Lista de obras - Thomas Krag - Dominio Público Uruguay

90-kDa ribosomal S6 kinase is phosphorylated and activated by 3-phosphoinositide-dependent protein kinase-1.

artículo científico publicado en 1999

A New Mouse Model of Limb-Girdle Muscular Dystrophy Type 2I Homozygous for the Common L276I Mutation Mimicking the Mild Phenotype in Humans

artículo científico publicado en 2015

A novel de novo mutation of the mitochondrial tRNAlys gene mt.8340G>a associated with pure myopathy.

artículo científico publicado en 2013

A pilot study of muscle plasma protein changes after exercise.

artículo científico publicado en 2013

Absence of p.R50X Pygm read-through in McArdle disease cellular models

scientific article published on 13 January 2020

Aerobic training is safe and improves exercise capacity in patients with mitochondrial myopathy

artículo científico publicado en 2006

BAG3 myopathy is not always associated with cardiomyopathy

scientific article published on 05 July 2018

Calpain 3 is important for muscle regeneration: evidence from patients with limb girdle muscular dystrophies.

artículo científico publicado en 2012

Clinical heterogeneity and phenotype/genotype findings in 5 families with GYG1 deficiency

artículo científico publicado en 2017

Collagen XII myopathy with rectus femoris atrophy and collagen XII retention in fibroblasts

artículo científico publicado en 2018

Deletion of exon 16 of the dystrophin gene is not associated with disease

artículo científico publicado en 2007

Differential Muscle Involvement in Mice and Humans Affected by McArdle Disease.

artículo científico publicado en 2016

Differential glucose metabolism in mice and humans affected by McArdle disease.

artículo científico publicado en 2016

Effect of Aerobic Exercise Training and Deconditioning on Oxidative Capacity and Muscle Mitochondrial Enzyme Machinery in Young and Elderly Individuals

artículo científico publicado en 2020

Effect of sildenafil on skeletal and cardiac muscle in Becker muscular dystrophy

artículo científico publicado en 2014

Electroporation Enhanced Effect of Dystrophin Splice Switching PNA Oligomers in Normal and Dystrophic Muscle

scientific article published on December 2015

Endurance training: an effective and safe treatment for patients with LGMD2I

artículo científico publicado en 2007

Exercising with blocked muscle glycogenolysis: Adaptation in the McArdle mouse.

artículo científico publicado en 2017

Expanding the phenotype of filamin-C-related myofibrillar myopathy

scientific article published on 19 November 2018

Functional improvement of dystrophic muscle by myostatin blockade.

artículo científico publicado en 2002

Glycogen Synthesis in Glycogenin 1-Deficient Patients: A Role for Glycogenin 2 in Muscle.

artículo científico publicado en 2017

Harnessing the potential of dystrophin-related proteins for ameliorating Duchenne's muscular dystrophy

artículo científico publicado en 2001

Identification of genes that are differentially expressed in extraocular and limb muscle.

artículo científico publicado en 2000

Level of muscle regeneration in limb-girdle muscular dystrophy type 2I relates to genotype and clinical severity

artículo científico publicado en 2011

Limb girdle muscular dystrophy due to mutations in POMT2.

artículo científico publicado en 2017

Low survival rate and muscle fiber-dependent aging effects in the McArdle disease mouse model

scientific article published on 26 March 2019

Muscle atrophy reversed by growth factor activation of satellite cells in a mouse muscle atrophy model

artículo científico publicado en 2014

Muscle biopsies off-set normal cellular signaling in surrounding musculature

artículo científico publicado en 2013

Muscle involvement in limb-girdle muscular dystrophy with GMPPB deficiency (LGMD2T).

artículo científico publicado en 2016

Muscle regeneration and inflammation in patients with facioscapulohumeral muscular dystrophy

artículo científico publicado en 2013

Muscle regeneration in mitochondrial myopathies

artículo científico publicado en 2013

Myostatin propeptide-mediated amelioration of dystrophic pathophysiology

scientific article published on 01 April 2005

No muscle involvement in myoclonus-dystonia caused by epsilon-sarcoglycan gene mutations

artículo científico publicado en 2008

Phenotype and clinical course in a family with a new de novo Twinkle gene mutation

artículo científico publicado en 2008

Preclinical Research in Glycogen Storage Diseases: A Comprehensive Review of Current Animal Models

artículo científico publicado en 2020

Preserved Capacity for Adaptations in Strength and Muscle Regulatory Factors in Elderly in Response to Resistance Exercise Training and Deconditioning

artículo científico publicado en 2020

Protein turnover and cellular stress in mildly and severely affected muscles from patients with limb girdle muscular dystrophy type 2I.

