Lista de obras - Marianna Paulis - Dominio Público Uruguay

A pre-screening FISH-based method to detect CRISPR/Cas9 off-targets in mouse embryonic stem cells.

artículo científico publicado en 2015

A set of duplicons on human chromosome 9 is involved in the origin of a supernumerary marker chromosome

artículo científico publicado en 2006

Anti-CD3ε mAb improves thymic architecture and prevents autoimmune manifestations in a mouse model of Omenn syndrome: therapeutic implications

artículo científico publicado en 2012

Autofluorescence properties of murine embryonic stem cells during spontaneous differentiation phases

artículo científico publicado en 2013

Chromosome Transplantation: Correction of the Chronic Granulomatous Disease Defect in Mouse Induced Pluripotent Stem Cells

scientific article published on 02 April 2019

Chromosome transfer via cell fusion.

artículo científico publicado en 2011

Chromosome transplantation as a novel approach for correcting complex genomic disorders

artículo científico publicado en 2015

Claspin inhibition leads to fragile site expression.

artículo científico publicado en 2009

Cloning of the bovine prion-like Shadoo (SPRN) gene by comparative analysis of the predicted genomic locus

artículo científico publicado en 2006

Cornelia de Lange syndrome mutations in SMC1A or SMC3 affect binding to DNA

artículo científico publicado en 2008

Correction of a Recessive Genetic Defect by CRISPR-Cas9-Mediated Endogenous Repair

artículo científico publicado en 2018

Frataxin gene editing rescues Friedreich's ataxia pathology in dorsal root ganglia organoid-derived sensory neurons

scientific article published on 21 August 2020

Fusion between cancer cells and macrophages occurs in a murine model of spontaneous neu+ breast cancer without increasing its metastatic potential

artículo científico publicado en 2016

Generation of Human Induced Pluripotent Stem Cell-Derived Bona Fide Neural Stem Cells for Ex Vivo Gene Therapy of Metachromatic Leukodystrophy

artículo científico publicado en 2016

Isolation from the horse genome of a new DNA transposon belonging to the Tigger family.

artículo científico publicado en 2004

Motor neuron degeneration, severe myopathy and TDP-43 increase in a transgenic pig model of SOD1-linked familiar ALS

scientific article published on 22 November 2018

Osteopetrosis rescue upon RANKL administration to Rankl(-/-) mice: a new therapy for human RANKL-dependent ARO.

artículo científico publicado en 2012

Prion-like Doppel gene (PRND) in the goat: genomic structure, cDNA, and polymorphisms

artículo científico publicado en 2005

Targeted Gene Correction in Osteopetrotic-Induced Pluripotent Stem Cells for the Generation of Functional Osteoclasts

artículo científico publicado en 2015

The K219T-Lamin mutation induces conduction defects through epigenetic inhibition of SCN5A in human cardiac laminopathy

artículo científico publicado en 2019

Transfer of a human chromosomal vector from a hamster cell line to a mouse embryonic stem cell line.

artículo científico publicado en 2007

Lista de obras de Marianna Paulis

A pre-screening FISH-based method to detect CRISPR/Cas9 off-targets in mouse embryonic stem cells.

A set of duplicons on human chromosome 9 is involved in the origin of a supernumerary marker chromosome

Anti-CD3ε mAb improves thymic architecture and prevents autoimmune manifestations in a mouse model of Omenn syndrome: therapeutic implications

Autofluorescence properties of murine embryonic stem cells during spontaneous differentiation phases

Chromosome Transplantation: Correction of the Chronic Granulomatous Disease Defect in Mouse Induced Pluripotent Stem Cells

Chromosome transfer via cell fusion.

Chromosome transplantation as a novel approach for correcting complex genomic disorders

Claspin inhibition leads to fragile site expression.

Cloning of the bovine prion-like Shadoo (SPRN) gene by comparative analysis of the predicted genomic locus

Cornelia de Lange syndrome mutations in SMC1A or SMC3 affect binding to DNA

Correction of a Recessive Genetic Defect by CRISPR-Cas9-Mediated Endogenous Repair

Frataxin gene editing rescues Friedreich's ataxia pathology in dorsal root ganglia organoid-derived sensory neurons

Fusion between cancer cells and macrophages occurs in a murine model of spontaneous neu+ breast cancer without increasing its metastatic potential

Generation of Human Induced Pluripotent Stem Cell-Derived Bona Fide Neural Stem Cells for Ex Vivo Gene Therapy of Metachromatic Leukodystrophy

Isolation from the horse genome of a new DNA transposon belonging to the Tigger family.

Motor neuron degeneration, severe myopathy and TDP-43 increase in a transgenic pig model of SOD1-linked familiar ALS

Osteopetrosis rescue upon RANKL administration to Rankl(-/-) mice: a new therapy for human RANKL-dependent ARO.

Prion-like Doppel gene (PRND) in the goat: genomic structure, cDNA, and polymorphisms

Targeted Gene Correction in Osteopetrotic-Induced Pluripotent Stem Cells for the Generation of Functional Osteoclasts

The K219T-Lamin mutation induces conduction defects through epigenetic inhibition of SCN5A in human cardiac laminopathy

Transfer of a human chromosomal vector from a hamster cell line to a mouse embryonic stem cell line.