Insights into Muscle Degeneration from Heritable Inclusion Body Myopathies
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Title
Insights into Muscle Degeneration from Heritable Inclusion Body Myopathies
Authors
Keywords
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Journal
Frontiers in Aging Neuroscience
Volume 7, Issue -, Pages -
Publisher
Frontiers Media SA
Online
2015-02-12
DOI
10.3389/fnagi.2015.00013
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Note: Only part of the references are listed.- Expression of sialic acids in human adult skeletal muscle tissue
- (2014) Mirca Marini et al. ACTA HISTOCHEMICA
- Molecular analyses provide insight into mechanisms underlying sarcopenia and myofibre denervation in old skeletal muscles of mice
- (2014) Mitchell Barns et al. INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY
- The VCP/p97 system at a glance: connecting cellular function to disease pathogenesis
- (2014) H. Meyer et al. JOURNAL OF CELL SCIENCE
- Chemical chaperone ameliorates pathological protein aggregation in plectin-deficient muscle
- (2014) Lilli Winter et al. JOURNAL OF CLINICAL INVESTIGATION
- GNE myopathy: current update and future therapy
- (2014) Ichizo Nishino et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- The role of senescent cells in ageing
- (2014) Jan M. van Deursen NATURE
- Abnormal distribution of heterogeneous nuclear ribonucleoproteins in sporadic inclusion body myositis
- (2014) Jack L. Pinkus et al. NEUROMUSCULAR DISORDERS
- The ubiquitin-selective chaperone Cdc48/p97 associates with Ubx3 to modulate monoubiquitylation of histone H2B
- (2014) Mélanie Bonizec et al. NUCLEIC ACIDS RESEARCH
- Vitamin D Signaling in Myogenesis: Potential for Treatment of Sarcopenia
- (2014) Akira Wagatsuma et al. Biomed Research International
- Novel region discovery method for Infinium 450K DNA methylation data reveals changes associated with aging in muscle and neuronal pathways
- (2013) Mei-Lyn Ong et al. AGING CELL
- Aging increases CCN1 expression leading to muscle senescence
- (2013) Jie Du et al. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
- Myosin chaperones
- (2013) Doris Hellerschmied et al. CURRENT OPINION IN STRUCTURAL BIOLOGY
- Elevated expression of activins promotes muscle wasting and cachexia
- (2013) Justin L. Chen et al. FASEB JOURNAL
- Mitochondrial dysfunction and sarcopenia of aging: From signaling pathways to clinical trials
- (2013) Emanuele Marzetti et al. INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY
- An Antibody Blocking Activin Type II Receptors Induces Strong Skeletal Muscle Hypertrophy and Protects from Atrophy
- (2013) E. Lach-Trifilieff et al. MOLECULAR AND CELLULAR BIOLOGY
- Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS
- (2013) Hong Joo Kim et al. NATURE
- 188th ENMC International Workshop: Inclusion Body Myositis, 2–4 December 2011, Naarden, The Netherlands
- (2013) M.R. Rose NEUROMUSCULAR DISORDERS
- VCP Is Essential for Mitochondrial Quality Control by PINK1/Parkin and this Function Is Impaired by VCP Mutations
- (2013) Nam Chul Kim et al. NEURON
- A three-state model for the regulation of telomerase by TERRA and hnRNPA1
- (2013) Sophie Redon et al. NUCLEIC ACIDS RESEARCH
- Skeletal muscle aging and the mitochondrion
- (2013) Matthew L. Johnson et al. TRENDS IN ENDOCRINOLOGY AND METABOLISM
- Biomarkers of sarcopenia in clinical trials-recommendations from the International Working Group on Sarcopenia
- (2012) Matteo Cesari et al. Journal of Cachexia Sarcopenia and Muscle
- Genes and the ageing muscle: a review on genetic association studies
- (2011) Nuria Garatachea et al. AGE
