Cargando…
Novel Genetic and Molecular Pathways in Pulmonary Arterial Hypertension Associated with Connective Tissue Disease
Pulmonary Arterial Hypertension (PAH) is a severe complication of Connective Tissue Disease (CTD), with remarkable morbidity and mortality. However, the molecular and genetic basis of CTD-PAH remains incompletely understood. This study aimed to screen for genetic defects in a cohort of patients with...
Autores principales: | Hernandez-Gonzalez, Ignacio, Tenorio-Castano, Jair, Ochoa-Parra, Nuria, Gallego, Natalia, Pérez-Olivares, Carmen, Lago-Docampo, Mauro, Palomino Doza, Julian, Valverde, Diana, Lapunzina, Pablo, Escribano-Subias, Pilar |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8231632/ https://www.ncbi.nlm.nih.gov/pubmed/34199176 http://dx.doi.org/10.3390/cells10061488 |
Ejemplares similares
-
Customized Massive Parallel Sequencing Panel for Diagnosis of Pulmonary Arterial Hypertension
por: Castaño, Jair Antonio Tenorio, et al.
Publicado: (2020) -
Characterization of rare ABCC8 variants identified in Spanish pulmonary arterial hypertension patients
por: Lago-Docampo, Mauro, et al.
Publicado: (2020) -
Description of Two New Cases of AQP1 Related Pulmonary Arterial Hypertension and Review of the Literature
por: Gallego-Zazo, Natalia, et al.
Publicado: (2022) -
Clinical heterogeneity of Pulmonary Arterial Hypertension associated with variants in TBX4
por: Hernandez-Gonzalez, Ignacio, et al.
Publicado: (2020) -
Expanding the Evidence of a Semi-Dominant Inheritance in GDF2 Associated with Pulmonary Arterial Hypertension
por: Gallego, Natalia, et al.
Publicado: (2021)