Lorraine A. Everett

Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)

Lorraine A. Everett, Benjamin Gläser, John C. Beck et al. · Nature Genetics · 1997 · 1.1K citations

Life Sciences, Genetics, Molecular Genetics +4

LIM-kinase1 Hemizygosity Implicated in Impaired Visuospatial Constructive Cognition

J.Michael Frangiskakis, Amanda K. Ewart, Colleen A. Morris et al. · Cell · 1996 · 561 citations · Full text

Life Sciences, Neuroscience, Psychology +11

Pendrin, encoded by the Pendred syndrome gene, resides in the apical region of renal intercalated cells and mediates bicarbonate secretion

Inès Royaux, Susan M. Wall, Lawrence P. Karniski et al. · Proceedings of the National Academy of Sciences · 2001 · 546 citations

Medicine, Molecular Biology, Molecular Genetics +16

Pendrin, the Protein Encoded by the Pendred Syndrome Gene (<i>PDS</i>), Is an Apical Porter of Iodide in the Thyroid and Is Regulated by Thyroglobulin in FRTL-5 Cells

Inès Royaux, Koichi Suzuki, Atsumi Mori et al. · Endocrinology · 2000 · 390 citations · Full text

Medicine, Endocrinology, Genetics +11

Expression pattern of the mouse ortholog of the Pendred’s syndrome gene ( <i>Pds</i> ) suggests a key role for pendrin in the inner ear

Lorraine A. Everett, Hakim Morsli, Doris K. Wu et al. · Proceedings of the National Academy of Sciences · 1999 · 304 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17