S.A. Rundle

Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member

J. David Brook, Mila E. McCurrach, H G Harley et al. · Cell · 1992 · 2.8K citations

Signal Transduction, Mendelian Disorder, Genetic Disorder +7

Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy

Helen G. Harley, J. David Brook, S.A. Rundle et al. · Nature · 1992 · 727 citations

Phenotypic Variation, Mendelian Disorder, Genetic Disorder +7

Unstable DNA sequence in myotonic dystrophy

H G Harley, S.A. Rundle, William Reardon et al. · The Lancet · 1992 · 201 citations

Mendelian Disorder, Genetic Disorder, Natural Sciences +5

The promoter of the latency-associated transcripts of herpes simplex virus type 1 contains a functional cAMP-response element: role of the latency-associated transcripts and cAMP in reactivation of viral latency.

David A. Leib, Kari C. Nadeau, S.A. Rundle et al. · Proceedings of the National Academy of Sciences · 1991 · 145 citations · Full text

Viral Replication, Latency-associated Transcripts, Molecular Biology +21

Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA marker.

H G Harley, J. David Brook, Jo L. Floyd et al. · PubMed · 1991 · 92 citations