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Elisa Di Pasquale
Elisa Di Pasquale
IRGB-CNR, UOS of Milan, Italy & Humanitas Research Hospital, Rozzano, Milan greater area, Italy
Verified email at irgb.cnr.it
Title
Cited by
Cited by
Year
Hypergonadotropic ovarian failure associated with an inherited mutation of human bone morphogenetic protein-15 (BMP15) gene
E Di Pasquale, P Beck-Peccoz, L Persani
The American Journal of Human Genetics 75 (1), 106-111, 2004
5822004
A novel mutation in the bone morphogenetic protein 15 gene causing defective protein secretion is associated with both increased ovulation rate and sterility in Lacaune sheep
L Bodin, E Di Pasquale, S Fabre, M Bontoux, P Monget, L Persani, ...
Endocrinology 148 (1), 393-400, 2007
2812007
Identification of New Variants of Human BMP15 Gene in a Large Cohort of Women with Premature Ovarian Failure
E Di Pasquale, R Rossetti, A Marozzi, B Bodega, S Borgato, L Cavallo, ...
The Journal of Clinical Endocrinology & Metabolism 91 (5), 1976-1979, 2006
2652006
Identification of New Variants of Human BMP15 Gene in a Large Cohort of Women with Premature Ovarian Failure
E Di Pasquale, R Rossetti, A Marozzi, B Bodega, S Borgato, L Cavallo, ...
The Journal of Clinical Endocrinology & Metabolism 91 (5), 1976-1979, 2006
2652006
Regulation of ovulation rate in mammals: contribution of sheep genetic models
S Fabre, A Pierre, P Mulsant, L Bodin, E Di Pasquale, L Persani, ...
Reproductive Biology and Endocrinology 4 (1), 1-12, 2006
2372006
The fundamental role of bone morphogenetic protein 15 in ovarian function and its involvement in female fertility disorders
L Persani, R Rossetti, E Di Pasquale, C Cacciatore, S Fabre
Human reproduction update 20 (6), 869-883, 2014
2252014
BMP15 mutations associated with primary ovarian insufficiency cause a defective production of bioactive protein
R Rossetti, E Di Pasquale, A Marozzi, S Bione, D Toniolo, P Grammatico, ...
Human mutation 30 (5), 804-810, 2009
1472009
T cell costimulation blockade blunts pressure overload-induced heart failure
M Kallikourdis, E Martini, P Carullo, C Sardi, G Roselli, CM Greco, ...
Nature communications 8 (1), 1-14, 2017
1262017
CaMKII inhibition rectifies arrhythmic phenotype in a patient-specific model of catecholaminergic polymorphic ventricular tachycardia
E Di Pasquale, F Lodola, M Miragoli, M Denegri, JE Avelino-Cruz, ...
Cell death & disease 4 (10), e843-e843, 2013
1242013
Doubly heterozygous LMNA and TTN mutations revealed by exome sequencing in a severe form of dilated cardiomyopathy
R Roncarati, C Viviani Anselmi, P Krawitz, G Lattanzi, Y Von Kodolitsch, ...
European Journal of Human Genetics 21 (10), 1105-1111, 2013
942013
Induced pluripotent stem cell–derived cardiomyocytes in studies of inherited arrhythmias
SG Priori, C Napolitano, E Di Pasquale, G Condorelli
The Journal of clinical investigation 123 (1), 84-91, 2013
792013
Post-natal cardiomyocytes can generate iPS cells with an enhanced capacity toward cardiomyogenic re-differentation
R Rizzi, E Di Pasquale, P Portararo, R Papait, P Cattaneo, MVG Latronico, ...
Cell Death & Differentiation 19 (7), 1162-1174, 2012
692012
The K219T-Lamin mutation induces conduction defects through epigenetic inhibition of SCN5A in human cardiac laminopathy
N Salvarani, S Crasto, M Miragoli, A Bertero, M Paulis, P Kunderfranco, ...
Nature communications 10 (1), 1-16, 2019
642019
DOT1L-mediated H3K79me2 modification critically regulates gene expression during cardiomyocyte differentiation
P Cattaneo, P Kunderfranco, C Greco, A Guffanti, GG Stirparo, F Rusconi, ...
Cell Death & Differentiation 23 (4), 555-564, 2016
632016
Adeno-associated virus-mediated CASQ2 delivery rescues phenotypic alterations in a patient-specific model of recessive catecholaminergic polymorphic ventricular tachycardia
F Lodola, D Morone, M Denegri, R Bongianino, H Nakahama, ...
Cell death & disease 7 (10), e2393-e2393, 2016
492016
Growth hormone-releasing hormone attenuates cardiac hypertrophy and improves heart function in pressure overload-induced heart failure
I Gesmundo, M Miragoli, P Carullo, L Trovato, V Larcher, E Di Pasquale, ...
Proceedings of the National Academy of Sciences 114 (45), 12033-12038, 2017
422017
Cofilin-1 phosphorylation catalyzed by ERK1/2 alters cardiac actin dynamics in dilated cardiomyopathy caused by lamin A/C gene mutation
M Chatzifrangkeskou, D Yadin, T Marais, S Chardonnet, ...
Human Molecular Genetics 27 (17), 3060-3078, 2018
412018
Peptidomimetic Targeting of Cavβ2 Overcomes Dysregulation of the L-Type Calcium Channel Density and Recovers Cardiac Function
F Rusconi, P Ceriotti, M Miragoli, P Carullo, N Salvarani, M Rocchetti, ...
Circulation 134 (7), 534-546, 2016
412016
Human iPSC modelling of a familial form of atrial fibrillation reveals a gain of function of If and ICaL in patient-derived cardiomyocytes
P Benzoni, G Campostrini, S Landi, V Bertini, E Marchina, M Iascone, ...
Cardiovascular research 116 (6), 1147-1160, 2020
372020
Toward cardiac regeneration: combination of pluripotent stem cell-based therapies and bioengineering strategies
M Mazzola, E Di Pasquale
Frontiers in Bioengineering and Biotechnology 8, 455, 2020
352020
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