A. Hayama

Disease-causing mutant WNK4 increases paracellular chloride permeability and phosphorylates claudins.

S. Sasaki, K. Yamauchi, T. Rai, 2004, Proceedings of the National Academy of Sciences of the United States of America.

Overt nephrogenic diabetes insipidus in mice lacking the CLC-K1 chloride channel

M. Arisawa, F. Marumo, S. Sasaki, 1999, Nature Genetics.

CLC‐3 deficiency leads to phenotypes similar to human neuronal ceroid lipofuscinosis

F. Marumo, M. Noda, S. Sasaki, 2002, Genes to cells : devoted to molecular & cellular mechanisms.

Intracellular localization of ClC chloride channels and their ability to form hetero‐oligomers

S. Sasaki, T. Rai, E. Sohara, 2006, Journal of cellular physiology.

Barttin binds to the outer lateral surface of the ClC-K2 chloride channel.

S. Sasaki, T. Rai, A. Hayama, 2007, Biochemical and biophysical research communications.

Molecular mechanisms of Bartter syndrome caused by mutations in the BSND gene

Shinichi Uchida, Sei Sasaki, Atsushi Hayama, 2003, Histochemistry and Cell Biology.

Purification and some properties of plant serine acetyltransferase

K. Fukushima, A. Hayama, M. Masada, 1988 .

Measurement of Serine Acetyltransferase Activity in Crude Plant Extracts by a Coupled Assay System Using Cysteine Synthase

K. Fukushima, A. Hayama, M. Masada, 1987 .

Isolation and characterization of the human CLC-5 chloride channel gene promoter.

F. Marumo, S. Sasaki, A. Hayama, 2000, Gene.