Search Results - Chakrabarti, Subhabrata

Variations in TIMP3 are associated with age-related macular degeneration by Kaur, Inderjeet, Rathi, Sonika, Chakrabarti, Subhabrata

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Lack of association of three primary open-angle glaucoma-susceptible loci with primary glaucomas in an Indian population by Rao, Kollu N., Kaur, Inderjeet, Chakrabarti, Subhabrata

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Complex genetic mechanisms in glaucoma: An overview by Rao, Kollu N, Nagireddy, Srujana, Chakrabarti, Subhabrata

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Primary Congenital Glaucoma and the Involvement of CYP1B1 by Kaur, Kiranpreet, Mandal, Anil K, Chakrabarti, Subhabrata

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Ocular Ciliopathies: Genetic and Mechanistic Insights into Developing Therapies by Shivanna, Mahesh, Anand, Manisha, Chakrabarti, Subhabrata, Khanna, Hemant

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FOXC1-associated phenotypes in humans may not always exhibit corneal neovascularization by Chakrabarti, Subhabrata, Ramappa, Muralidhar, Chaurasia, Sunita, Kaur, Inderjeet, Mandal, Anil K.

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Mutation spectrum of the FZD-4, TSPAN12 AND ZNF408 genes in Indian FEVR patients by Musada, Ganeswara Rao, Syed, Hameed, Jalali, Subhadra, Chakrabarti, Subhabrata, Kaur, Inderjeet

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Changing trends in the prevalence of blindness and visual impairment in a rural district of India: Systematic observations over a decade by Khanna, Rohit C, Marmamula, Srinivas, Krishnaiah, Sannapaneni, Giridhar, Pyda, Chakrabarti, Subhabrata, Rao, Gullapalli N

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­Exfoliation syndrome and exfoliation glaucoma-associated LOXL1 variations are not involved in pigment dispersion syndrome and pigmentary glaucoma by Rao, Kollu Nageswara, Ritch, Robert, Dorairaj, Syril K., Kaur, Inderjeet, Liebmann, Jeffrey M., Thomas, Ravi, Chakrabarti, Subhabrata

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Mutation spectrum of the Norrie disease pseudoglioma (NDP) gene in Indian patients with FEVR by Musada, Ganeswara Rao, Jalali, Subhadra, Hussain, Anjli, Chururu, Anupama Reddy, Gaddam, Pramod Reddy, Chakrabarti, Subhabrata, Kaur, Inderjeet

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A Systematic Investigation on Complement Pathway Activation in Diabetic Retinopathy by Shahulhameed, Shahna, Vishwakarma, Sushma, Chhablani, Jay, Tyagi, Mudit, Pappuru, Rajeev R., Jakati, Saumya, Chakrabarti, Subhabrata, Kaur, Inderjeet

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Evaluation of the OPTC gene in primary open angle glaucoma: functional significance of a silent change by Acharya, Moulinath, Mookherjee, Suddhasil, Bhattacharjee, Ashima, Thakur, Sanjay KD, Bandyopadhyay, Arun K, Sen, Abhijit, Chakrabarti, Subhabrata, Ray, Kunal

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Disease-Causing Mutations in Proteins: Structural Analysis of the CYP1b1 Mutations Causing Primary Congenital Glaucoma in Humans by 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.

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Cataract, Visual Impairment and Long-Term Mortality in a Rural Cohort in India: The Andhra Pradesh Eye Disease Study by Khanna, Rohit C., Murthy, Gudlavalleti V. S., Giridhar, Pyda, Krishnaiah, Sannapaneni, Pant, Hira B., Palamaner Subash Shantha, Ghanshyam, Chakrabarti, Subhabrata, Gilbert, Clare, Rao, Gullapalli N.

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Prevalence and Causes of Blindness and Visual Impairment and Their Associated Risk Factors, in Three Tribal Areas of Andhra Pradesh, India by Singh, Nakul, Eeda, Shiva Shankar, Gudapati, Bala Krishna, Reddy, Srinivasa, Kanade, Pushkar, Shantha, Ghanshyam Palamaner Subash, Rani, Padmaja Kumari, Chakrabarti, Subhabrata, Khanna, Rohit C

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A Robust Model System for Retinal Hypoxia: Live Imaging of Calcium Dynamics and Gene Expression Studies in Primary Human Mixed Retinal Culture by Shahulhameed, Shahna, Swain, Sarpras, Jana, Soumya, Chhablani, Jay, Ali, Mohammad Javed, Pappuru, Rajeev R., Tyagi, Mudit, Vishwakarma, Sushma, Sailaja, Nanda, Chakrabarti, Subhabrata, Giri, Lopamudra, Kaur, Inderjeet

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Population Based Outcomes of Cataract Surgery in Three Tribal Areas of Andhra Pradesh, India: Risk Factors for Poor Outcomes by Khanna, Rohit C., Pallerla, Srinivasa Reddy, Eeda, Shiva Shankar, Gudapati, Bala Krishna, Cassard, Sandra D., Rani, Padmaja Kumari, Shantha, Ghanshyam Palamaner Subash, Chakrabarti, Subhabrata, Schein, Oliver D.

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An interplay of microglia and matrix metalloproteinase MMP9 under hypoxic stress regulates the opticin expression in retina by Patnaik, Satish, Rai, Meenakshi, Jalali, Subhadra, Agarwal, Komal, Badakere, Akshay, Puppala, Lavanya, Vishwakarma, Sushma, Balakrishnan, Divya, Rani, Padmaja K., Kekunnaya, Ramesh, Chhablani, Preeti Patil, Chakrabarti, Subhabrata, Kaur, Inderjeet

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Abnormal Complement Activation and Inflammation in the Pathogenesis of Retinopathy of Prematurity by Rathi, Sonika, Jalali, Subhadra, Patnaik, Satish, Shahulhameed, Shahna, Musada, Ganeswara R., Balakrishnan, Divya, Rani, Padmaja K., Kekunnaya, Ramesh, Chhablani, Preeti Patil, Swain, Sarpras, Giri, Lopamudra, Chakrabarti, Subhabrata, Kaur, Inderjeet

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Binding of Gtf2i-β/δ transcription factors to the ARMS2 gene leads to increased circulating HTRA1 in AMD patients and in vitro by Pan, Yang, Iejima, Daisuke, Nakayama, Mao, Suga, Akiko, Noda, Toru, Kaur, Inderjeet, Das, Taraprasad, Chakrabarti, Subhabrata, Guymer, Robyn H., DeAngelis, Margaret M., Yamamoto, Megumi, Baird, Paul N., Iwata, Takeshi

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