artículo científico publicado en 2013

Protein-carbohydrate supplements improve muscle protein balance in muscular dystrophy patients after endurance exercise: a placebo-controlled crossover study

scientific article published on 19 November 2014

Resistance training in patients with limb-girdle and becker muscular dystrophies.

artículo científico publicado en 2012

Short- and long-term effects of endurance training in patients with mitochondrial myopathy

scientific article published on 27 May 2009

Sp1 and the ets-related transcription factor complex GABP alpha/beta functionally cooperate to activate the utrophin promoter.

artículo científico publicado en 2002

Therapeutics for Duchenne muscular dystrophy: current approaches and future directions.

artículo científico publicado en 2003

Lista de obras de Thomas Krag

90-kDa ribosomal S6 kinase is phosphorylated and activated by 3-phosphoinositide-dependent protein kinase-1.

A New Mouse Model of Limb-Girdle Muscular Dystrophy Type 2I Homozygous for the Common L276I Mutation Mimicking the Mild Phenotype in Humans

A novel de novo mutation of the mitochondrial tRNAlys gene mt.8340G>a associated with pure myopathy.

A pilot study of muscle plasma protein changes after exercise.

Absence of p.R50X Pygm read-through in McArdle disease cellular models

Aerobic training is safe and improves exercise capacity in patients with mitochondrial myopathy

BAG3 myopathy is not always associated with cardiomyopathy

Calpain 3 is important for muscle regeneration: evidence from patients with limb girdle muscular dystrophies.

Clinical heterogeneity and phenotype/genotype findings in 5 families with GYG1 deficiency

Collagen XII myopathy with rectus femoris atrophy and collagen XII retention in fibroblasts

Deletion of exon 16 of the dystrophin gene is not associated with disease

Differential Muscle Involvement in Mice and Humans Affected by McArdle Disease.

Differential glucose metabolism in mice and humans affected by McArdle disease.

Effect of Aerobic Exercise Training and Deconditioning on Oxidative Capacity and Muscle Mitochondrial Enzyme Machinery in Young and Elderly Individuals

Effect of sildenafil on skeletal and cardiac muscle in Becker muscular dystrophy

Electroporation Enhanced Effect of Dystrophin Splice Switching PNA Oligomers in Normal and Dystrophic Muscle

Endurance training: an effective and safe treatment for patients with LGMD2I

Exercising with blocked muscle glycogenolysis: Adaptation in the McArdle mouse.

Expanding the phenotype of filamin-C-related myofibrillar myopathy

Functional improvement of dystrophic muscle by myostatin blockade.

Glycogen Synthesis in Glycogenin 1-Deficient Patients: A Role for Glycogenin 2 in Muscle.

Harnessing the potential of dystrophin-related proteins for ameliorating Duchenne's muscular dystrophy

Identification of genes that are differentially expressed in extraocular and limb muscle.

Level of muscle regeneration in limb-girdle muscular dystrophy type 2I relates to genotype and clinical severity

Limb girdle muscular dystrophy due to mutations in POMT2.

Low survival rate and muscle fiber-dependent aging effects in the McArdle disease mouse model

Muscle atrophy reversed by growth factor activation of satellite cells in a mouse muscle atrophy model

Muscle biopsies off-set normal cellular signaling in surrounding musculature

Muscle involvement in limb-girdle muscular dystrophy with GMPPB deficiency (LGMD2T).

Muscle regeneration and inflammation in patients with facioscapulohumeral muscular dystrophy

Muscle regeneration in mitochondrial myopathies

Myostatin propeptide-mediated amelioration of dystrophic pathophysiology

No muscle involvement in myoclonus-dystonia caused by epsilon-sarcoglycan gene mutations

Phenotype and clinical course in a family with a new de novo Twinkle gene mutation

Preclinical Research in Glycogen Storage Diseases: A Comprehensive Review of Current Animal Models

Preserved Capacity for Adaptations in Strength and Muscle Regulatory Factors in Elderly in Response to Resistance Exercise Training and Deconditioning

Protein turnover and cellular stress in mildly and severely affected muscles from patients with limb girdle muscular dystrophy type 2I.

Protein-carbohydrate supplements improve muscle protein balance in muscular dystrophy patients after endurance exercise: a placebo-controlled crossover study

Resistance training in patients with limb-girdle and becker muscular dystrophies.

Short- and long-term effects of endurance training in patients with mitochondrial myopathy

Sp1 and the ets-related transcription factor complex GABP alpha/beta functionally cooperate to activate the utrophin promoter.

Therapeutics for Duchenne muscular dystrophy: current approaches and future directions.