Guillermo Pérez, PhD

Masonic Medical Research Laboratory, Utica, Frankfort, NY, United States 
"Guillermo Pérez"
Mean distance: 17.21 (cluster 32)
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Martínez-Moreno R, Carreras D, Aran B, et al. (2022) Generation of four induced pluripotent stem cell lines from a family harboring a single nucleotide variant in SCN5A. Stem Cell Research. 63: 102847
Martínez-Moreno R, Pérez-Serra A, Carreras D, et al. (2022) Generation of an induced pluripotent stem cell line from a healthy Caucasian male. Stem Cell Research. 60: 102717
Carreras D, Martinez-Moreno R, Pinsach-Abuin ML, et al. (2021) Epigenetic Changes Governing Expression in Denervated Skeletal Muscle. International Journal of Molecular Sciences. 22
Martinez-Moreno R, Selga E, Riuró H, et al. (2020) An Variant Affects Both Cardiac-Type (Na1.5) and Brain-Type (Na1.1) Sodium Currents and Contributes to Complex Concomitant Brain and Cardiac Disorders. Frontiers in Cell and Developmental Biology. 8: 528742
Martinez-Moreno R, Carreras D, Selga E, et al. (2020) Comparative Study of the Effects of an SCN5A Mutation within a Family Diagnosed with Brugada Syndrome using iPS-CM Biophysical Journal. 118: 500a
Carreras D, Martinez-Moreno R, Selga E, et al. (2020) CPVT-Associated Mutation P.G357S-RYR2 Promotes a Gain of Function in Patient-Specific Induced Pluripotent Stem Cell-Derived Cardiomyocytes (iPS-CM) Biophysical Journal. 118: 255a
Yeste M, Llavanera M, Pérez G, et al. (2019) Elucidating the Role of K Channels during In Vitro Capacitation of Boar Spermatozoa: Do SLO1 Channels Play a Crucial Role? International Journal of Molecular Sciences. 20
Santori M, Gil R, Blanco-Verea A, et al. (2019) Sudden infant death as the most severe phenotype caused by genetic modulation in a family with atrial fibrillation. Forensic Science International. Genetics. 43: 102159
Cuyàs E, Gumuzio J, Lozano-Sánchez J, et al. (2019) Extra Virgin Olive Oil Contains a Phenolic Inhibitor of the Histone Demethylase LSD1/KDM1A. Nutrients. 11
Sendfeld F, Selga E, Scornik FS, et al. (2019) Experimental Models of Brugada syndrome. International Journal of Molecular Sciences. 20
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