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Cell|November 15, 1991
Nucleoside triphosphates are required to open the CFTR chloride channelM P Anderson, H A Berger, D P Rich, et al.
Nature|March 11, 1993
Mutations in CFTR associated with mild-disease-form Cl- channels with altered pore propertiesD N Sheppard, D P Rich, L S Ostedgaard, et al.
Bio/Technology (Nature Publishing Company)|January 1, 1992
Production of cystic fibrosis transmembrane conductance regulator in the milk of transgenic miceP DiTullio, S H Cheng, J Marshall, et al.
The Journal of Biological Chemistry|August 12, 1994
The cystic fibrosis transmembrane conductance regulator is a dual ATP and chloride channelI L Reisin, A G Prat, E H Abraham, et al.
Journal of Molecular Biology|September 15, 1984
Interaction of ribosomal proteins S6, S8, S15 and S18 with the central domain of 16 S ribosomal RNA from Escherichia coliR J Gregory, M L Zeller, D L Thurlow, et al.
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