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Functional correction of adult mdx mouse muscle using gutted adenoviral  vectors expressing full-length dystrophin | PNAS
Functional correction of adult mdx mouse muscle using gutted adenoviral vectors expressing full-length dystrophin | PNAS

JCI - microRNA-206 promotes skeletal muscle regeneration and delays  progression of Duchenne muscular dystrophy in mice
JCI - microRNA-206 promotes skeletal muscle regeneration and delays progression of Duchenne muscular dystrophy in mice

Natural disease history of the D2‐mdx mouse model for Duchenne muscular  dystrophy - Putten - 2019 - The FASEB Journal - Wiley Online Library
Natural disease history of the D2‐mdx mouse model for Duchenne muscular dystrophy - Putten - 2019 - The FASEB Journal - Wiley Online Library

Cells | Free Full-Text | Oligonucleotide Enhancing Compound Increases  Tricyclo-DNA Mediated Exon-Skipping Efficacy in the Mdx Mouse Model
Cells | Free Full-Text | Oligonucleotide Enhancing Compound Increases Tricyclo-DNA Mediated Exon-Skipping Efficacy in the Mdx Mouse Model

Humanizing the mdx mouse model of DMD: the long and the short of it | npj  Regenerative Medicine
Humanizing the mdx mouse model of DMD: the long and the short of it | npj Regenerative Medicine

538. Transgenic Mini-Dystrophin Expression in Skeletal Muscles of Mdx:utrn-/-  Double KO Mice Ameliorates Dystrophic Phenotypes and Remarkably Extends  Life Span: Molecular Therapy
538. Transgenic Mini-Dystrophin Expression in Skeletal Muscles of Mdx:utrn-/- Double KO Mice Ameliorates Dystrophic Phenotypes and Remarkably Extends Life Span: Molecular Therapy

Cardiac Protection after Systemic Transplant of Dystrophin Expressing  Chimeric (DEC) Cells to the mdx Mouse Model of Duchenne Muscular Dystrophy  | Stem Cell Reviews and Reports
Cardiac Protection after Systemic Transplant of Dystrophin Expressing Chimeric (DEC) Cells to the mdx Mouse Model of Duchenne Muscular Dystrophy | Stem Cell Reviews and Reports

PTEN Inhibition Ameliorates Muscle Degeneration and Improves Muscle  Function in a Mouse Model of Duchenne Muscular Dystrophy | bioRxiv
PTEN Inhibition Ameliorates Muscle Degeneration and Improves Muscle Function in a Mouse Model of Duchenne Muscular Dystrophy | bioRxiv

B10-mdx
B10-mdx

JCI Insight - TGF-β–driven muscle degeneration and failed regeneration  underlie disease onset in a DMD mouse model
JCI Insight - TGF-β–driven muscle degeneration and failed regeneration underlie disease onset in a DMD mouse model

Murine models of Duchenne muscular dystrophy: is there a best model? |  American Journal of Physiology-Cell Physiology
Murine models of Duchenne muscular dystrophy: is there a best model? | American Journal of Physiology-Cell Physiology

JCI Insight - Lack of miR-378 attenuates muscular dystrophy in mdx mice
JCI Insight - Lack of miR-378 attenuates muscular dystrophy in mdx mice

Preclinical Studies in the mdx Mouse Model of Duchenne Muscular Dystrophy  with the Histone Deacetylase Inhibitor Givinostat | Molecular Medicine |  Full Text
Preclinical Studies in the mdx Mouse Model of Duchenne Muscular Dystrophy with the Histone Deacetylase Inhibitor Givinostat | Molecular Medicine | Full Text

Muscle Structure Influences Utrophin Expression in mdx Mice | PLOS Genetics
Muscle Structure Influences Utrophin Expression in mdx Mice | PLOS Genetics

Graphical representation showing the effects of cannabinoids in mdx mice. |  Download Scientific Diagram
Graphical representation showing the effects of cannabinoids in mdx mice. | Download Scientific Diagram

Duchenne Muscular Dystrophy Models | Charles River
Duchenne Muscular Dystrophy Models | Charles River

Micro-utrophin Improves Cardiac and Skeletal Muscle Function of Severely  Affected D2/mdx Mice: Molecular Therapy Methods & Clinical Development
Micro-utrophin Improves Cardiac and Skeletal Muscle Function of Severely Affected D2/mdx Mice: Molecular Therapy Methods & Clinical Development

Moderate exercise improves function and increases adiponectin in the mdx  mouse model of muscular dystrophy | Scientific Reports
Moderate exercise improves function and increases adiponectin in the mdx mouse model of muscular dystrophy | Scientific Reports

001801 - mdx Strain Details
001801 - mdx Strain Details

IJMS | Free Full-Text | Lipocalin 2 Influences Bone and Muscle Phenotype in  the MDX Mouse Model of Duchenne Muscular Dystrophy
IJMS | Free Full-Text | Lipocalin 2 Influences Bone and Muscle Phenotype in the MDX Mouse Model of Duchenne Muscular Dystrophy

The D2.mdx mouse as a preclinical model of the skeletal muscle pathology  associated with Duchenne muscular dystrophy | Scientific Reports
The D2.mdx mouse as a preclinical model of the skeletal muscle pathology associated with Duchenne muscular dystrophy | Scientific Reports

Myofiber / pro-inflammatory macrophage interplay controls muscle damage in mdx  mice | bioRxiv
Myofiber / pro-inflammatory macrophage interplay controls muscle damage in mdx mice | bioRxiv

Duchenne's muscular dystrophy involves a defective transsulfuration pathway  activity - ScienceDirect
Duchenne's muscular dystrophy involves a defective transsulfuration pathway activity - ScienceDirect

Whole-body clearing, staining and screening of calcium deposits in the mdx  mouse model of Duchenne muscular dystrophy | Skeletal Muscle | Full Text
Whole-body clearing, staining and screening of calcium deposits in the mdx mouse model of Duchenne muscular dystrophy | Skeletal Muscle | Full Text