Zobrazeno 1 - 10
of 48
pro vyhledávání: '"G. Fogu"'
Autor:
I. Borze, Hans Zischler, G. Utermann, R. Sanna, M. Kontodiou, A. Kinney, J. Kunz, A.W. Kuss, D. Kotzot, S.-Y. Kim, J. Cieslak, M. Tzimina, S.-Y. Park, B. Kociucka, M. Erdel, Shelby L. Brown, Y.-S. Park, V. Jobanputra, C. Yu, A.B. Hamid, Bianca Navarro, D. Warburton, E. Klein, A. Tzschach, R.G. Weber, H.-S. Lee, L. Thomaidis, F. Kasai, E. Elonen, F. Zölzer, S. Martin, Z. Freitinger Skalická, N. Kosyakova, J. Kline, S. Ninomiya, J. Zschocke, A. Tyybäkinoja, Eberhard Schneider, Satz Mengensatzproduktion, M.B. Petersen, E. Wohlleber, R. Havránková, A. Montella, V. Grossmann, N. El Hajj, E. Manolakos, I. Szczerbal, A. Dufke, Annette M. Müller, V. Kalscheuer, J. Škopek, Thomas Liehr, P. Bartmann, S. Orru, P. Nicolaides, D.-E. Lee, S. Mayer, Ivanela Kondova, M. Höckner, Ronald E. Bontrop, M.A. Moro, C. Fauth, U. Kordaß, C. Fozza, J.-W. Kim, E. Siomou, A. Spreiz, R.M. Nieddu, A. Frühmesser, L. Navrátil, P.M. Campus, L.R. Jensen, S. Knuutila, F. Cambosu, E. Engels, E. Fuchs, J. Rosina, Z. Hon, Druck Reinhardt Druck Basel, R. Räty, U. Zechner, B. Levy, S. Bağci, A. Usvasalo, M. Shirazi, Thomas Haaf, Ulla M. Saarinen-Pihkala, A.L. Berner, O. Rittinger, I. Saitis, I. Papoulidis, B.-Y. Lee, M. Longinotti, P.C.M. O’Brien, H.-M. Ryu, G. Fogu, M.A. Ferguson-Smith, J.-T. Seo, H. Reutter, S. Singer
Publikováno v:
Cytogenetic and Genome Research. 136:I-IV
Publikováno v:
Zeitschrift für allgemeine Mikrobiologie. 22:127-131
Indirect immunofluorescence with antibodies to microtubular proteins has been used to investigate the microtubule system of Dictyostelium discoideum vegetative amoebae and the action of several compounds that interfere with that system. All the inhib
Autor:
Vincenzo Nigro, Lucia Perone, Marco Savarese, Giulio Piluso, Laura Perrone, Giuseppina Di Fruscio, Emanuele Miraglia del Giudice, G Fogu, Francesca Del Vecchio Blanco, Giuseppina De Luca, Anna Grandone
Publikováno v:
American Journal of Medical Genetics Part A; Vol 161
Several patients with partial trisomy 6p resulting from parental balanced translocations or from a de novo duplication or insertion have already been described. Here, we report on the first case of familial pure trisomy 6p as a result of interstitial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b6990d4a032b33cf49f4690f65e53e1
http://hdl.handle.net/11591/320734
http://hdl.handle.net/11591/320734
Autor:
Annalisa Pezzolo, Giorgio Gimelli, Amnon Cohen, Cesare Romano, Orsetta Zuffardi, G Fogu, Antonella Lavaggetto
Publikováno v:
Human Genetics. 92:23-27
In situ hybridization of a telomeric (TTA-GGG)n sequence to metaphases from three cases of ring chromosome, involving respectively chromosomes 4, 16, and 20, showed the presence of the cognate sequences in all three rings. To investigate whether thes
Publikováno v:
Annali di chimica. 90(11-12)
In this study we report the results of cytogenetic tests, namely a search for chromosome aberrations (CA) and sister chromatid exchanges (SCEs), performed on human amniotic fluid cells cultured and treated with Cadmium chloride. The cells from primar
