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Challenges associated with homologous directed repair using CRISPR-Cas9 and TALEN to edit the DMD genetic mutation in canine Duchenne muscular dystrophy

PloS one, 2020-01, Vol.15 (1), p.e0228072-e0228072

2020

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Gene therapies in canine models for Duchenne muscular dystrophy

Human genetics, 2019-05, Vol.138 (5), p.483-489

2019

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Short-term treatment of golden retriever muscular dystrophy (GRMD) dogs with rAAVrh74.MHCK7.GALGT2 induces muscle glycosylation and utrophin expression but has no significant effect on muscle strength

PloS one, 2021-03, Vol.16 (3), p.e0248721-e0248721

2021

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Correction: Challenges associated with homologous directed repair using CRISPR-Cas9 and TALEN to edit the DMD genetic mutation in canine Duchenne muscular dystrophy

PloS one, 2020-10, Vol.15 (10), p.e0241430-e0241430

2020

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Oxidative damage to urinary proteins from the GRMD dog and mdx mouse as biomarkers of dystropathology in Duchenne muscular dystrophy

PloS one, 2020-10, Vol.15 (10), p.e0240317-e0240317

2020

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Towards efficient resource provisioning in MapReduce

Journal of parallel and distributed computing, 2016-09, Vol.95, p.29-41

2016

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Best Trade-Off Point Method for Efficient Resource Provisioning in Spark

Algorithms, 2018-12, Vol.11 (12), p.190

Nghiem, Peter P.

2018

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Non-immunogenic utrophin gene therapy for the treatment of muscular dystrophy animal models

Nature medicine, 2019-10, Vol.25 (10), p.1505-1511

2019

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Correction to: Gene therapies in canine models for Duchenne muscular dystrophy

Human genetics, 2019-05, Vol.138 (5), p.491-491

2019

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Creation and characterization of an immortalized canine myoblast cell line: Myok9

Mammalian genome, 2020-04, Vol.31 (3-4), p.95-109

2020

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Modulating fast skeletal muscle contraction protects skeletal muscle in animal models of Duchenne muscular dystrophy

The Journal of clinical investigation, 2023-05, Vol.133 (10), p.1-14

2023

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Whole genome sequencing reveals a 7 base-pair deletion in DMD exon 42 in a dog with muscular dystrophy

Mammalian genome, 2017-04, Vol.28 (3-4), p.106-113

2017

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Comprehensive assessment of physical activity correlated with muscle function in canine Duchenne muscular dystrophy

Annals of physical and rehabilitation medicine, 2022-09, Vol.65 (5), p.101611-101611, Article 101611

2022

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Sparing of the Dystrophin-Deficient Cranial Sartorius Muscle Is Associated with Classical and Novel Hypertrophy Pathways in GRMD Dogs

The American journal of pathology, 2013-11, Vol.183 (5), p.1411-1424

2013

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OPN‐a induces muscle inflammation by increasing recruitment and activation of pro‐inflammatory macrophages

Experimental physiology, 2016-10, Vol.101 (10), p.1285-1300

2016

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Osteopontin is linked with AKT, FoxO1, and myostatin in skeletal muscle cells

Muscle & nerve, 2017-12, Vol.56 (6), p.1119-1127

2017

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A novel canine model for Duchenne muscular dystrophy (DMD): single nucleotide deletion in DMD gene exon 20

Skeletal muscle, 2018-05, Vol.8 (1), p.16-16, Article 16

2018

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Glucose Metabolism as a Pre-clinical Biomarker for the Golden Retriever Model of Duchenne Muscular Dystrophy

Molecular imaging and biology, 2018-10, Vol.20 (5), p.780-788

2018

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The Paradox of Muscle Hypertrophy in Muscular Dystrophy

Physical medicine and rehabilitation clinics of North America, 2012-02, Vol.23 (1), p.149-172

2012

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Pharmacologic Management of Duchenne Muscular Dystrophy: Target Identification and Preclinical Trials

ILAR journal, 2014, Vol.55 (1), p.119-149

2014

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Use of the six-minute walk test to characterize golden retriever muscular dystrophy

Neuromuscular disorders : NMD, 2016-12, Vol.26 (12), p.865-872

2016

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Regulation of cellular anabolism by mTOR: or how I learned to stop worrying and love translation

Sports medicine and health science, 2020-12, Vol.2 (4), p.195-201

2020

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Changes in Muscle Metabolism are Associated with Phenotypic Variability in Golden Retriever Muscular Dystrophy

The Yale journal of biology & medicine, 2017-09, Vol.90 (3), p.351-360

2017

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Bioavailability of a novel midazolam gel after intranasal administration in dogs

American journal of veterinary research, 2012-04, Vol.73 (4), p.539-545

2012

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Challenges associated with homologous directed repair using CRISPR-Cas9 and TALEN to edit the DMD genetic mutation in canine Duchenne muscular dystrophy

Gene therapies in canine models for Duchenne muscular dystrophy

Short-term treatment of golden retriever muscular dystrophy (GRMD) dogs with rAAVrh74.MHCK7.GALGT2 induces muscle glycosylation and utrophin expression but has no significant effect on muscle strength

Correction: Challenges associated with homologous directed repair using CRISPR-Cas9 and TALEN to edit the DMD genetic mutation in canine Duchenne muscular dystrophy

Oxidative damage to urinary proteins from the GRMD dog and mdx mouse as biomarkers of dystropathology in Duchenne muscular dystrophy

Towards efficient resource provisioning in MapReduce

Best Trade-Off Point Method for Efficient Resource Provisioning in Spark

Non-immunogenic utrophin gene therapy for the treatment of muscular dystrophy animal models

Correction to: Gene therapies in canine models for Duchenne muscular dystrophy

Assessment of systemic AAV-microdystrophin gene therapy in the GRMD model of Duchenne muscular dystrophy

Creation and characterization of an immortalized canine myoblast cell line: Myok9

Modulating fast skeletal muscle contraction protects skeletal muscle in animal models of Duchenne muscular dystrophy

Whole genome sequencing reveals a 7 base-pair deletion in DMD exon 42 in a dog with muscular dystrophy

Comprehensive assessment of physical activity correlated with muscle function in canine Duchenne muscular dystrophy

Sparing of the Dystrophin-Deficient Cranial Sartorius Muscle Is Associated with Classical and Novel Hypertrophy Pathways in GRMD Dogs

OPN‐a induces muscle inflammation by increasing recruitment and activation of pro‐inflammatory macrophages

Osteopontin is linked with AKT, FoxO1, and myostatin in skeletal muscle cells

A novel canine model for Duchenne muscular dystrophy (DMD): single nucleotide deletion in DMD gene exon 20

Glucose Metabolism as a Pre-clinical Biomarker for the Golden Retriever Model of Duchenne Muscular Dystrophy

The Paradox of Muscle Hypertrophy in Muscular Dystrophy

Pharmacologic Management of Duchenne Muscular Dystrophy: Target Identification and Preclinical Trials

Use of the six-minute walk test to characterize golden retriever muscular dystrophy

Regulation of cellular anabolism by mTOR: or how I learned to stop worrying and love translation

Changes in Muscle Metabolism are Associated with Phenotypic Variability in Golden Retriever Muscular Dystrophy

Bioavailability of a novel midazolam gel after intranasal administration in dogs

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