Lista de obras -

A consolidated AAV system for single-cut CRISPR correction of a common Duchenne muscular dystrophy mutation

artículo científico publicado en 2021

A humanized knockin mouse model of Duchenne muscular dystrophy and its correction by CRISPR-Cas9 therapeutic gene editing

artículo científico publicado en 2022

Ablation of CaMKIIδ oxidation by CRISPR-Cas9 base editing as a therapy for cardiac disease

artículo científico publicado en 2023

Activities of arginase I and II are limiting for endothelial cell proliferation ⬇️

artículo científico publicado el 1 de enero de 2002

Altered ion transport by thyroid epithelia from CFTR(-/-) pigs suggests mechanisms for hypothyroidism in cystic fibrosis.

artículo científico publicado en 2010

Alternative mRNA splicing generates two distinct ADAM12 prodomain variants.

artículo científico publicado en 2013

An essential role of metalloprotease-disintegrin ADAM12 in triple-negative breast cancer

artículo científico publicado en 2012

Analysis of nitrite and nitrate in biological samples using high-performance liquid chromatography.

artículo científico publicado en 2006

CRISPR-Cas9 corrects Duchenne muscular dystrophy exon 44 deletion mutations in mice and human cells

artículo científico publicado en 2019

CRISPR-Cpf1 correction of muscular dystrophy mutations in human cardiomyocytes and mice.

artículo científico publicado en 2017

Control of muscle formation by the fusogenic micropeptide myomixer.

artículo científico publicado en 2017

Correction of Three Prominent Mutations in Mouse and Human Models of Duchenne Muscular Dystrophy by Single-Cut Genome Editing

artículo científico publicado en 2020

Correction of diverse muscular dystrophy mutations in human engineered heart muscle by single-site genome editing.

artículo científico publicado en 2018

Correction: Dynamic Transcriptional Responses to Injury of Regenerative and Non-regenerative Cardiomyocytes Revealed by Single-Nucleus RNA Sequencing

artículo científico publicado en 2020

Degenerative and regenerative pathways underlying Duchenne muscular dystrophy revealed by single-nucleus RNA sequencing

artículo científico publicado en 2020

Dynamic Transcriptional Responses to Injury of Regenerative and Non-regenerative Cardiomyocytes Revealed by Single-Nucleus RNA Sequencing

scientific article published on 26 March 2020

Enhanced CRISPR-Cas9 correction of Duchenne muscular dystrophy in mice by a self-complementary AAV delivery system

scientific article published on 19 February 2020

Gene editing restores dystrophin expression in a canine model of Duchenne muscular dystrophy

scientific article published in Science

In vivo non-invasive monitoring of dystrophin correction in a new Duchenne muscular dystrophy reporter mouse

scientific article published on 04 October 2019

Intracellular complexes of the early-onset torsion dystonia-associated AAA+ ATPase TorsinA.

artículo científico publicado en 2014

Intracellular sources of ornithine for polyamine synthesis in endothelial cells

scientific article published on 14 May 2016

Metalloprotease-disintegrin ADAM12 actively promotes the stem cell-like phenotype in claudin-low breast cancer

artículo científico publicado en 2017

Metalloproteinase-disintegrin ADAM12 is associated with a breast tumor-initiating cell phenotype.

artículo científico publicado en 2013

Phenotypic diversity of breast cancer-related mutations in metalloproteinase-disintegrin ADAM12

artículo científico publicado en 2014

Postnatal genome editing partially restores dystrophin expression in a mouse model of muscular dystrophy.

artículo científico publicado en 2015

Precise correction of Duchenne muscular dystrophy exon deletion mutations by base and prime editing

artículo científico publicado en 2021

Precise genomic editing of pathogenic mutations in rescues dilated cardiomyopathy

artículo científico publicado en 2022

Proteomic Characterization of the Heart and Skeletal Muscle Reveals Widespread Arginine ADP-Ribosylation by the ARTC1 Ectoenzyme

artículo científico publicado en 2018

Requirement of the fusogenic micropeptide myomixer for muscle formation in zebrafish.

