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American Journal of Medical Genetics|October 1, 1992
Additional dystrophin fragment in Becker muscular dystrophy may result from proteolytic cleavage at deletion junctionsA H Beggs, E P Hoffman, L M KunkelClinical Chemistry|July 1, 1989
Molecular genetics of Duchenne and Becker muscular dystrophy: emphasis on improved diagnosisL M Kunkel, A H Beggs, E P HoffmanProceedings of the National Academy of Sciences of the United States of America|October 1, 1988
Extinction of JC virus tumor-antigen expression in glial cell--fibroblast hybridsA H Beggs, R J Frisque, G A ScangosProceedings of the National Academy of Sciences of the United States of America|February 15, 1991
Dystrophin is transcribed in brain from a distant upstream promoterF M Boyce, A H Beggs, C Feener, et al.Human Genetics|November 1, 1990
Detection of 98% of DMD/BMD gene deletions by polymerase chain reactionA H Beggs, M Koenig, F M Boyce, et al.Biochemical and Biophysical Research Communications|July 24, 1998
Human skeletal muscle-specific alpha-actinin-2 and -3 isoforms form homodimers and heterodimers in vitro and in vivoY Chan, H Q Tong, A H Beggs, et al.Nature Genetics|May 1, 1994
Mapping a gene for congenital fibrosis of the extraocular muscles to the centromeric region of chromosome 12E C Engle, L M Kunkel, L A Specht, et al.Neurology|March 1, 1992
ELISA quantitation of dystrophin for the diagnosis of Duchenne and Becker muscular dystrophiesT J Byers, P E Neumann, A H Beggs, et al.The Journal of Biological Chemistry|July 21, 1995
Isoform cloning, actin binding, and chromosomal localization of human erythroid dematin, a member of the villin superfamilyA C Azim, J H Knoll, A H Beggs, et al.FEBS Letters|July 24, 1995
Novel actin crosslinker superfamily member identified by a two step degenerate PCR procedureT J Byers, A H Beggs, E M McNally, et al.Pageof 8