(Q34716334)

English

Alternative splicing of human insulin receptor gene (INSR) in type I and type II skeletal muscle fibers of patients with myotonic dystrophy type 1 and type 2.

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scholarly article

1 reference

Europe PubMed Central

4 August 2017

Alternative splicing of human insulin receptor gene (INSR) in type I and type II skeletal muscle fibers of patients with myotonic dystrophy type 1 and type 2. (English)

1 reference

Europe PubMed Central

4 August 2017

alternative mRNA splicing, via spliceosome

1 reference

based on heuristic

inferred from title

myotonic dystrophy

1 reference

based on heuristic

inferred from title

author name string

Massimo Santoro

1

1 reference

Europe PubMed Central

4 August 2017

Marcella Masciullo

2

1 reference

Europe PubMed Central

4 August 2017

Davide Bonvissuto

3

1 reference

Europe PubMed Central

4 August 2017

Maria Laura Ester Bianchi

4

1 reference

Europe PubMed Central

4 August 2017

Fabrizio Michetti

5

1 reference

Europe PubMed Central

4 August 2017

Gabriella Silvestri

6

1 reference

Europe PubMed Central

4 August 2017

publication date

11 May 2013

1 reference

Europe PubMed Central

4 August 2017

Molecular and Cellular Biochemistry

1 reference

Europe PubMed Central

4 August 2017

380

1 reference

Europe PubMed Central

4 August 2017

1-2

1 reference

Europe PubMed Central

4 August 2017

259-265

1 reference

Europe PubMed Central

4 August 2017

https://scigraph.springernature.com/pub.10.1007/s11010-013-1681-z

0 references

Myotonic dystrophy type 2: molecular, diagnostic and clinical spectrum

1 reference

https://api.crossref.org/works/10.1007%2FS11010-013-1681-Z

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS11010-013-1681-Z

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS11010-013-1681-Z

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS11010-013-1681-Z

21 January 2018

The myotonic dystrophies: molecular, clinical, and therapeutic challenges

1 reference

https://api.crossref.org/works/10.1007%2FS11010-013-1681-Z

21 January 2018

Foci of trinucleotide repeat transcripts in nuclei of myotonic dystrophy cells and tissues

1 reference

https://api.crossref.org/works/10.1007%2FS11010-013-1681-Z

21 January 2018

Expansion of a CUG trinucleotide repeat in the 3' untranslated region of myotonic dystrophy protein kinase transcripts results in nuclear retention of transcripts

1 reference

https://api.crossref.org/works/10.1007%2FS11010-013-1681-Z

21 January 2018

Myotonic dystrophy: emerging mechanisms for DM1 and DM2.

1 reference

https://api.crossref.org/works/10.1007%2FS11010-013-1681-Z

21 January 2018

Disruption of splicing regulated by a CUG-binding protein in myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1007%2FS11010-013-1681-Z

21 January 2018

Insulin receptor splicing alteration in myotonic dystrophy type 2.

1 reference

https://api.crossref.org/works/10.1007%2FS11010-013-1681-Z

21 January 2018

A muscleblind knockout model for myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1007%2FS11010-013-1681-Z

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS11010-013-1681-Z

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS11010-013-1681-Z

21 January 2018

Muscle-specific alternative splicing of myotubularin-related 1 gene is impaired in DM1 muscle cells

1 reference

https://api.crossref.org/works/10.1007%2FS11010-013-1681-Z

21 January 2018

Altered mRNA splicing of the skeletal muscle ryanodine receptor and sarcoplasmic/endoplasmic reticulum Ca2+-ATPase in myotonic dystrophy type 1.

1 reference

https://api.crossref.org/works/10.1007%2FS11010-013-1681-Z

21 January 2018

Analysis of MTMR1 expression and correlation with muscle pathological features in juvenile/adult onset myotonic dystrophy type 1 (DM1) and in myotonic dystrophy type 2 (DM2).

1 reference

https://api.crossref.org/works/10.1007%2FS11010-013-1681-Z

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS11010-013-1681-Z

21 January 2018

Differences in aberrant expression and splicing of sarcomeric proteins in the myotonic dystrophies DM1 and DM2.

1 reference

https://api.crossref.org/works/10.1007%2FS11010-013-1681-Z

21 January 2018

Deregulated microRNAs in myotonic dystrophy type 2

1 reference

https://api.crossref.org/works/10.1007%2FS11010-013-1681-Z

21 January 2018

Overexpression of microRNA-206 in the skeletal muscle from myotonic dystrophy type 1 patients.

1 reference

https://api.crossref.org/works/10.1007%2FS11010-013-1681-Z

21 January 2018

Insulin receptor isoforms and insulin receptor/insulin-like growth factor receptor hybrids in physiology and disease.

1 reference

https://api.crossref.org/works/10.1007%2FS11010-013-1681-Z

21 January 2018

Alternative splicing of human insulin receptor messenger RNA.

1 reference

https://api.crossref.org/works/10.1007%2FS11010-013-1681-Z

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS11010-013-1681-Z

21 January 2018

Signaling in muscle atrophy and hypertrophy

1 reference

https://api.crossref.org/works/10.1007%2FS11010-013-1681-Z

21 January 2018

Immuno-LCM: laser capture microdissection of immunostained frozen sections for mRNA analysis

1 reference

https://api.crossref.org/works/10.1007%2FS11010-013-1681-Z

21 January 2018

Improvement of tissue preparation for laser capture microdissection: application for cell type-specific miRNA expression profiling in colorectal tumors

1 reference

https://api.crossref.org/works/10.1007%2FS11010-013-1681-Z

21 January 2018

Laser capture microdissection and single-cell RT-PCR without RNA purification

1 reference

https://api.crossref.org/works/10.1007%2FS11010-013-1681-Z

21 January 2018

Technique for quantitative RT-PCR analysis directly from single muscle fibers.

1 reference

https://api.crossref.org/works/10.1007%2FS11010-013-1681-Z

21 January 2018

Etiology of limb girdle muscular dystrophy 1D/1E determined by laser capture microdissection proteomics

1 reference

https://api.crossref.org/works/10.1007%2FS11010-013-1681-Z

21 January 2018

Alternative splicing dysregulation secondary to skeletal muscle regeneration

1 reference

https://api.crossref.org/works/10.1007%2FS11010-013-1681-Z

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS11010-013-1681-Z

21 January 2018

Preferential central nucleation of type 2 myofibers is an invariable feature of myotonic dystrophy type 2

1 reference

https://api.crossref.org/works/10.1007%2FS11010-013-1681-Z

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS11010-013-1681-Z

21 January 2018

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/23666741

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Defective satellite cells in congenital myotonic dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/23666741

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ribonuclear inclusions in skeletal muscle in myotonic dystrophy types 1 and 2

1 reference

https://pubmed.ncbi.nlm.nih.gov/23666741

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S11010-013-1681-Z

1 reference

Europe PubMed Central

4 August 2017

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0 references

1 reference

Europe PubMed Central

4 August 2017

ResearchGate publication ID

0 references

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