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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

214 related items for PubMed ID: 18400105

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  • 25. Generation and phenotype of cell lines derived from CF and non-CF mice that carry the H-2K(b)-tsA58 transgene.
    Takacs-Jarrett M, Sweeney WE, Avner ED, Cotton CU.
    Am J Physiol Cell Physiol; 2001 Jan; 280(1):C228-36. PubMed ID: 11121394
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  • 26. Mapping of genetic factors influencing the weight of cystic fibrosis knockout mice.
    Haston CK, Corey M, Tsui LC.
    Mamm Genome; 2002 Nov; 13(11):614-8. PubMed ID: 12461646
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  • 27. cAMP- but not Ca(2+)-regulated Cl- conductance in the oviduct is defective in mouse model of cystic fibrosis.
    Leung AY, Wong PY, Gabriel SE, Yankaskas JR, Boucher RC.
    Am J Physiol; 1995 Mar; 268(3 Pt 1):C708-12. PubMed ID: 7534985
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  • 28. Ion-transporting activity in the murine colonic epithelium of normal animals and animals with cystic fibrosis.
    Cuthbert AW, MacVinish LJ, Hickman ME, Ratcliff R, Colledge WH, Evans MJ.
    Pflugers Arch; 1994 Oct; 428(5-6):508-15. PubMed ID: 7838673
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  • 30. Olfactory epithelia exhibit progressive functional and morphological defects in CF mice.
    Grubb BR, Rogers TD, Kulaga HM, Burns KA, Wonsetler RL, Reed RR, Ostrowski LE.
    Am J Physiol Cell Physiol; 2007 Aug; 293(2):C574-83. PubMed ID: 17428842
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  • 33. Restoration of CFTR function in patients with cystic fibrosis carrying the F508del-CFTR mutation.
    De Stefano D, Villella VR, Esposito S, Tosco A, Sepe A, De Gregorio F, Salvadori L, Grassia R, Leone CA, De Rosa G, Maiuri MC, Pettoello-Mantovani M, Guido S, Bossi A, Zolin A, Venerando A, Pinna LA, Mehta A, Bona G, Kroemer G, Maiuri L, Raia V.
    Autophagy; 2014 Aug; 10(11):2053-74. PubMed ID: 25350163
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  • 34. Long-term docosahexaenoic acid therapy in a congenic murine model of cystic fibrosis.
    Beharry S, Ackerley C, Corey M, Kent G, Heng YM, Christensen H, Luk C, Yantiss RK, Nasser IA, Zaman M, Freedman SD, Durie PR.
    Am J Physiol Gastrointest Liver Physiol; 2007 Mar; 292(3):G839-48. PubMed ID: 17095751
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  • 35. The severe G480C cystic fibrosis mutation, when replicated in the mouse, demonstrates mistrafficking, normal survival and organ-specific bioelectrics.
    Dickinson P, Smith SN, Webb S, Kilanowski FM, Campbell IJ, Taylor MS, Porteous DJ, Willemsen R, de Jonge HR, Farley R, Alton EW, Dorin JR.
    Hum Mol Genet; 2002 Feb 01; 11(3):243-51. PubMed ID: 11823443
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  • 36. The Effects of CFTR and Mucoid Phenotype on Susceptibility and Innate Immune Responses in a Mouse Model of Pneumococcal Lung Disease.
    Dennis EA, Coats MT, Griffin SE, Hale JY, Novak L, Briles DE, Crain MJ.
    PLoS One; 2015 Feb 01; 10(10):e0140335. PubMed ID: 26469863
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  • 37. Genotype and phenotype in cystic fibrosis.
    Zielenski J.
    Respiration; 2000 Feb 01; 67(2):117-33. PubMed ID: 10773783
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  • 38. Cystic fibrosis mice carrying the missense mutation G551D replicate human genotype-phenotype correlations.
    Delaney SJ, Alton EW, Smith SN, Lunn DP, Farley R, Lovelock PK, Thomson SA, Hume DA, Lamb D, Porteous DJ, Dorin JR, Wainwright BJ.
    EMBO J; 1996 Mar 01; 15(5):955-63. PubMed ID: 8605891
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  • 39. The in vivo effects of milrinone on the airways of cystic fibrosis mice and human subjects.
    Smith SN, Middleton PG, Chadwick S, Jaffe A, Bush KA, Rolleston S, Farley R, Delaney SJ, Wainwright B, Geddes DM, Alton EW.
    Am J Respir Cell Mol Biol; 1999 Jan 01; 20(1):129-34. PubMed ID: 9870926
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  • 40. Nasal abnormalities in cystic fibrosis mice independent of infection and inflammation.
    Hilliard TN, Zhu J, Farley R, Escudero-Garcia S, Wainwright BJ, Jeffery PK, Griesenbach U, Bush A, Davies JC, Alton EW.
    Am J Respir Cell Mol Biol; 2008 Jul 01; 39(1):19-25. PubMed ID: 18239192
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