Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Manuela Lanzafame"'
Autor:
Hajer Tlili, Anca Macovei, Daniela Buonocore, Manuela Lanzafame, Hanen Najjaa, Anita Lombardi, Andrea Pagano, Maurizia Dossena, Manuela Verri, Abdelkarim Ben Arfa, Mohamed Neffati, Enrico Doria
Publikováno v:
BMC Complementary Medicine and Therapies, Vol 21, Iss 1, Pp 1-13 (2021)
Abstract Background Hyperactivation of mechanistic target of rapamycin (mTOR) signaling pathway is involved in the regulation of cellular growth, proliferation, and more in general, is a common phenomenon in most types of cancers. Thus, natural subst
Externí odkaz:
https://doaj.org/article/89b77a523e07455ba760e6ee0c3e21ba
Autor:
Venkatesh Kancherla, Samir Abdullazade, Matthias S. Matter, Manuela Lanzafame, Luca Quagliata, Guglielmo Roma, Yujin Hoshida, Luigi M. Terracciano, Charlotte K. Y. Ng, Salvatore Piscuoglio
Publikováno v:
Frontiers in Genetics, Vol 9 (2018)
The TP53 gene is the most commonly mutated gene in human cancers and mutations in TP53 have been shown to have either gain-of-function or loss-of-function effects. Using the data generated by The Cancer Genome Atlas, we sought to define the spectrum
Externí odkaz:
https://doaj.org/article/72d96652e5ac4337856c9b70247960f1
Autor:
Manuela Lanzafame, Gaia Bianco, Luigi M. Terracciano, Charlotte K. Y. Ng, Salvatore Piscuoglio
Publikováno v:
International Journal of Molecular Sciences, Vol 19, Iss 3, p 682 (2018)
Whole-transcriptome analyses have revealed that a large proportion of the human genome is transcribed in non-protein-coding transcripts, designated as long non-coding RNAs (lncRNAs). Rather than being “transcriptional noise”, increasing evidence
Externí odkaz:
https://doaj.org/article/2ead261ae53844e9a975068a91cf287f
Autor:
Manuela Lanzafame, Tiziana Nardo, Roberta Ricotti, Chiara Pantaleoni, Stefano D'Arrigo, Franco Stanzial, Francesco Benedicenti, Mary A. Thomas, Miria Stefanini, Donata Orioli, Elena Botta
Publikováno v:
Human mutationREFERENCES. 43(12)
Trichothiodystrophy (TTD) is a rare hereditary disease whose prominent feature is brittle hair. Additional clinical signs are physical and neurodevelopmental abnormalities and in about half of the cases hypersensitivity to UV radiation. The photosens
Autor:
Bernhard Englinger, Salvatore Piscuoglio, Jean Rommelaere, Dominik Witzigmann, Sushilla van Schoonhoven, Walter Berger, David Grünig, Xue-Ting Tran, Patrick Hauswirth, Susanne H. Schenk, Stephan Krähenbühl, Jörg Huwyler, Luigi Terracciano, Manuela Lanzafame, Philip Grossen, Cristina Quintavalle, Jürg P. F. Nüesch, Luca Quagliata
Publikováno v:
Journal of Controlled Release. 334:138-152
Hepatocellular carcinoma (HCC) is related to increasing incidence rates and poor clinical outcomes due to lack of efficient treatment options and emerging resistance mechanisms. The aim of the present study is to exploit a non-viral gene therapy enab
Autor:
Giulia Branca, Miria Stefanini, Bruno Vaz, Fiorenzo A. Peverali, Tiziana Nardo, Manuela Mura, Manuela Lanzafame, Donata Orioli, Mingyue Qiang, Debora Ferri, Sebastian Iben, Luca Bini, Claudia Landi
Publikováno v:
Nucleic Acids Research
CSA and CSB proteins are key players in transcription-coupled nucleotide excision repair (TC-NER) pathway that removes UV-induced DNA lesions from the transcribed strands of expressed genes. Additionally, CS proteins play relevant but still elusive r
Autor:
Salvatore Piscuoglio, Stephanie Taha-Mehlitz, Antoine de Weck, Hesam Montazeri, Manuela Lanzafame, Sumana Srivatsa, Viola Paradiso, Guglielmo Roma, Charlotte K.Y. Ng, Ehsan Zangene, Niko Beerenwinkel, Gaia Bianco, Luigi Terracciano, Mairene Coto-Llerena, Markus von Flüe, Martin Bolli