artículo científico publicado en 2017

Severe muscle wasting and denervation in mice lacking the RNA-binding protein ZFP106.

artículo científico publicado en 2016

Single-cut genome editing restores dystrophin expression in a new mouse model of muscular dystrophy.

artículo científico publicado en 2017

The role of Delta-like 1 shedding in muscle cell self-renewal and differentiation.

artículo científico publicado en 2008

Lista de obras de

A consolidated AAV system for single-cut CRISPR correction of a common Duchenne muscular dystrophy mutation

A humanized knockin mouse model of Duchenne muscular dystrophy and its correction by CRISPR-Cas9 therapeutic gene editing

Ablation of CaMKIIδ oxidation by CRISPR-Cas9 base editing as a therapy for cardiac disease

Activities of arginase I and II are limiting for endothelial cell proliferation ⬇️

Altered ion transport by thyroid epithelia from CFTR(-/-) pigs suggests mechanisms for hypothyroidism in cystic fibrosis.

Alternative mRNA splicing generates two distinct ADAM12 prodomain variants.

An essential role of metalloprotease-disintegrin ADAM12 in triple-negative breast cancer

Analysis of nitrite and nitrate in biological samples using high-performance liquid chromatography.

CRISPR-Cas9 corrects Duchenne muscular dystrophy exon 44 deletion mutations in mice and human cells

CRISPR-Cpf1 correction of muscular dystrophy mutations in human cardiomyocytes and mice.

Control of muscle formation by the fusogenic micropeptide myomixer.

Correction of Three Prominent Mutations in Mouse and Human Models of Duchenne Muscular Dystrophy by Single-Cut Genome Editing

Correction of diverse muscular dystrophy mutations in human engineered heart muscle by single-site genome editing.

Correction: Dynamic Transcriptional Responses to Injury of Regenerative and Non-regenerative Cardiomyocytes Revealed by Single-Nucleus RNA Sequencing

Degenerative and regenerative pathways underlying Duchenne muscular dystrophy revealed by single-nucleus RNA sequencing

Dynamic Transcriptional Responses to Injury of Regenerative and Non-regenerative Cardiomyocytes Revealed by Single-Nucleus RNA Sequencing

Enhanced CRISPR-Cas9 correction of Duchenne muscular dystrophy in mice by a self-complementary AAV delivery system

Gene editing restores dystrophin expression in a canine model of Duchenne muscular dystrophy

In vivo non-invasive monitoring of dystrophin correction in a new Duchenne muscular dystrophy reporter mouse

Intracellular complexes of the early-onset torsion dystonia-associated AAA+ ATPase TorsinA.

Intracellular sources of ornithine for polyamine synthesis in endothelial cells

Metalloprotease-disintegrin ADAM12 actively promotes the stem cell-like phenotype in claudin-low breast cancer

Metalloproteinase-disintegrin ADAM12 is associated with a breast tumor-initiating cell phenotype.

Phenotypic diversity of breast cancer-related mutations in metalloproteinase-disintegrin ADAM12

Postnatal genome editing partially restores dystrophin expression in a mouse model of muscular dystrophy.

Precise correction of Duchenne muscular dystrophy exon deletion mutations by base and prime editing

Precise genomic editing of pathogenic mutations in rescues dilated cardiomyopathy

Proteomic Characterization of the Heart and Skeletal Muscle Reveals Widespread Arginine ADP-Ribosylation by the ARTC1 Ectoenzyme

Requirement of the fusogenic micropeptide myomixer for muscle formation in zebrafish.

Severe muscle wasting and denervation in mice lacking the RNA-binding protein ZFP106.

Single-cut genome editing restores dystrophin expression in a new mouse model of muscular dystrophy.

The role of Delta-like 1 shedding in muscle cell self-renewal and differentiation.