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Items: 17

1.

Characterization of the novel protein KIAA0564 (Von Willebrand Domain-containing Protein 8).

Luo M, Mengos AE, Ma W, Finlayson J, Bustos RZ, Xiao Zhu Y, Shi CX, Stubblefield TM, Willis WT, Mandarino LJ.

Biochem Biophys Res Commun. 2017 Jun 3;487(3):545-551. doi: 10.1016/j.bbrc.2017.04.067. Epub 2017 Apr 13.

2.

Association of liprin β-1 with kank proteins in melanoma.

Luo M, Mengos AE, Mandarino LJ, Sekulic A.

Exp Dermatol. 2016 Apr;25(4):321-3. doi: 10.1111/exd.12933. Epub 2016 Feb 26. No abstract available.

3.

Identification of a role for CLASP2 in insulin action.

Langlais P, Dillon JL, Mengos A, Baluch DP, Ardebili R, Miranda DN, Xie X, Heckmann BL, Liu J, Mandarino LJ.

J Biol Chem. 2012 Nov 9;287(46):39245-53. doi: 10.1074/jbc.M112.394148. Epub 2012 Sep 19.

4.

CFTR delivery to 25% of surface epithelial cells restores normal rates of mucus transport to human cystic fibrosis airway epithelium.

Zhang L, Button B, Gabriel SE, Burkett S, Yan Y, Skiadopoulos MH, Dang YL, Vogel LN, McKay T, Mengos A, Boucher RC, Collins PL, Pickles RJ.

PLoS Biol. 2009 Jul;7(7):e1000155. doi: 10.1371/journal.pbio.1000155. Epub 2009 Jul 21.

5.

Role of individual R domain phosphorylation sites in CFTR regulation by protein kinase A.

Hegedus T, Aleksandrov A, Mengos A, Cui L, Jensen TJ, Riordan JR.

Biochim Biophys Acta. 2009 Jun;1788(6):1341-9. doi: 10.1016/j.bbamem.2009.03.015. Epub 2009 Mar 26.

6.

Role of N-linked oligosaccharides in the biosynthetic processing of the cystic fibrosis membrane conductance regulator.

Chang XB, Mengos A, Hou YX, Cui L, Jensen TJ, Aleksandrov A, Riordan JR, Gentzsch M.

J Cell Sci. 2008 Sep 1;121(Pt 17):2814-23. doi: 10.1242/jcs.028951. Epub 2008 Aug 5.

7.

SERCA pump inhibitors do not correct biosynthetic arrest of deltaF508 CFTR in cystic fibrosis.

Grubb BR, Gabriel SE, Mengos A, Gentzsch M, Randell SH, Van Heeckeren AM, Knowles MR, Drumm ML, Riordan JR, Boucher RC.

Am J Respir Cell Mol Biol. 2006 Mar;34(3):355-63. Epub 2005 Nov 11.

8.

Characterization of wild-type and deltaF508 cystic fibrosis transmembrane regulator in human respiratory epithelia.

Kreda SM, Mall M, Mengos A, Rochelle L, Yankaskas J, Riordan JR, Boucher RC.

Mol Biol Cell. 2005 May;16(5):2154-67. Epub 2005 Feb 16.

9.

Bcr (breakpoint cluster region) protein binds to PDZ-domains of scaffold protein PDZK1 and vesicle coat protein Mint3.

Malmberg EK, Andersson CX, Gentzsch M, Chen JH, Mengos A, Cui L, Hansson GC, Riordan JR.

J Cell Sci. 2004 Nov 1;117(Pt 23):5535-41. Epub 2004 Oct 19.

10.

The DeltaF508 mutation results in loss of CFTR function and mature protein in native human colon.

Mall M, Kreda SM, Mengos A, Jensen TJ, Hirtz S, Seydewitz HH, Yankaskas J, Kunzelmann K, Riordan JR, Boucher RC.

Gastroenterology. 2004 Jan;126(1):32-41.

PMID:
14699484
11.

Comprehensive scanning of the ATM gene with DOVAM-S.

Buzin CH, Gatti RA, Nguyen VQ, Wen CY, Mitui M, Sanal O, Chen JS, Nozari G, Mengos A, Li X, Fujimura F, Sommer SS.

Hum Mutat. 2003 Feb;21(2):123-31.

PMID:
12552559
12.

The PDZ-binding chloride channel ClC-3B localizes to the Golgi and associates with cystic fibrosis transmembrane conductance regulator-interacting PDZ proteins.

Gentzsch M, Cui L, Mengos A, Chang XB, Chen JH, Riordan JR.

J Biol Chem. 2003 Feb 21;278(8):6440-9. Epub 2002 Dec 5.

13.

Frequency of recent retrotransposition events in the human factor IX gene.

Li X, Scaringe WA, Hill KA, Roberts S, Mengos A, Careri D, Pinto MT, Kasper CK, Sommer SS.

Hum Mutat. 2001 Jun;17(6):511-9.

PMID:
11385709
14.

Differential interactions of nucleotides at the two nucleotide binding domains of the cystic fibrosis transmembrane conductance regulator.

Aleksandrov L, Mengos A, Chang X, Aleksandrov A, Riordan JR.

J Biol Chem. 2001 Apr 20;276(16):12918-23. Epub 2001 Jan 29.

15.

Scanning by DOVAM-S detects all unique sequence changes in blinded analyses: evidence that the scanning conditions are generic.

Buzin CH, Wen CY, Nguyen VQ, Nozari G, Mengos A, Li X, Chen JS, Liu Q, Gatti RA, Fujimura FK, Sommer SS.

Biotechniques. 2000 Apr;28(4):746-50, 752-3.

16.

Removal of multiple arginine-framed trafficking signals overcomes misprocessing of delta F508 CFTR present in most patients with cystic fibrosis.

Chang XB, Cui L, Hou YX, Jensen TJ, Aleksandrov AA, Mengos A, Riordan JR.

Mol Cell. 1999 Jul;4(1):137-42.

17.

Detection of virtually all mutations-SSCP (DOVAM-S): a rapid method for mutation scanning with virtually 100% sensitivity.

Liu Q, Feng J, Buzin C, Wen C, Nozari G, Mengos A, Nguyen V, Liu J, Crawford L, Fujimura FK, Sommer SS.

Biotechniques. 1999 May;26(5):932, 936-8, 940-2.

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