- Apoptosis in Skeletal Myocytes: A Potential Target for Interventions against Sarcopenia and Physical Frailty – A Mini-Review
- (2011) Emanuele Marzetti et al. GERONTOLOGY
- Sarcopenia: An Undiagnosed Condition in Older Adults. Current Consensus Definition: Prevalence, Etiology, and Consequences. International Working Group on Sarcopenia
- (2011) Roger A. Fielding et al. Journal of the American Medical Directors Association
- The Proteomic Profile of Hereditary Inclusion Body Myopathy
- (2011) Ilan Sela et al. PLoS One
- Regulation of skeletal muscle growth by the IGF1-Akt/PKB pathway: insights from genetic models
- (2011) Stefano Schiaffino et al. Skeletal Muscle
- Sarcopenia: European consensus on definition and diagnosis: Report of the European Working Group on Sarcopenia in Older People
- (2010) A. J. Cruz-Jentoft et al. AGE AND AGEING
- VCP/p97 is essential for maturation of ubiquitin-containing autophagosomes and this function is impaired by mutations that cause IBMPFD
- (2010) Emilie Tresse et al. Autophagy
- A novel ATP-dependent conformation in p97 N–D1 fragment revealed by crystal structures of disease-related mutants
- (2010) Wai Kwan Tang et al. EMBO JOURNAL
- Imbalances in p97 co-factor interactions in human proteinopathy
- (2010) Vanesa Fernández-Sáiz et al. EMBO REPORTS
- Quantitation of selective autophagic protein aggregate degradation in vitro and in vivo using luciferase reporters
- (2009) Jeong-Sun Ju et al. Autophagy
- Alternative Splicing of Cyr61 Is Regulated by Hypoxia and Significantly Changed in Breast Cancer
- (2009) M. Hirschfeld et al. CANCER RESEARCH
- Valosin-containing protein (VCP) is required for autophagy and is disrupted in VCP disease
- (2009) Jeong-Sun Ju et al. JOURNAL OF CELL BIOLOGY
- Prophylactic treatment with sialic acid metabolites precludes the development of the myopathic phenotype in the DMRV-hIBM mouse model
- (2009) May Christine V Malicdan et al. NATURE MEDICINE
- Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources
- (2009) Da Wei Huang et al. Nature Protocols
- Valosin-containing protein disease: Inclusion body myopathy with Paget’s disease of the bone and fronto-temporal dementia
- (2009) Conrad C. Weihl et al. NEUROMUSCULAR DISORDERS
- Clinical outcome in 19 French and Spanish patients with valosin-containing protein myopathy associated with Paget’s disease of bone and frontotemporal dementia
- (2009) Tanya Stojkovic et al. NEUROMUSCULAR DISORDERS
- Valosin containing protein associated inclusion body myopathy: abnormal vacuolization, autophagy and cell fusion in myoblasts
- (2009) Jouni Vesa et al. NEUROMUSCULAR DISORDERS
- Clinical studies in familial VCP myopathy associated with Paget disease of bone and frontotemporal dementia
- (2008) Virginia. E. Kimonis et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Lectin-based proteomic profiling of aged skeletal muscle: Decreased pyruvate kinase isozyme M1 exhibits drastically increased levels of N-glycosylation
- (2008) Kathleen O’Connell et al. EUROPEAN JOURNAL OF CELL BIOLOGY
- Mitochondrial processes are impaired in hereditary inclusion body myopathy
- (2008) Iris Eisenberg et al. HUMAN MOLECULAR GENETICS
- Opposing roles for p16Ink4a and p19Arf in senescence and ageing caused by BubR1 insufficiency
- (2008) Darren J. Baker et al. NATURE CELL BIOLOGY
- Bioinformatics enrichment tools: paths toward the comprehensive functional analysis of large gene lists
- (2008) Da Wei Huang et al. NUCLEIC ACIDS RESEARCH
- UDP-N-Acetylglucosamine 2-Epimerase/N-Acetylmannosamine Kinase (GNE) Binds to Alpha-Actinin 1: Novel Pathways in Skeletal Muscle?
- (2008) Shira Amsili et al. PLoS One
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