Sodium and chloride absorptive defects in the small intestine in Slc26a6 null mice

Prestin is the motor protein of cochlear outer hair cells

Jing Zheng, Weixing Shen, David Z. Z. He et al. · Nature · 2000 · 1.3K citations

Molecular Physiology, Motor Protein, Molecular Biology +6

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

Renal and intestinal absorptive defects in mice lacking the NHE3 Na+/H+ exchanger

Patrick J. Schultheis, Lane L. Clarke, Pierre Meneton et al. · Nature Genetics · 1998 · 856 citations

Knockout Mouse, Nhe3 Na+/h+ Exchanger, Sodium Homeostasis +8

The diastrophic dysplasia gene encodes a novel sulfate transporter: Positional cloning by fine-structure linkage disequilibrium mapping

Johanna Hästbacka, Albert de la Chapelle, Melanie M. Mahtani et al. · Cell · 1994 · 761 citations

Natural Sciences, Genetics, Dna Replication +7

Gating of CFTR by the STAS domain of SLC26 transporters

Shigeru B. H. Ko, Weizhong Zeng, Michael R. Dorwart et al. · Nature Cell Biology · 2004 · 464 citations · Full text

Transport Phenomena, Engineering, Physics +1