Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Chiara Mazzanti"'
Autor:
Leonela Luce, Micaela Carcione, Chiara Mazzanti, Paula I. Buonfiglio, Viviana Dalamón, Lilia Mesa, Alberto Dubrovsky, José Corderí, Florencia Giliberto
Publikováno v:
Frontiers in Pharmacology, Vol 12 (2021)
Dystrophinopathies cover a spectrum of rare progressive X-linked muscle diseases, arising from DMD mutations. They are among the most common pediatric muscular dystrophies, being Duchenne muscular dystrophy (DMD) the most severe form. Despite the fac
Externí odkaz:
https://doaj.org/article/9670f28779b84c91968bfc80279f7db4
Autor:
James S. Lawson, Chiara Mazzanti, Prospero Civita, Michele Menicagli, Christopher C. Ngan, Noel J. Whitaker, Jacob Hochman, Ori Braitbard, Benafsha Yosufi, Wendy K. Glenn
Publikováno v:
Frontiers in Oncology, Vol 8 (2018)
PurposeThe purpose of this study is to determine whether mouse mammary tumor virus (MMTV)-associated human breast cancer has the same or similar histology to MMTV-associated mouse mammary tumors. Such associations may indicate a role for MMTV in huma
Externí odkaz:
https://doaj.org/article/f45fdce3eba840249b9f5f848d9533a3
Publikováno v:
International Journal of Emotional Education, Vol 7, Iss 1, Pp 69-83 (2015)
A considerable amount of research has examined the link between children’s peer acceptance, which refers to the degree of likability within the peer group, social functioning and emotional wellbeing, at a same age and in a long term perspective, p
Externí odkaz:
https://doaj.org/article/fee20b327c42407489e25055d5d4893e
Autor:
Monica Miari, Erika Valli, Martina Bazzocchi, Fiorella Bestetti, Laura Del Gatto, Chiara Mazzanti, Simona Padonello, Luca Tagliani
Publikováno v:
IpoTESI di Preistoria, Vol 2, Iss 1, Pp 37-74 (2009)
The paper summarized the main results of the extensive archaeology excavation in the prehistoric settlement of Cattolica, via Carpignola (RN). The site is located near the Adriatic coast and along an ancient river. Several structures were identified,
Externí odkaz:
https://doaj.org/article/fbbe6d333b9b48608cb40c4de5b0f9fe
Autor:
Chiara Mazzanti, Liliana Francipane, Carlos Daniel de Brasi, Leonela Natalia Luce, Florencia Giliberto, Sebastián Menazzi, Pablo Lapunzina, Irene Szijan, Micaela Carcione, Liliana Carmen Rossetti, Julián Nevado, M. M. Abelleyro, Pamela Radic
Publikováno v:
Neuromuscular disorders : NMD. 31(3)
This work describes a family with Duchenne muscular dystrophy (DMD) with a rare case of a symptomatic pregnant woman. The main aim was to perform prenatal molecular diagnosis to provide genetic counseling. The secondary aim was to suggest the molecul
Autor:
Leonela Luce, Miguel Abelleyro, Micaela Carcione, Chiara Mazzanti, Liliana Rossetti, Pamela Radic, Irene Szijan, Sebasti n Menazzi, Liliana Francipane, Juli n Nevado, Pablo Lapunzina, Carlos De Brasi, Florencia Giliberto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a992f352db222400b70a2105183cc17
https://doi.org/10.22541/au.159242061.16003967
https://doi.org/10.22541/au.159242061.16003967
Autor:
Nicola Riccardo Pugliese, Cristian Scatena, Rossella Di Stefano, G. Naccarato, Iacopo Fabiani, Claudia Scopelliti, Marco Angelillis, Vitantonio Di Bello, Matteo Passiatore, Enrico Calogero, Elena Tantillo, Maria Chiara Mazzanti, Anna Sonia Petronio, Lorenzo Conte
Publikováno v:
Scientific Reports, Vol 8, Iss 1, Pp 1-10 (2018)
Scientific Reports
Scientific Reports
Aortic valve stenosis (AVS) represents a cluster of different phenotypes, considering gradient and flow pattern. Circulating micro RNAs may reflect specific pathophysiological processes and could be useful biomarkers to identify disease. We assessed
Autor:
Florencia Giliberto, Alberto Dubrovsky, Lilia Mesa, Jose Corderi, Micaela Carcione, Leonela Natalia Luce, Chiara Mazzanti
Publikováno v:
Neuromuscular Disorders. 31:S83
Autor:
Marcela Maria Ferrer, Florencia Giliberto, Irene Szijan, María Micaela Carcione, Chiara Mazzanti, Leonela Natalia Luce
Dystrophinopathies are neuromuscular X-linked recessive diseases caused by mutations in the DMD gene. This study aimed to identify DMD gene small mutations by Whole Exome Sequencing (WES), in order to confirm clinical diagnosis, identify candidates f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee85e19ce00931deca2b1cea1ec920fb
https://www.sciencedirect.com/science/article/pii/S0960896618301202
https://www.sciencedirect.com/science/article/pii/S0960896618301202
Autor:
María Micaela Carcione, Carlos Daniel de Brasi, Liliana Francipane, Julián Nevado, Pablo Lapunzina, Irena Szijan, Leonela Natalia Luce, Miguel Martin Abelleyro, Chiara Mazzanti, Liliana Carmen Rossetti, Florencia Giliberto, Sebastián Menazzi, Claudia Pamela Radic
Publikováno v:
Neuromuscular Disorders. 29:S170-S171
Fil: Luce, Leonela Natalia. Universidad de Buenos Aires. Facultad de Farmacia y Bioquimica. Departamento de Microbiologia, Inmunologia y Biotecnologia. Catedra de Genetica y Biologia Molecular; Argentina. Consejo Nacional de Investigaciones Cientific