Epigenetics of Myotonic Dystrophy

Myotonic Dystrophy is an autosomal dominant neuromuscular disorder associated with the expansion of CTG trinucleotide repeats in the 3’ untranslated region of the myotonic dystrophy protein kinase (DMPK) gene. Here is the latest research focusing on epigenetic modifications in myotonic dystrophy.

June 11, 2016
Open Access

Identification of MyoD Interactome Using Tandem Affinity Purification Coupled to Mass Spectrometry

Journal of Visualized Experiments : JoVE
Ekaterina BoyarchukSlimane Ait-Si-Ali
February 3, 2016

DNA methylation status defines clinicopathological parameters including survival for patients with clear cell renal cell carcinoma (ccRCC)

Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine
Emma Andersson EvelönnGöran Roos
January 24, 2012
Review
Open Access

Epigenetics in nucleotide repeat expansion disorders

Seminars in Neurology
Fang He, Peter K Todd
April 25, 2009
Review
Open Access

The genetic signatures of noncoding RNAs

PLoS Genetics
John S Mattick
December 2, 2016
Review
Open Access

Are microRNAs true sensors of ageing and cellular senescence?

Ageing Research Reviews
Justin WilliamsP Hemachandra Reddy
July 13, 2018
Preprint
Open Access

Brachyury controls Ciona notochord fate as part of a feedforward network and not as a unitary master regulator

BioRxiv : the Preprint Server for Biology
W. M. ReevesMichael T Veeman
November 27, 2019
Open Access

Recovery in the Myogenic Program of Congenital Myotonic Dystrophy Myoblasts after Excision of the Expanded (CTG)n Repeat

International Journal of Molecular Sciences
Laurène M AndréBé Wieringa
July 5, 2015
Open Access

C9orf72 hexanucleotide repeat expansions in Chinese sporadic amyotrophic lateral sclerosis

Neurobiology of Aging
Ji HeDongsheng Fan
March 24, 2015
Review

Timing in neural maturation: arrest, delay, precociousness, and temporal determination of malformations

Pediatric Neurology
Harvey B SarnatXing-Chang Wei
August 21, 2013
Review

Epigenetic modifications in trinucleotide repeat diseases

Trends in Molecular Medicine
Marguerite V Evans-GaleaRichard Saffery
March 27, 2012
Review
Open Access

The role of CUGBP1 in age-dependent changes of liver functions

Ageing Research Reviews
Karlie JonesNikolai A Timchenko
February 23, 2010
Review
Open Access

Epigenetic changes and non-coding expanded repeats

Neurobiology of Disease
Masayuki Nakamori, Charles Thornton
January 21, 2017
Review

Nuclear Inositide Signaling Via Phospholipase C

Journal of Cellular Biochemistry
Stefano RattiLucia Manzoli
November 27, 2015
Open Access

Trans effects of chromosome aneuploidies on DNA methylation patterns in human Down syndrome and mouse models

Genome Biology
Maite MendiorozBenjamin Tycko
July 22, 2019
Review
Open Access

Molecular genetics of congenital myotonic dystrophy

Neurobiology of Disease
Stella Lanni, Christopher E Pearson
February 18, 2017
Open Access

Myotonic dystrophy type 1 patient-derived iPSCs for the investigation of CTG repeat instability

Scientific Reports
Junko UekiHidetoshi Sakurai
July 20, 2001
Open Access

Demethylation, reactivation, and destabilization of human fragile X full-mutation alleles in mouse embryocarcinoma cells

American Journal of Human Genetics
D WöhrleP Steinbach
September 8, 2020
Open Access

Epigenetic inactivation of IRX4 is responsible for acceleration of cell growth in human pancreatic cancer

Cancer Science
Kanchan ChakmaShinichi Fukushige
January 13, 2016
Open Access

Epigenetics of the myotonic dystrophy-associated DMPK gene neighborhood

Epigenomics
Lauren BuckleyMelanie Ehrlich

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