Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 39

1.

The short apical membrane half-life of rescued {Delta}F508-cystic fibrosis transmembrane conductance regulator (CFTR) results from accelerated endocytosis of {Delta}F508-CFTR in polarized human airway epithelial cells.

Swiatecka-Urban A, Brown A, Moreau-Marquis S, Renuka J, Coutermarsh B, Barnaby R, Karlson KH, Flotte TR, Fukuda M, Langford GM, Stanton BA.

J Biol Chem. 2005 Nov 4;280(44):36762-72. Epub 2005 Aug 30.

2.

Defects in processing and trafficking of cystic fibrosis transmembrane conductance regulator.

Kunzelmann K, Nitschke R.

Exp Nephrol. 2000 Nov-Dec;8(6):332-42. Review.

PMID:
11014930
3.

Control of cystic fibrosis transmembrane conductance regulator membrane trafficking: not just from the endoplasmic reticulum to the Golgi.

Farinha CM, Matos P, Amaral MD.

FEBS J. 2013 Sep;280(18):4396-406. doi: 10.1111/febs.12392. Epub 2013 Jul 5. Review.

4.

Cystic fibrosis transmembrane conductance regulator (CFTR) and renal function.

Stanton BA.

Wien Klin Wochenschr. 1997 Jun 27;109(12-13):457-64. Review.

PMID:
9261986
5.

CFTR, chloride concentration and cell volume: could mammalian protein histidine phosphorylation play a latent role?

Treharne KJ, Crawford RM, Mehta A.

Exp Physiol. 2006 Jan;91(1):131-9. Epub 2005 Oct 11. Review.

6.

Cystic fibrosis: a disease of altered protein folding.

Qu BH, Strickland E, Thomas PJ.

J Bioenerg Biomembr. 1997 Oct;29(5):483-90. Review.

PMID:
9511933
7.
8.

From the endoplasmic reticulum to the plasma membrane: mechanisms of CFTR folding and trafficking.

Farinha CM, Canato S.

Cell Mol Life Sci. 2017 Jan;74(1):39-55. doi: 10.1007/s00018-016-2387-7. Epub 2016 Oct 3. Review.

PMID:
27699454
9.

Endocytic trafficking of CFTR in health and disease.

Ameen N, Silvis M, Bradbury NA.

J Cyst Fibros. 2007 Jan;6(1):1-14. Epub 2006 Nov 13. Review.

10.

Acquired Cystic Fibrosis Transmembrane Conductance Regulator Deficiency.

Cho DY, Woodworth BA.

Adv Otorhinolaryngol. 2016;79:78-85. doi: 10.1159/000445134. Epub 2016 Jul 28. Review.

PMID:
27466849
11.

Emerging relationship between CFTR, actin and tight junction organization in cystic fibrosis airway epithelium.

Castellani S, Favia M, Guerra L, Carbone A, Abbattiscianni AC, Di Gioia S, Casavola V, Conese M.

Histol Histopathol. 2017 May;32(5):445-459. doi: 10.14670/HH-11-842. Epub 2016 Nov 11. Review.

PMID:
27834058
12.

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

Marunaka Y.

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

13.

The role of the UPS in cystic fibrosis.

Turnbull EL, Rosser MF, Cyr DM.

BMC Biochem. 2007 Nov 22;8 Suppl 1:S11. Review.

14.

Strategies for correcting the delta F508 CFTR protein-folding defect.

Brown CR, Hong-Brown LQ, Welch WJ.

J Bioenerg Biomembr. 1997 Oct;29(5):491-502. Review.

PMID:
9511934
15.

Divergent signaling via SUMO modification: potential for CFTR modulation.

Ahner A, Gong X, Frizzell RA.

Am J Physiol Cell Physiol. 2016 Feb 1;310(3):C175-80. doi: 10.1152/ajpcell.00124.2015. Epub 2015 Nov 18. Review.

16.

New insights into cystic fibrosis: molecular switches that regulate CFTR.

Guggino WB, Stanton BA.

Nat Rev Mol Cell Biol. 2006 Jun;7(6):426-36. doi: 10.1038/nrm1949. Review.

PMID:
16723978
17.

Cystic fibrosis transmembrane conductance regulator in teleost fish.

Marshall WS, Singer TD.

Biochim Biophys Acta. 2002 Nov 13;1566(1-2):16-27. Review.

18.

CFTR chloride channel in the apical compartments: spatiotemporal coupling to its interacting partners.

Li C, Naren AP.

Integr Biol (Camb). 2010 Apr;2(4):161-77. doi: 10.1039/b924455g. Epub 2010 Mar 5. Review.

19.

Regulation of epithelial ion channels by Rab GTPases.

Saxena SK, Kaur S.

Biochem Biophys Res Commun. 2006 Dec 22;351(3):582-7. Epub 2006 Oct 27. Review.

PMID:
17084813
20.

Cell surface dynamics of CFTR: the ins and outs.

Okiyoneda T, Lukacs GL.

Biochim Biophys Acta. 2007 Apr;1773(4):476-9. Epub 2007 Jan 19. Review.

Supplemental Content

Support Center