| scholarly article | Q13442814 |
| P2093 | author name string | Christina K Haston | |
| Sean M Cory | |||
| Daryl G Humes | |||
| Juan C Canale-Zambrano | |||
| Maya C Poffenberger | |||
| P2860 | cites work | Bioconductor: open software development for computational biology and bioinformatics | Q21194861 |
| Mechanisms of lipid malabsorption in Cystic Fibrosis: the impact of essential fatty acids deficiency | Q24806288 | ||
| A membrane lipid imbalance plays a role in the phenotypic expression of cystic fibrosis in cftr(-/-) mice | Q28505262 | ||
| Genetics of gene expression surveyed in maize, mouse and man | Q29617297 | ||
| Genotype and phenotype in cystic fibrosis | Q33895736 | ||
| An animal model for cystic fibrosis made by gene targeting | Q33970549 | ||
| Transcriptional gene silencing in plants: targets, inducers and regulators | Q34133334 | ||
| Characteristic multiorgan pathology of cystic fibrosis in a long-living cystic fibrosis transmembrane regulator knockout murine model | Q35097413 | ||
| Wasting as an independent predictor of mortality in patients with cystic fibrosis | Q35534184 | ||
| Genetics of Crohn disease, an archetypal inflammatory barrier disease | Q36110574 | ||
| Short bowel syndrome: current medical and surgical trends | Q36696607 | ||
| Lung disease in mice with cystic fibrosis | Q37376391 | ||
| Bacterial overgrowth in the cystic fibrosis transmembrane conductance regulator null mouse small intestine | Q37523964 | ||
| Gene expression profiling of intestinal epithelial cell maturation along the crypt-villus axis | Q38328111 | ||
| Strain-dependent pulmonary gene expression profiles of a cystic fibrosis mouse model | Q38518598 | ||
| Proliferation, not apoptosis, alters epithelial cell migration in small intestine of CFTR null mice | Q43716997 | ||
| Regulation by glucose and calcium of the carboxylmethylation of the catalytic subunit of protein phosphatase 2A in insulin-secreting INS-1 cells | Q44768350 | ||
| Fat absorption in cystic fibrosis mice is impeded by defective lipolysis and post-lipolytic events | Q45140576 | ||
| Mapping of genetic factors influencing the weight of cystic fibrosis knockout mice | Q47174927 | ||
| Abnormal Paneth cell granule dissolution and compromised resistance to bacterial colonization in the intestine of CF mice | Q50101740 | ||
| Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13. | Q55033106 | ||
| P433 | issue | 1 | |
| P921 | main subject | cystic fibrosis | Q178194 |
| knockout mouse | Q1364740 | ||
| phenotype | Q104053 | ||
| P304 | page(s) | G222-9 | |
| P577 | publication date | 2007-07-01 | |
| P1433 | published in | American Journal of Physiology - Gastrointestinal and Liver Physiology | Q15765756 |
| P1476 | title | Intestinal phenotype of variable-weight cystic fibrosis knockout mice | |
| P478 | volume | 293 |
| Q92624827 | A BAC Transgene Expressing Human CFTR under Control of Its Regulatory Elements Rescues Cftr Knockout Mice |
| Q60920753 | Animal Models in the Pathophysiology of Cystic Fibrosis |
| Q39790745 | CFTR knockdown stimulates lipid synthesis and transport in intestinal Caco-2/15 cells |
| Q35216745 | Cystic fibrosis growth retardation is not correlated with loss of Cftr in the intestinal epithelium |
| Q35568501 | Cystic fibrosis mouse model-dependent intestinal structure and gut microbiome |
| Q30628431 | Defective goblet cell exocytosis contributes to murine cystic fibrosis-associated intestinal disease |
| Q47406142 | IGF Binding Protein-3 Treatment Alters Intestinal Cell Proliferation But Not Body Weight of Adult Cystic Fibrosis Transmembrane Conductance Regulator Deficient Mice |
| Q46242283 | Insulin production and resistance in cystic fibrosis: effect of age, disease activity, and genotype |
| Q34533687 | Listeria monocytogenes exploits cystic fibrosis transmembrane conductance regulator (CFTR) to escape the phagosome. |
| Q42590406 | MicroRNA profiling implicates the insulin-like growth factor pathway in bleomycin-induced pulmonary fibrosis in mice |
| Q44675835 | MicroRNA profiling of cystic fibrosis intestinal disease in mice |
| Q36093336 | Recent advances in small bowel diseases: Part II. |
| Q56535583 | SLC6A14, an amino acid transporter, modifies the primary CF defect in fluid secretion |
| Q92377442 | Short-term CFTR inhibition reduces islet area in C57BL/6 mice |
| Q57124971 | Toll-like receptor-4 genotype influences the survival of cystic fibrosis mice |
| Q38005772 | Vitamin D bioavailability in cystic fibrosis: a cause for concern? |
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