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Items: 31

1.

Primary Open-Angle African American Glaucoma Genetics (POAAGG) Study: gender and risk of POAG in African Americans.

Khachatryan N, Pistilli M, Maguire MG, Salowe RJ, Fertig RM, Moore T, Gudiseva HV, Chavali VRM, Collins DW, Daniel E, Murphy W, Henderer JD, Lehman A, Cui Q, Addis V, Sankar PS, Miller-Ellis EG, O'Brien JM.

PLoS One. 2019 Aug 1;14(8):e0218804. doi: 10.1371/journal.pone.0218804. eCollection 2019.

2.

SNP located in an AluJb repeat downstream of TMCO1, rs4657473, is protective for POAG in African Americans.

Verkuil L, Danford I, Pistilli M, Collins DW, Gudiseva HV, Trachtman BT, He J, Rathi S, Haider N, Ying GS, Chavali VRM, O'Brien JM.

Br J Ophthalmol. 2019 Oct;103(10):1530-1536. doi: 10.1136/bjophthalmol-2018-313086. Epub 2019 Mar 12.

3.

The association of mitochondrial DNA haplogroups with POAG in African Americans.

Gudiseva HV, Pistilli M, Salowe R, Singh LN, Collins DW, Cole B, He J, Merriam S, Khachataryan N, Henderer J, Addis V, Cui QN, Sankar PS, Miller-Ellis E, Chavali VRM, Ying GS, Wallace D, O'Brien JM.

Exp Eye Res. 2019 Apr;181:85-89. doi: 10.1016/j.exer.2019.01.015. Epub 2019 Jan 15.

PMID:
30653964
4.

Whole-genome methylation profiling of the retinal pigment epithelium of individuals with age-related macular degeneration reveals differential methylation of the SKI, GTF2H4, and TNXB genes.

Porter LF, Saptarshi N, Fang Y, Rathi S, den Hollander AI, de Jong EK, Clark SJ, Bishop PN, Olsen TW, Liloglou T, Chavali VRM, Paraoan L.

Clin Epigenetics. 2019 Jan 14;11(1):6. doi: 10.1186/s13148-019-0608-2.

5.

Long-Term Effects of Gene Therapy in a Novel Mouse Model of Human MFRP-Associated Retinopathy.

Chekuri A, Sahu B, Chavali VRM, Voronchikhina M, Soto-Hermida A, Suk JJ, Alapati AN, Bartsch DU, Ayala-Ramirez R, Zenteno JC, Dinculescu A, Jablonski MM, Borooah S, Ayyagari R.

Hum Gene Ther. 2019 May;30(5):632-650. doi: 10.1089/hum.2018.192. Epub 2019 Jan 16.

PMID:
30499344
6.

Directional ABCA1-mediated cholesterol efflux and apoB-lipoprotein secretion in the retinal pigment epithelium.

Lyssenko NN, Haider N, Picataggi A, Cipollari E, Jiao W, Phillips MC, Rader DJ, Chavali VRM.

J Lipid Res. 2018 Oct;59(10):1927-1939. doi: 10.1194/jlr.M087361. Epub 2018 Aug 3.

7.

The MT-CO1 V83I Polymorphism is a Risk Factor for Primary Open-Angle Glaucoma in African American Men.

Collins DW, Gudiseva HV, Chavali VRM, Trachtman B, Ramakrishnan M, Merritt WT III, Pistilli M, Rossi RA, Blachon S, Sankar PS, Miller-Ellis E, Lehman A, Addis V, O'Brien JM.

Invest Ophthalmol Vis Sci. 2018 Apr 1;59(5):1751-1759. doi: 10.1167/iovs.17-23277.

8.

Complete Transcriptome Profiling of Normal and Age-Related Macular Degeneration Eye Tissues Reveals Dysregulation of Anti-Sense Transcription.

Kim EJ, Grant GR, Bowman AS, Haider N, Gudiseva HV, Chavali VRM.

Sci Rep. 2018 Feb 14;8(1):3040. doi: 10.1038/s41598-018-21104-7.

9.

Characterizing the "POAGome": A bioinformatics-driven approach to primary open-angle glaucoma.

Danford ID, Verkuil LD, Choi DJ, Collins DW, Gudiseva HV, Uyhazi KE, Lau MK, Kanu LN, Grant GR, Chavali VRM, O'Brien JM.

