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

Urology, Mendelian Disorder, Genetic Disorder +7

LIM-kinase1 Hemizygosity Implicated in Impaired Visuospatial Constructive Cognition

J.Michael Frangiskakis, Amanda K. Ewart, Colleen A. Morris et al. · Cell · 1996 · 559 citations · Full text

Neuropsychology, Cognitive Science, Brain Mechanism +8

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 · 540 citations · Full text

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 · 387 citations · Full text

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 · 302 citations · Full text