المؤلفون: Elena Sommariva, Ilaria Stadiotti, Michela Casella, Valentina Catto, Antonio Dello Russo, Corrado Carbucicchio, Lorenzo Arnaboldi, Simona De Metrio, Giuseppina Milano, Alessandro Scopece, Manuel Casaburo, Daniele Andreini, Saima Mushtaq, Edoardo Conte, Mattia Chiesa, Walter Birchmeier, Elisa Cogliati, Adolfo Paolin, Eva König, Viviana Meraviglia, Monica De Musso, Chiara Volani, Giada Cattelan, Werner Rauhe, Linda Turnu, Benedetta Porro, Matteo Pedrazzini, Marina Camera, Alberto Corsini, Claudio Tondo, Alessandra Rossini, Giulio Pompilio

المصدر: EMBO Molecular Medicine, Vol 13, Iss 9, Pp n/a-n/a (2021)

مصطلحات موضوعية: Arrhythmogenic Cardiomyopathy, ARVC, adipogenesis, oxidative stress, lipoproteins, Medicine (General), R5-920, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1757-4676; https://doaj.org/toc/1757-4684

URL الوصول: https://doaj.org/article/301c35b9793845e3942738060fda5380

المؤلفون: Luca Lavra, Fiorenza Magi, Alessandra Ulivieri, Alessandra Morgante, Marianna Paulis, Luca Sala, Matteo Pedrazzini, Patrizio Polisca, Marcella Rocchetti, Leonardo Calò, Salvatore Sciacchitano, Leila B. Salehi

المصدر: Stem Cell Research, Vol 54, Iss , Pp 102418- (2021)

مصطلحات موضوعية: Biology (General), QH301-705.5

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S1873506121002646; https://doaj.org/toc/1873-5061

URL الوصول: https://doaj.org/article/3dee8cd02ef6407b96a8a6deaf2c1067

المؤلفون: Melania Lippi, Mattia Chiesa, Ciro Ascione, Matteo Pedrazzini, Saima Mushtaq, Davide Rovina, Daniela Riggio, Anna Maria Di Blasio, Maria Luisa Biondi, Giulio Pompilio, Gualtiero I. Colombo, Michela Casella, Valeria Novelli, Elena Sommariva

المصدر: Biomolecules, Vol 12, Iss 8, p 1043 (2022)

مصطلحات موضوعية: arrhythmogenic cardiomyopathy, cardiovascular genetics, genotype-phenotype correlation, desmosomal genes, rare variants, common variants, Microbiology, QR1-502

وصف الملف: electronic resource

Relation: https://www.mdpi.com/2218-273X/12/8/1043; https://doaj.org/toc/2218-273X

URL الوصول: https://doaj.org/article/371c9cc628b542988473d2506becada5

المؤلفون: Paolo Catarsi, Vittorio Rosti, Giacomo Morreale, Valentina Poletto, Laura Villani, Roberto Bertorelli, Matteo Pedrazzini, Michele Zorzetto, Giovanni Barosi, AGIMM investigators

المصدر: PLoS ONE, Vol 10, Iss 1, p e0116636 (2015)

مصطلحات موضوعية: Medicine, Science

وصف الملف: electronic resource

Relation: http://europepmc.org/articles/PMC4305294?pdf=render; https://doaj.org/toc/1932-6203

URL الوصول: https://doaj.org/article/99ef3155e07f4776bba441adb5fa85ce

المؤلفون: Carla Spazzolini, Isabelle Denjoy, Roel L.H.M.G. Spätjens, Peter J. Schwartz, Maria Christina Kotta, Paul A. Brink, Cristina Moreno, Kristina H. Haugaa, Sandrine R.M. Seyen, Maria Shkolnikova, Federica Dagradi, Lia Crotti, Marshall Heradien, Paul G.A. Volders, Silvia Castelletti, Matteo Pedrazzini

المساهمون: Schwartz, P, Moreno, C, Kotta, M, Pedrazzini, M, Crotti, L, Dagradi, F, Castelletti, S, Haugaa, K, Denjoy, I, Shkolnikova, M, Brink, P, Heradien, M, Seyen, S, Spatjens, R, Spazzolini, C, Volders, P, RS: Carim - H04 Arrhythmogenesis and cardiogenetics, Cardiologie, MUMC+: MA Med Staf Spec Cardiologie (9)

المصدر: Eur Heart J
European Heart Journal, 42(46), 4743-4755. Oxford University Press

مصطلحات موضوعية: medicine.medical_specialty, Long QT syndrome, Romano-Ward Syndrome, Mutation, Missense, Fast Track Clinical Research, REQUIREMENT, Stimulation, VARIANTS, medicine.disease_cause, PHENOTYPE, QT interval, Sudden cardiac death, MECHANISMS, chemistry.chemical_compound, Genetic, CHANNEL, Internal medicine, medicine, Clinical endpoint, Genetics, Missense mutation, Humans, Cyclic adenosine monophosphate, Mutation, business.industry, KVLQT1, medicine.disease, GENOTYPE, DOMINANT-NEGATIVE SUPPRESSION, chemistry, KCNQ1 Potassium Channel, Cardiology, GENETIC MODIFIER, Cardiology and Cardiovascular Medicine, business, LANGE-NIELSEN-SYNDROME

