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204 related items for PubMed ID: 16571105
1. Spontaneous rescue from cystic fibrosis in a mouse model. Charizopoulou N, Wilke M, Dorsch M, Bot A, Jorna H, Jansen S, Stanke F, Hedrich HJ, de Jonge HR, Tümmler B. BMC Genet; 2006 Mar 29; 7():18. PubMed ID: 16571105 [Abstract] [Full Text] [Related]
2. Very mild disease phenotype of congenic CftrTgH(neoim)Hgu cystic fibrosis mice. Tóth B, Wilke M, Stanke F, Dorsch M, Jansen S, Wedekind D, Charizopoulou N, Bot A, Burmester M, Leonhard-Marek S, de Jonge HR, Hedrich HJ, Breves G, Tümmler B. BMC Genet; 2008 Apr 09; 9():28. PubMed ID: 18400105 [Abstract] [Full Text] [Related]
3. Instability of the insertional mutation in CftrTgH(neoim)Hgu cystic fibrosis mouse model. Charizopoulou N, Jansen S, Dorsch M, Stanke F, Dorin JR, Hedrich HJ, Tümmler B. BMC Genet; 2004 Apr 21; 5():6. PubMed ID: 15102331 [Abstract] [Full Text] [Related]
4. Characterisation of electrogenic nutrient absorption in the Cftr TgH(neoim)Hgu mouse model. Tóth B, Leonhard-Marek S, Hedrich HJ, Breves G. J Comp Physiol B; 2008 Aug 21; 178(6):705-12. PubMed ID: 18369642 [Abstract] [Full Text] [Related]
7. Rectal potential difference and the functional expression of CFTR in the gastrointestinal epithelia in cystic fibrosis mouse models. Weiner SA, Caputo C, Bruscia E, Ferreira EC, Price JE, Krause DS, Egan ME. Pediatr Res; 2008 Jan 21; 63(1):73-8. PubMed ID: 18043508 [Abstract] [Full Text] [Related]
8. Characterisation of chloride currents across the proximal colon in CftrTgH(neoim)1Hgu congenic mice. Bleich EM, Leonhard-Marek S, Beyerbach M, Breves G. J Comp Physiol B; 2007 Jan 21; 177(1):61-73. PubMed ID: 16868751 [Abstract] [Full Text] [Related]
9. Residual cftr expression varies with age in cftr(tm1Hgu) cystic fibrosis mice: impact on morphology and physiology. Larbig M, Jansen S, Dorsch M, Bernhard W, Bellmann B, Dorin JR, Porteous DJ, Von Der Hardt H, Steinmetz I, Hedrich HJ, Tuemmler B, Tschernig T. Pathobiology; 2007 Jan 21; 70(2):89-97. PubMed ID: 12476034 [Abstract] [Full Text] [Related]
10. Quantitative expression analyses of candidates for alternative anion conductance in cystic fibrosis mouse models. Braun J, Mundhenk L, Range F, Gruber AD. J Cyst Fibros; 2010 Sep 21; 9(5):351-64. PubMed ID: 20624691 [Abstract] [Full Text] [Related]
11. Correction of chloride transport and mislocalization of CFTR protein by vardenafil in the gastrointestinal tract of cystic fibrosis mice. Dhooghe B, Noël S, Bouzin C, Behets-Wydemans G, Leal T. PLoS One; 2013 Sep 21; 8(10):e77314. PubMed ID: 24204804 [Abstract] [Full Text] [Related]
13. Defective CFTR promotes intestinal proliferation via inhibition of the hedgehog pathway during cystic fibrosis. Liu K, Wang X, Zou C, Zhang J, Chen H, Tsang L, Yu MK, Chung YW, Wang J, Dai Y, Liu Y, Zhang X. Cancer Lett; 2019 Apr 01; 446():15-24. PubMed ID: 30639531 [Abstract] [Full Text] [Related]
16. Bioelectric characterization of epithelia from neonatal CFTR knockout ferrets. Fisher JT, Tyler SR, Zhang Y, Lee BJ, Liu X, Sun X, Sui H, Liang B, Luo M, Xie W, Yi Y, Zhou W, Song Y, Keiser N, Wang K, de Jonge HR, Engelhardt JF. Am J Respir Cell Mol Biol; 2013 Nov 01; 49(5):837-44. PubMed ID: 23782101 [Abstract] [Full Text] [Related]
17. Spliceosome-mediated RNA trans-splicing with recombinant adeno-associated virus partially restores cystic fibrosis transmembrane conductance regulator function to polarized human cystic fibrosis airway epithelial cells. Liu X, Luo M, Zhang LN, Yan Z, Zak R, Ding W, Mansfield SG, Mitchell LG, Engelhardt JF. Hum Gene Ther; 2005 Sep 01; 16(9):1116-23. PubMed ID: 16149910 [Abstract] [Full Text] [Related]
18. Differential expression of calcium-activated chloride channels (CLCA) gene family members in the small intestine of cystic fibrosis mouse models. Leverkoehne I, Holle H, Anton F, Gruber AD. Histochem Cell Biol; 2006 Aug 01; 126(2):239-50. PubMed ID: 16514548 [Abstract] [Full Text] [Related]