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Items: 1 to 20 of 23

1.

The truncated mutant HBsAg expression increases the tumorigenesis of hepatitis B virus by regulating TGF-β/Smad signaling pathway.

Wang ML, Wu DB, Tao YC, Chen LL, Liu CP, Chen EQ, Tang H.

Virol J. 2018 Apr 2;15(1):61. doi: 10.1186/s12985-018-0972-0.

2.

Restoration of type 1 iodothyronine deiodinase expression in renal cancer cells downregulates oncoproteins and affects key metabolic pathways as well as anti-oxidative system.

Popławski P, Wiśniewski JR, Rijntjes E, Richards K, Rybicka B, Köhrle J, Piekiełko-Witkowska A.

PLoS One. 2017 Dec 22;12(12):e0190179. doi: 10.1371/journal.pone.0190179. eCollection 2017.

3.

Post-LASIK exacerbation of granular corneal dystrophy type 2 in members of a chinese family.

Chao-Shern C, Me R, DeDionisio LA, Ke BL, Nesbit MA, Marshall J, Moore CBT.

Eye (Lond). 2018 Jan;32(1):39-43. doi: 10.1038/eye.2017.265. Epub 2017 Dec 1.

4.
5.

Loss of SPDEF and gain of TGFBI activity after androgen deprivation therapy promote EMT and bone metastasis of prostate cancer.

Chen WY, Tsai YC, Yeh HL, Suau F, Jiang KC, Shao AN, Huang J, Liu YN.

Sci Signal. 2017 Aug 15;10(492). pii: eaam6826. doi: 10.1126/scisignal.aam6826.

PMID:
28811384
6.

TGFBI functions similar to periostin but is uniquely dispensable during cardiac injury.

Schwanekamp JA, Lorts A, Sargent MA, York AJ, Grimes KM, Fischesser DM, Gokey JJ, Whitsett JA, Conway SJ, Molkentin JD.

PLoS One. 2017 Jul 27;12(7):e0181945. doi: 10.1371/journal.pone.0181945. eCollection 2017.

7.

Proteomic Analysis of Amyloid Corneal Aggregates from TGFBI-H626R Lattice Corneal Dystrophy Patient Implicates Serine-Protease HTRA1 in Mutation-Specific Pathogenesis of TGFBIp.

Venkatraman A, Dutta B, Murugan E, Piliang H, Lakshminaryanan R, Sook Yee AC, Pervushin KV, Sze SK, Mehta JS.

J Proteome Res. 2017 Aug 4;16(8):2899-2913. doi: 10.1021/acs.jproteome.7b00188. Epub 2017 Jul 20.

PMID:
28689406
8.

Microarray-based detection and expression analysis of new genes associated with drug resistance in ovarian cancer cell lines.

Januchowski R, Sterzyńska K, Zawierucha P, Ruciński M, Świerczewska M, Partyka M, Bednarek-Rajewska K, Brązert M, Nowicki M, Zabel M, Klejewski A.

Oncotarget. 2017 Jul 25;8(30):49944-49958. doi: 10.18632/oncotarget.18278.

9.

Mutation analysis of TGFBI and KRT12 in a case of concomitant keratoconus and granular corneal dystrophy.

Du X, Chen P, Sun D.

Graefes Arch Clin Exp Ophthalmol. 2017 Sep;255(9):1779-1786. doi: 10.1007/s00417-017-3699-5. Epub 2017 May 31.

PMID:
28567551
10.

Identification and characterization of biomarkers and their functions for Lapatinib-resistant breast cancer.

Zhang L, Huang Y, Zhuo W, Zhu Y, Zhu B, Chen Z.

Med Oncol. 2017 May;34(5):89. doi: 10.1007/s12032-017-0953-y. Epub 2017 Apr 9.

PMID:
28393315
11.

Effect of position-specific single-point mutations and biophysical characterization of amyloidogenic peptide fragments identified from lattice corneal dystrophy patients.

