Zobrazeno 1 - 10
of 165
pro vyhledávání: '"M, Montera"'
Autor:
R, Biassoni, Malnati, I, Vanni, A, Raso, F, Sironi, F, Broccolo, L, Garbarino, M, Mazzocco, M, Montera, P, Larghero, E, Di Marco, E, Ugolotti
Publikováno v:
In Journal of Immunological Methods November 2015 426:29-34
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Michela Mazzocco, Lucia Garbarino, Patrizia Larghero, Mauro S. Malnati, Francesca Sironi, M. Montera, Irene Vanni, Alessandro Raso, Roberto Biassoni, Francesco Broccolo, Elisabetta Ugolotti, E. Di Marco
A growing body of evidence links the analysis of the KIR genotype and the presence of their HLA-B and -C ligands to a wide repertoire of human diseases. We noticed that, using a panel of 184 Caucasoid donors, a limited number of HLA alleles were inco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e77abe0bb43c7872e14eb7666a1e43e4
http://hdl.handle.net/10281/135046
http://hdl.handle.net/10281/135046
Autor:
S. Daniele, Paola Mandich, M. Bianchi, G. P. Pelliccioli, C. Simoncelli, C Daniele, A. Cavaliere, M. Montera
Publikováno v:
European Journal of Neurology. 3:581-587
von Hippel Lindau disease is a familial syndrome transmitted as an autosomal dominant trait with variable penetrance and expression. It presents with vascular tumours that involve the central nervous system, visceral organs and other tissues. Althoug
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0dc4f54f634b952bd9151c6bb98a17d0
https://doi.org/10.1111/j.1468-1331.1996.tb00276.x
https://doi.org/10.1111/j.1468-1331.1996.tb00276.x
Autor:
M. Montera, Cristina Mareni, Giovanna Bianchi Scarrat, Paola Origone, Roberto Lerza, Giuseppina Fugazza, Elena D'Amato, Mario Sessarego, Vito Pistoia
Publikováno v:
Leukemia & Lymphoma. 15:135-141
Peripheral blood mononuclear cells from seventeen patients with primary myelodysplastic syndromes (MDS) in advanced stage were enriched for blasts and tested for (1) karyotype, (2) genomic configuration and (3) expression of IL-3, GM-CSF, FMS and EGR
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ec3d8d046c58fd4364550c041b1612b
https://doi.org/10.3109/10428199409051688
https://doi.org/10.3109/10428199409051688
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Marco Gobbi, Ombretta Rosso, M. Montera, Robin Foà, Marino Clavio, Enrico Balleari, Daniela de Totero
In B-cell chronic lymphocytic leukemia (CLL), accumulation of neoplastic B cells may be the result of dysregulated apoptosis. One of the major molecules triggering apoptosis, CD95 (FAS), is not expressed on CLL B cells at resting conditions. However,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f78009232713163c3a786715165abba3
http://hdl.handle.net/11567/211712
http://hdl.handle.net/11567/211712
Autor:
جواد صادقی بالون1 Sadeghi.javad@ut.ac.ir, حسین صادقی2 hosadeghi@ut.ac.ir, بابک ضیا3 bziyea@ut.ac.ir
Publikováno v:
Journal of Entrepreneurship Development. Dec2024, Vol. 17 Issue 3, p223-252. 30p.
Autor:
N, Resta, C, Simone, C, Mareni, M, Montera, M, Gentile, F, Susca, R, Gristina, S, Pozzi, L, Bertario, P, Bufo, N, Carlomagno, M, Ingrosso, F P, Rossini, R, Tenconi, G, Guanti
Publikováno v:
Cancer research. 58(21)
A potential tumor suppressor gene, STK11 , encoding a serine threonine kinase, has recently been identified on chromosome 19p13. Germ-line mutations of this gene have been found in patients with Peutz-Jeghers syndrome (PJS). To further investigate th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f758dad999827d5997be8855066b6e39
https://pubmed.ncbi.nlm.nih.gov/9809980
https://pubmed.ncbi.nlm.nih.gov/9809980
Publikováno v:
Arquivos brasileiros de cardiologia. 70(4)
To evaluate the arrhythmogenic profile of patients with dilated cardiomyopathy of low ejection fraction and its prognostic significance.Data from 40 patients (30 males; mean age: 52 +/- 13 years) were analysed including ventricular arrhythmias (24h -
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e3a26f1ea5f2368ade8d0eac03d6563c
https://pubmed.ncbi.nlm.nih.gov/9687622
https://pubmed.ncbi.nlm.nih.gov/9687622