Zobrazeno 1 - 10
of 59
pro vyhledávání: '"Ranzani, Guglielmina N."'
Autor:
De Gregori, Manuela, Diatchenko, Luda, Ingelmo, Pablo M., Napolioni, Valerio, Klepstad, Pal, Belfer, Inna, Molinaro, Valeria, Garbin, Giulia, Ranzani, Guglielmina N., Alberio, Giovanni, Normanno, Marco, Lovisari, Federica, Somaini, Marta, Govoni, Stefano, Mura, Elisa, Bugada, Dario, Niebel, Thekla, Zorzetto, Michele, De Gregori, Simona, Molinaro, Mariadelfina, Fanelli, Guido, Allegri, Massimo
Publikováno v:
In The Journal of Pain May 2016 17(5):628-636
Autor:
Venesio, Tiziana, Balsamo, Antonella, Errichiello, Edoardo, Ranzani, Guglielmina N, Risio, Mauro
Publikováno v:
In Modern Pathology October 2013 26(10):1371-1381
Autor:
De Gregori, Manuela, De Gregori, Simona, Ranzani, Guglielmina N., Allegri, Massimo, Govoni, Stefano, Regazzi, Mario
Publikováno v:
In European Journal of Pain Supplements 2010 4(4):245-250
Autor:
Venesio, Tiziana ∗, Molatore, Sara, Cattaneo, Francesca, Arrigoni, Arrigo, Risio, Mauro ∗, Ranzani, Guglielmina N. *
Publikováno v:
In Gastroenterology 2004 126(7):1681-1685
Autor:
Weren, Robbert D A, van der Post, Rachel S, Vogelaar, Ingrid P, van Krieken, J Han, Spruijt, Liesbeth, Lubinski, Jan, Jakubowska, Anna, Teodorczyk, Urszula, Aalfs, Cora M, van Hest, Liselotte P, Oliveira, Carla, Kamping, Eveline J, Schackert, Hans K, Ranzani, Guglielmina N, Gómez García, Encarna B, Hes, Frederik J, Holinski-Feder, Elke, Genuardi, Maurizio, Ausems, Margreet G E M, Sijmons, Rolf H, Wagner, Anja, van der Kolk, Lizet E, Cats, Annemieke, Bjørnevoll, Inga, Hoogerbrugge, Nicoline, Ligtenberg, Marjolijn J L
Publikováno v:
JOURNAL OF MEDICAL GENETICS, 55(10), 669-674. BMJ PUBLISHING GROUP
BACKGROUND: In approximately 10% of all gastric cancer (GC) cases, a heritable cause is suspected. A subset of these cases have a causative germlineCDH1mutation; however, in most cases the cause remains unknown. Our objective was to assess to what ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::1a22200ad379dc9ff7d211e315c4c738
https://research.rug.nl/en/publications/05c5a3d7-a064-4061-a7c1-71023585d6b6
https://research.rug.nl/en/publications/05c5a3d7-a064-4061-a7c1-71023585d6b6
Rb and TP53 Pathway Alterations in Sporadic and NF1-Related Malignant Peripheral Nerve Sheath Tumors
Autor:
Birindelli, Sarah, Perrone, Federica, Oggionni, Maria, Lavarino, Cinzia, Pasini, Barbara, Vergani, Barbara, Ranzani, Guglielmina N, Pierotti, Marco A, Pilotti, Silvana
Publikováno v:
In Laboratory Investigation 1 June 2001 81(6):833-844
Autor:
Matei Irina, Herlea Vlad, Ranzani Guglielmina N, Amadori Dino, Calin George, Barbanti-Brodano Giuseppe, Negrini Massimo
Publikováno v:
BMC Genetics, Vol 2, Iss 1, p 14 (2001)
Abstract Background Genomic instability has been reported at microsatellite tracts in few coding sequences. We have shown that the Bloom syndrome BLM gene may be a target of microsatelliteinstability (MSI) in a short poly-adenine repeat located in it
Externí odkaz:
https://doaj.org/article/baf1d33fe375473dadd03d5b919c83cd
Akademický článek
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Autor:
Calin, George1,2 George.Calin@mail.tju.edu, Ranzani, Guglielmina N.3 ranzani@jpvgen.unipv.it, Amadori, Dino4 dino.amadori@hotmail.com, Herlea, Vlad5 vlad_herlea@hotmail.com, Matei, Irina6,7 matei_irina@hotmail.com, Barbanti-Brodano, Giuseppe1 zcp@unife.it, Negrini, Massimo1 ngm@dns.umfe.it
Publikováno v:
BMC Genetics. 2001, Vol. 2, p1-7. 7p. 1 Diagram, 2 Charts.
Autor:
Vogelaar, Ingrid P., Ligtenberg, Marjolijn J. L., van der Post, Rachel S., de Voer, Richarda M., Kets, C. Marleen, Jansen, Trees J. G., Jacobs, Liesbeth, Schreibelt, Gerty, de Vries, I. Jolanda M., Netea, Mihai G., Hoogerbrugge, Nicoline, Lubinski, Jan, Jakubowska, Anna, Teodorczyk, Urszula, Schackert, Hans K., Aalfs, Cora M., Gómez García, Encarna B., Ranzani, Guglielmina N., Molinaro, Valeria, van Hest, Liselotte P., Hes, Frederik J., Holinski Feder, Elke, Genuardi, Maurizio, Ausems, Margreet G. E. M., Sijmons, Rolf H., Wagner, Anja, van der Kolk, Lizet E., Pinheiro, Hugo, Oliveira, Carla, Bjørnevoll, Inga, Høberg Vetti, Hildegunn, Han, J., van Krieken, J. M.
Publikováno v:
Familial Cancer, 15(2), 289-296. Springer Netherlands
Familial Cancer, 15(2), 289-296
Familial Cancer
Familial Cancer, 15(2), 289. Springer Netherlands
Familial Cancer, 15, 289-96
Vogelaar, I P, Ligtenberg, M J L, van der Post, R S, de Voer, R M, Kets, C M, Jansen, T J G, Jacobs, L, Schreibelt, G, de Vries, I J M, Netea, M G, Hoogerbrugge, N & International Gastric Cancer Genetics Group 2016, ' Recurrent candidiasis and early-onset gastric cancer in a patient with a genetically defined partial MYD88 defect ', Familial Cancer, vol. 15, no. 2, pp. 289-296 . https://doi.org/10.1007/s10689-015-9859-z
Familial Cancer, 15, 2, pp. 289-96
Familial Cancer, 15(2), 289-296
Familial Cancer
Familial Cancer, 15(2), 289. Springer Netherlands
Familial Cancer, 15, 289-96
Vogelaar, I P, Ligtenberg, M J L, van der Post, R S, de Voer, R M, Kets, C M, Jansen, T J G, Jacobs, L, Schreibelt, G, de Vries, I J M, Netea, M G, Hoogerbrugge, N & International Gastric Cancer Genetics Group 2016, ' Recurrent candidiasis and early-onset gastric cancer in a patient with a genetically defined partial MYD88 defect ', Familial Cancer, vol. 15, no. 2, pp. 289-296 . https://doi.org/10.1007/s10689-015-9859-z
Familial Cancer, 15, 2, pp. 289-96
Contains fulltext : 171354.pdf (Publisher’s version ) (Open Access) Gastric cancer is caused by both genetic and environmental factors. A woman who suffered from recurrent candidiasis throughout her life developed diffuse-type gastric cancer at the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::715f91b714f5bcf4addd2fb8bb2bd059
https://dspace.library.uu.nl/handle/1874/340480
https://dspace.library.uu.nl/handle/1874/340480