but the mechanisms remain unclear. Since in
Externí odkaz:
https://doaj.org/article/54f1216763544108b5edac3f8895dfb5