Publikováno v:
Nucleic Acids Research, 49 (15)
Montazeri, Hesam; Coto-Llerena, Mairene; Bianco, Gaia; Zangene, Ehsan; Taha-Mehlitz, Stephanie; Paradiso, Viola; Srivatsa, Sumana; de Weck, Antoine; Roma, Guglielmo; Lanzafame, Manuela; Bolli, Martin; Beerenwinkel, Niko; von Flüe, Markus; Terracciano, Luigi M; Piscuoglio, Salvatore; Ng, Charlotte K Y (2021). Systematic identification of novel cancer genes through analysis of deep shRNA perturbation screens. Nucleic acids research, 49(15), pp. 8488-8504. Oxford University Press 10.1093/nar/gkab627
Nucleic Acids Research
Montazeri, Hesam; Coto-Llerena, Mairene; Bianco, Gaia; Zangene, Ehsan; Taha-Mehlitz, Stephanie; Paradiso, Viola; Srivatsa, Sumana; de Weck, Antoine; Roma, Guglielmo; Lanzafame, Manuela; Bolli, Martin; Beerenwinkel, Niko; von Flüe, Markus; Terracciano, Luigi M; Piscuoglio, Salvatore; Ng, Charlotte K Y (2021). Systematic identification of novel cancer genes through analysis of deep shRNA perturbation screens. Nucleic acids research, 49(15), pp. 8488-8504. Oxford University Press 10.1093/nar/gkab627
Nucleic Acids Research
BackgroundSystematic perturbation screens provide comprehensive resources for the elucidation of cancer driver genes, including rarely mutated genes that are missed by approaches focused on frequently mutated genes and driver genes for which the basi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ea8828b498526269a1316bc3a3ec366
Autor:
Anita Lombardi, Anca Macovei, Hajer Tlili, Abdelkarim Ben Arfa, Mohamed Neffati, Daniela Buonocore, Hanen Najjaa, Manuela Verri, Enrico Doria, Andrea Pagano, Maurizia Dossena, Manuela Lanzafame
Publikováno v:
BMC Complementary Medicine and Therapies
BMC Complementary Medicine and Therapies, Vol 21, Iss 1, Pp 1-13 (2021)
BMC Complementary Medicine and Therapies, Vol 21, Iss 1, Pp 1-13 (2021)
Background Hyperactivation of mechanistic target of rapamycin (mTOR) signaling pathway is involved in the regulation of cellular growth, proliferation, and more in general, is a common phenomenon in most types of cancers. Thus, natural substances tar
Autor:
Ana Luísa Correia, Alexander Schmidt, Mihaela Zavolan, Joao C. Guimaraes, Anastasiya Börsch, Sébastien Pfeffer, Luigi Terracciano, Gunter Meister, Salvatore Piscuoglio, Thomas Montavon, Souvik Ghosh, Johannes Danner, Nitish Mittal, Beatrice Dimitriades, Afzal Pasha Syed, Shreemoyee Ghosh, Manuela Lanzafame
Publikováno v:
EMBO Journal
EMBO Journal, EMBO Press, 2020, 39 (18), ⟨10.15252/embj.2019103922⟩
The EMBO Journal
EMBO Journal, EMBO Press, 2020, 39 (18), ⟨10.15252/embj.2019103922⟩
The EMBO Journal
Translational readthrough, i.e., elongation of polypeptide chains beyond the stop codon, was initially reported for viral RNA, but later found also on eukaryotic transcripts, resulting in proteome diversification and protein‐level modulation. Here,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d47e999d1f62c666eb1f8b17ba27ab32
https://hal.archives-ouvertes.fr/hal-02954154/document
https://hal.archives-ouvertes.fr/hal-02954154/document
Autor:
Shinichi Moriwaki, Donata Orioli, Marie-Aude Spitz, Nadège Calmels, Nan Jia, Katsuo Sugita, Elena Botta, Alan R. Lehmann, Miria Stefanini, Vincent Laugel, Heather Fawcett, Masaya Kubota, Cathy Obringer, Tiziana Nardo, Tomoo Ogi, Yuka Nakazawa, Manuela Lanzafame
Publikováno v:
Journal of Medical Genetics. 55:329-343
BackgroundCockayne syndrome (CS) is a rare, autosomal recessive multisystem disorder characterised by prenatal or postnatal growth failure, progressive neurological dysfunction, ocular and skeletal abnormalities and premature ageing. About half of th