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LANZAFAME, MANUELA

LANZAFAME, MANUELA  

Istituto di Genetica Molecolare "Luigi Luca Cavalli Sforza"  

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Risultati 1 - 20 di 38 (tempo di esecuzione: 0.037 secondi).
Titolo Data di pubblicazione Autore(i) File
TFIIH stabilization recovers the DNA repair and transcription dysfunctions in thermo-sensitive trichothiodystrophy 1-gen-2022 Lanzafame M; Nardo T; Ricotti R; Pantaleoni C; D'Arrigo S; Stanzial F; Benedicenti F; Thomas MA; Stefanini M; Orioli D; Botta E
Cockayne syndrome group A and ferrochelatase finely tune ribosomal gene transcription and its response to UV irradiation 1-gen-2021 Lanzafame M; Branca G; Landi C; Qiang M; Vaz B; Nardo T; Ferri D; Mura M; Iben S; Stefanini M; Peverali FA; Bini L; Orioli D.
Non-viral gene delivery of the oncotoxic protein NS1 for treatment of hepatocellular carcinoma 1-gen-2021 Witzigmann, Dominik; Grossen, Philip; Quintavalle, Cristina; Lanzafame, Manuela; Schenk, Susanne H; Tran, Xue-Ting; Englinger, Bernhard; Hauswirth, Patrick; Grünig, David; van Schoonhoven, Sushilla; Krähenbühl, Stephan; Terracciano, Luigi M; Berger, Walter; Piscuoglio, Salvatore; Quagliata, Luca; Rommelaere, Jean; Nüesch, Jürg P F; Huwyler, Jörg
Functional and clinical relevance of novel mutations in a large cohort of patients with Cockayne syndrome. 1-gen-2018 Calmels, N; Botta, E; Jia, N; Fawcett, H; Nardo, T; Nakazawa, Y; Lanzafame, M; Moriwaki, S; Sugita, K; Kubota, M; Obringer, C; Spitz, Ma; Stefanini, M; Laugel, V; Orioli, D; Ogi, T; Lehmann, Ar
GTF2E2 Mutations Destabilize the General Transcription Factor Complex TFIIE in Individuals with DNA Repair-Proficient Trichothiodystrophy 1-gen-2016 Kuschal C.; Botta E.; Orioli D.; Digiovanna J.J.; Seneca S.; Keymolen K.; Tamura D.; Heller E.; Khan S.G.; Caligiuri G.; Lanzafame M.; Nardo T.; Ricotti R.; Peverali F.A.; Stephens R.; Zhao Y.; Lehmann A.R.; Baranello L.; Levens D.; Kraemer K.; Stefanini M.
Overexpression of parkin rescues the defective mitochondrial phenotype and the increased apoptosis of Cockayne Syndrome A cells. 1-gen-2016 Pascucci B.; D'Errico M.; Romagnoli A.; De Nuccio C.; Savino M.; Pietraforte D.; Lanzafame M.; Calcagnile A.S.; Fortini P.; Baccarini S.; Orioli D.; Degan P.; Visentin S.; Stefanini M.; Isidoro C.; Fimia G.M.; Dogliotti E.
Reference genes for gene expression analysis in proliferating and differentiating human keratinocytes 1-gen-2015 Lanzafame, M; Botta, E; Teson, M; Fortugno, P; Zambruno, G; Stefanini, M; Orioli, D
TFIIH-dependent MMP-1 overexpression in trichothiodystrophy leads to extracellular matrix alterations in patient skin 1-gen-2015 Arseni, L; Lanzafame, M; Compe, E; Fortugno, P; Afonsobarroso, A; Peverali, Fa; Lehmann, Ar; Zambruno, G; Egly, Jm; Stefanini, M; Orioli, D
The role of mitochondrial dysfunction in Cockayne Syndrome 1-gen-2015 Mariarosaria D'Errico; Barbara Pascucci; Alessandra Romagnoli; Chiara De Nuccio; Miriam Savino; Donatella Pietraforte; Manuela Lanzafame; Angelo Salvatore Calcagnile; Paola Fortini; Sara Baccarini; Donata Orioli; Paolo Degan; Sergio Visentin; Miria Stefanini; Ciro Isidoro; Gian Maria Fimia; Eugenia Dogliotti
TFIIH-dependent transcriptional impairments contribute to the phenotypic differences associated with distinct XPD mutations 1-gen-2014 Arseni L; Lanzafame M; Compe E; Fortugno P; AfonsoBarroso A; Peverali FA; Zambruno G; Egly JM; Stefanini M; Orioli D
TFIIH-dependent transcriptional impairments contribute to the phenotypic differences associated with distinct XPD mutations 1-gen-2014 Orioli, D; Arseni, L; Lanzafame, M; Nardo, T; Botta, E; Peverali, Fa; Compe, E; Egly, Jm; Stefanini, M
Dalla conferma della diagnosi clinica dei pazienti alla dissezione dei pathways coinvolti nella risposta a stress ossidativo e radiazione UV 1-gen-2013 Lanzafame M; Botta E; Nardo T; Garbelli M; Ricotti R; Orioli D; Stefanini M
Does CSA play a role in mitochondrial quality control? 1-gen-2013 Pascucci, B; Lanzafame, M; Orioli, D; Stefanini, M; Fimia, G; Romagnoli, A; Visentin, S; De Nuccio, C; Calcagnile, A; Vaz, B; Degan, P; Dogliotti, E; D'Errico, M
Does CSA play a role in mitochondrial quality control? 1-gen-2013 Pascucci B.; Lanzafame M.; Orioli D.; Stefanini M.; Fimia G.; Romagnoli A.; Visentin S.; De Nuccio C.; Calcagnile A.; Vaz B.; Degan P.; Dogliotti E.; D'Errico M.
From laboratory tests to functional characterisation of Cockayne syndrome 1-gen-2013 Lanzafame, M; Vaz, B; Nardo, T; Botta, E; Orioli, D; Stefanini, M
Identification of CSA-interacting proteins through a novel TAP/RMCE approach 1-gen-2013 Lanzafame M; Vaz B; Landi C; Peverali FA; Bini L; Stefanini M e Orioli D
TFIIH-mutated cells as a model system to dissect the multiple roles of TFIIH in chromatin dynamics 1-gen-2013 Lombardi A; Arseni L; Lanzafame M; Biamonti G; Stefanini M;Orioli D
Transcriptional alterations in trichotiodystrophy affect different components of the extracellular matrix 1-gen-2013 Arseni, L; Lanzafame, M; Barroso, A; Stefanini, M; Orioli, D
TFIIH-dependent transcription deregulation hampers the extracellular matrix in trichothiodystrophy 1-gen-2012 Arseni, L; Lanzafame, M; Botta, E; Stefanini, M; Orioli, D
Extracellular matrix defects in trichothiodystrophy 1-gen-2011 Arseni L; Lanzafame M; Stefanini M;Orioli D