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Items: 1 to 20 of 121

1.

Proteomics, bioinformatics and targeted gene expression analysis reveals up-regulation of cochlin and identifies other potential biomarkers in the mouse model for deafness in Usher syndrome type 1F.

Chance MR, Chang J, Liu S, Gokulrangan G, Chen DH, Lindsay A, Geng R, Zheng QY, Alagramam K.

Hum Mol Genet. 2010 Apr 15;19(8):1515-27. doi: 10.1093/hmg/ddq025.

2.

Proteomics reveal Cochlin deposits associated with glaucomatous trabecular meshwork.

Bhattacharya SK, Rockwood EJ, Smith SD, Bonilha VL, Crabb JS, Kuchtey RW, Robertson NG, Peachey NS, Morton CC, Crabb JW.

J Biol Chem. 2005 Feb 18;280(7):6080-4.

4.

Cochlin immunostaining of inner ear pathologic deposits and proteomic analysis in DFNA9 deafness and vestibular dysfunction.

Robertson NG, Cremers CW, Huygen PL, Ikezono T, Krastins B, Kremer H, Kuo SF, Liberman MC, Merchant SN, Miller CE, Nadol JB Jr, Sarracino DA, Verhagen WI, Morton CC.

Hum Mol Genet. 2006 Apr 1;15(7):1071-85.

PMID:
16481359
5.

iTRAQ-proteomics and bioinformatics analyses of mammary tissue from cows with clinical mastitis due to natural infection with Staphylococci aureus.

Huang J, Luo G, Zhang Z, Wang X, Ju Z, Qi C, Zhang Y, Wang C, Li R, Li J, Yin W, Xu Y, Moisá SJ, Loor JJ, Zhong J.

BMC Genomics. 2014 Oct 2;15:839. doi: 10.1186/1471-2164-15-839.

6.

Characterization of vestibular dysfunction in the mouse model for Usher syndrome 1F.

Alagramam KN, Stahl JS, Jones SM, Pawlowski KS, Wright CG.

J Assoc Res Otolaryngol. 2005 Jun;6(2):106-18.

7.

Molecular basis of human Usher syndrome: deciphering the meshes of the Usher protein network provides insights into the pathomechanisms of the Usher disease.

Reiners J, Nagel-Wolfrum K, Jürgens K, Märker T, Wolfrum U.

Exp Eye Res. 2006 Jul;83(1):97-119. Review.

PMID:
16545802
9.

Inner ear localization of mRNA and protein products of COCH, mutated in the sensorineural deafness and vestibular disorder, DFNA9.

Robertson NG, Resendes BL, Lin JS, Lee C, Aster JC, Adams JC, Morton CC.

Hum Mol Genet. 2001 Oct 15;10(22):2493-500.

PMID:
11709536
10.

Potential for transcriptional upregulation of cochlin in glaucomatous trabecular meshwork: a combinatorial bioinformatic and biochemical analytical approach.

Picciani RG, Diaz A, Lee RK, Bhattacharya SK.

Invest Ophthalmol Vis Sci. 2009 Jul;50(7):3106-11. doi: 10.1167/iovs.08-3106.

11.

Expression of cochlin mRNA splice variants in the inner ear.

Sekine K, Ikezono T, Matsumura T, Shindo S, Watanabe A, Li L, Pawankar R, Nishino T, Yagi T.

Audiol Neurootol. 2010;15(2):88-96. doi: 10.1159/000231634.

PMID:
19657184
12.

Identification of a novel Cochlin isoform in the perilymph: insights to Cochlin function and the pathogenesis of DFNA9.

Ikezono T, Shindo S, Li L, Omori A, Ichinose S, Watanabe A, Kobayashi T, Pawankar R, Yagi T.

Biochem Biophys Res Commun. 2004 Feb 6;314(2):440-6.

PMID:
14733925
13.

Identification of human hepatocellular carcinoma-related biomarkers by two-dimensional difference gel electrophoresis and mass spectrometry.

Lee IN, Chen CH, Sheu JC, Lee HS, Huang GT, Yu CY, Lu FJ, Chow LP.

J Proteome Res. 2005 Nov-Dec;4(6):2062-9.

PMID:
16335951
14.
15.

Cochlin expression in the rat perilymph during postnatal development.

Shiiba K, Shindo S, Ikezono T, Sekine K, Matsumura T, Sekiguchi S, Yagi T, Okubo K.

Acta Otolaryngol. 2012 Nov;132(11):1134-9. doi: 10.3109/00016489.2012.687456.

PMID:
23020749
16.

Proteomic analysis of propiconazole responses in mouse liver: comparison of genomic and proteomic profiles.

Ortiz PA, Bruno ME, Moore T, Nesnow S, Winnik W, Ge Y.

J Proteome Res. 2010 Mar 5;9(3):1268-78. doi: 10.1021/pr900755q.

PMID:
20095644
17.

Proteomic identification of altered proteins in skeletal muscle during chronic potassium depletion: Implications for hypokalemic myopathy.

Thongboonkerd V, Kanlaya R, Sinchaikul S, Parichatikanond P, Chen ST, Malasit P.

J Proteome Res. 2006 Dec;5(12):3326-35.

PMID:
17137334
19.

Proteomic analysis of Nrf2 deficient transgenic mice reveals cellular defence and lipid metabolism as primary Nrf2-dependent pathways in the liver.

Kitteringham NR, Abdullah A, Walsh J, Randle L, Jenkins RE, Sison R, Goldring CE, Powell H, Sanderson C, Williams S, Higgins L, Yamamoto M, Hayes J, Park BK.

J Proteomics. 2010 Jun 16;73(8):1612-31. doi: 10.1016/j.jprot.2010.03.018.

20.

Proteome changes in ovarian epithelial cells derived from women with BRCA1 mutations and family histories of cancer.

Smith-Beckerman DM, Fung KW, Williams KE, Auersperg N, Godwin AK, Burlingame AL.

Mol Cell Proteomics. 2005 Feb;4(2):156-68.

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