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Meloso Kilimanjaro vestir mdx mouse filósofo Grabar Diverso

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Human Galectin-1 Improves Sarcolemma Stability and Muscle Vascularization  in the mdx Mouse Model of Duchenne Muscular Dystrophy: Molecular Therapy -  Methods & Clinical Development
Human Galectin-1 Improves Sarcolemma Stability and Muscle Vascularization in the mdx Mouse Model of Duchenne Muscular Dystrophy: Molecular Therapy - Methods & Clinical Development

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

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

Full-length dystrophin restoration via targeted exon integration by  AAV-CRISPR in a humanized mouse model of Duchenne muscular dystrophy:  Molecular Therapy
Full-length dystrophin restoration via targeted exon integration by AAV-CRISPR in a humanized mouse model of Duchenne muscular dystrophy: Molecular Therapy

UA reduced muscle damage and improved muscle morphology in mdx mice. (A...  | Download Scientific Diagram
UA reduced muscle damage and improved muscle morphology in mdx mice. (A... | Download Scientific Diagram

pGz increases muscle strength and reduces muscle damage in mdx mice.
pGz increases muscle strength and reduces muscle damage in mdx mice.

Prevention of muscular dystrophy in mice by CRISPR/Cas9–mediated editing of  germline DNA | Science
Prevention of muscular dystrophy in mice by CRISPR/Cas9–mediated editing of germline DNA | Science

Utrophin Compensates dystrophin Loss during Mouse Spermatogenesis |  Scientific Reports
Utrophin Compensates dystrophin Loss during Mouse Spermatogenesis | Scientific Reports

Life | Free Full-Text | Deficiency of MMP-10 Aggravates the Diseased  Phenotype of Aged Dystrophic Mice
Life | Free Full-Text | Deficiency of MMP-10 Aggravates the Diseased Phenotype of Aged Dystrophic Mice

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

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

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

Akt1 activation increases muscle mass in mdx mice. (A) Timeline of... |  Download Scientific Diagram
Akt1 activation increases muscle mass in mdx mice. (A) Timeline of... | Download Scientific Diagram

Monitoring disease activity noninvasively in the mdx model of Duchenne  muscular dystrophy | PNAS
Monitoring disease activity noninvasively in the mdx model of Duchenne muscular dystrophy | PNAS

miR-146a deficiency does not aggravate muscular dystrophy in mdx mice |  Skeletal Muscle | Full Text
miR-146a deficiency does not aggravate muscular dystrophy in mdx mice | Skeletal Muscle | Full Text

IJMS | Free Full-Text | A Protocol for Simultaneous In Vivo Imaging of  Cardiac and Neuroinflammation in Dystrophin-Deficient MDX Mice Using  [18F]FEPPA PET
IJMS | Free Full-Text | A Protocol for Simultaneous In Vivo Imaging of Cardiac and Neuroinflammation in Dystrophin-Deficient MDX Mice Using [18F]FEPPA PET

001801 - mdx Strain Details
001801 - mdx Strain Details

A Morpholino Oligomer Therapy Regime That Restores Mitochondrial Function  and Prevents mdx Cardiomyopathy | JACC: Basic to Translational Science
A Morpholino Oligomer Therapy Regime That Restores Mitochondrial Function and Prevents mdx Cardiomyopathy | JACC: Basic to Translational Science

Muscular dystrophy research using the mdx mouse
Muscular dystrophy research using the mdx mouse

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

The tibialis anterior (TA) muscle of the mdx/FVB mouse displays... |  Download Scientific Diagram
The tibialis anterior (TA) muscle of the mdx/FVB mouse displays... | Download Scientific Diagram

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

PDF] Commentary : SU 9516 increases α 7 β 1 Integrin and Ameliorates  Disease Progression in the mdx Mouse Model of Duchenne Muscular Dystrophy |  Semantic Scholar
PDF] Commentary : SU 9516 increases α 7 β 1 Integrin and Ameliorates Disease Progression in the mdx Mouse Model of Duchenne Muscular Dystrophy | Semantic Scholar

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

Cardiac fibrosis starts at a young age (2 months) in mdx mice, but... |  Download Scientific Diagram
Cardiac fibrosis starts at a young age (2 months) in mdx mice, but... | Download Scientific Diagram

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

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

Assessing Functional Performance in the Mdx Mouse Model | Protocol  (Translated to Spanish)
Assessing Functional Performance in the Mdx Mouse Model | Protocol (Translated to Spanish)

Mechanics of dystrophin deficient skeletal muscles in very young mice and  effects of age | American Journal of Physiology-Cell Physiology
Mechanics of dystrophin deficient skeletal muscles in very young mice and effects of age | American Journal of Physiology-Cell Physiology