Chakrabarti S - Search Results

1

GLIS1 regulates trabecular meshwork function and intraocular pressure and is associated with glaucoma in humans.

Nair KS, Srivastava C, Brown RV, Koli S, Choquet H, Kang HS, Kuo YM, Grimm SA, Sutherland C, Badea A, Johnson GA, Zhao Y, Yin J, Okamoto K, Clark G, Borrás T, Zode G, Kizhatil K, Chakrabarti S, John SWM, Jorgenson E, Jetten AM. Nair KS, et al. Among authors: chakrabarti s. Nat Commun. 2021 Aug 12;12(1):4877. doi: 10.1038/s41467-021-25181-7. Nat Commun. 2021. PMID: 34385434 Free PMC article.

2

Loss of PRSS56 function leads to ocular angle defects and increased susceptibility to high intraocular pressure.

Labelle-Dumais C, Pyatla G, Paylakhi S, Tolman NG, Hameed S, Seymens Y, Dang E, Mandal AK, Senthil S, Khanna RC, Kabra M, Kaur I, John SWM, Chakrabarti S, Nair KS. Labelle-Dumais C, et al. Among authors: chakrabarti s. Dis Model Mech. 2020 May 29;13(5):dmm042853. doi: 10.1242/dmm.042853. Dis Model Mech. 2020. PMID: 32152063 Free PMC article.

3

[No title available]

[No authors listed] [No authors listed] PMID: 34005051

4

A polymorphism in the CYP1B1 promoter is functionally associated with primary congenital glaucoma.

Chakrabarti S, Ghanekar Y, Kaur K, Kaur I, Mandal AK, Rao KN, Parikh RS, Thomas R, Majumder PP. Chakrabarti S, et al. Hum Mol Genet. 2010 Oct 15;19(20):4083-90. doi: 10.1093/hmg/ddq309. Epub 2010 Jul 21. Hum Mol Genet. 2010. PMID: 20660114

5

Exfoliation syndrome and exfoliation glaucoma-associated LOXL1 variations are not involved in pigment dispersion syndrome and pigmentary glaucoma.

Rao KN, Ritch R, Dorairaj SK, Kaur I, Liebmann JM, Thomas R, Chakrabarti S. Rao KN, et al. Among authors: chakrabarti s. Mol Vis. 2008 Jul 9;14:1254-62. Mol Vis. 2008. PMID: 18618003 Free PMC article.

6

Variations in NTF4, VAV2, and VAV3 genes are not involved with primary open-angle and primary angle-closure glaucomas in an indian population.

Rao KN, Kaur I, Parikh RS, Mandal AK, Chandrasekhar G, Thomas R, Chakrabarti S. Rao KN, et al. Among authors: chakrabarti s. Invest Ophthalmol Vis Sci. 2010 Oct;51(10):4937-41. doi: 10.1167/iovs.10-5553. Epub 2010 May 12. Invest Ophthalmol Vis Sci. 2010. PMID: 20463313

7

Complex genetic mechanisms in glaucoma: an overview.

Rao KN, Nagireddy S, Chakrabarti S. Rao KN, et al. Among authors: chakrabarti s. Indian J Ophthalmol. 2011 Jan;59 Suppl(Suppl1):S31-42. doi: 10.4103/0301-4738.73685. Indian J Ophthalmol. 2011. PMID: 21150032 Free PMC article. Review.

8

Primary Congenital Glaucoma and the Involvement of CYP1B1.

Kaur K, Mandal AK, Chakrabarti S. Kaur K, et al. Among authors: chakrabarti s. Middle East Afr J Ophthalmol. 2011 Jan;18(1):7-16. doi: 10.4103/0974-9233.75878. Middle East Afr J Ophthalmol. 2011. PMID: 21572728 Free PMC article.

9

Genotype-Phenotype Correlations in CYP1B1-Associated Primary Congenital Glaucoma Patients Representing Two Large Cohorts from India and Brazil.

de Melo MB, Mandal AK, Tavares IM, Ali MH, Kabra M, de Vasconcellos JP, Senthil S, Sallum JM, Kaur I, Betinjane AJ, Moura CR, Paula JS, Costa KA, Sarfarazi M, Paolera MD, Finzi S, Ferraz VE, Costa VP, Belfort R Jr, Chakrabarti S. de Melo MB, et al. Among authors: chakrabarti s. PLoS One. 2015 May 15;10(5):e0127147. doi: 10.1371/journal.pone.0127147. eCollection 2015. PLoS One. 2015. PMID: 25978063 Free PMC article.

10

The molecular genetic basis of age-related macular degeneration: an overview.

Katta S, Kaur I, Chakrabarti S. Katta S, et al. Among authors: chakrabarti s. J Genet. 2009 Dec;88(4):425-49. doi: 10.1007/s12041-009-0064-4. J Genet. 2009. PMID: 20090206 Free article. Review.

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