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Biosynthesis of surfactant protein C (SP-C). Sorting of SP-C proprotein involves homomeric association via a signal anchor domain.

Wang WJ, Russo SJ, Mulugeta S, Beers MF.

J Biol Chem. 2002 May 31;277(22):19929-37. Epub 2002 Mar 20.


Folding and Intramembraneous BRICHOS Binding of the Prosurfactant Protein C Transmembrane Segment.

Sáenz A, Presto J, Lara P, Akinyi-Oloo L, García-Fojeda B, Nilsson I, Johansson J, Casals C.

J Biol Chem. 2015 Jun 3. pii: jbc.M114.630343. [Epub ahead of print]


Clinical and ultrastructural spectrum of diffuse lung disease associated with surfactant protein C mutations.

Peca D, Boldrini R, Johannson J, Shieh JT, Citti A, Petrini S, Salerno T, Cazzato S, Testa R, Messina F, Onofri A, Cenacchi G, Westermark P, Ullman N, Cogo P, Cutrera R, Danhaive O.

Eur J Hum Genet. 2015 Mar 18. doi: 10.1038/ejhg.2015.45. [Epub ahead of print]


High-Efficiency Type II Cell-Enhanced Green Fluorescent Protein Expression Facilitates Cellular Identification, Tracking, and Isolation.

Vanderbilt JN, Gonzalez RF, Allen L, Gillespie A, Leaffer D, Dean WB, Chapin C, Dobbs LG.

Am J Respir Cell Mol Biol. 2015 Jul;53(1):14-21. doi: 10.1165/rcmb.2014-0348MA.


Trafficking of excitatory amino acid transporter 2-laden vesicles in cultured astrocytes: a comparison between approximate and exact determination of trajectory angles.

Cavender CE, Gottipati MK, Parpura V.

Amino Acids. 2015 Feb;47(2):357-67. doi: 10.1007/s00726-014-1868-y. Epub 2014 Nov 19.


An uncleaved signal peptide directs the Malus xiaojinensis iron transporter protein Mx IRT1 into the ER for the PM secretory pathway.

Zhang P, Tan S, Berry JO, Li P, Ren N, Li S, Yang G, Wang WB, Qi XT, Yin LP.

Int J Mol Sci. 2014 Nov 7;15(11):20413-33. doi: 10.3390/ijms151120413.


Mutations of rat surfactant protein A have distinct effects on its glycosylation, secretion, aggregation and degradation.

Yang W, Shen H, Fang G, Li H, Li L, Deng F, Gu W, Li K, Ma L, Gu J, Wang Y.

Life Sci. 2014 Nov 11;117(2):47-55. doi: 10.1016/j.lfs.2014.09.006. Epub 2014 Sep 19.


Unexpected transcellular protein crossover occurs during canonical DNA transfection.

Arsenault J, Cuijpers SA, Niranjan D, Davletov B.

J Cell Biochem. 2014 Dec;115(12):2047-54. doi: 10.1002/jcb.24884.


Allele-specific N-glycosylation delays human surfactant protein B secretion in vitro and associates with decreased protein levels in vivo.

Taponen S, Huusko JM, Petäjä-Repo UE, Paananen R, Guttentag SH, Hallman M, Haataja R.

Pediatr Res. 2013 Dec;74(6):646-51. doi: 10.1038/pr.2013.151. Epub 2013 Sep 3.


SFTPC mutations cause SP-C degradation and aggregate formation without increasing ER stress.

Thurm T, Kaltenborn E, Kern S, Griese M, Zarbock R.

Eur J Clin Invest. 2013 Aug;43(8):791-800. doi: 10.1111/eci.12107. Epub 2013 May 24.


DNA-mediated assembly of protein heterodimers on membrane surfaces.

Coyle MP, Xu Q, Chiang S, Francis MB, Groves JT.

J Am Chem Soc. 2013 Apr 3;135(13):5012-6. doi: 10.1021/ja3101215. Epub 2013 Mar 26.


An amphipathic alpha-helix in the prodomain of cocaine and amphetamine regulated transcript peptide precursor serves as its sorting signal to the regulated secretory pathway.

Blanco EH, Lagos CF, Andrés ME, Gysling K.

PLoS One. 2013;8(3):e59695. doi: 10.1371/journal.pone.0059695. Epub 2013 Mar 19.


Human surfactant protein A2 gene mutations impair dimmer/trimer assembly leading to deficiency in protein sialylation and secretion.

Song Y, Fang G, Shen H, Li H, Yang W, Pan B, Huang G, Lin G, Ma L, Willard B, Gu J, Zheng L, Wang Y.

PLoS One. 2012;7(10):e46559. doi: 10.1371/journal.pone.0046559. Epub 2012 Oct 3.


4-Phenylbutyric acid treatment rescues trafficking and processing of a mutant surfactant protein-C.

Stewart GA, Ridsdale R, Martin EP, Na CL, Xu Y, Mandapaka K, Weaver TE.

Am J Respir Cell Mol Biol. 2012 Sep;47(3):324-31. doi: 10.1165/rcmb.2012-0003OC. Epub 2012 Mar 29.


High-resolution structure of a BRICHOS domain and its implications for anti-amyloid chaperone activity on lung surfactant protein C.

Willander H, Askarieh G, Landreh M, Westermark P, Nordling K, Keränen H, Hermansson E, Hamvas A, Nogee LM, Bergman T, Saenz A, Casals C, Åqvistg J, Jörnvall H, Berglund H, Presto J, Knight SD, Johansson J.

Proc Natl Acad Sci U S A. 2012 Feb 14;109(7):2325-9. doi: 10.1073/pnas.1114740109. Epub 2012 Feb 2.


Assessing the tendency of fluorescent proteins to oligomerize under physiologic conditions.

Costantini LM, Fossati M, Francolini M, Snapp EL.

Traffic. 2012 May;13(5):643-9. doi: 10.1111/j.1600-0854.2012.01336.x. Epub 2012 Feb 20.


A glutathione peroxidase 4 (GPx4) homologue from southern bluefin tuna is a secreted protein: first report of a secreted GPx4 isoform in vertebrates.

Bain PA, Schuller KA.

Comp Biochem Physiol B Biochem Mol Biol. 2012 Apr;161(4):392-7. doi: 10.1016/j.cbpb.2012.01.004. Epub 2012 Jan 12.


A nonaggregating surfactant protein C mutant is misdirected to early endosomes and disrupts phospholipid recycling.

Beers MF, Hawkins A, Maguire JA, Kotorashvili A, Zhao M, Newitt JL, Ding W, Russo S, Guttentag S, Gonzales L, Mulugeta S.

Traffic. 2011 Sep;12(9):1196-210. doi: 10.1111/j.1600-0854.2011.01223.x. Epub 2011 Jun 28.


BRICHOS domain associated with lung fibrosis, dementia and cancer--a chaperone that prevents amyloid fibril formation?

Willander H, Hermansson E, Johansson J, Presto J.

FEBS J. 2011 Oct;278(20):3893-904. doi: 10.1111/j.1742-4658.2011.08209.x. Epub 2011 Jul 5. Review.


A non-BRICHOS surfactant protein c mutation disrupts epithelial cell function and intercellular signaling.

Woischnik M, Sparr C, Kern S, Thurm T, Hector A, Hartl D, Liebisch G, Mulugeta S, Beers MF, Schmitz G, Griese M.

BMC Cell Biol. 2010 Nov 20;11:88. doi: 10.1186/1471-2121-11-88.

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