Ignacia Fuentes
Santiago, RM, Chile
Last Updated: 09/26/2026
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Found 40 publications
N-acetylcysteine exerts senescence-selective antifibrotic effects in fibroblast from chronic wounds in recessive dystrophic epidermolysis bullosa.
Journal: The British journal of dermatology
Published: December 11, 2025
Impaired skin reinnervation in epidermolysis bullosa due to neurotrophic deficiency.
Journal: Pain
Published: October 23, 2025
Sephardic origins revealed for rare skin disorder, recessive dystrophic epidermolysis bullosa, in individuals carrying the unique c.6527insC mutation.
Journal: Journal of medical genetics
Published: June 01, 2025
A Novel Homozygous 9385 bp Deletion in the FERMT1 (KIND1) Gene in a Malaysian Family with Kindler Epidermolysis bullosa and a Review of Large Deletions.
Journal: International journal of molecular sciences
Published: April 02, 2025
KLHL24 mutation drives intermediate filament degradation, mitochondrial dysfunction and fibrosis in heart failure patients.
Journal: Cardiovascular research
Published: November 04, 2024
Prevalence of Crown Resorption in Amelogenesis Imperfecta due to Junctional Epidermolysis Bullosa.
Journal: Oral diseases
Published: June 19, 2024
Novel variants impairing Sp1 transcription factor binding in the COL7A1 promoter cause mild cases of recessive dystrophic epidermolysis bullosa.
Journal: European journal of human genetics : EJHG
Published: May 01, 2024
Epidemiology of epidermolysis bullosa in Chile.
Journal: The British journal of dermatology
Published: March 30, 2024
Orofacial Anomalies in Kindler Epidermolysis Bullosa.
Journal: JAMA dermatology
Published: March 20, 2024
Skin in the game: a review of single-cell and spatial transcriptomics in dermatological research.
Journal: Clinical chemistry and laboratory medicine
Published: November 03, 2023
Last Updated: 09/26/2026