Cargando…

Increased Expression of CC16 in Patients with Idiopathic Pulmonary Fibrosis

Idiopathic pulmonary fibrosis (IPF) is a devastating disease of unknown etiology. The pathogenic mechanisms are unclear, but evidence indicates that aberrantly activated alveolar epithelial cells secrete a variety of mediators which induce the migration, proliferation and activation of fibroblasts a...

Descripción completa

Detalles Bibliográficos
Autores principales:	Buendía-Roldán, Ivette, Ruiz, Víctor, Sierra, Patricia, Montes, Eduardo, Ramírez, Remedios, Vega, Anita, Salgado, Alfonso, Vargas, Mario H., Mejía, Mayra, Pardo, Annie, Selman, Moisés
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2016
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5158056/ https://www.ncbi.nlm.nih.gov/pubmed/27977812 http://dx.doi.org/10.1371/journal.pone.0168552

Ejemplares similares

Lower levels of α-Klotho in serum are associated with decreased lung function in individuals with interstitial lung abnormalities
por: Buendia-Roldan, Ivette, et al.
Publicado: (2019)

Identification of MMP28 as a biomarker for the differential diagnosis of idiopathic pulmonary fibrosis
por: Maldonado, Mariel, et al.
Publicado: (2018)

Fibroblasts From Idiopathic Pulmonary Fibrosis Induce Apoptosis and Reduce the Migration Capacity of T Lymphocytes
por: Chavez-Galan, Leslie, et al.
Publicado: (2022)

Immunoglobulin Free Light Chains Are Increased in Hypersensitivity Pneumonitis and Idiopathic Pulmonary Fibrosis
por: Groot Kormelink, Tom, et al.
Publicado: (2011)

Pulmonary Fibrosis in the Time of COVID-19
por: Buendia-Roldan, Ivette, et al.
Publicado: (2022)

Role of matrix metaloproteases in idiopathic pulmonary fibrosis
por: Pardo, Annie, et al.
Publicado: (2012)

Idiopathic pulmonary fibrosis: an epithelial/fibroblastic cross-talk disorder
por: Selman, Moisés, et al.
Publicado: (2002)

Idiopathic Pulmonary Fibrosis: Aberrant Recapitulation of Developmental Programs?
por: Selman, Moisés, et al.
Publicado: (2008)

Role of matrix metalloproteinases in the pathogenesis of idiopathic pulmonary fibrosis
por: Pardo, Annie, et al.
Publicado: (2016)

One Molecule, Two Opposite Biological Effects: The Many Faces of Matrix Metalloproteases in the Pathogenesis of Idiopathic Pulmonary Fibrosis
por: Pardo, Annie, et al.
Publicado: (2021)

Inflammatory pathways are upregulated in the nasal epithelium in patients with idiopathic pulmonary fibrosis
por: Sala, Marc A., et al.
Publicado: (2018)

CX3CL1 and CX3CR1 could be a relevant molecular axis in the pathophysiology of idiopathic pulmonary fibrosis
por: Rivas-Fuentes, Selma, et al.
Publicado: (2020)

Transmembrane protease, serine 4 (TMPRSS4) is upregulated in IPF lungs and increases the fibrotic response in bleomycin-induced lung injury
por: Valero-Jiménez, Ana, et al.
Publicado: (2018)

CD4+T cells in ageing-associated interstitial lung abnormalities show evidence of pro-inflammatory phenotypic and functional profile
por: Machahua, Carlos, et al.
Publicado: (2021)

Effects of Supplemental Oxygen on Cardiovascular and Respiratory Interactions by Extended Partial Directed Coherence in Idiopathic Pulmonary Fibrosis
por: Santiago-Fuentes, Laura M., et al.
Publicado: (2022)

Accelerated Variant of Idiopathic Pulmonary Fibrosis: Clinical Behavior and Gene Expression Pattern
por: Selman, Moisés, et al.
Publicado: (2007)

Determination of the phenotypic age in residents of Mexico City: effect of accelerated ageing on lung function and structure
por: Buendía-Roldan, Ivette, et al.
Publicado: (2020)

Risk factors associated with the detection of pulmonary emphysema in older asymptomatic respiratory subjects
por: Buendia-Roldan, Ivette, et al.
Publicado: (2020)

mTORC1 activation decreases autophagy in aging and idiopathic pulmonary fibrosis and contributes to apoptosis resistance in IPF fibroblasts
por: Romero, Yair, et al.
Publicado: (2016)

