Aberrant insulin receptor expression is associated with insulin resistance and skeletal muscle atrophy in myotonic dystrophies (Q64063436)

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scientific article published on 22 March 2019

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English	Aberrant insulin receptor expression is associated with insulin resistance and skeletal muscle atrophy in myotonic dystrophies	scientific article published on 22 March 2019

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6430513

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30 April 2020

title

Aberrant insulin receptor expression is associated with insulin resistance and skeletal muscle atrophy in myotonic dystrophies (English)

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6430513

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30 April 2020

main subject

preproinsulin

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insulin resistance

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author

Rosanna Cardani

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6

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6430513

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author name string

Laura Valentina Renna

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1

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6430513

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Francesca Bosè

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2

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6430513

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Elisa Brigonzi

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3

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6430513

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Barbara Fossati

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4

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6430513

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30 April 2020

Giovanni Meola

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5

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6430513

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English

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22 March 2019

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PLOS One

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6430513

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30 April 2020

volume

14

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6430513

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3

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30 April 2020

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e0214254

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Creative Commons Attribution 4.0 International

start time

22 March 2019

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cites work

Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

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12 December 2020

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Distinct alpha-subunit structures of human insulin receptor A and B variants determine differences in tyrosine kinase activities

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30901379

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12 December 2020

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Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/30901379

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12 December 2020

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An unstable triplet repeat in a gene related to myotonic muscular dystrophy

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30901379

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12 December 2020

based on heuristic

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Mechanism of muscle wasting in myotonic dystrophy

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https://pubmed.ncbi.nlm.nih.gov/30901379

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12 December 2020

based on heuristic

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In vivo estimation of muscle protein synthesis in myotonic dystrophy

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/30901379

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal regulation of monocyte insulin-binding affinity after glucose ingestion in patients with myotonic dystrophy

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/30901379

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12 December 2020

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The B Isoform of the Insulin Receptor Signals More Efficiently Than the A Isoform in HepG2 Cells

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30901379

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12 December 2020

based on heuristic

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RNA metabolism in myotonic dystrophy: patient muscle shows decreased insulin receptor RNA and protein consistent with abnormal insulin resistance.

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/30901379

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12 December 2020

based on heuristic

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Evaluation of signals activating ubiquitin-proteasome proteolysis in a model of muscle wasting

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/30901379

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12 December 2020

based on heuristic

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Insulin-like growth factor I circumvents defective insulin action in human myotonic dystrophy skeletal muscle cells

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/30901379

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12 December 2020

based on heuristic

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Clinical and genetic heterogeneity in myotonic dystrophies

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30901379

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12 December 2020

based on heuristic

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Assessment of a disease-specific muscular impairment rating scale in myotonic dystrophy

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https://pubmed.ncbi.nlm.nih.gov/30901379

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12 December 2020

based on heuristic

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Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9

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PubMed

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12 December 2020

based on heuristic

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Aberrant regulation of insulin receptor alternative splicing is associated with insulin resistance in myotonic dystrophy

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30901379

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12 December 2020

based on heuristic

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Identification of ubiquitin ligases required for skeletal muscle atrophy

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30901379

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12 December 2020

based on heuristic

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Akt/mTOR pathway is a crucial regulator of skeletal muscle hypertrophy and can prevent muscle atrophy in vivo

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/30901379

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12 December 2020

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Atrogin-1, a muscle-specific F-box protein highly expressed during muscle atrophy

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30901379

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12 December 2020

based on heuristic

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Report of the 84th ENMC Workshop: PROMM (Proximal Myotonic Myopathy) and Other Myotonic Dystrophy-Like Syndromes: 2nd Workshop. 13–15th October, 2000, Loosdrecht, The Netherlands

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https://pubmed.ncbi.nlm.nih.gov/30901379

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12 December 2020

based on heuristic

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Expanded CUG repeats trigger aberrant splicing of ClC-1 chloride channel pre-mRNA and hyperexcitability of skeletal muscle in myotonic dystrophy

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30901379

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12 December 2020

based on heuristic

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Loss of the muscle-specific chloride channel in type 1 myotonic dystrophy due to misregulated alternative splicing

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https://pubmed.ncbi.nlm.nih.gov/30901379

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12 December 2020

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Ageing and local growth factors in muscle

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12 December 2020

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Insulin-stimulated phosphorylation of a Rab GTPase-activating protein regulates GLUT4 translocation

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https://pubmed.ncbi.nlm.nih.gov/30901379

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12 December 2020

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Histopathological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30901379

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12 December 2020

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inferred from PubMed ID database lookup

Muscle- and fibre type-specific expression of glucose transporter 4, glycogen synthase and glycogen phosphorylase proteins in human skeletal muscle

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/30901379

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12 December 2020

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inferred from PubMed ID database lookup

Foxo transcription factors induce the atrophy-related ubiquitin ligase atrogin-1 and cause skeletal muscle atrophy