Autor:
A.W. Kuss, A. Tyybäkinoja, S. Ninomiya, A. Usvasalo, Eberhard Schneider, J. Cieslak, A. Frühmesser, P. Nicolaides, D.-E. Lee, R. Havránková, U. Zechner, M. Kontodiou, I. Saitis, A. Montella, V. Grossmann, G. Utermann, J.-T. Seo, H. Reutter, S. Singer, S. Knuutila, M. Shirazi, M. Höckner, Ronald E. Bontrop, J. Kunz, S. Mayer, Ivanela Kondova, C. Fozza, B. Levy, M. Erdel, E. Klein, A. Kinney, B. Kociucka, F. Zölzer, P. Bartmann, V. Kalscheuer, J. Škopek, Thomas Liehr, A.B. Hamid, N. El Hajj, Annette M. Müller, M. Tzimina, U. Kordaß, Z. Hon, A. Tzschach, Thomas Haaf, R.G. Weber, R.M. Nieddu, H.-S. Lee, Y.-S. Park, M. Longinotti, D. Warburton, P.C.M. O’Brien, H.-M. Ryu, G. Fogu, Z. Freitinger Skalická, L. Navrátil, I. Borze, M.A. Ferguson-Smith, Druck Reinhardt Druck Basel, Shelby L. Brown, N. Kosyakova, M.B. Petersen, Hans Zischler, Satz Mengensatzproduktion, E. Manolakos, M.A. Moro, A. Dufke, C. Fauth, J. Rosina, I. Szczerbal, S. Martin, S. Bağci, V. Jobanputra, E. Siomou, J. Zschocke, D. Kotzot, A. Spreiz, S.-Y. Park, P.M. Campus, L.R. Jensen, F. Cambosu, J.-W. Kim, L. Thomaidis, O. Rittinger, I. Papoulidis, S. Orru, S.-Y. Kim, R. Räty, B.-Y. Lee, E. Engels, E. Fuchs, Bianca Navarro, F. Kasai, J. Kline, Ulla M. Saarinen-Pihkala, A.L. Berner, C. Yu, E. Elonen, R. Sanna, E. Wohlleber
Publikováno v:
Digestion. 87:X-X
Autor:
Giancarlo Latte, Rosangela Invernizzi, Attilio Gabbas, Monica Casali, Raimonda Sanna, Edoardo Ascari, Francesco Pasquali, Emanuela Maserati, Paolo Simi, G Fogu
Publikováno v:
Cancer genetics and cytogenetics. 61(2)
Two male patients with Philadelphia-chromosome (Ph+) chronic myelogenous leukemia (CML) underwent allogeneic bone marrow transplantation (ABMT) in the first chronic phase after busulfan treatment. In both cases, the donor was a sister, and engrafting
Autor:
G, Fogu, B, Spano, R, Sanna, A G, Angius, P M, Campus, M G, Olzai, M G, Sanna, A, Balata, A, Chiarolini
Publikováno v:
La Pediatria medica e chirurgica : Medical and surgical pediatrics. 13(4)
We report a case of Edward's syndrome showing some symptoms infrequently described in trisomy 18. The authors suggest that the phenotypic expression of symptoms rarely observed in the syndrome may be better interpreted as non specific consequence of
Publikováno v:
La Pediatria medica e chirurgica : Medical and surgical pediatrics. 12(4)
The study of gene/dosage effect may be essential in tracing the pathogenetic steps which lead from an unbalanced chromosome anomaly to a pathological phenotype. We present a newborn with a clinical and pathological picture compatible with a diagnosis
Autor:
B, Spano, G, Fogu, R, Sanna, A G, Angius, P M, Campus, A, Cattina, A, Chiarolini, M G, Olzai, A, Balata
Publikováno v:
La Pediatria medica e chirurgica : Medical and surgical pediatrics. 12(1)
The study of gene/dosage effect may be essential in tracing the pathogenetic steps which lead from an unbalanced chromosome anomaly to a pathological phenotype. We present a newborn with a clinical and pathological picture compatible with a diagnosis