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FABIANA SILVIA SCORNIK GERZENSTEIN

Firma
FABIANA SILVIA SCORNIK-GERZENSTEIN
Posición
Investigador/a Consolidat - R3
Investigador/a Consolidado - R3

Publicacions

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Generation of four induced pluripotent stem cell lines from a family harboring a single nucleotide variant in SCN5A

STEM CELL RESEARCH, 2022, 63, 102847-102847 dx.doi.org/10.1016/j.scr.2022.102847
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Generation of an induced pluripotent stem cell line from a healthy Caucasian male

STEM CELL RESEARCH, 2022, 60, 102717-102717 dx.doi.org/10.1016/j.scr.2022.102717

Carreras D, Martinez-Moreno R, Pinsach-Abuin ML, Santafe MM, Gomà P, Brugada R, Scornik FS, Pérez GJ, Pagans S

Epigenetic Changes Governing Scn5a Expression in Denervated Skeletal Muscle

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2021, 22 dx.doi.org/10.3390/ijms22052755

Martinez-Moreno R, Selga E, Riuró H, Carreras D, Parnes M, Srinivasan C, Wangler MF, Pérez GJ, Scornik FS, Brugada R

An SCN1B Variant Affects Both Cardiac-Type (Na(V)1.5) and Brain-Type (Na(V)1.1) Sodium Currents and Contributes to Complex Concomitant Brain and Cardiac Disorders

Frontiers in Cell and Developmental Biology, 2020, 8, 528742-528742 dx.doi.org/10.3389/fcell.2020.528742

Cuyàs E, Gumuzio J, Lozano-Sánchez J, Carreras D, Verdura S, Llorach-Parés L, Sanchez-Martinez M, Selga E, Pérez GJ, Scornik FS, Brugada R, Bosch-Barrera J, Segura-Carretero A, Martin ÁG, Encinar JA, Menendez JA

Extra Virgin Olive Oil Contains a Phenolic Inhibitor of the Histone Demethylase LSD1/KDM1A

Nutrients, 2019, 11 dx.doi.org/10.3390/nu11071656

Sendfeld F, Selga E, Scornik FS, Pérez GJ, Mills NL, Brugada R

Experimental Models of Brugada syndrome

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2019, 20 dx.doi.org/10.3390/ijms20092123

Yeste M, Llavanera M, Pérez G, Scornik F, Puig-Parri J, Brugada R, Bonet S, Pinart E

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, 2019, 20 dx.doi.org/10.3390/ijms20246330

Santori M, Gil R, Blanco-Verea A, Riuró H, Díaz-Castro Ó, López-Abel B, Brugada R, Carracedo Á, Pérez GJ, Scornik FS, Brion M

Sudden infant death as the most severe phenotype caused by genetic modulation in a family with atrial fibrillation

FORENSIC SCIENCE INTERNATIONAL-GENETICS, 2019, 43, 102159-102159 dx.doi.org/10.1016/j.fsigen.2019.102159

Selga E, Sendfeld F, Martinez-Moreno R, Medine CN, Tura-Ceide O, Wilmut SI, Pérez GJ, Scornik FS, Brugada R, Mills NL

Sodium channel current loss of function in induced pluripotent stem cell-derived cardiomyocytes from a Brugada syndrome patient

JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2018, 114, 10-19 dx.doi.org/10.1016/j.yjmcc.2017.10.002

Riuró H, Campuzano O, Berne P, Arbelo E, Iglesias A, Pérez-Serra A, Coll-Vidal M, Partemi S, Mademont-Soler I, Picó F, Allegue C, Oliva A, Gerstenfeld E, Sarquella-Brugada G, Castro-Urda V, Fernández-Lozano I, Mont L, Brugada J, Scornik FS, Brugada R

Genetic analysis, in silico prediction, and family segregation in long QT syndrome.

EUROPEAN JOURNAL OF HUMAN GENETICS, 2015, 23, 79-85 dx.doi.org/10.1038/ejhg.2014.54

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