खोज परिणाम - Chakrabarti, Subhabrata
- प्रदर्शित 1 - 20 परिणाम 28
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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 द्वारा Khanna, Rohit C, Marmamula, Srinivas, Krishnaiah, Sannapaneni, Giridhar, Pyda, Chakrabarti, Subhabrata, Rao, Gullapalli N
प्रकाशित 2012मूलपाठ -
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Exfoliation syndrome and exfoliation glaucoma-associated LOXL1 variations are not involved in pigment dispersion syndrome and pigmentary glaucoma द्वारा Rao, Kollu Nageswara, Ritch, Robert, Dorairaj, Syril K., Kaur, Inderjeet, Liebmann, Jeffrey M., Thomas, Ravi, Chakrabarti, Subhabrata
प्रकाशित 2008मूलपाठ -
10
Mutation spectrum of the Norrie disease pseudoglioma (NDP) gene in Indian patients with FEVR द्वारा Musada, Ganeswara Rao, Jalali, Subhadra, Hussain, Anjli, Chururu, Anupama Reddy, Gaddam, Pramod Reddy, Chakrabarti, Subhabrata, Kaur, Inderjeet
प्रकाशित 2016मूलपाठ -
11
A Systematic Investigation on Complement Pathway Activation in Diabetic Retinopathy द्वारा Shahulhameed, Shahna, Vishwakarma, Sushma, Chhablani, Jay, Tyagi, Mudit, Pappuru, Rajeev R., Jakati, Saumya, Chakrabarti, Subhabrata, Kaur, Inderjeet
प्रकाशित 2020मूलपाठ -
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Evaluation of the OPTC gene in primary open angle glaucoma: functional significance of a silent change द्वारा Acharya, Moulinath, Mookherjee, Suddhasil, Bhattacharjee, Ashima, Thakur, Sanjay KD, Bandyopadhyay, Arun K, Sen, Abhijit, Chakrabarti, Subhabrata, Ray, Kunal
प्रकाशित 2007मूलपाठ -
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Disease-Causing Mutations in Proteins: Structural Analysis of the CYP1b1 Mutations Causing Primary Congenital Glaucoma in Humans द्वारा 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.
प्रकाशित 2006मूलपाठ -
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Cataract, Visual Impairment and Long-Term Mortality in a Rural Cohort in India: The Andhra Pradesh Eye Disease Study द्वारा 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.
प्रकाशित 2013मूलपाठ -
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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 द्वारा Singh, Nakul, Eeda, Shiva Shankar, Gudapati, Bala Krishna, Reddy, Srinivasa, Kanade, Pushkar, Shantha, Ghanshyam Palamaner Subash, Rani, Padmaja Kumari, Chakrabarti, Subhabrata, Khanna, Rohit C
प्रकाशित 2014मूलपाठ -
16
A Robust Model System for Retinal Hypoxia: Live Imaging of Calcium Dynamics and Gene Expression Studies in Primary Human Mixed Retinal Culture द्वारा 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
प्रकाशित 2020मूलपाठ -
17
Population Based Outcomes of Cataract Surgery in Three Tribal Areas of Andhra Pradesh, India: Risk Factors for Poor Outcomes द्वारा 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.
प्रकाशित 2012मूलपाठ -
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An interplay of microglia and matrix metalloproteinase MMP9 under hypoxic stress regulates the opticin expression in retina द्वारा 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
प्रकाशित 2021मूलपाठ -
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Abnormal Complement Activation and Inflammation in the Pathogenesis of Retinopathy of Prematurity द्वारा 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
प्रकाशित 2017मूलपाठ -
20
Binding of Gtf2i-β/δ transcription factors to the ARMS2 gene leads to increased circulating HTRA1 in AMD patients and in vitro द्वारा 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
प्रकाशित 2021मूलपाठ