Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Roberta Iannitti"'
Publikováno v:
Cells, Vol 11, Iss 3, p 354 (2022)
The Golgi complex of mammalian cells is organized in a ribbon-like structure often closely associated with the centrosome during interphase. Conversely, the Golgi complex assumes a fragmented and dispersed configuration away from the centrosome durin
Externí odkaz:
https://doaj.org/article/e07f32f28eab49cd8f96b07c97d1a000
The decision to enter mitosis requires not only the control of DNA replication but also additional and crucial preparatory steps such as, for example, partial disassembly of the Golgi complex during G2. The Golgi complex is fundamental for the proces
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6674c960d412db52cd2cbb5786c8d309
https://doi.org/10.1101/2023.03.05.531163
https://doi.org/10.1101/2023.03.05.531163
Publikováno v:
Cells, Vol 11, Iss 354, p 354 (2022)
The Golgi complex of mammalian cells is organized in a ribbon-like structure often closely associated with the centrosome during interphase. Conversely, the Golgi complex assumes a fragmented and dispersed configuration away from the centrosome durin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f6709b33842602e25c9a5c9a733e833
https://pubmed.ncbi.nlm.nih.gov/35159164
https://pubmed.ncbi.nlm.nih.gov/35159164
Autor:
Giancarlo Morelli, Francesco Ruffo, Maria Elena Cucciolito, Roberta Iannitti, Rosanna Palumbo, Angela D'Amora, Diego Tesauro
Publikováno v:
Journal of Drug Delivery Science and Technology. 51:552-558
The first aim of the present study is the development of a new ruthenium(III) complex, belonging to NAMI-A class, with a potentially high cytotoxic ability. The presence of a fully protected sugar moiety as ruthenium ligand should increase the comple
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::feb31eb5b38af05d4470ff61c33fe11e
https://doi.org/10.1016/j.jddst.2019.02.009
https://doi.org/10.1016/j.jddst.2019.02.009
Autor:
Valentina Roviello, Antonio Carella, Rosita Diana, Giovanni N. Roviello, Sara La Manna, Rosanna Palumbo, Daniela Marasco, Marco Trifuoggi, Roberta Iannitti
Publikováno v:
International journal of biological macromolecules 121 (2019): 77–88. doi:10.1016/j.ijbiomac.2018.09.153
info:cnr-pdr/source/autori:Carella, Antonio; Roviello, Valentina; Iannitti, Roberta; Palumbo, Rosanna; La Manna, Sara; Marasco, Daniela; Trifuoggi, Marco; Diana, Rosita; Roviello, Giovanni N./titolo:Evaluating the biological properties of synthetic 4-nitrophenyl functionalized benzofuran derivatives with telomeric DNA binding and antiproliferative activities/doi:10.1016%2Fj.ijbiomac.2018.09.153/rivista:International journal of biological macromolecules/anno:2019/pagina_da:77/pagina_a:88/intervallo_pagine:77–88/volume:121
info:cnr-pdr/source/autori:Carella, Antonio; Roviello, Valentina; Iannitti, Roberta; Palumbo, Rosanna; La Manna, Sara; Marasco, Daniela; Trifuoggi, Marco; Diana, Rosita; Roviello, Giovanni N./titolo:Evaluating the biological properties of synthetic 4-nitrophenyl functionalized benzofuran derivatives with telomeric DNA binding and antiproliferative activities/doi:10.1016%2Fj.ijbiomac.2018.09.153/rivista:International journal of biological macromolecules/anno:2019/pagina_da:77/pagina_a:88/intervallo_pagine:77–88/volume:121
Four 4-nitrophenyl-functionalized benzofuran (BF1, BF2) and benzodifuran (BDF1, BDF2) compounds were synthesized by a convenient route based on the Craven reaction. All the compounds underwent a detailed chemical physical characterization to evaluate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95a3f4dba3c17b775e0eda41b3196b77
https://doi.org/10.1016/j.ijbiomac.2018.09.153
https://doi.org/10.1016/j.ijbiomac.2018.09.153
Autor:
Idolo Tedesco, Carmela Spagnuolo, Maria Russo, Roberta Iannitti, Annunziata Nappo, Gian Luigi Russo
Publikováno v:
Dose-Response, Vol 11 (2013)
Radiations may trigger protective response within a threshold of doses applied. Exposures above an upper threshold are generally detrimental, while exposures below a lower threshold may or may not increase risks for health. We recently reported that
Externí odkaz:
https://doaj.org/article/e6b1302d25a34dc39529f0444df48d2f
Autor:
Luciano Pirone, Emilia Pedone, Rosanna Palumbo, Roberta Iannitti, Concetta Di Natale, Daniela Marasco, Marilisa Leone, Flavia Anna Mercurio
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-11 (2017)
Scientific reports (Nature Publishing Group) 7 (2017). doi:10.1038/s41598-017-17684-5
