publication venue for
- Retinoids Assist the Cellular Folding of the Autosomal Dominant Retinitis Pigmentosa. Opsin Mutant P23H.. 79:16278-16284. 2004
- Electrophysiological and Biochemical Evidence that DEG/ENaC Cation Channels are Composed of Nine Subunits. 273:681-685. 19998
- Properties of the reaction of cis-dichlorodiammineplatinum(II) with metallothionein.. 267:16121. 15,
- Assembly of the Epithelial Na+ Channel Evaluated Using Sucrose Gradient Sedimentation Analysis. 273:22693-22701.
- Basolateral Localization of Fiber Receptors Limits Adenovirus Infection From the Apical Surface of Airway Epithelia. 274:10219-10227.
- Binding of Adeno-Associated Virus Type 5 to 2, 3-Linked Sialic Acid is Required for Gene Transfer. 276:20610-20617.
- Biochemical Basis of Touch Perception: Mechanosensory Function of Degnerin/Epithelial Na+ Channels. 277:2369-2373.
- Cellular and Molecular Barriers to Gene Transfer by a Cationic Lipid. 270:18997-19008.
- Cloning and Expression of a Novel Human Brain Na+ Channel. 271:7879-7883.
- Complexes of Adenovirus with Polycationic Polymers and Cationic Lipids Increase the Efflciency of Gene Transfer in Vitro and in Vivo. 272:6479-6490.
- Contribution of Proline Residues in the Membrand-Spanning Domains of Systic Fibrosis Transmembrane Conductance Regulator to Cloride Channel Function. 271:14995-15002.
- Covalent Modification of the Nucleotide Binding Domains of Cystic Fibrosis Transmembrane Conductance Regulator. 273:31873-31880.
- Covalent Modification of the Regulatory Domain Irreversibly Stimulates Cystic Fibrosis Transmembrane Conductance Regulator. 272:25617-25623.
- Curcumin Stimulates Cystic Fibrosis Transmembrane Conductance Regulator CI-Channel Activity. 280:5221-5227.
- Cystic Fibrosis Transmembrane Conductance Regulator Cl-Channels with R Domain Deletions and Translocations Show Phosphorylation-Dependent and -Independent Activity. 276:1904-1911.
- Cystic Fibrosis-Associated Mutations at Arginine 347 Alter the Pore Architecture of CFTR. Evidence for Disruption of a Salt Bridge. 274:5429-5436.
- Difference Between Cystic Fibrosis Transmembrane Conductance Regulator and HisP in the Interaction with the Adenine Ring of ATP. 275:29407-29413.
- Effect of Cystic Fibrosis-Associated Mutations in the Fourth Intracellular Loop of Cystic Fibrosis Transmembrane Conductance Regulator. 271:21279-21285.
- Engineering Novel Cell Surface Receptors for Virus-Mediated Gene Transfer. 274:21878-21885.
- Function of Xenopus Cystic Fibrosis Transmembrane Conductance Regulator (CF R) Cl-Channels and Use of Human-Xenopus Chimeras to Investigate the Pore. 271:25187-25192.
- HSP22, a New Member of the Small Heat Shock Protein Superfamily, Interacts with Mimic of Phosphorylated HSP27 (3D HSP27). 276:26753-26762.
- Identification and Characterization of Hic-5/ARA55 as an HSP27 Binding Protein. 276:39911-39919.
- Interaction of Nucleotides with Membrane-Associated Cystic Fibrosis Transmembrane Conductance Regulator. 268.
- Isolation, Characterization, and Localization of the Inositol 1, 4, 5-Trisphosphate Receptor Protein in Xenopus Laevis Oocytes. 267.
- Number of Subunits Comprising the Epithelial Sodium Channel. 274:27281-27287.
- Paradoxical Stimulation of a DEG/ENaC Channel by Amiloride. 274:15500-15505.
- Partial Purification of the Cystic Fibrosis Transmembrane Conductance Regulator. 267.
- Protons Activate Brain Na+ Channel 1 by Inducing a Conformational Change that Exposes a Residue Associated with Neurodegeneration. 273:30204-30208.
- Pyrophosphate Stimulates Wild-Type and Mutant Cystic Fibrosis Transmembrane Conductance Regulator Cl-Channels. 270:20466-20473.
- Regulation of the Cystic Fibrosis Transmembrane Conductance Regulator Cl-Channel by its R Domain. 276:7689-7693.
- Regulation of the Cystic Fibrosis Transmembrane Conductance Regulator Cl{sup}- Channel by Specific Protein Kinases and Protein Phosphatases. 268.
- The Involvement of MAPK Signaling Pathways in Determining the Cellular Response to p53 Activation: Cell Cycle Arrets or Apoptosis. 281:3832-3840.