Laura Fugazzola

Functional Characterization of Wild-Type and a Mutated Form of SLC26A4 Identified in a Patient with Pendred Syndrome

Markus Ritter, Luca Persani, Johannes Fürst, 2006, Cellular Physiology and Biochemistry.

Fast Fluorometric Method for Measuring Pendrin (SLC26A4) Cl-/I- Transport Activity

Markus Ritter, Paolo Beck-Peccoz, Luca Persani, 2006, Cellular Physiology and Biochemistry.

Molecular and functional studies of 4 candidate loci in Pendred syndrome and nonsyndromic hearing loss

Paolo Beck-Peccoz, Luca Persani, P. Beck‐Peccoz, 2012, Molecular and Cellular Endocrinology.

High phenotypic intrafamilial variability in patients with Pendred syndrome and a novel duplication in the SLC26A4 gene: clinical characterization and functional studies of the mutated SLC26A4 protein.

Umberto Ambrosetti, Paolo Beck-Peccoz, P. Beck‐Peccoz, 2007, European journal of endocrinology.

Induction of a proinflammatory program in normal human thyrocytes by the RET/PTC1 oncogene.

Manuela Gariboldi, Angela Greco, Alberto Mantovani, 2005, Proceedings of the National Academy of Sciences of the United States of America.