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Mutation Research. Reviews in Mutation Research|July 30, 2025
Trichothiodystrophy: Molecular insights and mechanisms of pathogenicityManuela Lanzafame, Francesca Brevi, Gaia Veniali, et al.
Mechanisms of Ageing and Development|April 10, 2013
From laboratory tests to functional characterisation of Cockayne syndromeManuela Lanzafame, Bruno Vaz, Tiziana Nardo, et al.
International Journal of Molecular Sciences|March 3, 2018
The Role of Long Non-Coding RNAs in HepatocarcinogenesisManuela Lanzafame, Gaia Bianco, Luigi M Terracciano, et al.
Experimental Dermatology|February 6, 2015
Reference genes for gene expression analysis in proliferating and differentiating human keratinocytesManuela Lanzafame, Elena Botta, Massimo Teson, et al.
Human Mutation|October 19, 2022
TFIIH stabilization recovers the DNA repair and transcription dysfunctions in thermo-sensitive trichothiodystrophyManuela Lanzafame, Tiziana Nardo, Roberta Ricotti, et al.
Frontiers in Genetics|February 20, 2018
Genomic Analysis Revealed New Oncogenic Signatures in TP53-Mutant Hepatocellular CarcinomaVenkatesh Kancherla, Samir Abdullazade, Matthias S Matter, et al.
BMC Complementary Medicine and Therapies|May 28, 2021
The polyphenol/saponin-rich Rhus tripartita extract has an apoptotic effect on THP-1 cells through the PI3K/AKT/mTOR signaling pathwayHajer Tlili, Anca Macovei, Daniela Buonocore, et al.
Melanoma Research|July 16, 2008
SPANX-B and SPANX-C (Xq27 region) gene dosage analysis in Sicilian patients with melanomaMichele Salemi, Paolo Bosco, Francesco Calì, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 22, 2015
TFIIH-dependent MMP-1 overexpression in trichothiodystrophy leads to extracellular matrix alterations in patient skinLavinia Arseni, Manuela Lanzafame, Emmanuel Compe, et al.
Nucleic Acids Research|September 28, 2021
Cockayne syndrome group A and ferrochelatase finely tune ribosomal gene transcription and its response to UV irradiationManuela Lanzafame, Giulia Branca, Claudia Landi, et al.
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