| scholarly article | Q13442814 |
| P2093 | author name string | Etienne Hollande | |
| Laetitia Alvarez | |||
| Marjorie Fanjul | |||
| Christel Salvador-Cartier | |||
| P2860 | cites work | Centrosomal abnormalities, multipolar mitoses, and chromosomal instability in head and neck tumours with dysfunctional telomeres | Q24641868 |
| The machinery of mitochondrial inheritance and behavior | Q33538526 | ||
| A cystic fibrosis pancreatic adenocarcinoma cell line | Q33598519 | ||
| Microtubule perturbation retards both the direct and the indirect apical pathway but does not affect sorting of plasma membrane proteins in intestinal epithelial cells (Caco-2). | Q33922061 | ||
| Organellar relationships in the Golgi region of the pancreatic beta cell line, HIT-T15, visualized by high resolution electron tomography | Q33935943 | ||
| The Golgi complex is a microtubule-organizing organelle | Q33937465 | ||
| cAMP stimulates bicarbonate secretion across normal, but not cystic fibrosis airway epithelia | Q35600394 | ||
| Associations of elements of the Golgi apparatus with microtubules | Q36211367 | ||
| Abnormal subcellular localization of mutated CFTR protein in a cystic fibrosis epithelial cell line. | Q36677828 | ||
| Golgi dispersal during microtubule disruption: regeneration of Golgi stacks at peripheral endoplasmic reticulum exit sites | Q37380591 | ||
| Immunocytochemical localization of the cystic fibrosis gene product CFTR | Q37609030 | ||
| Three-dimensional electron microscopy: structure of the Golgi apparatus | Q37930289 | ||
| Structural integrity of the Golgi stack is essential for normal secretory functions of rat parotid acinar cells: effects of brefeldin A and okadaic acid | Q38359706 | ||
| Microtubules and the organization of the Golgi complex | Q39827448 | ||
| Targeting of carbonic anhydrase IV to plasma membranes is altered in cultured human pancreatic duct cells expressing a mutated (deltaF508) CFTR. | Q40704066 | ||
| Abnormal glycosylation and altered Golgi structure in colorectal cancer: dependence on intra-Golgi pH. | Q40737573 | ||
| Downregulated in adenoma and putative anion transporter are regulated by CFTR in cultured pancreatic duct cells | Q40773534 | ||
| Regulatory interaction between the cystic fibrosis transmembrane conductance regulator and HCO3- salvage mechanisms in model systems and the mouse pancreatic duct | Q40816480 | ||
| Aberrant CFTR-dependent HCO3- transport in mutations associated with cystic fibrosis | Q40821697 | ||
| Traffic pattern of cystic fibrosis transmembrane regulator through the early exocytic pathway | Q40826405 | ||
| Low cytoplasmic pH causes fragmentation and dispersal of the Golgi apparatus in human hepatoma cells. | Q40948746 | ||
| Presence of MRP8 and MRP14 in pancreatic cell lines: differential expression and localization in CFPAC-1 cells | Q41348223 | ||
| The expression of carbonic anhydrases II and IV in the human pancreatic cancer cell line (Capan 1) is associated with bicarbonate ion channels | Q41506567 | ||
| Relationship between the Golgi complex and microtubules enriched in detyrosinated or acetylated alpha-tubulin: studies on cells recovering from nocodazole and cells in the terminal phase of cytokinesis | Q41528823 | ||
| High intracellular pH in CFPAC: A pancreas cell line from a patient with cystic fibrosis is lowered by retrovirus-mediated CFTR gene transfer | Q41661082 | ||
| Defective acidification of intracellular organelles in cystic fibrosis | Q41675496 | ||
| Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis | Q41714520 | ||
| Correction of the cystic fibrosis defect in vitro by retrovirus-mediated gene transfer | Q41721279 | ||
| Partitioning of cytoplasmic organelles during mitosis with special reference to the Golgi complex | Q41732124 | ||
| Identification of transport abnormalities in duodenal mucosa and duodenal enterocytes from patients with cystic fibrosis | Q41738688 | ||
| Brefeldin A causes disassembly of the Golgi complex and accumulation of secretory proteins in the endoplasmic reticulum | Q41810951 | ||
| Stable Golgi-mitochondria complexes and formation of Golgi Ca(2+) gradients in pancreatic acinar cells. | Q42474574 | ||
| Misfolded growth hormone causes fragmentation of the Golgi apparatus and disrupts endoplasmic reticulum-to-Golgi traffic | Q43798616 | ||
| Evidence for a membrane carbonic anhydrase IV anchored by its C-terminal peptide in normal human pancreatic ductal cells | Q44739880 | ||
| Delta F508 CFTR localizes in the endoplasmic reticulum-Golgi intermediate compartment in cystic fibrosis cells | Q47838383 | ||
| Multiple proteolytic systems, including the proteasome, contribute to CFTR processing | Q50337154 | ||
| Effect of microtubule network disturbance by nocodazole and docetaxel (Taxotere) on protein secretion in rat extraorbital lacrimal and parotid glands | Q52508333 | ||
| Okadaic acid induces Golgi apparatus fragmentation and arrest of intracellular transport | Q54284500 | ||
| Evidence for reduced Cl- and increased Na+ permeability in cystic fibrosis human primary cell cultures. | Q54373452 | ||
| Mislocalization of ΔF508 CFTR in cystic fibrosis sweat gland | Q67468902 | ||
| Impaired chloride secretion, as well as bicarbonate secretion, underlies the fluid secretory defect in the cystic fibrosis pancreas | Q68434984 | ||
| Polarity and nucleation of microtubules in polarized epithelial cells | Q71018409 | ||
| Bicarbonate secretion in interlobular ducts from guinea-pig pancreas | Q71673999 | ||
| [Targeting of type IV carbonic anhydrases in Capan-1 human pancreatic duct cells is concomitant of the polarization] | Q71706785 | ||
| Correlation between centrosome abnormalities and chromosomal instability in human pancreatic cancer cells | Q73852548 | ||
| Altered intracellular pH regulation in neutrophils from patients with cystic fibrosis | Q73992821 | ||
| Golgi division and membrane traffic | Q77057718 | ||
| Role of microtubules in the organization of the Golgi complex | Q77928235 | ||
| P433 | issue | 12 | |
| P921 | main subject | cystic fibrosis | Q178194 |
| P304 | page(s) | 1539-1552 | |
| P577 | publication date | 2005-06-13 | |
| P1433 | published in | Journal of Histochemistry and Cytochemistry | Q1523992 |
| P1476 | title | Expression of a wild-type CFTR maintains the integrity of the biosynthetic/secretory pathway in human cystic fibrosis pancreatic duct cells | |
| P478 | volume | 53 |
| Q33818738 | Bioinformatic analyses identifies novel protein-coding pharmacogenomic markers associated with paclitaxel sensitivity in NCI60 cancer cell lines. |
| Q39961011 | Characterization of primary cilia and Hedgehog signaling during development of the human pancreas and in human pancreatic duct cancer cell lines |
| Q27320511 | Expression and in vivo rescue of human ABCC6 disease-causing mutants in mouse liver |
| Q37401745 | Pancreatic duct secretion: experimental methods, ion transport mechanisms and regulation |
| Q33569399 | Reduced GM1 ganglioside in CFTR-deficient human airway cells results in decreased β1-integrin signaling and delayed wound repair |
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