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
5162004
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
2372006
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
2372006
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
2282007
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), 20, 2006
1872006
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
1482014
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
1262009
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
872013
Doubly heterozygous LMNA and TTN mutations revealed by exome sequencing in a severe form of dilated cardiomyopathy
R Roncarati, CV Anselmi, P Krawitz, G Lattanzi, Y Von Kodolitsch, ...
European journal of human genetics 21 (10), 1105-1111, 2013
742013
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
682013
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
532017
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
522012
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
292016
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
292016
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
252016
Positive selection in bone morphogenetic protein 15 targets a natural mutation associated with primary ovarian insufficiency in human
S Auclair, R Rossetti, C Meslin, O Monestier, E Di Pasquale, G Pascal, ...
PLoS One 8 (10), 2013
212013
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
202018
Generation of human cardiomyocytes: a differentiation protocol from feeder-free human induced pluripotent stem cells
E Di Pasquale, B Song, G Condorelli
JoVE (Journal of Visualized Experiments), e50429, 2013
202013
Lentiviral vectors and cardiovascular diseases: a genetic tool for manipulating cardiomyocyte differentiation and function
E Di Pasquale, MVG Latronico, GS Jotti, G Condorelli
Gene therapy 19 (6), 642-648, 2012
202012
A novel mutation in the BMP15 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, ...
192007
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