Facioscapulohumeral muscular dystrophy
AM DeSimone, A Pakula, A Lek… - Comprehensive …, 2011 - Wiley Online Library
ABSTRACT Facioscapulohumeral Muscular Dystrophy is a common form of muscular
dystrophy that presents clinically with progressive weakness of the facial, scapular, and …
dystrophy that presents clinically with progressive weakness of the facial, scapular, and …
DUX4c, an FSHD candidate gene, interferes with myogenic regulators and abolishes myoblast differentiation
D Bosnakovski, S Lamb, T Simsek, Z Xu… - Experimental …, 2008 - Elsevier
Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant neuromuscular
disease. It maps to the D4Z4 repeat array at 4q35, and correlates with a repeat contraction …
disease. It maps to the D4Z4 repeat array at 4q35, and correlates with a repeat contraction …
Cellular and animal models for facioscapulohumeral muscular dystrophy
Facioscapulohumeral muscular dystrophy (FSHD) is one of the most common forms of
muscular dystrophy and presents with weakness of the facial, scapular and humeral …
muscular dystrophy and presents with weakness of the facial, scapular and humeral …
Hypermethylation of genomic 3.3-kb repeats is frequent event in HPV-positive cervical cancer
AN Katargin, LS Pavlova, FL Kisseljov… - BMC medical …, 2009 - Springer
Background Large-scale screening methods are widely used to reveal cancer-specific DNA
methylation markers. We previously identified non-satellite 3.3-kb repeats associated with …
methylation markers. We previously identified non-satellite 3.3-kb repeats associated with …