Prog Retin Eye Res. 2017 May;58:89-114. doi: 10.1016/j.preteyeres.2017.02.001. Epub 2017 Feb 20. Review.

10.

Risk Factors Associated with Progression to Blindness from Primary Open-Angle Glaucoma in an African-American Population.

Pleet A, Sulewski M, Salowe RJ, Fertig R, Salinas J, Rhodes A, Merritt Iii W, Natesh V, Huang J, Gudiseva HV, Collins DW, Chavali VR, Tapino P, Lehman A, Regina-Gigiliotti M, Miller-Ellis E, Sankar P, Ying GS, O'Brien JM.

Ophthalmic Epidemiol. 2016 Aug;23(4):248-56. doi: 10.1080/09286586.2016.1193207. Epub 2016 Jun 27.

11.

A missense mutation in ASRGL1 is involved in causing autosomal recessive retinal degeneration.

Biswas P, Chavali VR, Agnello G, Stone E, Chakarova C, Duncan JL, Kannabiran C, Homsher M, Bhattacharya SS, Naeem MA, Kimchi A, Sharon D, Iwata T, Riazuddin S, Reddy GB, Hejtmancik JF, Georgiou G, Riazuddin SA, Ayyagari R.

Hum Mol Genet. 2016 Jun 15;25(12):2483-2497. Epub 2016 Apr 22.

12.

Association of OCT derived drusen measurements with AMD associated-genotypic SNPs in Amish population.

Chavali VR, Diniz B, Huang J, Ying GS, Sadda SR, Stambolian D.

J Clin Med. 2015;4(2):304-317.

13.

Presence of rd8 mutation does not alter the ocular phenotype of late-onset retinal degeneration mouse model.

Sahu B, Chavali VR, Alapati A, Suk J, Bartsch DU, Jablonski MM, Ayyagari R.

Mol Vis. 2015 Mar 13;21:273-84. eCollection 2015.

14.

Drusen and RPE atrophy automated quantification by optical coherence tomography in an elderly population.

Diniz B, Rodger DC, Chavali VR, MacKay T, Lee SY, Stambolian D, Sadda SV.

Eye (Lond). 2015 Feb;29(2):300. doi: 10.1038/eye.2014.307. No abstract available.

15.

The primary open-angle african american glaucoma genetics study: baseline demographics.

Charlson ES, Sankar PS, Miller-Ellis E, Regina M, Fertig R, Salinas J, Pistilli M, Salowe RJ, Rhodes AL, Merritt WT 3rd, Chua M, Trachtman BT, Gudiseva HV, Collins DW, Chavali VR, Nichols C, Henderer J, Ying GS, Varma R, Jorgenson E, O'Brien JM.

Ophthalmology. 2015 Apr;122(4):711-20. doi: 10.1016/j.ophtha.2014.11.015. Epub 2015 Jan 8.

16.

Drusen and RPE atrophy automated quantification by optical coherence tomography in an elderly population.

Diniz B, Rodger DC, Chavali VR, MacKay T, Lee SY, Stambolian D, Sadda SV.

Eye (Lond). 2015 Feb;29(2):272-9. doi: 10.1038/eye.2014.260. Epub 2014 Nov 7. Erratum in: Eye (Lond). 2015 Feb;29(2):300.

17.

Exome analysis identified a novel mutation in the RBP4 gene in a consanguineous pedigree with retinal dystrophy and developmental abnormalities.

Cukras C, Gaasterland T, Lee P, Gudiseva HV, Chavali VR, Pullakhandam R, Maranhao B, Edsall L, Soares S, Reddy GB, Sieving PA, Ayyagari R.

PLoS One. 2012;7(11):e50205. doi: 10.1371/journal.pone.0050205. Epub 2012 Nov 26.

18.

Cloning, characterization, and expression analysis of the pig (Sus scrofa) C1q tumor necrosis factor-related protein-5 gene.

Sommer JR, Chavali VR, Simpson SG, Ayyagari R, Petters RM.

Mol Vis. 2012;18:92-102. Epub 2012 Jan 17.

19.

GNAT1 associated with autosomal recessive congenital stationary night blindness.

Naeem MA, Chavali VR, Ali S, Iqbal M, Riazuddin S, Khan SN, Husnain T, Sieving PA, Ayyagari R, Riazuddin S, Hejtmancik JF, Riazuddin SA.

