Fabiana Scornik, PhD
Affiliations: | Masonic Medical Research Laboratory, Utica, Frankfort, NY, United States |
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"Fabiana Scornik"Mean distance: 17.21 (cluster 32) | S | N | B | C | P |
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Publications
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| Martínez-Moreno R, Carreras D, Sarquella-Brugada G, et al. (2023) Loss of sodium current caused by a Brugada syndrome-associated variant is determined by patient-specific genetic background. Heart Rhythm |
| Martínez-Moreno R, Pérez-Serra A, Selga E, et al. (2023) Generation of the induced pluripotent stem cell line ESi108-A from a familial atrial fibrillation patient. Stem Cell Research. 73: 103239 |
| 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 |