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Select item 234093891.

Pulmonology: CFTR modulators for cystic fibrosis.

Bertoncini E, Colomb-Lippa D.

JAAPA. 2013 Feb;26(2):59-60. No abstract available.

PMID:: 23409389; [PubMed - indexed for MEDLINE]

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Select item 233258542.

Nucleosome mapping across the CFTR locus identifies novel regulatory factors.

Yigit E, Bischof JM, Zhang Z, Ott CJ, Kerschner JL, Leir SH, Buitrago-Delgado E, Zhang Q, Wang JP, Widom J, Harris A.

Nucleic Acids Res. 2013 Mar 1;41(5):2857-68. doi: 10.1093/nar/gks1462. Epub 2013 Jan 15.

PMID:: 23325854; [PubMed - indexed for MEDLINE]

Free PMC Article

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Select item 232091793.

Assessing the Disease-Liability of Mutations in CFTR.

Ferec C, Cutting GR.

Cold Spring Harb Perspect Med. 2012 Dec 1;2(12):a009480. doi: 10.1101/cshperspect.a009480.

PMID:: 23209179; [PubMed - indexed for MEDLINE]

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Select item 231852474.

The mitochondrial complex I activity is reduced in cells with impaired cystic fibrosis transmembrane conductance regulator (CFTR) function.

Valdivieso AG, Clauzure M, Marín MC, Taminelli GL, Massip Copiz MM, Sánchez F, Schulman G, Teiber ML, Santa-Coloma TA.

PLoS One. 2012;7(11):e48059. doi: 10.1371/journal.pone.0048059. Epub 2012 Nov 21.

PMID:: 23185247; [PubMed - indexed for MEDLINE]

Free PMC Article

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Select item 231482145.

Depletion of the ubiquitin-binding adaptor molecule SQSTM1/p62 from macrophages harboring cftr ΔF508 mutation improves the delivery of Burkholderia cenocepacia to the autophagic machinery.

Abdulrahman BA, Khweek AA, Akhter A, Caution K, Tazi M, Hassan H, Zhang Y, Rowland PD, Malhotra S, Aeffner F, Davis IC, Valvano MA, Amer AO.

J Biol Chem. 2013 Jan 18;288(3):2049-58. doi: 10.1074/jbc.M112.411728. Epub 2012 Nov 12.

PMID:: 23148214; [PubMed - indexed for MEDLINE]

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Select item 231049836.

Correctors of ΔF508 CFTR restore global conformational maturation without thermally stabilizing the mutant protein.

He L, Kota P, Aleksandrov AA, Cui L, Jensen T, Dokholyan NV, Riordan JR.

FASEB J. 2013 Feb;27(2):536-45. doi: 10.1096/fj.12-216119. Epub 2012 Oct 26.

PMID:: 23104983; [PubMed - indexed for MEDLINE]

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Select item 231022227.

Correction of F508del-CFTR trafficking by the sponge alkaloid latonduine is modulated by interaction with PARP.

Carlile GW, Keyzers RA, Teske KA, Robert R, Williams DE, Linington RG, Gray CA, Centko RM, Yan L, Anjos SM, Sampson HM, Zhang D, Liao J, Hanrahan JW, Andersen RJ, Thomas DY.

Chem Biol. 2012 Oct 26;19(10):1288-99. doi: 10.1016/j.chembiol.2012.08.014.

PMID:: 23102222; [PubMed - indexed for MEDLINE]

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Select item 230921028.

CFTR polymorphisms of healthy individuals in two Chinese cities--Changchun and Nanjing.

Jin CX, Fujiki K, Song Y, Ping Z, Nakakuki M, Wei MX, Zhang SM, Ishiguro H, Naruse S.

Nagoya J Med Sci. 2012 Aug;74(3-4):293-301.

PMID:: 23092102; [PubMed - indexed for MEDLINE]

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Select item 230821989.

Measurements of CFTR-mediated Cl- secretion in human rectal biopsies constitute a robust biomarker for Cystic Fibrosis diagnosis and prognosis.

Sousa M, Servidoni MF, Vinagre AM, Ramalho AS, Bonadia LC, Felício V, Ribeiro MA, Uliyakina I, Marson FA, Kmit A, Cardoso SR, Ribeiro JD, Bertuzzo CS, Sousa L, Kunzelmann K, Ribeiro AF, Amaral MD.

PLoS One. 2012;7(10):e47708. doi: 10.1371/journal.pone.0047708. Epub 2012 Oct 17.

PMID:: 23082198; [PubMed - indexed for MEDLINE]

Free PMC Article

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Select item 2307114910.

Fixing cystic fibrosis by correcting CFTR domain assembly.

Okiyoneda T, Lukacs GL.

J Cell Biol. 2012 Oct 15;199(2):199-204. doi: 10.1083/jcb.201208083.

PMID:: 23071149; [PubMed - indexed for MEDLINE]

Free PMC Article

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Select item 2306044411.

Regulation of activation and processing of the cystic fibrosis transmembrane conductance regulator (CFTR) by a complex electrostatic interaction between the regulatory domain and cytoplasmic loop 3.

Wang G, Duan DD.

J Biol Chem. 2012 Nov 23;287(48):40484-92. doi: 10.1074/jbc.M112.360214. Epub 2012 Oct 11.

PMID:: 23060444; [PubMed - indexed for MEDLINE]

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Select item 2304393212.

CFTR haplotypes in northern Iranian population.

Kholghi Oskooei V, Esmaeili Dooki MR, Tabaripour R, Mirzajani S, Pourbagher R, Akhavan-Niaki H.

