Elisa Di Pasquale
Elisa Di Pasquale
IRGB-CNR, UOS of Milan, Italy & Humanitas Research Hospital, Rozzano, Milan greater area, Italy
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Cited by
Cited by
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
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
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
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
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, 1-12, 2006
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
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
American heart association council on E, prevention statistics c, stroke statistics s. heart disease and stroke statistics-2019 update: a report from the American heart association
EJ Benjamin, P Muntner, A Alonso, MS Bittencourt, CW Callaway, ...
Circulation 139 (10), e56-e528, 2019
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), 14680, 2017
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
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
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), 2267, 2019
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
The broad spectrum of LMNA cardiac diseases: from molecular mechanisms to clinical phenotype
S Crasto, I My, E Di Pasquale
Frontiers in Physiology 11, 538082, 2020
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
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
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
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
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
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
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