Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Guglielmina Ranzani"'
Autor:
Baffa, R., Negrini, M., Mandes, B., Rugge, M., Guglielmina Ranzani, Hirohashi, S., Croce, C. M.
Publikováno v:
Scopus-Elsevier
Loss of heterozygosity (LOH) at several chromosomal loci is a common feature of the malignant progression of human tumors. In the case of chromosome 11, LOH has been well documented in several types of solid neoplasms, including gastric carcinoma, su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::bd97a2b5c0893271d4be57eaf2b49c84
https://pubmed.ncbi.nlm.nih.gov/8542579
https://pubmed.ncbi.nlm.nih.gov/8542579
Autor:
Guglielmina Ranzani, Padovan, L. S., Calistri, D., Renault, B., Luinetti, O., Burrel, M., Fiocca, R., Solcia, E., Amadori, D.
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::74a56f936af397bec5757ef28138cf4e
http://hdl.handle.net/11567/184866
http://hdl.handle.net/11567/184866
Publikováno v:
Scopus-Elsevier
A group of Babinga Pygmies from the Central African Republic have been analyzed for the acid phosphatase polymorphism with special reference to the ACPR allele. The frequency of this allele (17%) is one of the highest observed in Africa and is compar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::170d49d02290d3372a696806bc44c4d2
https://europepmc.org/articles/PMC1685514/
https://europepmc.org/articles/PMC1685514/
Autor:
Renault, B., Den Broek, M., Fodde, R., Wijnen, J., Pellegata, N. S., Amadori, D., Han, P. M., Guglielmina Ranzani
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::40818527f591cb184105349be8b99755
http://www.scopus.com/inward/record.url?eid=2-s2.0-0027175653&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0027175653&partnerID=MN8TOARS
Autor:
Guglielmina Ranzani, Pellegata, N. S., Previderè, C., Saragoni, A., Vio, A., Maltoni, M., Amadori, D.
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::137fcad8ef62e8077d6ceaa3329c2228
http://www.scopus.com/inward/record.url?eid=2-s2.0-0025672611&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0025672611&partnerID=MN8TOARS
Autor:
Avato, F. M., Peloso, G., Lucarini, N., Ballarini, P., Aloia, A., Previderè, C., Guglielmina Ranzani
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::8792b290a8a8d2d440b296c2d872d3ae
http://www.scopus.com/inward/record.url?eid=2-s2.0-0025673650&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0025673650&partnerID=MN8TOARS
Publikováno v:
Scopus-Elsevier
Some populations of Rwanda (South Twa Pygmies, Hutu, and Tutsi) have been analyzed by acid starch gel electrophoresis for the subtyping of PGM1 polymorphism. The new polymorphic third PGM11 allele, the PGM1(1Twa), which we recently detected in Twa Py
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::f87daad1e0bd6d5557b9fd0723c1605e
http://www.scopus.com/inward/record.url?eid=2-s2.0-0020066408&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0020066408&partnerID=MN8TOARS
Autor:
Guglielmina Ranzani, Salerno-Mele, P., Maltoni, M., Talarico, D., Della Valle, G., Amadori, D.
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::dabc0d6f7d59a38a4e451bea0d23b02a
http://www.scopus.com/inward/record.url?eid=2-s2.0-0024239725&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0024239725&partnerID=MN8TOARS
Autor:
Benedetti, L., Varesco, L., Pellegata, N. S., Losi, L., Gismondi, V., Casarino, L., Sciallero, S., Bonelli, L., Biticchi, R., Bafico, A., Masetti, E., James, R., Heouaine, A., Guglielmina Ranzani, Aste, H., Ferrara, G.
Publikováno v:
Scopus-Elsevier
Publons
Publons
Twenty-four sporadic colorectal adenomas were analysed for the presence of allelic loss on the short arm of chromosome 17 as well as mutations in the K-ras and p53 genes. Chromosome 17p13 allelic loss was not present in 14 out of 14 informative cases
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::cd5bd79ee1ee4bb4a726120f05ad10e8
http://www.scopus.com/inward/record.url?eid=2-s2.0-0027201180&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0027201180&partnerID=MN8TOARS
Autor:
Tenti, P., Vesentini, N., Rondo Spaudo, M., Zappatore, R., Migliora, P., Carnevali, L., Guglielmina Ranzani
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::86784cc6dd61756c9c5fa73f4f1b9574
http://www.scopus.com/inward/record.url?eid=2-s2.0-0034100911&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0034100911&partnerID=MN8TOARS