Mandal AK - Search Results

1

Potential Involvements of Cilia-Centrosomal Genes in Primary Congenital Glaucoma.

Pyatla G, Kabra M, Mandal AK, Zhang W, Mishra A, Bera S, Rathi S, Patnaik S, Anthony AA, Dixit R, Banerjee S, Shekhar K, Marmamula S, Kaur I, Khanna RC, Chakrabarti S. Pyatla G, et al. Among authors: mandal ak. Int J Mol Sci. 2024 Sep 18;25(18):10028. doi: 10.3390/ijms251810028. Int J Mol Sci. 2024. PMID: 39337513 Free PMC article.

2

Identification of novel mutations causing familial primary congenital glaucoma in Indian pedigrees.

Panicker SG, Reddy AB, Mandal AK, Ahmed N, Nagarajaram HA, Hasnain SE, Balasubramanian D. Panicker SG, et al. Among authors: mandal ak. Invest Ophthalmol Vis Sci. 2002 May;43(5):1358-66. Invest Ophthalmol Vis Sci. 2002. PMID: 11980847

3

Mutation spectrum of FOXC1 and clinical genetic heterogeneity of Axenfeld-Rieger anomaly in India.

Komatireddy S, Chakrabarti S, Mandal AK, Reddy AB, Sampath S, Panicker SG, Balasubramanian D. Komatireddy S, et al. Among authors: mandal ak. Mol Vis. 2003 Feb 18;9:43-8. Mol Vis. 2003. PMID: 12592227 Free article.

4

PAX6 gene mutations and genotype-phenotype correlations in sporadic cases of aniridia from India.

Dharmaraj N, Reddy A, Kiran V, Mandal A, Panicker S, Chakrabarti S. Dharmaraj N, et al. Ophthalmic Genet. 2003 Sep;24(3):161-5. doi: 10.1076/opge.24.3.161.15607. Ophthalmic Genet. 2003. PMID: 12868034

5

Identification of R368H as a predominant CYP1B1 allele causing primary congenital glaucoma in Indian patients.

Reddy AB, Panicker SG, Mandal AK, Hasnain SE, Balasubramanian D. Reddy AB, et al. Among authors: mandal ak. Invest Ophthalmol Vis Sci. 2003 Oct;44(10):4200-3. doi: 10.1167/iovs.02-0945. Invest Ophthalmol Vis Sci. 2003. PMID: 14507861

6

Gene symbol: CYP1B1. Disease: glaucoma, primary congenital.

Chakrabarti S, Komatireddy S, Mandal AK, Balasubramanian D. Chakrabarti S, et al. Among authors: mandal ak. Hum Genet. 2003 Nov;113(6):556. Hum Genet. 2003. PMID: 14640114 No abstract available.

7

Gene symbol: MY0C (GLC1A). Disease: glaucoma 1, open angle.

Chakrabarti S, Komatireddy S, Mandal AK, Balasubramanian D. Chakrabarti S, et al. Among authors: mandal ak. Hum Genet. 2003 Nov;113(6):557. Hum Genet. 2003. PMID: 14640116 No abstract available.

8

Correlations of genotype with phenotype in Indian patients with primary congenital glaucoma.

Panicker SG, Mandal AK, Reddy AB, Gothwal VK, Hasnain SE. Panicker SG, et al. Among authors: mandal ak. Invest Ophthalmol Vis Sci. 2004 Apr;45(4):1149-56. doi: 10.1167/iovs.03-0404. Invest Ophthalmol Vis Sci. 2004. PMID: 15037581

9

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: mandal ak. Mol Vis. 2004 Sep 30;10:696-702. Mol Vis. 2004. PMID: 15475877 Free article.

10

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: mandal ak. Mol Vis. 2005 Feb 4;11:111-3. Mol Vis. 2005. PMID: 15723004 Free article.

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