Kaur K - Search Results

1

Globally, CYP1B1 mutations in primary congenital glaucoma are strongly structured by geographic and haplotype backgrounds.

Chakrabarti S, Kaur K, Kaur I, Mandal AK, Parikh RS, Thomas R, Majumder PP. Chakrabarti S, et al. Among authors: kaur i, kaur k. Invest Ophthalmol Vis Sci. 2006 Jan;47(1):43-7. doi: 10.1167/iovs.05-0912. Invest Ophthalmol Vis Sci. 2006. PMID: 16384942

2

Myocilin gene implicated in primary congenital glaucoma.

Kaur K, Reddy AB, Mukhopadhyay A, Mandal AK, Hasnain SE, Ray K, Thomas R, Balasubramanian D, Chakrabarti S. Kaur K, et al. Clin Genet. 2005 Apr;67(4):335-40. doi: 10.1111/j.1399-0004.2005.00411.x. Clin Genet. 2005. PMID: 15733270

3

Mutation spectrum of the CYP1B1 gene in Indian primary congenital glaucoma patients.

Reddy AB, Kaur K, Mandal AK, Panicker SG, Thomas R, Hasnain SE, Balasubramanian D, Chakrabarti S. Reddy AB, et al. Among authors: kaur k. Mol Vis. 2004 Sep 30;10:696-702. Mol Vis. 2004. PMID: 15475877 Free article.

4

Gln48His is the prevalent myocilin mutation in primary open angle and primary congenital glaucoma phenotypes in India.

Chakrabarti S, Kaur K, Komatireddy S, Acharya M, Devi KR, Mukhopadhyay A, Mandal AK, Hasnain SE, Chandrasekhar G, Thomas R, Ray K. Chakrabarti S, et al. Among authors: kaur k. Mol Vis. 2005 Feb 4;11:111-3. Mol Vis. 2005. PMID: 15723004 Free article.

5

Glaucoma-associated CYP1B1 mutations share similar haplotype backgrounds in POAG and PACG phenotypes.

Chakrabarti S, Devi KR, Komatireddy S, Kaur K, Parikh RS, Mandal AK, Chandrasekhar G, Thomas R. Chakrabarti S, et al. Among authors: kaur k. Invest Ophthalmol Vis Sci. 2007 Dec;48(12):5439-44. doi: 10.1167/iovs.07-0629. Invest Ophthalmol Vis Sci. 2007. PMID: 18055790

6

The transcription factor gene FOXC1 exhibits a limited role in primary congenital glaucoma.

Chakrabarti S, Kaur K, Rao KN, Mandal AK, Kaur I, Parikh RS, Thomas R. Chakrabarti S, et al. Among authors: kaur i, kaur k. Invest Ophthalmol Vis Sci. 2009 Jan;50(1):75-83. doi: 10.1167/iovs.08-2253. Epub 2008 Aug 15. Invest Ophthalmol Vis Sci. 2009. PMID: 18708620

7

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. Among authors: kaur i, kaur k. 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

8

Primary Congenital Glaucoma and the Involvement of CYP1B1.

Kaur K, Mandal AK, Chakrabarti S. Kaur K, et al. 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

Acceptability and Satisfaction of Patients and Providers With Telemedicine During the COVID-19 Pandemic: A Systematic Review.

Saeed S, Singhal M, Kaur KN, Shannawaz M, Koul A, Arora K, Kumar B, Sethiya NK, Hasan S. Saeed S, et al. Among authors: kaur kn. Cureus. 2024 Mar 17;16(3):e56308. doi: 10.7759/cureus.56308. eCollection 2024 Mar. Cureus. 2024. PMID: 38628988 Free PMC article. Review.

10

Role of Natural Killer Cells as Cell-Based Immunotherapy in Oral Tumor Eradication and Differentiation Both In Vivo and In Vitro.

Kaur K, Jewett A. Kaur K, et al. Crit Rev Immunol. 2024;44(5):87-98. doi: 10.1615/CritRevImmunol.2024052389. Crit Rev Immunol. 2024. PMID: 38618731 Review.

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