Marianna Paulis
Rozzano, Italy
Last Updated: 09/26/2026
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Found 27 publications
Chromosomal Instability in Mouse-Induced Pluripotent Stem Cells: Insights into X and Y Aneuploidies.
Chromosomal Instability in Mouse-Induced Pluripotent Stem Cells: Insights into X and Y Aneuploidies.
Journal: Cytogenetic and genome research
Published: July 24, 2025
Detecting Telomeric DNA Damage by Immuno-Telo FISH.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: March 14, 2025
Generation of iPSC lines (ICHi001-A, ICHi002-A, ICHi003-A, ICHi004-A) from four patients carrying Titin truncating variants associated with dilated cardiomyopathy.
Journal: Stem cell research
Published: January 27, 2025
Generation and characterization of human iPSC lines from two patients with therapy-resistant epilepsy carrying nonsense heterozygous variants in the SMC1A gene.
Journal: Stem cell research
Published: January 23, 2025
Generation of the human iPSC line UNIPDi006-A from a patient with arrhythmogenic cardiomyopathy carrying the DSG2 c.1672C > T pathogenic variant.
Journal: Stem cell research
Published: December 09, 2024
Exonic knockout and knockin gene editing in hematopoietic stem and progenitor cells rescues RAG1 immunodeficiency.
Journal: Science translational medicine
Published: February 07, 2024
Unbiased assessment of genome integrity and purging of adverse outcomes at the target locus upon editing of CD4+ T-cells for the treatment of Hyper IgM1.
Journal: The EMBO journal
Published: April 04, 2023
Dysfunctional Extracellular Matrix Remodeling Supports Perianal Fistulizing Crohn's Disease by a Mechanoregulated Activation of the Epithelial-to-Mesenchymal Transition.
Journal: Cellular and molecular gastroenterology and hepatology
Published: May 26, 2022
Where Are We with RPE Replacement Therapy? A Translational Review from the Ophthalmologist Perspective.
Journal: International journal of molecular sciences
Published: December 10, 2021
Generation and characterization of the human induced pluripotent stem cell (hiPSC) line NCUFi001-A from a patient carrying KCNQ1 G314S mutation.
Journal: Stem cell research
Published: April 08, 2021
Last Updated: 09/26/2026