Insights into muscle degeneration from heritable inclusion body myopathies (Q26851967)

language of work or name

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2015

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Frontiers in Aging Neuroscience

published in

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volume

7

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page(s)

13

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Vitamin D signaling in myogenesis: potential for treatment of sarcopenia

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The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy

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The proteomic profile of hereditary inclusion body myopathy

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28 September 2017

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28 September 2017

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28 September 2017

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Prophylactic treatment with sialic acid metabolites precludes the development of the myopathic phenotype in the DMRV-hIBM mouse model

28 September 2017

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Valosin-containing protein disease: inclusion body myopathy with Paget's disease of the bone and fronto-temporal dementia

28 September 2017

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28 September 2017

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28 September 2017

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28 September 2017

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28 September 2017

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28 September 2017

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GNE protein expression and subcellular distribution are unaltered in HIBM.

28 September 2017

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The ubiquitin-selective chaperone CDC-48/p97 links myosin assembly to human myopathy

28 September 2017

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28 September 2017

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28 September 2017

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Chaperoning myosin assembly in muscle formation and aging

28 September 2017

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Characterization of hereditary inclusion body myopathy myoblasts: possible primary impairment of apoptotic events

31 May 2018

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Molecular analyses provide insight into mechanisms underlying sarcopenia and myofibre denervation in old skeletal muscles of mice.

21 January 2018

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Mitochondrial processes are impaired in hereditary inclusion body myopathy.

21 January 2018

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Clinical studies in familial VCP myopathy associated with Paget disease of bone and frontotemporal dementia.

21 January 2018

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Localization of UDP-GlcNAc 2-epimerase/ManAc kinase (GNE) in the Golgi complex and the nucleus of mammalian cells

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A novel homozygous missense mutation in the GNE gene of a patient with quadriceps-sparing hereditary inclusion body myopathy associated with muscle inflammation

21 January 2018

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Abnormal distribution of heterogeneous nuclear ribonucleoproteins in sporadic inclusion body myositis

21 January 2018

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188th ENMC International Workshop: Inclusion Body Myositis, 2-4 December 2011, Naarden, The Netherlands

21 January 2018

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Clinical outcome in 19 French and Spanish patients with valosin-containing protein myopathy associated with Paget's disease of bone and frontotemporal dementia

21 January 2018

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Roles for UDP-GlcNAc 2-epimerase/ManNAc 6-kinase outside of sialic acid biosynthesis: modulation of sialyltransferase and BiP expression, GM3 and GD3 biosynthesis, proliferation, and apoptosis, and ERK1/2 phosphorylation

21 January 2018

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H2B Ubiquitylation Acts as a Barrier to Ctk1 Nucleosomal Recruitment Prior to Removal by Ubp8 within a SAGA-Related Complex

21 January 2018

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GNE mutations causing distal myopathy with rimmed vacuoles with inflammation

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12 December 2020

Expression of sialic acids in human adult skeletal muscle tissue

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12 December 2020

Proteomic profiling reveals a severely perturbed protein expression pattern in aged skeletal muscle

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12 December 2020

The human muscle proteome in aging

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12 December 2020

Identifiers

DOI

10.3389/FNAGI.2015.00013

0 references

1 reference

PubMed publication ID

25729363

1 reference