Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 20 of 9306

1.

Signaling Cascade Involved in Rapid Stimulation of Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) by Dexamethasone.

Bossmann M, Ackermann BW, Thome UH, Laube M.

Int J Mol Sci. 2017 Aug 19;18(8). pii: E1807. doi: 10.3390/ijms18081807.

PMID:
28825630
2.

Stem cell-derived organoids to model gastrointestinal facets of cystic fibrosis.

Hohwieler M, Perkhofer L, Liebau S, Seufferlein T, Müller M, Illing A, Kleger A.

United European Gastroenterol J. 2017 Aug;5(5):609-624. doi: 10.1177/2050640616670565. Epub 2016 Sep 21. Review.

PMID:
28815024
3.

Pathogenic role of ADGRG2 in CBAVD patients replicated in Chinese population.

Yang B, Wang J, Zhang W, Pan H, Li T, Liu B, Li H, Wang B.

Andrology. 2017 Aug 14. doi: 10.1111/andr.12407. [Epub ahead of print]

PMID:
28805948
4.

The Mechanistic Links between Insulin and Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Cl<sup>-</sup> Channel.

Marunaka Y.

Int J Mol Sci. 2017 Aug 14;18(8). pii: E1767. doi: 10.3390/ijms18081767. Review.

5.

Increased Expression of Plasma-Induced ABCC1 mRNA in Cystic Fibrosis.

Ideozu JE, Zhang X, Pan A, Ashrafi Z, Woods KJ, Hessner MJ, Simpson P, Levy H.

Int J Mol Sci. 2017 Aug 11;18(8). pii: E1752. doi: 10.3390/ijms18081752.

6.

Children and adolescents with cystic fibrosis display moderate bone microarchitecture abnormalities: data from high-resolution peripheral quantitative computed tomography.

Braun C, Bacchetta J, Braillon P, Chapurlat R, Drai J, Reix P.

Osteoporos Int. 2017 Aug 9. doi: 10.1007/s00198-017-4179-9. [Epub ahead of print]

PMID:
28795206
7.

Targeting the PI3K/Akt/mTOR signalling pathway in Cystic Fibrosis.

Reilly R, Mroz MS, Dempsey E, Wynne K, Keely SJ, McKone EF, Hiebel C, Behl C, Coppinger JA.

Sci Rep. 2017 Aug 9;7(1):7642. doi: 10.1038/s41598-017-06588-z.

8.

<i>Pseudomonas aeruginosa</i> LasB protease impairs innate immunity in mice and humans by targeting a lung epithelial cystic fibrosis transmembrane regulator-IL-6-antimicrobial-repair pathway.

Saint-Criq V, Villeret B, Bastaert F, Kheir S, Hatton A, Cazes A, Xing Z, Sermet-Gaudelus I, Garcia-Verdugo I, Edelman A, Sallenave JM.

Thorax. 2017 Aug 8. pii: thoraxjnl-2017-210298. doi: 10.1136/thoraxjnl-2017-210298. [Epub ahead of print]

PMID:
28790180
9.

Correction of CFTR function in nasal epithelial cells from cystic fibrosis patients predicts improvement of respiratory function by CFTR modulators.

Pranke IM, Hatton A, Simonin J, Jais JP, Le Pimpec-Barthes F, Carsin A, Bonnette P, Fayon M, Stremler-Le Bel N, Grenet D, Thumerel M, Mazenq J, Urbach V, Mesbahi M, Girodon-Boulandet E, Hinzpeter A, Edelman A, Sermet-Gaudelus I.

Sci Rep. 2017 Aug 7;7(1):7375. doi: 10.1038/s41598-017-07504-1.

10.

CFTR reduces microtubule-dependent Campylobacter jejuni invasion.

Kido J, Shimohata T, Amano S, Hatayama S, Nguyen AQ, Sato Y, Kanda Y, Tentaku A, Fukushima S, Nakahashi M, Uebanso T, Mawatari K, Takahashi A.

Infect Immun. 2017 Aug 7. pii: IAI.00311-17. doi: 10.1128/IAI.00311-17. [Epub ahead of print]

PMID:
28784926
11.

