| P50 | author | Maria Pellegrini | Q41824510 |
| | Prisca Boisguerin | Q55117843 |
| P2093 | author name string | Dean R Madden | |
| | Patrick R Cushing | |
| | Lars Vouilleme | |
| P2860 | cites work | Lack of acrosome formation in mice lacking a Golgi protein, GOPC. | Q24534997 |
| | Accessory protein facilitated CFTR-CFTR interaction, a molecular mechanism to potentiate the chloride channel activity | Q28142263 |
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| | Lung infections associated with cystic fibrosis | Q30080000 |
| | Small molecule pharmacological chaperones: From thermodynamic stabilization to pharmaceutical drugs. | Q30357485 |
| | An improved method for the synthesis of cellulose membrane-bound peptides with free C termini is useful for PDZ domain binding studies | Q31056625 |
| | Characterization of a putative phosphorylation switch: adaptation of SPOT synthesis to analyze PDZ domain regulation mechanisms | Q33304541 |
| | A specificity map for the PDZ domain family | Q33373127 |
| | Differential roles of NHERF1, NHERF2, and PDZK1 in regulating CFTR-mediated intestinal anion secretion in mice | Q33409811 |
| | Modulation of endocytic trafficking and apical stability of CFTR in primary human airway epithelial cultures | Q33728190 |
| | E3KARP mediates the association of ezrin and protein kinase A with the cystic fibrosis transmembrane conductance regulator in airway cells | Q33909378 |
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| | The Cystic Fibrosis Transmembrane Conductance Regulator | Q40486029 |
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| | Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis | Q41714520 |
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| P433 | issue | 51 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 9907-9911 | |
| P577 | publication date | 2010-12-01 | |
| P1433 | published in | Angewandte Chemie International Edition | Q62023953 |
| P1476 | title | A stabilizing influence: CAL PDZ inhibition extends the half-life of ΔF508-CFTR | |
| P478 | volume | 49 | |