(Q45869968)

17 December 2017

title

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

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17 December 2017

Hereditary inclusion body myopathy

main subject

myoblast

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5

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17 December 2017

author name string

Amsili S

1

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17 December 2017

Shlomai Z

2

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17 December 2017

Levitzki R

3

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17 December 2017

Krause S

4

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17 December 2017

Ben-Bassat H

6

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17 December 2017

Mitrani-Rosenbaum S

7

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17 December 2017

publication date

3 August 2007

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17 December 2017

Cell Death & Differentiation

published in

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17 December 2017

volume

14

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17 December 2017

issue

11

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17 December 2017

page(s)

1916-1924

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17 December 2017

https://scigraph.springernature.com/pub.10.1038/sj.cdd.4402208

exact match

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cites work

Distal myopathy with rimmed vacuoles is allelic to hereditary inclusion body myopathy

1 reference

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Distal myopathy with rimmed vacuoles (DMRV): new GNE mutations and splice variant

21 January 2018

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Caspase-independent phosphatidylserine exposure during apoptosis of primary T lymphocytes

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Insulin-like growth factor I in inclusion-body myositis and human muscle cultures.

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Akt: versatile mediator of cell survival and beyond

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Skeletal muscle hypertrophy and atrophy signaling pathways

21 January 2018

1 reference

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"Rimmed vacuole myopathy" sparing the quadriceps. A unique disorder in Iranian Jews

21 January 2018

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7 January 2021

Genetics of inclusion body myopathies

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402208

7 January 2021

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

1 reference

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7 January 2021

Mutations spectrum of GNE in hereditary inclusion body myopathy sparing the quadriceps.

1 reference

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7 January 2021

Novel GNE mutations in Italian families with autosomal recessive hereditary inclusion-body myopathy

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7 January 2021

A bifunctional enzyme catalyzes the first two steps in N-acetylneuraminic acid biosynthesis of rat liver. Purification and characterization of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase

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7 January 2021

Sialic acids: fascinating sugars in higher animals and man

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7 January 2021

The homozygous M712T mutation of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase results in reduced enzyme activities but not in altered overall cellular sialylation in hereditary inclusion body myopathy

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402208

7 January 2021

Reduction of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase activity and sialylation in distal myopathy with rimmed vacuoles

1 reference

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7 January 2021

No overall hyposialylation in hereditary inclusion body myopathy myoblasts carrying the homozygous M712T GNE mutation

1 reference

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7 January 2021

Cellular and molecular regulation of muscle regeneration

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7 January 2021

Human skeletal muscle cell differentiation is associated with changes in myogenic markers and enhanced insulin-mediated MAPK and PKB phosphorylation.

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7 January 2021

Signaling satellite-cell activation in skeletal muscle: markers, models, stretch, and potential alternate pathways

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7 January 2021

Tubulyzine, a novel tri-substituted triazine, prevents the early cell death of transplanted myogenic cells and improves transplantation success.

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7 January 2021

Increased apoptosis, Huntingtin inclusions and altered differentiation in muscle cell cultures from Huntington's disease subjects

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Molecular basis for impaired muscle differentiation in myotonic dystrophy

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7 January 2021

Defective satellite cells in congenital myotonic dystrophy

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7 January 2021

Accelerated age-related decline in replicative life-span of Duchenne muscular dystrophy myoblasts: implications for cell and gene therapy

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7 January 2021

Reduced expression of nicotinic AChRs in myotubes from spinal muscular atrophy I patients.

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7 January 2021

Apoptotic muscle fiber degeneration in distal myopathy with rimmed vacuoles

1 reference

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7 January 2021

Apoptosis and muscle fibre loss in neuromuscular disorders

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7 January 2021

Inhibition of caspase-mediated apoptosis by peroxynitrite in traumatic brain injury.

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7 January 2021

Reasons for the degeneration of ageing skeletal muscle: a central role for IGF-1 signalling.

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7 January 2021

Intracellular signaling during skeletal muscle atrophy

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7 January 2021

The IGF-1/Akt pathway is neuroprotective in Huntington's disease and involves Huntingtin phosphorylation by Akt.

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7 January 2021

Potential roles of insulin and IGF-1 in Alzheimer's disease.

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7 January 2021

Free insulin-like growth factor (IGF)-I and IGF binding proteins 2, 5, and 6 in spinal motor neurons in amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402208

7 January 2021

Autocrine and/or paracrine insulin-like growth factor-I activity in skeletal muscle.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402208

7 January 2021

Mammalian MAP kinase signalling cascades

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402208

7 January 2021

Akt/protein kinase B.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402208

7 January 2021

Expression of the E6 and E7 genes of human papillomavirus (HPV16) extends the life span of human myoblasts

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4402208

7 January 2021

Identifiers

DOI

10.1038/SJ.CDD.4402208

1 reference

17 December 2017

Dimensions Publication ID

1015011272

0 references

1 reference

17 December 2017