In cellulo analyses of the p.Val322Ala mutation on the CFTR protein conformation and activity.

Farhat R, El-Seedy A, Sari AIP, Norez C, Pasquet MC, Becq F, Kitzis A, Ladevèze V.

C R Biol. 2017 Aug 4. pii: S1631-0691(17)30100-2. doi: 10.1016/j.crvi.2017.06.001. [Epub ahead of print]

PMID:
28784578
12.

Association between F508 deletion in CFTR and chronic pancreatitis risk.

Zhao D, Xu Y, Li J, Fu S, Xiao F, Song X, Xie Z, Jiang M, He Y, Liu C, Wen Q, Yang X.

Dig Liver Dis. 2017 Jul 1. pii: S1590-8658(17)30943-X. doi: 10.1016/j.dld.2017.06.013. [Epub ahead of print] Review.

PMID:
28780053
13.

The CFTR gene mild variants poly-T, TG repeats and M470V detection in Indian men with congenital bilateral absence of vas deferens.

Gaikwad A, Khan S, Kadam S, Kadam K, Dighe V, Shah R, Kulkarni V, Kumaraswamy R, Gajbhiye R.

Andrologia. 2017 Aug 3. doi: 10.1111/and.12858. [Epub ahead of print]

PMID:
28776713
14.

Influenza virus infection alters ion channel function of Airway and alveolar cells: Mechanisms and physiological sequelae.

Londino JD, Lazrak A, Collawn JF, Bebok Z, Harrod KS, Matalon S.

Am J Physiol Lung Cell Mol Physiol. 2017 Aug 3:ajplung.00244.2017. doi: 10.1152/ajplung.00244.2017. [Epub ahead of print]

PMID:
28775098
15.

Molecular dynamics of the cryo-EM CFTR structure.

Tordai H, Leveles I, Hegedűs T.

Biochem Biophys Res Commun. 2017 Jul 31. pii: S0006-291X(17)31532-2. doi: 10.1016/j.bbrc.2017.07.165. [Epub ahead of print]

PMID:
28774558
16.

Characterization of primary rat nasal epithelial cultures in CFTR knockout rats as a model for CF sinus disease.

Tipirneni KE, Cho DY, Skinner DF, Zhang S, Mackey C, Lim DJ, Woodworth BA.

Laryngoscope. 2017 Aug 3. doi: 10.1002/lary.26720. [Epub ahead of print]

PMID:
28771736
17.

The cubicon method for concentrating membrane proteins in the cubic mesophase.

Ma P, Weichert D, Aleksandrov LA, Jensen TJ, Riordan JR, Liu X, Kobilka BK, Caffrey M.

Nat Protoc. 2017 Sep;12(9):1745-1762. doi: 10.1038/nprot.2017.057. Epub 2017 Aug 3.

PMID:
28771236
18.

Drug-induced dyspnea versus cystic fibrosis exacerbation: a diagnostic dilemma.

Walayat S, Hussain N, Patel J, Hussain F, Patel P, Dhillon S, Aulakh B, Chittivelu S.

Int Med Case Rep J. 2017 Jul 19;10:243-246. doi: 10.2147/IMCRJ.S139022. eCollection 2017.

19.

Sperm cystic fibrosis transmembrane conductance regulator expression level is relevant to fecundity of healthy couples.

Sun PB, Xu HM, Li K, Li HC, Chen AJ, Chen MJ, Dai HT, Ni Y.

Andrologia. 2017 Aug 1. doi: 10.1111/and.12865. [Epub ahead of print]

PMID:
28762521
20.

Establishment and long-term culture of human cystic fibrosis endothelial cells.

Plebani R, Tripaldi R, Lanuti P, Recchiuti A, Patruno S, Di Silvestre S, Simeone P, Anile M, Venuta F, Prioletta M, Mucilli F, Del Porto P, Marchisio M, Pandolfi A, Romano M.

Lab Invest. 2017 Jul 31. doi: 10.1038/labinvest.2017.74. [Epub ahead of print]

PMID:
28759010

Supplemental Content

Loading ...
Support Center