Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Samantha Zongaro"'
Autor:
Sabiha Abekhoukh, H. Bahar Sahin, Mauro Grossi, Samantha Zongaro, Thomas Maurin, Irene Madrigal, Daniele Kazue-Sugioka, Annick Raas-Rothschild, Mohamed Doulazmi, Pilar Carrera, Andrea Stachon, Steven Scherer, Maria Rita Drula Do Nascimento, Alain Trembleau, Ignacio Arroyo, Peter Szatmari, Isabel M. Smith, Montserrat Milà, Adam C. Smith, Angela Giangrande, Isabelle Caillé, Barbara Bardoni
Publikováno v:
Disease Models & Mechanisms, Vol 10, Iss 4, Pp 463-474 (2017)
Cytoplasmic FMRP interacting protein 1 (CYFIP1) is a candidate gene for intellectual disability (ID), autism, schizophrenia and epilepsy. It is a member of a family of proteins that is highly conserved during evolution, sharing high homology with its
Externí odkaz:
https://doaj.org/article/b879a391863543d5b04344b33425077a
Autor:
Roberto Ugolotti, Pablo Mesejo, Samantha Zongaro, Barbara Bardoni, Gaia Berto, Federico Bianchi, Ivan Molineris, Mario Giacobini, Stefano Cagnoni, Ferdinando Di Cunto
Publikováno v:
PLoS ONE, Vol 8, Iss 9, p e74481 (2013)
RNA molecules specifically enriched in the neuropil of neuronal cells and in particular in dendritic spines are of great interest for neurobiology in virtue of their involvement in synaptic structure and plasticity. The systematic recognition of such
Externí odkaz:
https://doaj.org/article/b199eee2c6254bc5ba48af6090f9dce5
Autor:
Chiara Mondello, Elena Giulotto, Maurizio D'Incalci, Tina Colombo, Elisa de Stanchina, Samantha Zongaro
Supplementary Figure Legend from Stepwise Neoplastic Transformation of a Telomerase Immortalized Fibroblast Cell Line
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c505fba4f11b52a1f02e50569e07e723
https://doi.org/10.1158/0008-5472.22364219.v1
https://doi.org/10.1158/0008-5472.22364219.v1
Autor:
Chiara Mondello, Elena Giulotto, Maurizio D'Incalci, Tina Colombo, Elisa de Stanchina, Samantha Zongaro
We have described recently a human fibroblast cell line immortalized through ectopic telomerase expression (cen3tel), in which the extension of the life span was associated with the appearance of chromosomal aberrations and with the ability to grow i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::706e6830d45b8e80dd732d0c9b49e89d
https://doi.org/10.1158/0008-5472.c.6494078.v1
https://doi.org/10.1158/0008-5472.c.6494078.v1
Autor:
Chiara Mondello, Elena Giulotto, Maurizio D'Incalci, Tina Colombo, Elisa de Stanchina, Samantha Zongaro
Supplementary Figure 1 from Stepwise Neoplastic Transformation of a Telomerase Immortalized Fibroblast Cell Line
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4cd170e504e68cf1d651b367ea0b97b8
https://doi.org/10.1158/0008-5472.22364222
https://doi.org/10.1158/0008-5472.22364222
Publikováno v:
Neuroscience & Biobehavioral Reviews. 46:242-255
Fragile X Syndrome (FXS) is the most common form of inherited intellectual disability due to the silencing of the FMR1 gene encoding FMRP (Fragile X Mental Retardation Protein), an RNA-binding protein involved in different steps of RNA metabolism. Of
Autor:
Andrea Lossani, Béatrice Horard, Ilaria Chiodi, Roberta Ricotti, Cristina Belgiovine, Chiara Mondello, Eric Gilson, Federico Focher, Samantha Zongaro, Elena Giulotto
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1833(8):1885-1893
Telomere length maintenance is critical for organisms' long-term survival and cancer cell proliferation. Telomeres are kept within species-specific length ranges by the interplay between telomerase activity and telomeric chromatin organization. In th
Autor:
Mireille Melko, Samantha Zongaro, Jozef Gecz, Dominique Douguet, Barbara Bardoni, Céline Verheggen, Mounia Bensaid
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2011, 20 (10), pp.1873-85. 〈10.1093/hmg/ddr069〉
Human Molecular Genetics, Oxford University Press (OUP), 2011, 20 (10), pp.1873-85. ⟨10.1093/hmg/ddr069⟩
Human Molecular Genetics, Oxford University Press (OUP), 2011, 20 (10), pp.1873-85. 〈10.1093/hmg/ddr069〉
Human Molecular Genetics, Oxford University Press (OUP), 2011, 20 (10), pp.1873-85. ⟨10.1093/hmg/ddr069⟩
International audience; The AFF (AF4/FMR2) family of genes includes four members: AFF1/AF4, AFF2/FMR2, AFF3/LAF4 and AFF4/AF5q31. AFF2/FMR2 is silenced in FRAXE intellectual disability, while the other three members have been reported to form fusion
Autor:
Mario Giacobini, Barbara Bardoni, Gaia Berto, Samantha Zongaro, F. Bianchi, Roberto Ugolotti, Pablo Mesejo, Ivan Molineris, Stefano Cagnoni, Ferdinando Di Cunto
Publikováno v:
PLoS ONE
PLoS ONE, Public Library of Science, 2013, 8 (9), ⟨10.1371/journal.pone.0074481⟩
PLoS ONE, Vol 8, Iss 9, p e74481 (2013)
PLoS ONE, 2013, 8 (9), ⟨10.1371/journal.pone.0074481⟩
PLoS ONE, Public Library of Science, 2013, 8 (9), ⟨10.1371/journal.pone.0074481⟩
PLoS ONE, Vol 8, Iss 9, p e74481 (2013)
PLoS ONE, 2013, 8 (9), ⟨10.1371/journal.pone.0074481⟩
International audience; Motivation: RNA molecules specifically enriched in the neuropil of neuronal cells and in particular in dendritic spines are of great interest for neurobiology in virtue of their involvement in synaptic structure and plasticity
Intellectual disability (ID) is the most frequent cause of serious handicap in children and young adults and interests 2-3% of worldwide population, representing a serious problem from the medical, social, and economic points of view. The causes are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c57f6786cb1b3c234ee5e4cad4b49abd
https://doi.org/10.1016/b978-0-444-54299-1.00003-0
https://doi.org/10.1016/b978-0-444-54299-1.00003-0