(Q72896182)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8358430%20AND%20SRC:MED&resulttype=core&format=json

30 October 2019

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8358430%20AND%20SRC:MED&resulttype=core&format=json

30 October 2019

1 reference

Sabouri LA

1

1 reference

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30 October 2019

Mahadevan MS

2

1 reference

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30 October 2019

Narang M

3

1 reference

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30 October 2019

Lee DS

4

1 reference

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30 October 2019

Surh LC

5

1 reference

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30 October 2019

Korneluk RG

6

1 reference

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30 October 2019

publication date

1 July 1993

1 reference

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30 October 2019

1 reference

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30 October 2019

volume

4

1 reference

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30 October 2019

issue

3

1 reference

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30 October 2019

page(s)

233-238

1 reference

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Dystrophia myotonica in childhood

30 October 2019

cites work

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7 January 2021

Maturational arrest of fetal muscle in neonatal myotonic dystrophy. A pathologic study of four cases

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7 January 2021

Distinct contractile protein profile in congenital myotonic dystrophy and X-linked myotubular myopathy

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7 January 2021

Cloning of the essential myotonic dystrophy region and mapping of the putative defect

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7 January 2021

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

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7 January 2021

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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7 January 2021

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

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7 January 2021

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

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7 January 2021

Characterization of the myotonic dystrophy region predicts multiple protein isoform-encoding mRNAs

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7 January 2021

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

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7 January 2021

Correlation between CTG trinucleotide repeat length and frequency of severe congenital myotonic dystrophy

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7 January 2021

Intergenerational stability of the myotonic dystrophy protomutation

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7 January 2021

Triplet repeat mutations in human disease

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7 January 2021

Dynamic mutations: a new class of mutations causing human disease

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7 January 2021

Anticipation in myotonic dystrophy: fact or fiction?

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7 January 2021

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

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7 January 2021

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

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7 January 2021

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

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7 January 2021

Physical mapping across the fragile X: hypermethylation and clinical expression of the fragile X syndrome

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7 January 2021

DNA methylation represses FMR-1 transcription in fragile X syndrome

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7 January 2021

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy

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7 January 2021

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

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7 January 2021

Cultivation in vitro of cells derived from a human rhabdomyosarcoma

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7 January 2021

Analysis of cytokine mRNA and DNA: detection and quantitation by competitive polymerase chain reaction

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7 January 2021

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

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7 January 2021

Optimal computer folding of large RNA sequences using thermodynamics and auxiliary information

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7 January 2021

A stem-loop in the 3' untranslated region mediates iron-dependent regulation of transferrin receptor mRNA stability in the cytoplasm.

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7 January 2021

A specific mRNA binding factor regulates the iron-dependent stability of cytoplasmic transferrin receptor mRNA.

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7 January 2021

Control of c-myc mRNA half-life in vitro by a protein capable of binding to a coding region stability determinant

1 reference

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7 January 2021

The iron regulatory region of ferritin mRNA is also a positive control element for iron-independent translation

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-233

7 January 2021

Direct evidence for translational regulation by leader RNA and Tat protein of human immunodeficiency virus type 1.

1 reference

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7 January 2021

Mechanism of interferon action: identification of a RNA binding domain within the N-terminal region of the human RNA-dependent P1/eIF-2 alpha protein kinase

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7 January 2021

cAMP-dependent protein kinase: framework for a diverse family of regulatory enzymes

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7 January 2021

Immaturity of muscle fibers in the congenital form of myotonic dystrophy: its consequences and its origin

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7 January 2021

Cyclic AMP-dependent protein kinase inhibits the activity of myogenic helix-loop-helix proteins

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7 January 2021

FGF inactivates myogenic helix-loop-helix proteins through phosphorylation of a conserved protein kinase C site in their DNA-binding domains

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7 January 2021

Post-transcriptional regulation of glyceraldehyde-3-phosphate-dehydrogenase gene expression in rat tissues

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7 January 2021

Rapid extraction of high molecular weight RNA from cultured cells and granulocytes for Northern analysis.

1 reference

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7 January 2021

Suppression of programmed death and G1 arrest in B-cell hybridomas by interleukin-6 is not accompanied by altered expression of immediate early response genes

1 reference

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7 January 2021

A reliable method for the recovery of DNA fragments from agarose and acrylamide gels

1 reference

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7 January 2021

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1 reference

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7 January 2021

Structure and genomic sequence of the myotonic dystrophy (DM kinase) gene

1 reference

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7 January 2021

Identifiers

DOI

10.1038/NG0793-233

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8358430%20AND%20SRC:MED&resulttype=core&format=json

30 October 2019

1 reference