Search | OpenScholar

Search results

356 results found

A (CA)n repeat polymorphism for the human skeletal muscle alpha-actinin gene ACTN2 and its localization on the linkage map of chromosome 1.

Publication: Journal Article

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.

Publication: Journal Article

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.

Publication: Journal Article

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.

Publication: Journal Article

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.

Publication: Journal Article

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.

Publication: Journal Article

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.

Publication: Journal Article

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.

Population-Level Evidence for an Autoimmune Etiology of Epilepsy

Publication: Journal Article

Ong, Kohane, Cai, Gorman, and Mandl. 2014. “Population-Level Evidence for an Autoimmune Etiology of Epilepsy”. JAMA Neurol.

Is Biblioleaks inevitable?

Publication: Journal Article

Dunn, Coiera, and Mandl. 2014. “Is Biblioleaks Inevitable?”. J Med Internet Res 16: e112.

HarvardX

Link

Harvard online resources including open courses.