Dystrophin analysis in idiopathic dilated cardiomyopathy.
Michels, Pastores, Moll, Driscoll, Miller, Burnett, Rodeheffer, Tajik, AH Beggs, and Kunkel. 1993. “Dystrophin Analysis in Idiopathic Dilated Cardiomyopathy.”. J Med Genet 30 (11): 955-7.
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A (CA)n repeat polymorphism for the human skeletal muscle alpha-actinin gene ACTN2 and its localization on the linkage map of chromosome 1.
Beggs, AH, Phillips, Kozman, Mulley, Wilton, Kunkel, and Laing. 1992. “A (CA)n Repeat Polymorphism for the Human Skeletal Muscle Alpha-Actinin Gene ACTN2 and Its Localization on the Linkage Map of Chromosome 1.”. Genomics 13 (4): 1314-5.
Cloning and characterization of two human skeletal muscle alpha-actinin genes located on chromosomes 1 and 11.
Beggs, AH, Byers, Knoll, Boyce, Bruns, and Kunkel. 1992. “Cloning and Characterization of Two Human Skeletal Muscle Alpha-Actinin Genes Located on Chromosomes 1 and 11.”. J Biol Chem 267 (13): 9281-8.
Assignment of a gene (NEMI) for autosomal dominant nemaline myopathy to chromosome I.
Laing, Majda, Akkari, Layton, Mulley, Phillips, Haan, White, AH Beggs, and Kunkel. 1992. “Assignment of a Gene (NEMI) for Autosomal Dominant Nemaline Myopathy to Chromosome I.”. Am J Hum Genet 50 (3): 576-83.
Possible influences on the expression of X chromosome-linked dystrophin abnormalities by heterozygosity for autosomal recessive Fukuyama congenital muscular dystrophy.
Beggs, AH, Neumann, Arahata, Arikawa, Nonaka, Anderson, and Kunkel. 1992. “Possible Influences on the Expression of X Chromosome-Linked Dystrophin Abnormalities by Heterozygosity for Autosomal Recessive Fukuyama Congenital Muscular Dystrophy.”. Proc Natl Acad Sci U S A 89 (2): 623-7.
Dystrophin is transcribed in brain from a distant upstream promoter.
Boyce, AH Beggs, Feener, and Kunkel. 1991. “Dystrophin Is Transcribed in Brain from a Distant Upstream Promoter.”. Proc Natl Acad Sci U S A 88 (4): 1276-80.
Effect of ageing on reactivation of the human X-linked HPRT locus.
Migeon, Axelman, and AH Beggs. 1988. “Effect of Ageing on Reactivation of the Human X-Linked HPRT Locus.”. Nature 335 (6185): 93-6.
Reactivation of X-linked genes in human fibroblasts transformed by origin-defective SV40.
Beggs, AH, Axelman, and Migeon. 1986. “Reactivation of X-Linked Genes in Human Fibroblasts Transformed by Origin-Defective SV40.”. Somat Cell Mol Genet 12 (6): 585-94.
Skeletal muscle microRNA and messenger RNA profiling in cofilin-2 deficient mice reveals cell cycle dysregulation hindering muscle regeneration.
Morton, Sarah, Mugdha Joshi, Talia Savic, Alan Beggs, and Pankaj Agrawal. 2015. “Skeletal Muscle MicroRNA and Messenger RNA Profiling in Cofilin-2 Deficient Mice Reveals Cell Cycle Dysregulation Hindering Muscle Regeneration.”. PLoS One 10 (4): e0123829.
Whole Exome Sequencing Reveals DYSF, FKTN, and ISPD Mutations in Congenital Muscular Dystrophy Without Brain or Eye Involvement.
Ceyhan-Birsoy, Ozge, Beril Talim, Lindsay Swanson, Mert Karakaya, Michelle Graff, Alan Beggs, and Haluk Topaloglu. 2015. “Whole Exome Sequencing Reveals DYSF, FKTN, and ISPD Mutations in Congenital Muscular Dystrophy Without Brain or Eye Involvement.”. J Neuromuscul Dis 2 (1): 87-92.