Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Monica Sancandi"'
Autor:
Paolo Degan, Federico Cesarone, Proto Pippia, Annalisa Zunino, Silvia Viaggi, Angelo Abbondandolo, Laura Ottaggio, Monica Sancandi, Grazia Galleri
Publikováno v:
Journal of Cellular Biochemistry. 94:460-469
Exposure of freshly drawn lymphocytes and lymphoblastoid cells (LB and COR3) to simulated microgravity decreased the intracellular ATP concentration to 50%-40% of the value found in normal growth conditions. The decrease was reversible although recov
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78b66f0a57aab4e77c8494792e37d7ec
https://doi.org/10.1002/jcb.20302
https://doi.org/10.1002/jcb.20302
Autor:
Barbara Pesce, Jan Osinga, Giovanna Patrone, Robert M.W. Hofstra, Francesca Puppo, Roberto Ravazzolo, Marcella Devoto, Paola Griseri, Monica Sancandi, Isabella Ceccherini, Giovanni Romeo
Publikováno v:
American Journal of Human Genetics, 71(4), 969-974. CELL PRESS
Scopus-Elsevier
Scopus-Elsevier
Hirschsprung disease (HSCR) is a common genetic disorder characterized by intestinal obstruction secondary to enteric aganglionosis. HSCR demonstrates a complex pattern of inheritance, with the RET proto-oncogene acting as a major gene and with sever
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d397a4459136640b490080fabc98f10f
https://hdl.handle.net/11370/9c99e261-2d46-4e39-b06f-be6c3e57d4c8
https://hdl.handle.net/11370/9c99e261-2d46-4e39-b06f-be6c3e57d4c8
Autor:
Marcella Devoto, Giovanna Patrone, Robert M.W. Hofstra, Roberto Ravazzolo, Renata Bocciardi, Isabella Ceccherini, Monica Sancandi, Paola Griseri, Giovanni Romeo
Publikováno v:
European Journal of Human Genetics, 8(9), 721-724. Nature Publishing Group
Hirschsprung disease (HSCR) is an inherited disorder characterised by absence of intrinsic ganglion cells in the distal gastrointestinal tract. Different susceptibility genes, involved in either the Ret-tyrosine kinase or the endothelin signalling pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e04decb4c40f04db6cfe9e2df5ca6c76
https://research.rug.nl/en/publications/06a9d83b-e873-4528-8369-590d198383c5
https://research.rug.nl/en/publications/06a9d83b-e873-4528-8369-590d198383c5
Publikováno v:
Journal of Biomedical Science
Journal of Biomedical Science, Vol 17, Iss 1, p 63 (2010)
Journal of Biomedical Science, Vol 17, Iss 1, p 63 (2010)
Background Whether microgravity might influence tumour growth and carcinogenesis is still an open issue. It is not clear also if and how normal and transformed cells are differently solicited by microgravity. The present study was designed to verify
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d726f357ed41a4c2af687c456feb0004
https://pubmed.ncbi.nlm.nih.gov/20667080
https://pubmed.ncbi.nlm.nih.gov/20667080
Autor:
Andrea Armirotti, Laura Ottaggio, Alessandro Balbi, Gianluca Damonte, Federica Bestoso, Monica Sancandi, Mariangela Miele, Mauro Mazzei
Publikováno v:
Journal of natural products. 71(1)
Paclitaxel is an effective antineoplastic agent originally extracted in low yield from the bark of Taxus brevifolia. Although it was generally considered a particular metabolite of Taxus sp., paclitaxel was recently found in hazel cell cultures. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5946c1faa753500eeeacc602b24b9c90
https://pubmed.ncbi.nlm.nih.gov/18163585
https://pubmed.ncbi.nlm.nih.gov/18163585
Autor:
N. Lemort, Jean-Pierre Hugot, Pierre-Simon Jouk, Isabella Ceccherini, Nadege Bondurand, Michel Goossens, Monica Sancandi, Veronique Pingault
Editor—Hirschsprung disease and Waardenburg syndrome are congenital malformations involving neural crest derivatives. Several genes are involved in these diseases, defining a complex pattern of inheritance. Hirschsprung disease (HSCR) is characteri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcc54855356a5bea917e30341993a873
https://europepmc.org/articles/PMC1734825/
https://europepmc.org/articles/PMC1734825/
Autor:
Giovanna Patrone, Isabella Ceccherini, Giovanni Romeo, Giuseppe Martucciello, F Puppo, B Pesce, Marcella Devoto, Paola Griseri, Monica Sancandi, Roberto Ravazzolo, Margherita Lerone
Publikováno v:
Scopus-Elsevier
Hirschsprung’s disease is a congenital disorder characterised by intestinal obstruction caused by the absence of parasympathetic intrinsic ganglion cells along variable lengths of the colon.1 The high proportion of sporadic cases (80–90%), the va
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a4c38b170121337499ad71aa1813cb5
http://www.scopus.com/inward/record.url?eid=2-s2.0-0042329921&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0042329921&partnerID=MN8TOARS