info:cnr-pdr/source/autori:Mercurio, Flavia Anna; Di Natale, Concetta; Pirone, Luciano; Iannitti, Roberta; Marasco, Daniela; Pedone, Emilia Maria; Palumbo, Rosanna; Leone, Marilisa/titolo:The Sam-Sam interaction between Ship2 and the EphA2 receptor: design and analysis of peptide inhibitors/doi:10.1038%2Fs41598-017-17684-5/rivista:Scientific reports (Nature Publishing Group)/anno:2017/pagina_da:/pagina_a:/intervallo_pagine:/volume:7
Scientific Reports
Scientific reports (Nature Publishing Group) 7 (2017). doi:10.1038/s41598-017-17684-5
info:cnr-pdr/source/autori:Mercurio, Flavia Anna; Di Natale, Concetta; Pirone, Luciano; Iannitti, Roberta; Marasco, Daniela; Pedone, Emilia Maria; Palumbo, Rosanna; Leone, Marilisa/titolo:The Sam-Sam interaction between Ship2 and the EphA2 receptor: design and analysis of peptide inhibitors/doi:10.1038%2Fs41598-017-17684-5/rivista:Scientific reports (Nature Publishing Group)/anno:2017/pagina_da:/pagina_a:/intervallo_pagine:/volume:7
Scientific Reports
The lipid phosphatase Ship2 represents a drug discovery target for the treatment of different diseases, including cancer. Its C-terminal sterile alpha motif domain (Ship2-Sam) associates with the Sam domain from the EphA2 receptor (EphA2-Sam). This i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f8cb18a177897ef6396bdd6d1e4ba27
http://link.springer.com/article/10.1038/s41598-017-17684-5
http://link.springer.com/article/10.1038/s41598-017-17684-5
Autor:
Hayarpi M. Simonyan, Roberta Iannitti, Valentina Roviello, Caterina Vicidomini, Giovanni N. Roviello, Rosanna Palumbo
Publikováno v:
Amino Acids. 49:1347-1353
Here we describe the synthesis, chromatographic purification, MS and NMR characterization of a new lactosyl-derivative, i.e. a lactosyl thiophenyl-substituted triazolyl-thione l-alanine (Lac-L-TTA). This amino acid–sugar conjugate was prepared by s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bbbc21ed7873af3febbfc4801bb3e7e0
https://doi.org/10.1007/s00726-017-2433-2
https://doi.org/10.1007/s00726-017-2433-2
Autor:
Diego Tesauro, Maria Elena Cucciolito, Roberta Iannitti, Rosanna Palumbo, Giancarlo Morelli, Angela D'Amora, Francesco Ruffo
The success of platinum complexes as chemiotherapeutic drugs pushed the scientific community to design new transition metal based complexes. to fight cancer and overcome the severe side effects and the insurgence of platinum resistance [1]..Among the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3730::7dc382fb9b03698b7aaf52fef9cab7c4
http://hdl.handle.net/11588/775186
http://hdl.handle.net/11588/775186
New Anti-Nodal Monoclonal Antibodies Targeting the Nodal Pre-Helix Loop Involved in Cripto-1 Binding
Autor:
Giuseppina Focà, Antonio Leonardi, Mary J.C. Hendrix, Menotti Ruvo, Annalia Focà, Rosanna Palumbo, Roberta Iannitti, Annamaria Sandomenico, Luigi Strizzi, Luca Sanguigno
Publikováno v:
International Journal of Molecular Sciences
Volume 16
Issue 9
Pages 21342-21362
International Journal of Molecular Sciences, Vol 16, Iss 9, Pp 21342-21362 (2015)
International journal of molecular sciences (Online) 16 (2015): 21342–62. doi:10.3390/ijms160921342
info:cnr-pdr/source/autori:Foca, Annalia; Sanguigno, Luca; Foca, Giuseppina; Strizzi, Luigi; Iannitti, Roberta; Palumbo, Rosanna; Hendrix, Mary J C; Leonardi, Antonio; Ruvo, Menotti; Sandomenico, Annamaria/titolo:New Anti-Nodal Monoclonal Antibodies Targeting the Nodal Pre-Helix Loop Involved in Cripto-1 Binding./doi:10.3390%2Fijms160921342/rivista:International journal of molecular sciences (Online)/anno:2015/pagina_da:21342/pagina_a:62/intervallo_pagine:21342–62/volume:16
Volume 16
Issue 9
Pages 21342-21362
International Journal of Molecular Sciences, Vol 16, Iss 9, Pp 21342-21362 (2015)
International journal of molecular sciences (Online) 16 (2015): 21342–62. doi:10.3390/ijms160921342
info:cnr-pdr/source/autori:Foca, Annalia; Sanguigno, Luca; Foca, Giuseppina; Strizzi, Luigi; Iannitti, Roberta; Palumbo, Rosanna; Hendrix, Mary J C; Leonardi, Antonio; Ruvo, Menotti; Sandomenico, Annamaria/titolo:New Anti-Nodal Monoclonal Antibodies Targeting the Nodal Pre-Helix Loop Involved in Cripto-1 Binding./doi:10.3390%2Fijms160921342/rivista:International journal of molecular sciences (Online)/anno:2015/pagina_da:21342/pagina_a:62/intervallo_pagine:21342–62/volume:16
Nodal is a potent embryonic morphogen belonging to the TGF-beta superfamily. Typically, it also binds to the ALK4/ActRIIB receptor complex in the presence of the co-receptor Cripto-1. Nodal expression is physiologically restricted to embryonic tissue
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a3aa1f8b6a4b3a935c2e53b5eb606ee
https://doi.org/10.3390/ijms160921342
https://doi.org/10.3390/ijms160921342