Mukhopadhyay A - Search Results

1

Evaluation of genetic association of the INK4 locus with primary open angle glaucoma in East Indian population.

Vishal M, Sharma A, Kaurani L, Chakraborty S, Ray J, Sen A, Mukhopadhyay A, Ray K. Vishal M, et al. Among authors: mukhopadhyay a. Sci Rep. 2014 May 30;4:5115. doi: 10.1038/srep05115. Sci Rep. 2014. PMID: 24875940 Free PMC article.

2

Did myocilin evolve from two different primordial proteins?

Mukhopadhyay A, Gupta A, Mukherjee S, Chaudhuri K, Ray K. Mukhopadhyay A, et al. Mol Vis. 2002 Jul 22;8:271-9. Mol Vis. 2002. PMID: 12142865 Free article.

3

Distribution of p53 codon 72 polymorphism in Indian primary open angle glaucoma patients.

Acharya M, Mitra S, Mukhopadhyay A, Khan M, Roychoudhury S, Ray K. Acharya M, et al. Among authors: mukhopadhyay a. Mol Vis. 2002 Sep 30;8:367-71. Mol Vis. 2002. PMID: 12368717 Free article.

4

Mutations in MYOC gene of Indian primary open angle glaucoma patients.

Mukhopadhyay A, Acharya M, Mukherjee S, Ray J, Choudhury S, Khan M, Ray K. Mukhopadhyay A, et al. Mol Vis. 2002 Nov 15;8:442-8. Mol Vis. 2002. PMID: 12447164 Free article.

5

Analysis of haemophilia B database and strategies for identification of common point mutations in the factor IX gene.

Mukherjee S, Mukhopadhyay A, Chaudhuri K, Ray K. Mukherjee S, et al. Among authors: mukhopadhyay a. Haemophilia. 2003 Mar;9(2):187-92. doi: 10.1046/j.1365-2516.2003.00727.x. Haemophilia. 2003. PMID: 12614370

6

Myocilin mutation 1109 C>T (Pro 370 Leu) is the most common gene defect causing early onset primary open angle glaucoma.

Mukhopadhyay A, Acharya M, Ray J, Khan M, Sarkar K, Banerjee AR, Ray K. Mukhopadhyay A, et al. Indian J Ophthalmol. 2003 Sep;51(3):279-81. Indian J Ophthalmol. 2003. PMID: 14601861 Free article. No abstract available.

7

Recent advances in molecular genetics of glaucoma.

Ray K, Mukhopadhyay A, Acharya M. Ray K, et al. Among authors: mukhopadhyay a. Mol Cell Biochem. 2003 Nov;253(1-2):223-31. doi: 10.1023/a:1026059800470. Mol Cell Biochem. 2003. PMID: 14619973 Review.

8

DNA linkage based diagnosis of Wilson disease in asymptomatic siblings.

Gupta A, Neogi R, Mukherjea M, Mukhopadhyay A, Roychoudhury S, Senapati A, Gangopadhyay PK, Ray K. Gupta A, et al. Among authors: mukhopadhyay a. Indian J Med Res. 2003 Nov;118:208-14. Indian J Med Res. 2003. PMID: 14723487

9

Molecular pathology of haemophilia B: identification of five novel mutations including a LINE 1 insertion in Indian patients.

Mukherjee S, Mukhopadhyay A, Banerjee D, Chandak GR, Ray K. Mukherjee S, et al. Among authors: mukhopadhyay a. Haemophilia. 2004 May;10(3):259-63. doi: 10.1111/j.1365-2516.2004.00895.x. Haemophilia. 2004. PMID: 15086324

10

Bioinformatic approaches for identification and characterization of olfactomedin related genes with a potential role in pathogenesis of ocular disorders.

Mukhopadhyay A, Talukdar S, Bhattacharjee A, Ray K. Mukhopadhyay A, et al. Mol Vis. 2004 Apr 20;10:304-14. Mol Vis. 2004. PMID: 15123989 Free article.

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