Karen Sloan‐Brown

Translational activation of the non-AUG-initiated c-myc 1 protein at high cell densities due to methionine deprivation.

Stephan Hann, Karen Sloan‐Brown, Gerald D. Spotts · Genes & Development · 1992 · 110 citations · Full text

C-myc Belongs, Molecular Regulation, Molecular Biology +22

Nonsense and missense mutations of the muscle chloride channel gene in patients with myotonia congenita.

Alfred L. George, Karen Sloan‐Brown, Gerald M. Fenichel et al. · PubMed · 1994 · 98 citations

Channelopathies, Missense Mutations, Muscle Function +9

A novel muscle sodium channel mutation causes painful congenital myotonia

Jeffrey Rosenfeld, Karen Sloan‐Brown, Alfred L. George · Annals of Neurology · 1997 · 83 citations

Genomic Organization and Chromosomal Assignment of the Human Voltage-Gated Na+ Channel β1 Subunit Gene (SCN1B)

Naomasa Makita, Karen Sloan‐Brown, D. Olde Weghuis et al. · Genomics · 1994 · 57 citations

Chromosomal Assignment, Genomic Organization, Hyperpolarization (Biology) +9

Inheritance of three distinct muscle chloride channel gene (CLCN1) mutations in a single recessive myotonia congenita family

Karen Sloan‐Brown, Alfred L. George · Neurology · 1997 · 25 citations

Biology, Rheumatology, Mendelian Disorder +15