Gene. 2013 Jan 1;512(1):55-60. doi: 10.1016/j.gene.2012.09.096. Epub 2012 Oct 5.

PMID:: 23043932; [PubMed - indexed for MEDLINE]

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Select item 2294228913.

Cystic fibrosis transmembrane conductance regulator (CFTR) potentiator VX-770 (ivacaftor) opens the defective channel gate of mutant CFTR in a phosphorylation-dependent but ATP-independent manner.

Eckford PD, Li C, Ramjeesingh M, Bear CE.

J Biol Chem. 2012 Oct 26;287(44):36639-49. doi: 10.1074/jbc.M112.393637. Epub 2012 Aug 31.

PMID:: 22942289; [PubMed - indexed for MEDLINE]

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Select item 2292267214.

Directed differentiation of human pluripotent stem cells into mature airway epithelia expressing functional CFTR protein.

Wong AP, Bear CE, Chin S, Pasceri P, Thompson TO, Huan LJ, Ratjen F, Ellis J, Rossant J.

Nat Biotechnol. 2012 Sep;30(9):876-82.

PMID:: 22922672; [PubMed - indexed for MEDLINE]

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Select item 2290417015.

Nedd4-2 does not regulate wt-CFTR in human airway epithelial cells.

Koeppen K, Chapline C, Sato JD, Stanton BA.

Am J Physiol Lung Cell Mol Physiol. 2012 Oct 15;303(8):L720-7. doi: 10.1152/ajplung.00409.2011. Epub 2012 Aug 17.

PMID:: 22904170; [PubMed - indexed for MEDLINE]

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Select item 2289671016.

Genotyping efficiency of 2 primer sets and an unlabeled oligonucleotide probe for the p.Phe508del in exon 10 of the CFTR gene as determined with high-resolution melting analysis.

Poulou M, Destouni A, Fylaktou I, Kanavakis E, Tzetis M.

Clin Chem. 2012 Oct;58(10):1490-2. Epub 2012 Aug 15. No abstract available.

PMID:: 22896710; [PubMed - indexed for MEDLINE]

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Select item 2288955717.

Ligand-based design, in silico ADME-Tox filtering, synthesis and biological evaluation to discover new soluble 1,4-DHP-based CFTR activators.

Visentin S, Ermondi G, Medana C, Pedemonte N, Galietta L, Caron G.

Eur J Med Chem. 2012 Sep;55:188-94. doi: 10.1016/j.ejmech.2012.07.017. Epub 2012 Jul 23.

PMID:: 22889557; [PubMed - indexed for MEDLINE]

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Select item 2287994418.

Relating the disease mutation spectrum to the evolution of the cystic fibrosis transmembrane conductance regulator (CFTR).

Rishishwar L, Varghese N, Tyagi E, Harvey SC, Jordan IK, McCarty NA.

PLoS One. 2012;7(8):e42336. doi: 10.1371/journal.pone.0042336. Epub 2012 Aug 7.

PMID:: 22879944; [PubMed - indexed for MEDLINE]

Free PMC Article

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Select item 2284672019.

CFTR is involved in the fine tuning of intracellular redox status: physiological implications in cystic fibrosis.

Duranton C, Rubera I, Cougnon M, Melis N, Chargui A, Mograbi B, Tauc M.

Am J Pathol. 2012 Oct;181(4):1367-77. doi: 10.1016/j.ajpath.2012.06.017. Epub 2012 Jul 28.

PMID:: 22846720; [PubMed - indexed for MEDLINE]

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Select item 2284270220.

The CFTR polymorphisms poly-T, TG-repeats and M470V in Chinese males with congenital bilateral absence of the vas deferens.

Ni WH, Jiang L, Fei QJ, Jin JY, Yang X, Huang XF.

Asian J Androl. 2012 Sep;14(5):687-90. doi: 10.1038/aja.2012.43. Epub 2012 Jul 30.

PMID:: 22842702; [PubMed - indexed for MEDLINE]

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Supplemental Content

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6 free full-text articles in PubMed Central

Nucleosome mapping across the CFTR locus identifies novel regulatory factors. [Nucleic Acids Res. 2013]
Nucleosome mapping across the CFTR locus identifies novel regulatory factors.
Yigit E, Bischof JM, Zhang Z, Ott CJ, Kerschner JL, Leir SH, Buitrago-Delgado E, Zhang Q, Wang JP, Widom J, et al. Nucleic Acids Res. 2013 Mar 1; 41(5):2857-68. Epub 2013 Jan 15.
The mitochondrial complex I activity is reduced in cells with impaired cystic fibrosis transmembrane conductance regulator (CFTR) function. [PLoS One. 2012]
The mitochondrial complex I activity is reduced in cells with impaired cystic fibrosis transmembrane conductance regulator (CFTR) function.
Valdivieso AG, Clauzure M, Marín MC, Taminelli GL, Massip Copiz MM, Sánchez F, Schulman G, Teiber ML, Santa-Coloma TA. PLoS One. 2012; 7(11):e48059. Epub 2012 Nov 21.
Measurements of CFTR-mediated Cl- secretion in human rectal biopsies constitute a robust biomarker for Cystic Fibrosis diagnosis and prognosis. [PLoS One. 2012]
Measurements of CFTR-mediated Cl- secretion in human rectal biopsies constitute a robust biomarker for Cystic Fibrosis diagnosis and prognosis.
Sousa M, Servidoni MF, Vinagre AM, Ramalho AS, Bonadia LC, Felício V, Ribeiro MA, Uliyakina I, Marson FA, Kmit A, et al. PLoS One. 2012; 7(10):e47708. Epub 2012 Oct 17.

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