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::844d33f416c443ba9630554a3eb61ac2
https://doi.org/10.1093/eurheartj/ehab582

المؤلفون: Enrico Ammirati, Francesca Raimondi, Nicolas Piriou, Loren Sardo Infirri, Saidi A. Mohiddin, Andrea Mazzanti, Chetan Shenoy, Ugo A. Cavallari, Massimo Imazio, Giovanni Donato Aquaro, Iacopo Olivotto, Patrizia Pedrotti, Neha Sekhri, Caroline M. Van de Heyning, Glenn Broeckx, Giovanni Peretto, Oliver Guttmann, Santo Dellegrottaglie, Alessandra Scatteia, Piero Gentile, Marco Merlo, Randal I. Goldberg, Alex Reyentovich, Christopher Sciamanna, Sabine Klaassen, Wolfgang Poller, Cory R. Trankle, Antonio Abbate, Andre Keren, Smadar Horowitz-Cederboim, Julia Cadrin-Tourigny, Rafik Tadros, Giuseppe A. Annoni, Emanuela Bonoldi, Claire Toquet, Lara Marteau, Vincent Probst, Jean Noël Trochu, Antheia Kissopoulou, Aurelia Grosu, Deni Kukavica, Alessandro Trancuccio, Cristina Gil, Giacomo Tini, Matteo Pedrazzini, Margherita Torchio, Gianfranco Sinagra, Juan Ramón Gimeno, Davide Bernasconi, Maria Grazia Valsecchi, Karin Klingel, Eric D. Adler, Paolo G. Camici, Leslie T. Cooper

المساهمون: Ammirati, Enrico, Raimondi, Francesca, Piriou, Nicola, Sardo Infirri, Loren, Mohiddin, Saidi A, Mazzanti, Andrea, Shenoy, Chetan, Cavallari, Ugo A, Imazio, Massimo, Aquaro, Giovanni Donato, Olivotto, Iacopo, Pedrotti, Patrizia, Sekhri, Neha, Van de Heyning, Caroline M, Broeckx, Glenn, Peretto, Giovanni, Guttmann, Oliver, Dellegrottaglie, Santo, Scatteia, Alessandra, Gentile, Piero, Merlo, Marco, Goldberg, Randal I, Reyentovich, Alex, Sciamanna, Christopher, Klaassen, Sabine, Poller, Wolfgang, Trankle, Cory R, Abbate, Antonio, Keren, Andre, Horowitz-Cederboim, Smadar, Cadrin-Tourigny, Julia, Tadros, Rafik, Annoni, Giuseppe A, Bonoldi, Emanuela, Toquet, Claire, Marteau, Lara, Probst, Vincent, Trochu, Jean Noël, Kissopoulou, Antheia, Grosu, Aurelia, Kukavica, Deni, Trancuccio, Alessandro, Gil, Cristina, Tini, Giacomo, Pedrazzini, Matteo, Torchio, Margherita, Sinagra, Gianfranco, Gimeno, Juan Ramón, Bernasconi, Davide, Valsecchi, Maria Grazia, Klingel, Karin, Adler, Eric D, Camici, Paolo G, Cooper, Leslie T

المصدر: JACC : heart failure

مصطلحات موضوعية: acute myocarditi, acute myocarditis, desmoplakin, desmosomal gene variant, desmosomal gene variants, cardiac magnetic resonance, prognosis, Human medicine, Cardiology and Cardiovascular Medicine

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca408b33ad40045ee3045463d0bf5c37

المؤلفون: Eleonora Torre, Peter J. Schwartz, Lia Crotti, Yee-Ki Lee, Matteo Pedrazzini, Pak C. Sham, Massimiliano Gnecchi, Xinru Ran, Hung-Fat Tse, Manuela Mura, Timothy Shin Heng Mak, Marcella Rocchetti, Luca Sala, Antonio Zaza

المساهمون: Lee, Y, Sala, L, Mura, M, Rocchetti, M, Pedrazzini, M, Ran, X, Mak, T, Crotti, L, Sham, P, Torre, E, Zaza, A, Schwartz, P, Tse, H, Gnecchi, M

المصدر: Cardiovascular Research

مصطلحات موضوعية: Physiology, Nedd4 Ubiquitin Protein Ligases, Arrhythmias, 030204 cardiovascular system & hematology, medicine.disease_cause, Electrocardiography, 0302 clinical medicine, BIO/09 - FISIOLOGIA, AcademicSubjects/MED00200, Myocytes, Cardiac, KvLQT1, Variant, Cells, Cultured, Exome sequencing, Genetics, 0303 health sciences, Mutation, biology, Variants, Protein Tyrosine Phosphatases, Non-Receptor, Phenotype, 3. Good health, KCNQ1 Potassium Channel, Long QT syndrome, Cardiology and Cardiovascular Medicine, Arrhythmia, Induced Pluripotent Stem Cells, hERG, Protein degradation, Polymorphism, Single Nucleotide, Cardiac Electrophysiology and Arrhythmia, 03 medical and health sciences, Physiology (medical), Nedd4L, medicine, Humans, Genetic Predisposition to Disease, 030304 developmental biology, NEDD4L, Genes, Modifier, business.industry, Induced pluripotent stem cell, Original Articles, medicine.disease, MTMR4, Proteolysis, biology.protein, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32cc88419b4b4f81213718f89e0eb94d
https://doi.org/10.1093/cvr/cvaa019

