Anna Cereseto

Trento, 38123, Italy

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 41 publications

Functional correction of the untreatable CFTR 1717-1G>A mutation through mRNA- and sgRNA-optimized base editing.

Functional correction of the untreatable CFTR 1717-1G>A mutation through mRNA- and sgRNA-optimized base editing.

Journal: Science translational medicine

Published: April 22, 2026

Progress and challenges in cystic fibrosis gene editing.

Progress and challenges in cystic fibrosis gene editing.

Journal: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society

Published: January 09, 2026

Germline-Somatic Liaison Dictates Cancer Subtypes via de novo Steroid Biosynthesis.

Germline-Somatic Liaison Dictates Cancer Subtypes via de novo Steroid Biosynthesis.

Journal: Cancer discovery

Published: December 31, 2024

Functional rescue of F508del-CFTR through revertant mutations introduced by CRISPR base editing.

Functional rescue of F508del-CFTR through revertant mutations introduced by CRISPR base editing.

Journal: Molecular therapy : the journal of the American Society of Gene Therapy

Published: September 06, 2024

Discovering and exploring the hidden diversity of human gut viruses using highly enriched virome samples.

Discovering and exploring the hidden diversity of human gut viruses using highly enriched virome samples.

Journal: bioRxiv : the preprint server for biology

Published: March 11, 2024

CoCas9 is a compact nuclease from the human microbiome for efficient and precise genome editing.

CoCas9 is a compact nuclease from the human microbiome for efficient and precise genome editing.

Journal: Nature communications

Published: January 05, 2024

Eukaryotic-driven directed evolution of Cas9 nucleases.

Eukaryotic-driven directed evolution of Cas9 nucleases.

Journal: Genome biology

Published: September 26, 2023

The NIPBL-gene mutation of a Cornelia de Lange Syndrome patient causes deficits in the hepatocyte differentiation of induced Pluripotent Stem Cells via altered chromatin-accessibility.

The NIPBL-gene mutation of a Cornelia de Lange Syndrome patient causes deficits in the hepatocyte differentiation of induced Pluripotent Stem Cells via altered chromatin-accessibility.

Journal: Cellular and molecular life sciences : CMLS

Published: September 14, 2023

Prime editing functionally corrects cystic fibrosis-causing CFTR mutations in human organoids and airway epithelial cells.

Prime editing functionally corrects cystic fibrosis-causing CFTR mutations in human organoids and airway epithelial cells.

Journal: Cell reports. Medicine

Published: July 26, 2023

An optimized SpCas9 high-fidelity variant for direct protein delivery.

An optimized SpCas9 high-fidelity variant for direct protein delivery.

Journal: Molecular therapy : the journal of the American Society of Gene Therapy

Published: December 08, 2022

Functional restoration of a CFTR splicing mutation through RNA delivery of CRISPR adenine base editor.

Functional restoration of a CFTR splicing mutation through RNA delivery of CRISPR adenine base editor.

Journal: Molecular therapy : the journal of the American Society of Gene Therapy

Published: November 04, 2022

Automated identification of sequence-tailored Cas9 proteins using massive metagenomic data.

Automated identification of sequence-tailored Cas9 proteins using massive metagenomic data.

Journal: Nature communications

Published: August 31, 2022

Showing 1-12 of 41

Last Updated: 09/26/2026