Showing results (51-60 of 62) with videos related to
Sort By:
Pageof 7
Photochemistry and Photobiology|February 20, 2008
The Arg160Trp allele of melanocortin-1 receptor gene might protect against vitiligoMárta Széll, Eszter Baltás, László Bodai, et al.International Journal of Molecular Sciences|January 27, 2024
Missing Heritability in Albinism: Deep Characterization of a Hungarian Albinism Cohort Raises the Possibility of the Digenic Genetic Background of the DiseaseNikoletta Nagy, Margit Pal, Jozsef Kun, et al.American Journal of Human Genetics|February 21, 2012
Germline mutation in ATR in autosomal- dominant oropharyngeal cancer syndromeAkio Tanaka, Sarah Weinel, Nikoletta Nagy, et al.Experimental Dermatology|May 29, 2010
The molecular skin pathology of familial primary localized cutaneous amyloidosisAkio Tanaka, Joey E Lai-Cheong, Peter C van den Akker, et al.The Journal of Allergy and Clinical Immunology|July 6, 2014
MicroRNA-146a alleviates chronic skin inflammation in atopic dermatitis through suppression of innate immune responses in keratinocytesAna Rebane, Toomas Runnel, Alar Aab, et al.International Journal of Molecular Sciences|March 14, 2026
A Unique Patient Stratification Method Combined with a Machine Learning Approach Identifies Novel Genetic Susceptibility and Protective Factors for Severe COVID-19 in a Hungarian PopulationAlexandra Neller, Mátyás Bukva, Bence Gálik, et al.The Journal of Allergy and Clinical Immunology|March 27, 2012
Mechanisms of IFN-γ-induced apoptosis of human skin keratinocytes in patients with atopic dermatitisAna Rebane, Maya Zimmermann, Alar Aab, et al.Clinical Chemistry|April 28, 2016
Cell-Free DNA Analysis of Targeted Genomic Regions in Maternal Plasma for Non-Invasive Prenatal Testing of Trisomy 21, Trisomy 18, Trisomy 13, and Fetal SexGeorge Koumbaris, Elena Kypri, Kyriakos Tsangaras, et al.BMC Genetics|February 11, 2016
The CYLD p.R758X worldwide recurrent nonsense mutation detected in patients with multiple familial trichoepithelioma type 1, Brooke-Spiegler syndrome and familial cylindromatosis represents a mutational hotspot in the geneKatalin Farkas, Barbara Kocsis Deák, Laura Cubells Sánchez, et al.The British Journal of Dermatology|March 4, 2026
Targeting non-canonical NF-κB signalling in CYLD cutaneous syndrome by selective inhibition of IκB kinase alphaKirsty Hodgson, Joseph Inns, Gary Reynolds, et al.Pageof 7