Differential induction of muscle atrophy pathways in two mouse models of spinal muscular atrophy
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Title
Differential induction of muscle atrophy pathways in two mouse models of spinal muscular atrophy
Authors
Keywords
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Journal
Scientific Reports
Volume 6, Issue 1, Pages -
Publisher
Springer Nature
Online
2016-06-28
DOI
10.1038/srep28846
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Note: Only part of the references are listed.- Regulation of autophagy and the ubiquitin–proteasome system by the FoxO transcriptional network during muscle atrophy
- (2015) Giulia Milan et al. Nature Communications
- Myogenic program dysregulation is contributory to disease pathogenesis in spinal muscular atrophy
- (2014) Justin G. Boyer et al. HUMAN MOLECULAR GENETICS
- Survival motor neuron protein deficiency impairs myotube formation by altering myogenic gene expression and focal adhesion dynamics
- (2014) Katherine V. Bricceno et al. HUMAN MOLECULAR GENETICS
- HDAC1 activates FoxO and is both sufficient and required for skeletal muscle atrophy
- (2014) A. W. Beharry et al. JOURNAL OF CELL SCIENCE
- Deletion of atrophy enhancing genes fails to ameliorate the phenotype in a mouse model of spinal muscular atrophy
- (2014) Chitra C. Iyer et al. NEUROMUSCULAR DISORDERS
- The Smn-Independent Beneficial Effects of Trichostatin A on an Intermediate Mouse Model of Spinal Muscular Atrophy
- (2014) Hong Liu et al. PLoS One
- Protein breakdown in muscle wasting: Role of autophagy-lysosome and ubiquitin-proteasome
- (2013) Marco Sandri INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY
- Early onset muscle weakness and disruption of muscle proteins in mouse models of spinal muscular atrophy
- (2013) Justin G Boyer et al. Skeletal Muscle
- Guidelines for the use and interpretation of assays for monitoring autophagy
- (2012) Daniel J. Klionsky et al. Autophagy
- Perilipin 2 Improves Insulin Sensitivity in Skeletal Muscle Despite Elevated Intramuscular Lipid Levels
- (2012) M. Bosma et al. DIABETES
- Histone deacetylase inhibition suppresses myogenin-dependent atrogene activation in spinal muscular atrophy mice
- (2012) Katherine V. Bricceno et al. HUMAN MOLECULAR GENETICS
- Partial restoration of cardio-vascular defects in a rescued severe model of spinal muscular atrophy
- (2012) Monir Shababi et al. JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY
- p300 Acetyltransferase activity differentially regulates the localization and activity of the FOXO homologues in skeletal muscle
- (2011) Sarah M. Senf et al. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
- Posttranslational modifications control FoxO3 activity during denervation
- (2011) Enrico Bertaggia et al. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
- FoxO3 induces reversible cardiac atrophy and autophagy in a transgenic mouse model
- (2011) Tobias G. Schips et al. CARDIOVASCULAR RESEARCH
- Increased IGF-1 in muscle modulates the phenotype of severe SMA mice
- (2011) Marta Bosch-Marcé et al. HUMAN MOLECULAR GENETICS
- Severe neuromuscular denervation of clinically relevant muscles in a mouse model of spinal muscular atrophy
- (2011) K. K. Y. Ling et al. HUMAN MOLECULAR GENETICS
- Myogenin regulates denervation-dependent muscle atrophy in mouse soleus muscle
- (2011) Peter C. D. Macpherson et al. JOURNAL OF CELLULAR BIOCHEMISTRY
- A critical smn threshold in mice dictates onset of an intermediate spinal muscular atrophy phenotype associated with a distinct neuromuscular junction pathology
- (2011) Mélissa Bowerman et al. NEUROMUSCULAR DISORDERS
- Regulation of skeletal muscle growth by the IGF1-Akt/PKB pathway: insights from genetic models
- (2011) Stefano Schiaffino et al. Skeletal Muscle
- Newborn and carrier screening for spinal muscular atrophy
- (2010) Thomas W. Prior et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Myogenin and Class II HDACs Control Neurogenic Muscle Atrophy by Inducing E3 Ubiquitin Ligases
- (2010) Viviana Moresi et al. CELL
- Spinal muscular atrophy type I combined with atrial septal defect in three sibs
- (2010) P. Møller et al. CLINICAL GENETICS
- LC3 and GATE-16/GABARAP subfamilies are both essential yet act differently in autophagosome biogenesis
- (2010) Hilla Weidberg et al. EMBO JOURNAL
- Arrhythmia and cardiac defects are a feature of spinal muscular atrophy model mice
- (2010) Christopher R. Heier et al. HUMAN MOLECULAR GENETICS
- Cardiac defects contribute to the pathology of spinal muscular atrophy models
- (2010) Monir Shababi et al. HUMAN MOLECULAR GENETICS
- Early heart failure in the SMNΔ7 model of spinal muscular atrophy and correction by postnatal scAAV9-SMN delivery
- (2010) Adam K. Bevan et al. HUMAN MOLECULAR GENETICS
- Identification of Novel Interacting Protein Partners of SMN Using Tandem Affinity Purification
- (2010) Dina Shafey et al. JOURNAL OF PROTEOME RESEARCH
- Rescue of the spinal muscular atrophy phenotype in a mouse model by early postnatal delivery of SMN
- (2010) Kevin D Foust et al. NATURE BIOTECHNOLOGY
- Mouse Survival Motor Neuron Alleles That Mimic SMN2 Splicing and Are Inducible Rescue Embryonic Lethality Early in Development but Not Late
- (2010) Suzan M. Hammond et al. PLoS One
- FOXO signaling is required for disuse muscle atrophy and is directly regulated by Hsp70
- (2009) Sarah M. Senf et al. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
- Different atrophy-hypertrophy transcription pathways in muscles affected by severe and mild spinal muscular atrophy
- (2009) Caterina Millino et al. BMC Medicine
- Inhibition of myostatin does not ameliorate disease features of severe spinal muscular atrophy mice
- (2009) Charlotte J. Sumner et al. HUMAN MOLECULAR GENETICS
- FoxO Transcription Factors Promote Autophagy in Cardiomyocytes
- (2009) Arunima Sengupta et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- The Transcription of FOXO Genes Is Stimulated by FOXO3 and Repressed by Growth Factors
- (2009) Ahmed Essaghir et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- The Developmental Pattern of Myotubes in Spinal Muscular Atrophy Indicates Prenatal Delay of Muscle Maturation
- (2009) Rebeca Martínez-Hernández et al. JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
- Congenital heart defects in spinal muscular atrophy type I: A clinical report of two siblings and a review of the literature
- (2008) Leonie A. Menke et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Delivery of recombinant follistatin lessens disease severity in a mouse model of spinal muscular atrophy
- (2008) Ferrill F. Rose et al. HUMAN MOLECULAR GENETICS
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