(Q34252137)

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Does (CUG)n repeat in DMPK mRNA 'paint' chromosome 19 to suppress distant genes to create the diverse phenotype of myotonic dystrophy?: A new hypothesis of long-range cis autosomal inactivation

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Europe PubMed Central

PubMed publication ID

31 July 2017

1 reference

Europe PubMed Central

Does (CUG)n repeat in DMPK mRNA 'paint' chromosome 19 to suppress distant genes to create the diverse phenotype of myotonic dystrophy?: A new hypothesis of long-range cis autosomal inactivation (English)

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

1 reference

based on heuristic

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author name string

Junghans RP

1

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Ebralidze A

2

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Tiwari B

3

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

publication date

1 March 2001

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

59-67

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Anticipating anticipation

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

Transgenic mice carrying large human genomic sequences with expanded CTG repeat mimic closely the DM CTG repeat intergenerational and somatic instability.

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

Transcriptional abnormality in myotonic dystrophy affects DMPK but not neighboring genes

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

DMPK dosage alterations result in atrioventricular conduction abnormalities in a mouse myotonic dystrophy model

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

Genomic organization and transcriptional units at the myotonic dystrophy locus

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

Expansion of the myotonic dystrophy CTG repeat reduces expression of the flanking DMAHP gene

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

Trinucleotide repeat expansion at the myotonic dystrophy locus reduces expression of DMAHP.

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

Myotonic dystrophy is associated with a reduced level of RNA from the DMWD allele adjacent to the expanded repeat

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

Mice deficient in Six5 develop cataracts: implications for myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

Heterozygous loss of Six5 in mice is sufficient to cause ocular cataracts

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

Accelerated breakdown of immunoglobulin G (IgG) in myotonic dystrophy: a hereditary error of immunoglobulin catabolism

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

Finally! The Brambell receptor (FcRB). Mediator of transmission of immunity and protection from catabolism for IgG.

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

Functional expression of the MHC class I-related receptor, FcRn, in endothelial cells of mice.

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

The protection receptor for IgG catabolism is the beta2-microglobulin-containing neonatal intestinal transport receptor

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

The human gene encoding the heavy chain of the major histocompatibility complex class I-like Fc receptor (FCGRT) maps to 19q13.3

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

Characterization of the expression of DMPK and SIX5 in the human eye and implications for pathogenesis in myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

Altered phosphorylation and intracellular distribution of a (CUG)n triplet repeat RNA-binding protein in patients with myotonic dystrophy and in myotonin protein kinase knockout mice

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

Remodelling chromatin with RNA.

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

XIST RNA paints the inactive X chromosome at interphase: evidence for a novel RNA involved in nuclear/chromosome structure

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

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%2FS100480000103

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

Long-range cis effects of ectopic X-inactivation centres on a mouse autosome

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

X-chromosome inactivation spreads itself: effects in autosomes

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

The spreading of X inactivation into autosomal material of an x;autosome translocation: evidence for a difference between autosomal and X-chromosomal DNA

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

H4 acetylation, XIST RNA and replication timing are coincident and define x;autosome boundaries in two abnormal X chromosomes

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

LINE-1 elements and X chromosome inactivation: a function for "junk" DNA?

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

Escapees on the X chromosome

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

A first-generation X-inactivation profile of the human X chromosome

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

Early recognition of heterozygotes for the gene for dystrophia myotonica

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

Immunological Function in Dystrophia Myotonica

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

Hyperresponsivness of patients with clinical and premyopathic myotonic dystrophy to human growth hormone.

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

Simultaneous analysis of expression of the three myotonic dystrophy locus genes in adult skeletal muscle samples: the CTG expansion correlates inversely with DMPK and 59 expression levels, but not DMAHP levels

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

Myotonic dystrophy in transgenic mice expressing an expanded CUG repeat

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

New nomenclature and DNA testing guidelines for myotonic dystrophy type 1 (DM1). The International Myotonic Dystrophy Consortium (IDMC)

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

Reduction of serum IgG level and peripheral T-cell counts are correlated with CTG repeat lengths in myotonic dystrophy patients.

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

The behavior of I 131-labeled plasma proteins in vivo

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

Abnormally short serum half-lives of IgG in beta 2-microglobulin-deficient mice

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

Serum proteins, lipoproteins, and glycoproteins in muscular dystrophy and related diseases

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

Immunologic derangement in myotonic dystrophy--abnormal contact sensitization to dinitrochlorobenzene

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

Immunoglobulin concentration and Gm allotypes in a family with thirty-three cases of myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

Normal platelet aggregation in myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

Immunoglobulin abnormalities in patients with myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

Sialic acid content in serum IgG from patients with myotonic dystrophy compared with healthy controls

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

Myotonic dystrophy with no trinucleotide repeat expansion

1 reference

https://api.crossref.org/works/10.1007%2FS100480000103

21 January 2018

Immunoglobulin levels in dystrophia myotonica

1 reference

https://pubmed.ncbi.nlm.nih.gov/11354827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Immunologic changes in Steinert disease]

1 reference

https://pubmed.ncbi.nlm.nih.gov/11354827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Metabolism of immunoglobulins

1 reference

https://pubmed.ncbi.nlm.nih.gov/11354827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A study of gamma globulins in dystrophia myotonica

1 reference

https://pubmed.ncbi.nlm.nih.gov/11354827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

IgG biosynthesis: no "immunoregulatory feedback"

1 reference

https://pubmed.ncbi.nlm.nih.gov/11354827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypo-IgG in myotonic dystrophy is due to a selective reduction of the IgG1-subclass serum level

1 reference

https://pubmed.ncbi.nlm.nih.gov/11354827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cerebrospinal fluid proteins in muscular dystrophy patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/11354827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S100480000103

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

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