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/30901379

retrieved

12 December 2020

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inferred from PubMed ID database lookup

Insulin receptor splicing alteration in myotonic dystrophy type 2.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30901379

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12 December 2020

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inferred from PubMed ID database lookup

The IGF-1/PI3K/Akt pathway prevents expression of muscle atrophy-induced ubiquitin ligases by inhibiting FOXO transcription factors

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30901379

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biomolecular identification of (CCTG)n mutation in myotonic dystrophy type 2 (DM2) by FISH on muscle biopsy

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30901379

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12 December 2020

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inferred from PubMed ID database lookup

Insulin Signaling and Glucose Transport in Skeletal Muscle From First-Degree Relatives of Type 2 Diabetic Patients

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30901379

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12 December 2020

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inferred from PubMed ID database lookup

Interaction of the Akt substrate, AS160, with the glucose transporter 4 vesicle marker protein, insulin-regulated aminopeptidase

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30901379

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12 December 2020

based on heuristic

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Distinct signals regulate AS160 phosphorylation in response to insulin, AICAR, and contraction in mouse skeletal muscle

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30901379

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The effect of exercise and insulin on AS160 phosphorylation and 14-3-3 binding capacity in human skeletal muscle.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/30901379

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression of RNA CCUG repeats dysregulates translation and degradation of proteins in myotonic dystrophy 2 patients

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/30901379

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Proteome profile in Myotonic Dystrophy type 2 myotubes reveals dysfunction in protein processing and mitochondrial pathways

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30901379

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12 December 2020

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Normal myogenesis and increased apoptosis in myotonic dystrophy type-1 muscle cells

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30901379

retrieved

12 December 2020

based on heuristic

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Altered signal transduction pathways and induction of autophagy in human myotonic dystrophy type 1 myoblasts

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/30901379

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophy.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/30901379

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regulation of skeletal muscle growth by the IGF1-Akt/PKB pathway: insights from genetic models

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/30901379

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inhibition of FoxO transcriptional activity prevents muscle fiber atrophy during cachexia and induces hypertrophy

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/30901379

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

mTOR-dependent proliferation defect in human ES-derived neural stem cells affected by myotonic dystrophy type 1.

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30901379

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Slow-twitch fiber proportion in skeletal muscle correlates with insulin responsiveness

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/30901379

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification and characterization of DM1 patients by a new diagnostic certified assay: neuromuscular and cardiac assessments

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/30901379

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reexpression of pyruvate kinase M2 in type 1 myofibers correlates with altered glucose metabolism in myotonic dystrophy.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/30901379

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Muscle insulin sensitivity and glucose metabolism are controlled by the intrinsic muscle clock

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/30901379

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Altered Ca2+ homeostasis and endoplasmic reticulum stress in myotonic dystrophy type 1 muscle cells.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/30901379

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myotonic dystrophies: An update on clinical aspects, genetic, pathology, and molecular pathomechanisms

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/30901379

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human muscle fiber type-specific insulin signaling: impact of obesity and type 2 diabetes

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/30901379

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased autophagy and apoptosis contribute to muscle atrophy in a myotonic dystrophy type 1 Drosophila model.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/30901379

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Development and Validation of a New Molecular Diagnostic Assay for Detection of Myotonic Dystrophy Type 2.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/30901379

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Muscle atrophy in patients with Type 2 Diabetes Mellitus: roles of inflammatory pathways, physical activity and exercise

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/30901379

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The ubiquitin proteasome system in atrophying skeletal muscle: roles and regulation

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/30901379

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Targeting deregulated AMPK/mTORC1 pathways improves muscle function in myotonic dystrophy type I.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/30901379

retrieved

12 December 2020

based on heuristic

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Receptor and post-receptor abnormalities contribute to insulin resistance in myotonic dystrophy type 1 and type 2 skeletal muscle.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/30901379

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Exercise Protects Against Defective Insulin Signaling and Insulin Resistance of Glucose Transport in Skeletal Muscle of Angiotensin II-Infused Rat.

1 reference

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reference URL

https://pubmed.ncbi.nlm.nih.gov/30901379

retrieved

12 December 2020

based on heuristic

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Abnormalities in Skeletal Muscle Myogenesis, Growth, and Regeneration in Myotonic Dystrophy.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/30901379

retrieved

12 December 2020

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Identifiers

DOI

10.1371/JOURNAL.PONE.0214254

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stated in

Europe PubMed Central

PMC publication ID

6430513

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30901379%20AND%20SRC:MED&resulttype=core&format=json

retrieved

30 April 2020

PMC publication ID

6430513

1 reference

stated in

Europe PubMed Central

PMC publication ID

6430513

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30901379%20AND%20SRC:MED&resulttype=core&format=json

retrieved

30 April 2020

PubMed publication ID

30901379

1 reference

stated in

Europe PubMed Central

PMC publication ID

6430513

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30901379%20AND%20SRC:MED&resulttype=core&format=json

retrieved

30 April 2020

 

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