Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Rita Shulman"'
Autor:
Yuval Shemer, Lucy N. Mekies, Ronen Ben Jehuda, Polina Baskin, Rita Shulman, Binyamin Eisen, Danielle Regev, Eloisa Arbustini, Brenda Gerull, Mihaela Gherghiceanu, Eyal Gottlieb, Michael Arad, Ofer Binah
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 15, p 7874 (2021)
LMNA-related dilated cardiomyopathy is an inherited heart disease caused by mutations in the LMNA gene encoding for lamin A/C. The disease is characterized by left ventricular enlargement and impaired systolic function associated with conduction defe
Externí odkaz:
https://doaj.org/article/163d673b362e41caa67adca85983e315
Autor:
Revital Schick, Lucy N Mekies, Yuval Shemer, Binyamin Eisen, Tova Hallas, Ronen Ben Jehuda, Meital Ben-Ari, Agnes Szantai, Lubna Willi, Rita Shulman, Michael Gramlich, Luna Simona Pane, Ilaria My, Dov Freimark, Marta Murgia, Gianluca Santamaria, Mihaela Gherghiceanu, Michael Arad, Alessandra Moretti, Ofer Binah
Publikováno v:
PLoS ONE, Vol 13, Iss 10, p e0205719 (2018)
AIMS:Dilated cardiomyopathy (DCM), a myocardial disorder that can result in progressive heart failure and arrhythmias, is defined by ventricular chamber enlargement and dilatation, and systolic dysfunction. Despite extensive research, the pathologica
Externí odkaz:
https://doaj.org/article/e1a99e6238e543028fefdc138f726611
Autor:
Ofer Binah, Raz Palty, Rita Shulman, Polina Baskin, Jonatan Fernandez‐Gracia, Binyamin Eisen, Ronen Ben Jehuda, Lucy N. Mekies, Irina Reiter, Eyal Gottlieb, Danielle Regev, Michael Arad
Publikováno v:
Journal of Cellular and Molecular Medicine
Duchenne muscular dystrophy (DMD), caused by mutations in the dystrophin gene, is an X‐linked disease affecting male and rarely adult heterozygous females, resulting in death by the late 20s to early 30s. Previous studies reported depressed left ve
Autor:
Polina Baskin, Eloisa Arbustini, Ofer Binah, Mihaela Gherghiceanu, Binyamin Eisen, Michael Arad, Yuval Shemer, Lucy N. Mekies, Rita Shulman, Brenda Gerull, Danielle Regev, Eyal Gottlieb, Ronen Ben Jehuda
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 22, Iss 7874, p 7874 (2021)
Volume 22
Issue 15
International Journal of Molecular Sciences, Vol 22, Iss 7874, p 7874 (2021)
Volume 22
Issue 15
LMNA-related dilated cardiomyopathy is an inherited heart disease caused by mutations in the LMNA gene encoding for lamin A/C. The disease is characterized by left ventricular enlargement and impaired systolic function associated with conduction defe
Autor:
Yuval Shemer, Lubna Willi, Michael Arad, Michael Gramlich, Ofer Binah, Mihaela Gherghiceanu, Alessandra Moretti, Dov Freimark, Ronen Ben Jehuda, Rita Shulman, Meital Ben-Ari, Luna Simona Pane, Binyamin Eisen, Tova Hallas, Gianluca Santamaria, Revital Schick, Agnes Szantai, Lucy N. Mekies, Ilaria My, Marta Murgia
Publikováno v:
PLoS One
PLOS ONE
PLoS ONE
PLOS ONE 13(10), e0205719 (2018). doi:10.1371/journal.pone.0205719
PLoS ONE, Vol 13, Iss 10, p e0205719 (2018)
PLOS ONE
PLoS ONE
PLOS ONE 13(10), e0205719 (2018). doi:10.1371/journal.pone.0205719
PLoS ONE, Vol 13, Iss 10, p e0205719 (2018)
Aims Dilated cardiomyopathy (DCM), a myocardial disorder that can result in progressive heart failure and arrhythmias, is defined by ventricular chamber enlargement and dilatation, and systolic dysfunction. Despite extensive research, the pathologica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3123d25edbfb721332acd04884d6e3c7
https://hdl.handle.net/21.11116/0000-0002-F13F-821.11116/0000-0002-F140-521.11116/0000-0002-F13D-A
https://hdl.handle.net/21.11116/0000-0002-F13F-821.11116/0000-0002-F140-521.11116/0000-0002-F13D-A
Autor:
Ronit Shtrichman, Eyal Zussman, Ron Avrahami, Atara Novak, Bettina Fishman, Naama Zeevi-Levin, Lior Lowenstein, Efrat Barak, Rinat Zaid, Anna Ziskind, Erella Livne, Joseph Itskovitz-Eldor, Rita Shulman
Publikováno v:
Tissue engineering. Part A. 20(19-20)
Extracellular matrix (ECM) has been utilized as a biological scaffold for tissue engineering applications in a variety of body systems, due to its bioactivity and biocompatibility. In the current study we developed a modified protocol for the efficie