Items where Author is "Chakrabarti, Subhabrata"

Article

Chakrabarti, Subhabrata ; Ghanekar, Yashoda ; Kaur, Kiranpreet ; Kaur, Inderjeet ; Mandal, Anil K. ; Rao, Kollu N. ; Parikh, Rajul S. ; Thomas, Ravi ; Majumder, Partha P. (2010) A polymorphism in the CYP1B1 promoter is functionally associated with primary congenital glaucoma Human Molecular Genetics, 19 (20). pp. 4083-4090. ISSN 0964-6906

Achary, Malkaram S. ; Reddy, Aramati B. M. ; Chakrabarti, Subhabrata ; Panicker, Shirly G. ; Mandal, Anil K. ; Ahmed, Niyaz ; Balasubramanian, Dorairajan ; Hasnain, Seyed E. ; Nagarajaram, Hampapathalu A. (2006) Disease-causing mutations in proteins: structural analysis of the CYP1b1 mutations causing primary congenital glaucoma in humans Biophysical Journal, 91 (12). pp. 4329-4339. ISSN 0006-3495

Chakrabarti, Subhabrata ; Kaur, Kiranpreet ; Kaur, Inderjeet ; Mandal, Anil K. ; Parikh, Rajul S. ; Thomas, Ravi ; Majumder, Partha P. (2006) Globally, CYP1B1 mutations in primary congenital glaucoma are strongly structured by geographic and haplotype backgrounds Investigative Ophthalmology and Visual Science, 47 . pp. 43-47. ISSN 0146-0404

Chakrabarti, Subhabrata ; Kaur, Kiranpreet ; Komatireddy, Sreelatha ; Acharya, Moulinath ; Devi, Koilkonda R. ; Mukhopadhyay, Arijit ; Mandal, Anil K. ; Hasnain, Seyed E. ; Chandrasekhar, Garudadri ; Thomas, Ravi ; Ray, Kunal (2005) Gln48His is the prevalent myocilin mutation in primary open angle and primary congenital glaucoma phenotypes in India Molecular Vision, 11 . pp. 111-113. ISSN 1090-0535

Reddy, Aramati Bindu Madhava ; Kaur, Kiranpreet ; Mandal, Anil Kumar ; Panicker, Shirly George ; Thomas, Ravi ; Hasnain, Seyed Ehtesham ; Balasubramanian, Dorairajan ; Chakrabarti, Subhabrata (2004) Mutation spectrum of the CYP1B1 gene in Indian primary congenital glaucoma patients Molecular Vision, 10 . pp. 696-702. ISSN 1090-0535

Ragothaman, Mona ; Sarangmath, Nagaraja ; Chaudhary, Shashi ; Khare, Vishwamohini ; Mittal, Uma ; Sharma, Sangeeta ; Komatireddy, Sreelatha ; Chakrabarti, Subhabrata ; Mukerji, Mitali ; Juyal, Ramesh C. ; Thelma, B. K. ; Muthane, Uday B. (2004) Complex phenotypes in an Indian family with homozygous SCA2 mutations Annals of Neurology, 55 (1). pp. 130-133. ISSN 0364-5134