Lina Cipolla

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 7

Top Topics

Intellectual Disability

Single Molecule

Human Immunodeficiency Virus

Top Venues

Scientific reports

Journal of cell science

This page only lists publications with an associated author ORCID identifier.

Publications

Roberto Ricciardiello, Giulia Forleo, Lina Cipolla, Geraldine van Winckel, Caterina Marconi, Thierry Nouspikel, Thanos D Halazonetis, Omar Zgheib, Simone Sabbioneda
Homozygous substitution of threonine 191 by proline in polymerase η causes Xeroderma pigmentosum variant. Scientific reports 14 (1) (2024)
Roberto Ricciardiello, Giulia Forleo, Lina Cipolla, Geraldine van Winckel, Caterina Marconi, Thierry Nouspikel, Thanos D Halazonetis, Omar Zgheib, Simone Sabbioneda
Homozygous substitution of threonine 191 by proline in polymerase η causes Xeroderma pigmentosum variant. Scientific reports 14 (1) (2024)
Roberto Ricciardiello, Giulia Forleo, Lina Cipolla, Geraldine van Winckel, Caterina Marconi, Thierry Nouspikel, Thanos D Halazonetis, Omar Zgheib, Simone Sabbioneda
Homozygous substitution of threonine 191 by proline in polymerase η causes Xeroderma pigmentosum variant. Scientific reports 14 (1) (2024)
Roberto Ricciardiello, Giulia Forleo, Lina Cipolla, Geraldine van Winckel, Caterina Marconi, Thierry Nouspikel, Thanos D Halazonetis, Omar Zgheib, Simone Sabbioneda
Homozygous substitution of threonine 191 by proline in polymerase η causes Xeroderma pigmentosum variant. Scientific reports 14 (1) (2024)
Roberto Ricciardiello, Giulia Forleo, Lina Cipolla, Geraldine van Winckel, Caterina Marconi, Thierry Nouspikel, Thanos D Halazonetis, Omar Zgheib, Simone Sabbioneda
Homozygous substitution of threonine 191 by proline in polymerase η causes Xeroderma pigmentosum variant. Scientific reports 14 (1) (2024)
Roberto Ricciardiello, Giulia Forleo, Lina Cipolla, Geraldine van Winckel, Caterina Marconi, Thierry Nouspikel, Thanos D Halazonetis, Omar Zgheib, Simone Sabbioneda
Homozygous substitution of threonine 191 by proline in polymerase η causes Xeroderma pigmentosum variant. Scientific reports 14 (1) (2024)
Matteo Cabrini, Marco Roncador, Alessandro Galbiati, Lina Cipolla, Antonio Maffia, Fabio Iannelli, Simone Sabbioneda, Fabrizio d'Adda di Fagagna, Sofia Francia
DROSHA is recruited to DNA damage sites by the MRN complex to promote non-homologous end joining. Journal of cell science 134 (6) (2021)