Giulia Forleo

Publication Activity (10 Years)

Years Active: 2024-2024
Publications (10 Years): 6

Top Topics

Hepatitis C Virus

Single Molecule

Top Venues

Scientific reports

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)