RNA metabolism in myotonic dystrophy: patient muscle shows decreased insulin receptor RNA and protein consistent with abnormal insulin resistance. (Q37365699)

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scientific article published on April 1997

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English	RNA metabolism in myotonic dystrophy: patient muscle shows decreased insulin receptor RNA and protein consistent with abnormal insulin resistance.	scientific article published on April 1997

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9120013%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

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

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2 November 2019

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

myotonic dystrophy

1 reference

based on heuristic

inferred from title

insulin resistance

1 reference

based on heuristic

inferred from title

author name string

A Morrone

1

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2 November 2019

E Pegoraro

2

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2 November 2019

E Zammarchi

4

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Europe PubMed Central

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2 November 2019

G Marconi

5

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2 November 2019

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publication date

1 April 1997

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2 November 2019

Journal of Clinical Investigation

1 reference

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2 November 2019

99

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2 November 2019

7

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Europe PubMed Central

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2 November 2019

1691-1698

1 reference

Europe PubMed Central

PMC publication ID

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2 November 2019

Novel proteins with binding specificity for DNA CTG repeats and RNA CUG repeats: implications for myotonic dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507989

6 September 2017

Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507989

6 September 2017

Isolation of a novel G protein-coupled receptor (GPR4) localized to chromosome 19q13.3

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507989

6 September 2017

A novel homeodomain-encoding gene is associated with a large CpG island interrupted by the myotonic dystrophy unstable (CTG)n repeat

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507989

6 September 2017

Decreased expression of myotonin-protein kinase messenger RNA and protein in adult form of myotonic dystrophy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507989

6 September 2017

Absence of myotonic dystrophy protein kinase (DMPK) mRNA as a result of a triplet repeat expansion in myotonic dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507989

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507989

6 September 2017

Triplet repeat expansion in myotonic dystrophy alters the adjacent chromatin structure

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507989

6 September 2017

Structural organization and developmental expression pattern of the mouse WD-repeat gene DMR-N9 immediately upstream of the myotonic dystrophy locus.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507989

6 September 2017

Slow and fast myosin heavy chain content defines three types of myotubes in early muscle cell cultures

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507989

6 September 2017

Isolation and sequence analysis of a full-length cDNA for human M creatine kinase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507989

6 September 2017

Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507989

6 September 2017

The human insulin receptor cDNA: the structural basis for hormone-activated transmembrane signalling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507989

6 September 2017

Physical mapping and cloning of the proximal segment of the myotonic dystrophy gene region.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507989

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507989

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507989

6 September 2017

Fluorescent multiplex linkage analysis and carrier detection for Duchenne/Becker muscular dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507989

6 September 2017

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://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507989

6 September 2017

Sequence and genomic structure of the human adult skeletal muscle sodium channel alpha subunit gene on 17q

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507989

6 September 2017

Brefeldin A inhibits insulin-dependent receptor redistribution in HIRcB cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507989

28 September 2017

IGF-I and insulin receptors in bovine skeletal muscle: comparisons of different developmental ages, two different genotypes and various individual muscles.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507989

26 June 2018

The role of insulin resistance in the pathogenesis of myotonic muscular dystrophy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507989

26 June 2018

Expression of fast and slow isoforms of the Ca2+-ATPase in developing chick skeletal muscle

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507989

26 June 2018

Abnormal regulation of intermediary metabolism after oral glucose ingestion in myotonic dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507989

26 June 2018

Absence of expression of the FMR-1 gene in fragile X syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507989

26 June 2018

Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507989

27 July 2018

Abnormal myotonic dystrophy protein kinase levels produce only mild myopathy in mice.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507989

2 September 2018

Pathophysiology of sodium channelopathies. Studies of sodium channel expression by quantitative multiplex fluorescence polymerase chain reaction.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507989

2 September 2018

Decreased myotonin-protein kinase in the skeletal and cardiac muscles in myotonic dystrophy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507989

2 September 2018

The human transferrin receptor gene: genomic organization, and the complete primary structure of the receptor deduced from a cDNA sequence.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507989

2 September 2018

Lack of rapid enhancement of insulin action after oral glucose challenge in myotonic dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507989

2 September 2018

Environmental influence on altered receptor function in a genetic disease: insulin and glucose affect insulin receptors in myotonic dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/9120013

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Preferential nucleosome assembly at DNA triplet repeats from the myotonic dystrophy gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/9120013

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Insulin Resistance in Myotonie Dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/9120013

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expanded CTG triplet blocks from the myotonic dystrophy gene create the strongest known natural nucleosome positioning elements

1 reference

https://pubmed.ncbi.nlm.nih.gov/9120013

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effect of the myotonic dystrophy (DM) mutation on mRNA levels of the DM gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/9120013

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myotonic dystrophy: evidence for a possible dominant-negative RNA mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/9120013

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Insulin receptors in myotonic dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/9120013

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/9120013

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Stutter, stumble, or fall of a kinase?

1 reference

https://pubmed.ncbi.nlm.nih.gov/9120013

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mice lacking the myotonic dystrophy protein kinase develop a late onset progressive myopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/9120013

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Failure in detecting mRNA transcripts from the mutated allele in myotonic dystrophy muscle

1 reference

https://pubmed.ncbi.nlm.nih.gov/9120013

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myotonic dystrophy: absence of CTG enlarged transcript in congenital forms, and low expression of the normal allele

1 reference

https://pubmed.ncbi.nlm.nih.gov/9120013

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of dystrophin in muscle-biopsy specimens from patients with Duchenne's or Becker's muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/9120013

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effect of Myotonic Dystrophy Trinucleotide Repeat Expansion on DMPK Transcription and Processing

1 reference

https://pubmed.ncbi.nlm.nih.gov/9120013

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1172/JCI119332

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9120013%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9120013%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9120013%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

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