Appearance of Water Channels in Xenopus Oocytes Expressing Red Cell CHIP28 Protein
Gregory M. Preston;Tiziana Piazza Carroll;William B. Guggino;Peter Agre.
In vivo transfer of the human cystic fibrosis transmembrane conductance regulator gene to the airway epithelium
Melissa A. Rosenfeld;Kunihiko Yoshimura;Bruce C. Trapnell;Koichi Yoneyama.
Aquaporin CHIP: the archetypal molecular water channel
P. Agre;G. M. Preston;B. L. Smith;Jin Sup Jung.
American Journal of Physiology-renal Physiology (1993)
Co-assembly of polycystin-1 and -2 produces unique cation-permeable currents
Kazushige Hanaoka;Feng Qian;Alessandra Boletta;Anil K. Bhunia.
Molecular characterization of an aquaporin cDNA from brain: candidate osmoreceptor and regulator of water balance
Jin Sup Jung;Ratan V. Bhat;Gregory M. Preston;William B. Guggino.
Proceedings of the National Academy of Sciences of the United States of America (1994)
Molecular structure of the water channel through aquaporin CHIP. The hourglass model.
Jin Sup Jung;G. M. Preston;B. L. Smith;W. B. Guggino.
Journal of Biological Chemistry (1994)
CFTR regulates outwardly rectifying chloride channels through an autocrine mechanism involving ATP.
Erik M. Schwiebert;Marie E. Egan;Tae Ho Hwang;Stephanie B. Fulmer.
Stable in vivo expression of the cystic fibrosis transmembrane conductance regulator with an adeno-associated virus vector.
Terence R. Flotte;Sandra A. Afione;Carol Conrad;Sharon A. McGrath.
Proceedings of the National Academy of Sciences of the United States of America (1993)
Identification of a urate transporter, ABCG2, with a common functional polymorphism causing gout
Owen M. Woodward;Anna Köttgen;Josef Coresh;Eric Boerwinkle.
Proceedings of the National Academy of Sciences of the United States of America (2009)
The mercury-sensitive residue at cysteine 189 in the CHIP28 water channel.
G. M. Preston;Jin Sup Jung;W. B. Guggino;P. Agre.
Journal of Biological Chemistry (1993)
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