Macroglossia and less advanced dystrophic change in the tongue muscle of the Duchenne muscular dystrophy rat

[1] Ariga M(2000)Signalling pathways of insulin-like growth factor-I that are augmented by cAMP in FRTL-5 cells Biochem J 348 409-416

[2] Nedachi T(2001)Identification of ubiquitin ligases required for skeletal muscle atrophy Science 294 1704-1708

[3] Akahori M(2009)Orofacial dysfunction in Duchenne muscular dystrophy Arch Oral Biol 54 26-31

[4] Sakamoto H(1988)The mdx mouse skeletal muscle myopathy: II. Contractile properties Neuropathol Appl Neurobiol 14 299-314

[5] Ito Y(2018)Dysphagia due to macroglossia in a patient with amyloidosis associated with multiple myeloma: a case report Spec Care Dentist 38 255-258

[6] Hakuno F(2016)ROS, cell senescence, and novel molecular mechanisms in aging and age-related diseases Oxid Med Cell Longev 2016 3565127-727

[7] Takahashi S(1997)Utrophin-dystrophin-deficient mice as a model for Duchenne muscular dystrophy Cell 90 717-321

[8] Bodine SC(1991)Fiber regeneration is not persistent in dystrophic (MDX) mouse skeletal muscle Dev Biol 148 314-1059

[9] Latres E(2021)Duchenne muscular dystrophy Nat Rev Dis Primers 7 13-738

[10] Baumhueter S(2015)Muscular dystrophy in the mdx mouse is a severe myopathy compounded by hypotrophy, hypertrophy and hyperplasia Skelet Muscle 5 16-951

[1] Ariga M(2000)Signalling pathways of insulin-like growth factor-I that are augmented by cAMP in FRTL-5 cells Biochem J 348 409-416

[2] Nedachi T(2001)Identification of ubiquitin ligases required for skeletal muscle atrophy Science 294 1704-1708

[3] Akahori M(2009)Orofacial dysfunction in Duchenne muscular dystrophy Arch Oral Biol 54 26-31

[4] Sakamoto H(1988)The mdx mouse skeletal muscle myopathy: II. Contractile properties Neuropathol Appl Neurobiol 14 299-314

[5] Ito Y(2018)Dysphagia due to macroglossia in a patient with amyloidosis associated with multiple myeloma: a case report Spec Care Dentist 38 255-258

[6] Hakuno F(2016)ROS, cell senescence, and novel molecular mechanisms in aging and age-related diseases Oxid Med Cell Longev 2016 3565127-727

[7] Takahashi S(1997)Utrophin-dystrophin-deficient mice as a model for Duchenne muscular dystrophy Cell 90 717-321

[8] Bodine SC(1991)Fiber regeneration is not persistent in dystrophic (MDX) mouse skeletal muscle Dev Biol 148 314-1059

[9] Latres E(2021)Duchenne muscular dystrophy Nat Rev Dis Primers 7 13-738

[10] Baumhueter S(2015)Muscular dystrophy in the mdx mouse is a severe myopathy compounded by hypotrophy, hypertrophy and hyperplasia Skelet Muscle 5 16-951