Invest Ophthalmol Vis Sci. 2012 Mar 13;53(3):1353-61. doi: 10.1167/iovs.11-8026. Print 2012 Mar.

20.

Silencing the expression of CTRP5/C1QTNF5 and ELOVL4 genes by small interfering RNA.

Chavali VR, Vasireddy V, Ayyagari R.

Adv Exp Med Biol. 2012;723:225-33. doi: 10.1007/978-1-4614-0631-0_30. No abstract available.

PMID:
22183337
21.

Rescue of photoreceptor degeneration by curcumin in transgenic rats with P23H rhodopsin mutation.

Vasireddy V, Chavali VR, Joseph VT, Kadam R, Lin JH, Jamison JA, Kompella UB, Reddy GB, Ayyagari R.

PLoS One. 2011;6(6):e21193. doi: 10.1371/journal.pone.0021193. Epub 2011 Jun 29.

22.

A CTRP5 gene S163R mutation knock-in mouse model for late-onset retinal degeneration.

Chavali VR, Khan NW, Cukras CA, Bartsch DU, Jablonski MM, Ayyagari R.

Hum Mol Genet. 2011 May 15;20(10):2000-14. doi: 10.1093/hmg/ddr080. Epub 2011 Feb 24.

23.

A mutation in SLC24A1 implicated in autosomal-recessive congenital stationary night blindness.

Riazuddin SA, Shahzadi A, Zeitz C, Ahmed ZM, Ayyagari R, Chavali VR, Ponferrada VG, Audo I, Michiels C, Lancelot ME, Nasir IA, Zafar AU, Khan SN, Husnain T, Jiao X, MacDonald IM, Riazuddin S, Sieving PA, Katsanis N, Hejtmancik JF.

Am J Hum Genet. 2010 Oct 8;87(4):523-31. doi: 10.1016/j.ajhg.2010.08.013. Epub 2010 Sep 16.

24.

A mutation in ZNF513, a putative regulator of photoreceptor development, causes autosomal-recessive retinitis pigmentosa.

Li L, Nakaya N, Chavali VR, Ma Z, Jiao X, Sieving PA, Riazuddin S, Tomarev SI, Ayyagari R, Riazuddin SA, Hejtmancik JF.

Am J Hum Genet. 2010 Sep 10;87(3):400-9. doi: 10.1016/j.ajhg.2010.08.003.

25.

Identification of a promoter for the human C1Q-tumor necrosis factor-related protein-5 gene associated with late-onset retinal degeneration.

Chavali VR, Sommer JR, Petters RM, Ayyagari R.

Invest Ophthalmol Vis Sci. 2010 Nov;51(11):5499-507. doi: 10.1167/iovs.10-5543. Epub 2010 Jun 16.

26.

Molecular characterization of genome segment 2 encoding RNA dependent RNA polymerase of Antheraea mylitta cytoplasmic polyhedrosis virus.

Ghorai S, Chakrabarti M, Roy S, Chavali VR, Bagchi A, Ghosh AK.

Virology. 2010 Aug 15;404(1):21-31. doi: 10.1016/j.virol.2010.04.019. Epub 2010 May 20.

27.

Age-related retinal degeneration (arrd2) in a novel mouse model due to a nonsense mutation in the Mdm1 gene.

Chang B, Mandal MN, Chavali VR, Hawes NL, Khan NW, Hurd RE, Smith RS, Davisson ML, Kopplin L, Klein BE, Klein R, Iyengar SK, Heckenlively JR, Ayyagari R.

Hum Mol Genet. 2008 Dec 15;17(24):3929-41. doi: 10.1093/hmg/ddn295. Epub 2008 Sep 18.

28.

Genome segment 6 of Antheraea mylitta cypovirus encodes a structural protein with ATPase activity.

Chavali VR, Madhurantakam C, Ghorai S, Roy S, Das AK, Ghosh AK.

Virology. 2008 Jul 20;377(1):7-18. doi: 10.1016/j.virol.2008.03.038. Epub 2008 May 16.

31.

Molecular cloning and characterization of Antheraea mylitta cytoplasmic polyhedrosis virus polyhedrin gene and its variant forms.

Sinha-Datta U, Chavali VR, Ghosh AK.

Biochem Biophys Res Commun. 2005 Jul 8;332(3):710-8.

PMID:
15907799

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