Anandalakshmi V, Murugan E, Leng EGT, Ting LW, Chaurasia SS, Yamazaki T, Nagashima T, George BL, Peh GSL, Pervushin K, Lakshminarayanan R, Mehta JS.

Biochem J. 2017 May 9;474(10):1705-1725. doi: 10.1042/BCJ20170125.

12.

TGFBI Gene Mutation Analysis of Clinically Diagnosed Granular Corneal Dystrophy Patients Prior to PTK: A Pilot Study from Eastern China.

Zeng L, Zhao J, Chen Y, Zhao F, Li M, Chao-Shern C, Moore T, Marshall J, Zhou X.

Sci Rep. 2017 Apr 4;7(1):596. doi: 10.1038/s41598-017-00716-5.

13.

TGFBI gene mutations analysis in Chinese families with corneal dystrophies.

Wang X, Ying M, Fu C, Wang Y, Li N.

Mol Med Rep. 2017 May;15(5):3198-3202. doi: 10.3892/mmr.2017.6414. Epub 2017 Mar 30.

PMID:
28358433
14.

Analysis of gene expression changes associated with human carcinoma-associated fibroblasts in non-small cell lung carcinoma.

Wu X, Ruan L, Yang Y, Mei Q.

Biol Res. 2017 Feb 23;50(1):6. doi: 10.1186/s40659-017-0108-9.

15.

Quantitative liver proteomics identifies FGF19 targets that couple metabolism and proliferation.

Massafra V, Milona A, Vos HR, Burgering BM, van Mil SW.

PLoS One. 2017 Feb 8;12(2):e0171185. doi: 10.1371/journal.pone.0171185. eCollection 2017.

16.

Vortex Pattern of Corneal Deposits in Granular Corneal Dystrophy Associated With the p.(Arg555Trp) Mutation in TGFBI.

Kattan JM, Serna-Ojeda JC, Sharma A, Kim EK, Ramirez-Miranda A, Cruz-Aguilar M, Cervantes AE, Frausto RF, Zenteno JC, Graue-Hernandez EO, Aldave AJ.

Cornea. 2017 Feb;36(2):210-216. doi: 10.1097/ICO.0000000000001045.

17.

Genome-wide association analyses of sleep disturbance traits identify new loci and highlight shared genetics with neuropsychiatric and metabolic traits.

Lane JM, Liang J, Vlasac I, Anderson SG, Bechtold DA, Bowden J, Emsley R, Gill S, Little MA, Luik AI, Loudon A, Scheer FA, Purcell SM, Kyle SD, Lawlor DA, Zhu X, Redline S, Ray DW, Rutter MK, Saxena R.

Nat Genet. 2017 Feb;49(2):274-281. doi: 10.1038/ng.3749. Epub 2016 Dec 19.

18.

Genetic analysis of CHST6 and TGFBI in Turkish patients with corneal dystrophies: Five novel variations in CHST6.

Yaylacioglu Tuncay F, Kayman Kurekci G, Guntekin Ergun S, Pasaoglu OT, Akata RF, Dincer PR.

Mol Vis. 2016 Oct 26;22:1267-1279. eCollection 2016.

19.

Novel TGFBI mutation p.(Leu558Arg) in a lattice corneal dystrophy patient.

Dudakova L, Palos M, Jirsova K, Skalicka P, Dundr P, Liskova P.

Ophthalmic Genet. 2016 Dec;37(4):473-474. Epub 2016 Mar 30. No abstract available.

PMID:
27028151
20.

WOMEN IN CANCER THEMATIC REVIEW: Ovarian cancer-peritoneal cell interactions promote extracellular matrix processing.

Ricciardelli C, Lokman NA, Ween MP, Oehler MK.

Endocr Relat Cancer. 2016 Nov;23(11):T155-T168. Epub 2016 Aug 30. Review.

PMID:
27578826

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