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Items: 1 to 20 of 104

1.

Identification of proteins that interact with TANK binding kinase 1 and testing for mutations associated with glaucoma.

Seo S, Solivan-Timpe F, Roos BR, Robin AL, Stone EM, Kwon YH, Alward WL, Fingert JH.

Curr Eye Res. 2013 Feb;38(2):310-5. doi: 10.3109/02713683.2012.754047. Epub 2013 Jan 3.

2.

SQSTM1 Mutations and Glaucoma.

Scheetz TE, Roos BR, Solivan-Timpe F, Miller K, DeLuca AP, Stone EM, Kwon YH, Alward WL, Wang K, Fingert JH.

PLoS One. 2016 Jun 8;11(6):e0156001. doi: 10.1371/journal.pone.0156001. eCollection 2016.

3.

TBK1 gene duplication and normal-tension glaucoma.

Ritch R, Darbro B, Menon G, Khanna CL, Solivan-Timpe F, Roos BR, Sarfarzi M, Kawase K, Yamamoto T, Robin AL, Lotery AJ, Fingert JH.

JAMA Ophthalmol. 2014 May;132(5):544-8. doi: 10.1001/jamaophthalmol.2014.104.

4.

Copy number variations on chromosome 12q14 in patients with normal tension glaucoma.

Fingert JH, Robin AL, Stone JL, Roos BR, Davis LK, Scheetz TE, Bennett SR, Wassink TH, Kwon YH, Alward WL, Mullins RF, Sheffield VC, Stone EM.

Hum Mol Genet. 2011 Jun 15;20(12):2482-94. doi: 10.1093/hmg/ddr123. Epub 2011 Mar 29.

5.

Genomic Organization of TBK1 Copy Number Variations in Glaucoma Patients.

DeLuca AP, Alward WLM, Liebmann J, Ritch R, Kawase K, Kwon YH, Robin AL, Stone EM, Scheetz TE, Fingert JH.

J Glaucoma. 2017 Dec;26(12):1063-1067. doi: 10.1097/IJG.0000000000000792.

PMID:
28984711
6.

Tank-Binding Kinase 1 (TBK1) Gene and Open-Angle Glaucomas (An American Ophthalmological Society Thesis).

Fingert JH, Robin AL, Scheetz TE, Kwon YH, Liebmann JM, Ritch R, Alward WL.

Trans Am Ophthalmol Soc. 2016 Aug;114:T6.

7.

Human TBK1: A Gatekeeper of Neuroinflammation.

Ahmad L, Zhang SY, Casanova JL, Sancho-Shimizu V.

Trends Mol Med. 2016 Jun;22(6):511-527. doi: 10.1016/j.molmed.2016.04.006. Review.

8.

Significance of optineurin mutations in glaucoma and other diseases.

Minegishi Y, Nakayama M, Iejima D, Kawase K, Iwata T.

Prog Retin Eye Res. 2016 Nov;55:149-181. doi: 10.1016/j.preteyeres.2016.08.002. Epub 2016 Sep 29. Review.

PMID:
27693724
9.

Enhanced optineurin E50K-TBK1 interaction evokes protein insolubility and initiates familial primary open-angle glaucoma.

Minegishi Y, Iejima D, Kobayashi H, Chi ZL, Kawase K, Yamamoto T, Seki T, Yuasa S, Fukuda K, Iwata T.

Hum Mol Genet. 2013 Sep 1;22(17):3559-67. doi: 10.1093/hmg/ddt210. Epub 2013 May 12.

PMID:
23669351
10.

TBK1 and flanking genes in human retina.

Fingert JH, Darbro BW, Qian Q, Van Rheeden R, Miller K, Riker M, Solivan-Timpe F, Roos BR, Robin AL, Mullins RF.

Ophthalmic Genet. 2014 Mar;35(1):35-40. doi: 10.3109/13816810.2013.768674. Epub 2013 Feb 20.

11.

Association of HK2 and NCK2 with normal tension glaucoma in the Japanese population.

Shi D, Funayama T, Mashima Y, Takano Y, Shimizu A, Yamamoto K, Mengkegale M, Miyazawa A, Yasuda N, Fukuchi T, Abe H, Ideta H, Nishida K, Nakazawa T, Richards JE, Fuse N.

PLoS One. 2013;8(1):e54115. doi: 10.1371/journal.pone.0054115. Epub 2013 Jan 22.

12.

Copy number variations of TBK1 in Australian patients with primary open-angle glaucoma.

Awadalla MS, Fingert JH, Roos BE, Chen S, Holmes R, Graham SL, Chehade M, Galanopolous A, Ridge B, Souzeau E, Zhou T, Siggs OM, Hewitt AW, Mackey DA, Burdon KP, Craig JE.

Am J Ophthalmol. 2015 Jan;159(1):124-30.e1. doi: 10.1016/j.ajo.2014.09.044. Epub 2014 Oct 2.

13.

Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease.

Pottier C, Bieniek KF, Finch N, van de Vorst M, Baker M, Perkersen R, Brown P, Ravenscroft T, van Blitterswijk M, Nicholson AM, DeTure M, Knopman DS, Josephs KA, Parisi JE, Petersen RC, Boylan KB, Boeve BF, Graff-Radford NR, Veltman JA, Gilissen C, Murray ME, Dickson DW, Rademakers R.

Acta Neuropathol. 2015 Jul;130(1):77-92. doi: 10.1007/s00401-015-1436-x. Epub 2015 May 6.

14.

Functional dissection of the TBK1 molecular network.

Goncalves A, Bürckstümmer T, Dixit E, Scheicher R, Górna MW, Karayel E, Sugar C, Stukalov A, Berg T, Kralovics R, Planyavsky M, Bennett KL, Colinge J, Superti-Furga G.

PLoS One. 2011;6(9):e23971. doi: 10.1371/journal.pone.0023971. Epub 2011 Sep 8.

15.
16.

Evidence for RPGRIP1 gene as risk factor for primary open angle glaucoma.

Fernández-Martínez L, Letteboer S, Mardin CY, Weisschuh N, Gramer E, Weber BH, Rautenstrauss B, Ferreira PA, Kruse FE, Reis A, Roepman R, Pasutto F.

Eur J Hum Genet. 2011 Apr;19(4):445-51. doi: 10.1038/ejhg.2010.217. Epub 2011 Jan 12.

17.

Enhanced binding of TBK1 by an optineurin mutant that causes a familial form of primary open angle glaucoma.

Morton S, Hesson L, Peggie M, Cohen P.

FEBS Lett. 2008 Mar 19;582(6):997-1002. doi: 10.1016/j.febslet.2008.02.047. Epub 2008 Feb 26.

18.
19.

Mitochondrial DNA variant discovery in normal-tension glaucoma patients by next-generation sequencing.

Jeoung JW, Seong MW, Park SS, Kim DM, Kim SH, Park KH.

Invest Ophthalmol Vis Sci. 2014 Feb 24;55(2):986-92. doi: 10.1167/iovs.13-12968.

PMID:
24448266
20.

A Glaucoma-Associated Variant of Optineurin, M98K, Activates Tbk1 to Enhance Autophagosome Formation and Retinal Cell Death Dependent on Ser177 Phosphorylation of Optineurin.

Sirohi K, Kumari A, Radha V, Swarup G.

PLoS One. 2015 Sep 16;10(9):e0138289. doi: 10.1371/journal.pone.0138289. eCollection 2015.

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