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Items: 1 to 20 of 72

1.

Restoration of proper trafficking to the cell surface for membrane proteins harboring cysteine mutations.

Lopez-Rodriguez A, Holmgren M.

PLoS One. 2012;7(10):e47693. doi: 10.1371/journal.pone.0047693. Epub 2012 Oct 17.

3.

Structural and functional determinants in the S5-P region of HCN-encoded pacemaker channels revealed by cysteine-scanning substitutions.

Au KW, Siu CW, Lau CP, Tse HF, Li RA.

Am J Physiol Cell Physiol. 2008 Jan;294(1):C136-44. Epub 2007 Nov 7.

4.

The mitochondrial oxoglutarate carrier: cysteine-scanning mutagenesis of transmembrane domain IV and sensitivity of Cys mutants to sulfhydryl reagents.

Stipani V, Cappello AR, Daddabbo L, Natuzzi D, Miniero DV, Stipani I, Palmieri F.

Biochemistry. 2001 Dec 25;40(51):15805-10.

PMID:
11747458
5.
6.

Mutations in CNGA3 impair trafficking or function of cone cyclic nucleotide-gated channels, resulting in achromatopsia.

Reuter P, Koeppen K, Ladewig T, Kohl S, Baumann B, Wissinger B; Achromatopsia Clinical Study Group.

Hum Mutat. 2008 Oct;29(10):1228-36. doi: 10.1002/humu.20790.

PMID:
18521937
7.

Dissecting the pathogenic mechanisms of mutations in the pore region of the human cone photoreceptor cyclic nucleotide-gated channel.

Koeppen K, Reuter P, Ladewig T, Kohl S, Baumann B, Jacobson SG, Plomp AS, Hamel CP, Janecke AR, Wissinger B.

Hum Mutat. 2010 Jul;31(7):830-9. doi: 10.1002/humu.21283.

PMID:
20506298
8.

Disease-causing mutations in the CLRN1 gene alter normal CLRN1 protein trafficking to the plasma membrane.

Isosomppi J, Västinsalo H, Geller SF, Heon E, Flannery JG, Sankila EM.

Mol Vis. 2009 Sep 8;15:1806-18.

9.

Transmembrane S1 mutations in CNGA3 from achromatopsia 2 patients cause loss of function and impaired cellular trafficking of the cone CNG channel.

Patel KA, Bartoli KM, Fandino RA, Ngatchou AN, Woch G, Carey J, Tanaka JC.

Invest Ophthalmol Vis Sci. 2005 Jul;46(7):2282-90.

PMID:
15980212
10.

Cysteine residues and the structure of the rat renal proximal tubular type II sodium phosphate cotransporter (rat NaPi IIa).

Lambert G, Forster IC, Biber J, Murer H.

J Membr Biol. 2000 Jul 15;176(2):133-41.

PMID:
10926678
11.

Topology of the P segments in the sodium channel pore revealed by cysteine mutagenesis.

Yamagishi T, Janecki M, Marban E, Tomaselli GF.

Biophys J. 1997 Jul;73(1):195-204.

12.
13.

Ligand-induced movements of inner transmembrane helices of Glut1 revealed by chemical cross-linking of di-cysteine mutants.

Mueckler M, Makepeace C.

PLoS One. 2012;7(2):e31412. doi: 10.1371/journal.pone.0031412. Epub 2012 Feb 20.

14.

Conserved glutamate residues are critically involved in Na+/nucleoside cotransport by human concentrative nucleoside transporter 1 (hCNT1).

Yao SY, Ng AM, Slugoski MD, Smith KM, Mulinta R, Karpinski E, Cass CE, Baldwin SA, Young JD.

J Biol Chem. 2007 Oct 19;282(42):30607-17. Epub 2007 Aug 17.

15.
16.

Cellular processing of cone photoreceptor cyclic GMP-gated ion channels: a role for the S4 structural motif.

Faillace MP, Bernabeu RO, Korenbrot JI.

J Biol Chem. 2004 May 21;279(21):22643-53. Epub 2004 Mar 15.

17.

CNGA3 achromatopsia-associated mutation potentiates the phosphoinositide sensitivity of cone photoreceptor CNG channels by altering intersubunit interactions.

Dai G, Varnum MD.

Am J Physiol Cell Physiol. 2013 Jul 15;305(2):C147-59. doi: 10.1152/ajpcell.00037.2013. Epub 2013 Apr 3.

18.

Functional analysis of human CNGA3 mutations associated with colour blindness suggests impaired surface expression of channel mutants A3(R427C) and A3(R563C).

Koeppen K, Reuter P, Kohl S, Baumann B, Ladewig T, Wissinger B.

Eur J Neurosci. 2008 May;27(9):2391-401. doi: 10.1111/j.1460-9568.2008.06195.x.

PMID:
18445228
19.

Voltage profile along the permeation pathway of an open channel.

Contreras JE, Chen J, Lau AY, Jogini V, Roux B, Holmgren M.

Biophys J. 2010 Nov 3;99(9):2863-9. doi: 10.1016/j.bpj.2010.08.053.

20.

Agonist-driven conformational changes in the inner beta-sheet of alpha7 nicotinic receptors.

McLaughlin JT, Fu J, Rosenberg RL.

Mol Pharmacol. 2007 May;71(5):1312-8. Epub 2007 Feb 26.

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