Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Ivana Magnani"'
Autor:
Gaia Roversi, Elisa Adele Colombo, Ivana Magnani, Cristina Gervasini, Giuseppe Maggiore, Mauro Paradisi, Lidia Larizza
Publikováno v:
Genetics and Molecular Biology, Vol 44, Iss 3 (2021)
Abstract Two Italian patients with the initial clinical diagnosis of Rothmund-Thomson syndrome were negative for RECQL4 mutations but showed in peripheral blood cells a spontaneous chromosomal instability significantly higher than controls. Revisitin
Externí odkaz:
https://doaj.org/article/f355c2d615214ae2a034fac99a1ecd9f
Autor:
Ivana Magnani, Chiara Novielli, Laura Fontana, Silvia Tabano, Davide Rovina, Ramona F. Moroni, Dario Bauer, Stefania Mazzoleni, Elisa A. Colombo, Gabriella Tedeschi, Laura Monti, Giovanni Porta, Silvano Bosari, Carolina Frassoni, Rossella Galli, Lorenzo Bello, Lidia Larizza
Publikováno v:
Analytical Cellular Pathology, Vol 34, Iss 6, Pp 319-338 (2011)
Background: MAP/microtubule affinity-regulating kinase 4 (MARK4) is a serine-threonine kinase expressed in two spliced isoforms, MARK4L and MARK4S, of which MARK4L is a candidate for a role in neoplastic transformation. Methods: We performed mutation
Externí odkaz:
https://doaj.org/article/3ecf17df987948d4be7f551ce0a409e5
Publikováno v:
Cellular Oncology, Vol 31, Iss 5, Pp 357-370 (2009)
Background: We have previously shown that the sustained expression of MARK4L transcripts in glioma and neural progenitors (NHNPs) declines after exposure to antisense MARK4L oligonucleotides in glioblastoma cell lines. Array-CGH confirmed the genomic
Externí odkaz:
https://doaj.org/article/663a3569a7c04011a02ce2fe0a278fd5
Autor:
Cristina Gervasini, Ivana Magnani, Lidia Larizza, Mauro Paradisi, Gaia Roversi, Elisa Colombo, Giuseppe Maggiore
Publikováno v:
Genetics and Molecular Biology
Genetics and Molecular Biology v.44 n.3 2021
Sociedade Brasileira de Genética (SBG)
instacron:SBG
Genetics and Molecular Biology, Vol 44, Iss 3 (2021)
Genetics and Molecular Biology, Volume: 44, Issue: 3, Article number: e20200332, Published: 06 AUG 2021
Genetics and Molecular Biology v.44 n.3 2021
Sociedade Brasileira de Genética (SBG)
instacron:SBG
Genetics and Molecular Biology, Vol 44, Iss 3 (2021)
Genetics and Molecular Biology, Volume: 44, Issue: 3, Article number: e20200332, Published: 06 AUG 2021
Two Italian patients with the initial clinical diagnosis of Rothmund-Thomson syndrome were negative for RECQL4 mutations but showed in peripheral blood cells a spontaneous chromosomal instability significantly higher than controls. Revisiting after t
Autor:
Lidia Larizza, Gabriella Tedeschi, Davide Rovina, Chiara Novielli, Laura Fontana, Elisa Maffioli, Ivana Magnani
Publikováno v:
Cancer Letters. 359:87-96
MAP/microtubule affinity-regulating kinase 4 (MARK4) is a serine-threonine kinase that phosphorylates microtubule-associated proteins taking part in the regulation of microtubule dynamics. MARK4 is expressed in two spliced isoforms characterized by i
Autor:
Ivana Magnani, Wassil Nowicky, C. Torri, Francesco Costa, Nicoletta Gagliano, Claudia Moscheni, Magda Gioia, Elena Donetti
Publikováno v:
Anti-Cancer Drugs. 18:669-676
Glioblastoma is a highly malignant tumor, characterized by an unfavorable prognosis even in response to multidisciplinary treatment strategies, owing to its high-invasive phenotype. Ukrain, a semisynthetic thiophosphoric acid derivative of the purifi
Autor:
Silvia M. Sirchia, Laura Fontana, Laura Monti, Nicolò Panini, Chiara Novielli, Davide Rovina, Lidia Larizza, Ivana Magnani, Eugenio Erba
Publikováno v:
European journal of cell biology. 93(8-9)
MARK4 is a serine-threonine kinase that phosphorylates MAP proteins, increasing microtubule dynamics. MARK4 differs from the other members of the MARK family for encoding two isoforms (MARK4L and MARK4S), differentially expressed in the nervous syste
Autor:
Ivana Magnani, C. Bassi, Anna Marozzi, A. Ventura, Raffaella Meneveri, Nicoletta Sacchi, Enrico Ginelli, Mariano Rocchi, Salvatore Saccone
Publikováno v:
Gene. 256:43-50
We have isolated and characterised one PAC clone (dJ233C1) containing a linkage between alphoid and non-alphoid DNA. The non-alphoid DNA was found to map at the pericentromeric region of chromosome 20, both on p and q sides, and to contain homologies
Publikováno v:
Cytogenetic and Genome Research. 73:123-129
Centromere activation, an important mechanism in karyotype evolution, is occasionally observed in some human chromosome rearrangements. We report a possible occurrence of centromere activation in a marker chromosome containing an atypical centromere
Publikováno v:
Cell Biology International. 19:9-16
A new cell line was established from the bone marrow of a patient with chronic myeloid leukemia. The cells were attributed an intermediate myeloid phenotype on the basis of their cytochemical features and membrane antigen expression. These cells resp