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Results: 20

1.

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.

2.

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.

3.

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.

4.

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.

PMID:
25576993
5.

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.

PMID:
25376121
6.

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.

7.

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.

8.

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.

9.

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
10.

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.

11.

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.

12.

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.

13.

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.

14.

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.

15.

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.

16.

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.

17.

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.

20.

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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