Zobrazeno 1 - 10
of 62
pro vyhledávání: '"R, Colognola"'
Autor:
L.J.M. Van Haarlem, Sven O. Warnaar, M.A. Nedelman, K.Y. Pak, P.E. Daddona, S.H. Tam, E. Wilson, R. Colognola, W.E. Fogler
Publikováno v:
International Journal of Radiation Applications and Instrumentation. Part B. Nuclear Medicine and Biology. 18:483-497
The 323 A3 murine monoclonal antibody, initially described as reactive to breast carcinomas, is found by immunohistological analyses to have broad cross reactivity with adenocarcinomas of diverse histologic origin. The 323 A3 antigen is similar to th
Autor:
K Y, Pak, M A, Nedelman, W E, Fogler, S H, Tam, E, Wilson, L J, Van Haarlem, R, Colognola, S O, Warnaar, P E, Daddona
Publikováno v:
International journal of radiation applications and instrumentation. Part B, Nuclear medicine and biology. 18(5)
The 323/A3 murine monoclonal antibody, initially described as reactive to breast carcinomas, is found by immunohistological analyses to have broad cross reactivity with adenocarcinomas of diverse histologic origin. The 323/A3 antigen is similar to th
Autor:
A S Santachiara, R. Colognola, F Nuzzo, Miria Stefanini, L Salvaneschi, P. Lagomarsini, G Zei, S. Marinoni
Publikováno v:
Journal of medical genetics. 27(1)
The association of two rare hereditary disorders, trichothiodystrophy (TTD) and xeroderma pigmentosum (XP), was found in four patients from three families, apparently unrelated but living in the same geographical area. In order to test the hypothesis
Publikováno v:
Biogeographia – The Journal of Integrative Biogeography. 7
13. DE MATTHAEXS, R. COLOGNOLA, M. COBOLLI SBORDONI, L. PESCE q‘, V. SBORDONI Istituto di Zoologia de1l’Universitz‘1 di Roma 7q‘ Istituto di Zoologia de]l’Universit51 di L’Aqui1a Divergenza genetica tra popolazioni di Spelaeomysis bottazz
Autor:
R. Scozzari, Fiorella Nuzzo, S. Marinoni, A. Casati, M. Rocchi, Miria Stefanini, P. Lagomarsini, R. Colognola
Publikováno v:
Mutation Research Letters. 208:159-161
Chromosome and blood marker studies were performed in the families of 4 patients in which the association of 2 rare recessive Mendelian disorders, xeroderma pigmentosum (XP-D) and trichothiodystrophy (TTD), was present. Blood genotypes did not indica
Autor:
David M. Segal, J.G. van Dijk, R. Colognola, R. J. van de Griendleuren, Reinder L. H. Bolhuis, Takashi Tsuruo, Gert Jan Fleuren, Sven O. Warnaar
Publikováno v:
International journal of cancer. 44(4)
We describe the lysis of multidrug-resistant (MDR) tumor cells by various lymphocytic effector cells, retargeted with bispecific antibodies (heteroconjugates). The Ab-heteroconjugate used was prepared by chemically cross-linking the OKT3 monoclonal a
Autor:
Pavone, Piero1 (AUTHOR), Polizzi, Agata2 (AUTHOR), Marino, Simona Domenica3 (AUTHOR), Corsello, Giovanni4 (AUTHOR), Falsaperla, Raffaele4 (AUTHOR), Marino, Silvia3 (AUTHOR), Ruggieri, Martino5 (AUTHOR) m.ruggieri@unict.it
Publikováno v:
Neurological Sciences. Dec2020, Vol. 41 Issue 12, p3547-3562. 16p. 3 Color Photographs, 1 Chart.
Autor:
Carotenuto, Marco1, Roccella, Michele2, Pisani, Francesco3, Matricardi, Sara4, Verrotti, Alberto5, Farello, Giovanni6, Operto, Francesca Felicia7, Bitetti, Ilaria1, Precenzano, Francesco1, Messina, Giovanni8, Ruberto, Maria9, Ciunfrini, Cristiana1, Riccardi, Mariagrazia1, Merolla, Eugenio1, Pastorino, Grazia Maria Giovanna1,7, Polito, Anna Nunzia10, Marotta, Rosa11
Publikováno v:
Behavioural Neurology. 12/3/2019, p1-8. 8p.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.