Hypersensitivity Pneumonitis: Diagnostic and Therapeutic Challenges
por: Alberti, Maria Laura, et al.
Publicado: (2021)

A major genetic determinant of autoimmune diseases is associated with the presence of autoantibodies in hypersensitivity pneumonitis
por: Buendía-Roldán, Ivette, et al.
Publicado: (2020)

The HLA-DRB1*07 Allele Is Associated with Interstitial Lung Abnormalities (ILA) and Subpleural Location in a Mexican Mestizo Population
por: Buendia-Roldan, Ivette, et al.
Publicado: (2022)

Pharmacokinetic evaluation of two pirfenidone formulations in patients with idiopathic pulmonary fibrosis and chronic hypersensitivity pneumonitis
por: Barranco-Garduño, Lina Marcela, et al.
Publicado: (2020)

SNP and Haplotype Interaction Models Reveal Association of Surfactant Protein Gene Polymorphisms With Hypersensitivity Pneumonitis of Mexican Population
por: Gandhi, Chintan K., et al.
Publicado: (2021)

Up-Regulation and Profibrotic Role of Osteopontin in Human Idiopathic Pulmonary Fibrosis
por: Pardo, Annie, et al.
Publicado: (2005)

Mortality in patients with interstitial lung diseases hospitalized by severe or critical COVID-19
por: Pruneda, Ana Karem S., et al.
Publicado: (2023)

Improving biocuration of microRNAs in diseases: a case study in idiopathic pulmonary fibrosis
por: Balderas-Martínez, Yalbi Itzel, et al.
Publicado: (2017)

Loss of MT1-MMP in Alveolar Epithelial Cells Exacerbates Pulmonary Fibrosis
por: Placido, Luis, et al.
Publicado: (2021)

Lack of ZNF365 Drives Senescence and Exacerbates Experimental Lung Fibrosis
por: Urista, Juan, et al.
Publicado: (2022)

Activated MC(TC )mast cells infiltrate diseased lung areas in cystic fibrosis and idiopathic pulmonary fibrosis
por: Andersson, Cecilia K, et al.
Publicado: (2011)

Single Nucleotide Polymorphisms (SNP) and SNP-SNP Interactions of the Surfactant Protein Genes Are Associated With Idiopathic Pulmonary Fibrosis in a Mexican Study Group; Comparison With Hypersensitivity Pneumonitis
por: Abbasi, Ata, et al.
Publicado: (2022)

Mitochondrial Dysfunction and Alterations in Mitochondrial Permeability Transition Pore (mPTP) Contribute to Apoptosis Resistance in Idiopathic Pulmonary Fibrosis Fibroblasts
por: Luis-García, Erika Rubí, et al.
Publicado: (2021)

Comorbidities of Patients With Idiopathic Pulmonary Fibrosis in Four Latin American Countries. Are There Differences by Country and Altitude?
por: Gonzalez-Garcia, Mauricio, et al.
Publicado: (2021)

CC Chemokines in Idiopathic Pulmonary Fibrosis: Pathogenic Role and Therapeutic Potential
por: Liu, Shanshan, et al.
Publicado: (2023)

MMP1 and MMP7 as Potential Peripheral Blood Biomarkers in Idiopathic Pulmonary Fibrosis
por: Rosas, Ivan O, et al.
Publicado: (2008)

MMP2 Polymorphism Affects Plasma Matrix Metalloproteinase (MMP)-2 Levels, and Correlates with the Decline in Lung Function in Hypersensitivity Pneumonitis Positive to Autoantibodies Patients
por: Santiago-Ruiz, Luis, et al.
Publicado: (2019)

Serum AGE/RAGEs as potential biomarker in idiopathic pulmonary fibrosis
por: Machahua, Carlos, et al.
Publicado: (2018)

Circulating microRNA Signature Associated to Interstitial Lung Abnormalities in Respiratory Asymptomatic Subjects
por: Ortiz-Quintero, Blanca, et al.
Publicado: (2020)

CC16 augmentation reduces exaggerated COPD-like disease in Cc16-deficient mice
por: Rojas-Quintero, Joselyn, et al.
Publicado: (2023)

Circulating Levels of PD-L1, TIM-3 and MMP-7 Are Promising Biomarkers to Differentiate COVID-19 Patients That Require Invasive Mechanical Ventilation
por: Chavez-Galan, Leslie, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_49f0hsc376vq383r3u4qsbrfu4