A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the...

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© 1997 Nature Publishing Group http://www.nature.com/naturegenetics

Transcript of A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the...

Page 1: A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator

© 1997 Nature Publishing Group http://www.nature.com/naturegenetics

Page 2: A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator

© 1997 Nature Publishing Group http://www.nature.com/naturegenetics

Page 3: A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator

© 1997 Nature Publishing Group http://www.nature.com/naturegenetics

Page 4: A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator

© 1997 Nature Publishing Group http://www.nature.com/naturegenetics

Page 5: A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator

© 1997 Nature Publishing Group http://www.nature.com/naturegenetics

Page 6: A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator

© 1997 Nature Publishing Group http://www.nature.com/naturegenetics

Page 7: A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator

© 1997 Nature Publishing Group http://www.nature.com/naturegenetics

Page 8: A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator

© 1997 Nature Publishing Group http://www.nature.com/naturegenetics

Page 9: A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator

© 1997 Nature Publishing Group http://www.nature.com/naturegenetics


The Caulobacter crescentus DNA-(adenine-N6)-methyltransferase CcrM methylates DNA in a distributive manner

The Caulobacter crescentus DNA-(adenine-N6)-methyltransferase CcrM methylates DNA in a distributive manner

Mutations in the Sarcoglycan Genes in Patients with Myopathy

Mutations in the Sarcoglycan Genes in Patients with Myopathy

Nebulin expression in patients with nemaline myopathy

Nebulin expression in patients with nemaline myopathy

Hereditary myopathy with early respiratory failure is associated with misfolding of the titin fibronectin III 119 subdomain

Hereditary myopathy with early respiratory failure is associated with misfolding of the titin fibronectin III 119 subdomain

TPC2 Proteins Mediate Nicotinic Acid Adenine Dinucleotide Phosphate (NAADP)- and Agonist-evoked Contractions of Smooth Muscle

TPC2 Proteins Mediate Nicotinic Acid Adenine Dinucleotide Phosphate (NAADP)- and Agonist-evoked Contractions of Smooth Muscle

A TPM3 mutation causing cap myopathy

A TPM3 mutation causing cap myopathy

Structural Probing of Off-Target G Protein-Coupled Receptor Activities within a Series of Adenosine/Adenine Congeners

Structural Probing of Off-Target G Protein-Coupled Receptor Activities within a Series of Adenosine/Adenine Congeners

Adsorption of Adenine and Thymine on Zeolites: FT-IR and EPR Spectroscopy and X-Ray Diffractometry and SEM Studies

Adsorption of Adenine and Thymine on Zeolites: FT-IR and EPR Spectroscopy and X-Ray Diffractometry and SEM Studies

The Arabidopsis Plastidic Glucose 6Phosphate/Phosphate Translocator GPT1 Is Essential for Pollen Maturation and Embryo Sac Development

The Arabidopsis Plastidic Glucose 6Phosphate/Phosphate Translocator GPT1 Is Essential for Pollen Maturation and Embryo Sac Development

Electrochemical detection of adenine and guanine using a self-assembled copper(II)–thiophenyl-azoimidazole complex monolayer modified gold electrode

Electrochemical detection of adenine and guanine using a self-assembled copper(II)–thiophenyl-azoimidazole complex monolayer modified gold electrode

Metformin activates the AMP-activated protein kinase in hepatocytes by changes in adenine nucleotides

Metformin activates the AMP-activated protein kinase in hepatocytes by changes in adenine nucleotides

Safety and efficacy of exercise training in patients with an idiopathic inflammatory myopathy--a systematic review

Safety and efficacy of exercise training in patients with an idiopathic inflammatory myopathy--a systematic review

Assessing function and endurance in adults with spinal and bulbar muscular atrophy: validity of the adult myopathy assessment tool

Assessing function and endurance in adults with spinal and bulbar muscular atrophy: validity of the adult myopathy assessment tool

Flavin Adenine Dinucleotide Rescues the Phenotype of Frataxin Deficiency

Flavin Adenine Dinucleotide Rescues the Phenotype of Frataxin Deficiency

Myofiber adaptational response to exercise in a mouse model of nemaline myopathy

Myofiber adaptational response to exercise in a mouse model of nemaline myopathy

Elevated zinc induces endothelial apoptosis via disruption of glutathione metabolism: role of the ADP translocator

Elevated zinc induces endothelial apoptosis via disruption of glutathione metabolism: role of the ADP translocator

The Transcription Factor Aryl Hydrocarbon Receptor Nuclear Translocator Functions as an Estrogen Receptor Selective Coactivator, and Its Recruitment to Alternative Pathways Mediates

The Transcription Factor Aryl Hydrocarbon Receptor Nuclear Translocator Functions as an Estrogen Receptor Selective Coactivator, and Its Recruitment to Alternative Pathways Mediates

Ultrafast Dynamics of Adenine Derivatives Studied by Time ...

Ultrafast Dynamics of Adenine Derivatives Studied by Time ...

Transgenic overexpression of human DMPK accumulates into hypertrophic cardiomyopathy, myotonic myopathy and hypotension traits of myotonic dystrophy

Transgenic overexpression of human DMPK accumulates into hypertrophic cardiomyopathy, myotonic myopathy and hypotension traits of myotonic dystrophy

Care of Congenital Myopathy: A Guide for Families

Care of Congenital Myopathy: A Guide for Families