Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Cristina Nodale"'
Autor:
Simona Ceccarelli, Cristina Nodale, Enrica Vescarelli, Paola Pontecorvi, Valeria Manganelli, Giovanni Casella, Maria Giuseppina Onesti, Maurizio Sorice, Ferdinando Romano, Antonio Angeloni, Cinzia Marchese
Publikováno v:
Stem Cells International, Vol 2018 (2018)
Adipogenesis is regulated by a complex network of molecules, including fibroblast growth factors. Keratinocyte growth factor (KGF) has been previously reported to promote proliferation on rat preadipocytes, although the expression of its specific rec
Externí odkaz:
https://doaj.org/article/7e0aa6a2f3874ee18dc50330cef62dda
Autor:
Cristina Nodale, Simona Ceccarelli, Mariateresa Giuliano, Marcella Cammarota, Sirio D'Amici, Enrica Vescarelli, Diana Maffucci, Filippo Bellati, Pierluigi Benedetti Panici, Ferdinando Romano, Antonio Angeloni, Cinzia Marchese
Publikováno v:
PLoS ONE, Vol 9, Iss 3, p e91010 (2014)
Mayer-Rokitansky-Küster-Hauser syndrome (MRKHS) is a rare disease characterized by congenital aplasia of uterus and vagina. Although many studies have investigated several candidate genes, up to now none of them seem to be responsible for the aetiol
Externí odkaz:
https://doaj.org/article/a68533579709469cb53d334b04136b6c
Autor:
David Givol, Valentina Folgiero, Cristina Nodale, Aurora Aiello, Alessia Garufi, Rita Falcioni, Gideon Rechavi, Jasmine Jacob-Hirsch, Gabriella D'Orazi, Michal Sheffer
Publikováno v:
Cancer Biology & Therapy. 13:198-205
Vimentin, a mesenchymal marker, is frequently overexpressed in epithelial carcinomas undergoing epithelial to mesenchymal transition (EMT), a condition correlated with invasiveness and poor prognosis. Therefore, vimentin is a potential molecular targ
Autor:
Filippo Bellati, Ferdinando Romano, Enrica Vescarelli, Simona Ceccarelli, Diana Maffucci, Cinzia Marchese, Antonio Angeloni, Pierluigi Benedetti Panici, Mariateresa Giuliano, Cristina Nodale, Sirio D'Amici, Marcella Cammarota
Publikováno v:
PLoS ONE, Vol 9, Iss 3, p e91010 (2014)
PLoS ONE
PLoS ONE
Mayer-Rokitansky-Kuster-Hauser syndrome (MRKHS) is a rare disease characterized by congenital aplasia of uterus and vagina. Although many studies have investigated several candidate genes, up to now none of them seem to be responsible for the aetiolo
Autor:
Simona Ceccarelli, Ferdinando Romano, Pierluigi Benedetti Panici, Sirio D'Amici, Diana Maffucci, Cristina Nodale, Cinzia Marchese, Antonio Angeloni, Enrica Vescarelli, Marco Monti
Publikováno v:
BioMed Research International, Vol 2014 (2014)
BioMed Research International
BioMed Research International
Mayer-Rokitansky-Küster-Hauser (MRKH) is a rare syndrome characterized by congenital aplasia of the uterus and vagina. The most common procedure used for surgical reconstruction of the neovagina is the McIndoe vaginoplasty, which consists in creatio