المؤلفون: Alberto Corsini, Lorenzo Arnaboldi, Ilaria Stadiotti, Giuseppina Milano, Edoardo Conte, Claudio Tondo, Saima Mushtaq, Giada Cattelan, Eva König, Daniele Andreini, Elena Sommariva, Giulio Pompilio, Elisa Cogliati, Monica De Musso, Adolfo Paolin, Walter Birchmeier, Alessandro Scopece, Viviana Meraviglia, Valentina Catto, Corrado Carbucicchio, Chiara Volani, Linda Turnu, Mattia Chiesa, Antonio Russo, Werner Rauhe, Manuel Casaburo, Simona De Metrio, Alessandra Rossini, Michela Casella, Matteo Pedrazzini, Benedetta Porro, Marina Camera

المصدر: EMBO Molecular Medicine
EMBO Molecular Medicine, Vol 13, Iss 9, Pp n/a-n/a (2021)

مصطلحات موضوعية: Medicine (General), Cancer Research, media_common.quotation_subject, CD36, Cell, Cardiomyopathy, QH426-470, medicine.disease_cause, Cardiovascular System, Article, adipogenesis, Mice, R5-920, Downregulation and upregulation, Risk Factors, Genetics, medicine, ARVC, oxidative stress, Animals, Humans, News & Views, Internalization, Arrhythmogenic Cardiomyopathy, Arrhythmogenic Right Ventricular Dysplasia, media_common, biology, business.industry, Arrhythmias, Cardiac, Articles, medicine.disease, lipoproteins, Lipoproteins, LDL, medicine.anatomical_structure, Phenotype, Adipogenesis, Cancer research, biology.protein, Molecular Medicine, lipids (amino acids, peptides, and proteins), business, Oxidative stress, Lipoprotein

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2520b864a94d36a506fdb28f0baf3022
http://edoc.mdc-berlin.de/20806/8/20806oa.pdf

المؤلفون: Krystian, Kozek, Yuko, Wada, Luca, Sala, Isabelle, Denjoy, Christian, Egly, Matthew J, O'Neill, Takeshi, Aiba, Wataru, Shimizu, Naomasa, Makita, Taisuke, Ishikawa, Lia, Crotti, Carla, Spazzolini, Maria-Christina, Kotta, Federica, Dagradi, Silvia, Castelletti, Matteo, Pedrazzini, Massimiliano, Gnecchi, Antoine, Leenhardt, Joe-Elie, Salem, Seiko, Ohno, Yi, Zuo, Andrew M, Glazer, Jonathan D, Mosley, Dan M, Roden, Bjorn C, Knollmann, Jeffrey D, Blume, Fabrice, Extramiana, Peter J, Schwartz, Minoru, Horie, Brett M, Kroncke

المصدر: Circ Genom Precis Med

مصطلحات موضوعية: ERG1 Potassium Channel, Heterozygote, Long QT Syndrome, INDEL Mutation, Mutation, Missense, Humans, Article

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::f027932df3a42415a51e33c8d5e261f4
https://pubmed.ncbi.nlm.nih.gov/34309407

المؤلفون: Matteo Pedrazzini, Alessandra Morgante, Marianna Paulis, Salvatore Sciacchitano, Fiorenza Magi, Leonardo Calò, Alessandra Ulivieri, Marcella Rocchetti, Luca Lavra, Leila B. Salehi, Luca Sala, Patrizio Polisca

المساهمون: Lavra, L, Magi, F, Ulivieri, A, Morgante, A, Paulis, M, Sala, L, Pedrazzini, M, Polisca, P, Rocchetti, M, Calo, L, Sciacchitano, S, Salehi, L

المصدر: Stem Cell Research, Vol 54, Iss, Pp 102418-(2021)

مصطلحات موضوعية: 0301 basic medicine, QH301-705.5, induced pluripotent stem cells, Romano-Ward Syndrome, Germ layer, Biology, medicine.disease_cause, Induced Pluripotent Stem Cell, Cell Line, 03 medical and health sciences, 0302 clinical medicine, cell Line, humans, KCNQ1 potassium channel, mutation, medicine, Biology (General), Induced pluripotent stem cell, Mutation, Cell Biology, General Medicine, Cell biology, 030104 developmental biology, KCNQ1 Potassium Channel, Reprogramming, Ipsc line, 030217 neurology & neurosurgery, Developmental Biology, Human

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd04edd4aa821b1df06bf4d020d8ac89
http://hdl.handle.net/10281/339398