Canlyniadau Chwilio - Chakrabarti, Subhabrata
- Dangos 1 - 20 canlyniadau o 28
- Ewch i'r Dudalen Nesaf
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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 gan Khanna, Rohit C, Marmamula, Srinivas, Krishnaiah, Sannapaneni, Giridhar, Pyda, Chakrabarti, Subhabrata, Rao, Gullapalli N
Cyhoeddwyd 2012Text -
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Exfoliation syndrome and exfoliation glaucoma-associated LOXL1 variations are not involved in pigment dispersion syndrome and pigmentary glaucoma gan Rao, Kollu Nageswara, Ritch, Robert, Dorairaj, Syril K., Kaur, Inderjeet, Liebmann, Jeffrey M., Thomas, Ravi, Chakrabarti, Subhabrata
Cyhoeddwyd 2008Text -
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Mutation spectrum of the Norrie disease pseudoglioma (NDP) gene in Indian patients with FEVR gan Musada, Ganeswara Rao, Jalali, Subhadra, Hussain, Anjli, Chururu, Anupama Reddy, Gaddam, Pramod Reddy, Chakrabarti, Subhabrata, Kaur, Inderjeet
Cyhoeddwyd 2016Text -
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A Systematic Investigation on Complement Pathway Activation in Diabetic Retinopathy gan Shahulhameed, Shahna, Vishwakarma, Sushma, Chhablani, Jay, Tyagi, Mudit, Pappuru, Rajeev R., Jakati, Saumya, Chakrabarti, Subhabrata, Kaur, Inderjeet
Cyhoeddwyd 2020Text -
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Evaluation of the OPTC gene in primary open angle glaucoma: functional significance of a silent change gan Acharya, Moulinath, Mookherjee, Suddhasil, Bhattacharjee, Ashima, Thakur, Sanjay KD, Bandyopadhyay, Arun K, Sen, Abhijit, Chakrabarti, Subhabrata, Ray, Kunal
Cyhoeddwyd 2007Text -
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Disease-Causing Mutations in Proteins: Structural Analysis of the CYP1b1 Mutations Causing Primary Congenital Glaucoma in Humans gan 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.
Cyhoeddwyd 2006Text -
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Cataract, Visual Impairment and Long-Term Mortality in a Rural Cohort in India: The Andhra Pradesh Eye Disease Study gan 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.
Cyhoeddwyd 2013Text -
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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 gan Singh, Nakul, Eeda, Shiva Shankar, Gudapati, Bala Krishna, Reddy, Srinivasa, Kanade, Pushkar, Shantha, Ghanshyam Palamaner Subash, Rani, Padmaja Kumari, Chakrabarti, Subhabrata, Khanna, Rohit C
Cyhoeddwyd 2014Text -
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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 gan 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
Cyhoeddwyd 2020Text -
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Population Based Outcomes of Cataract Surgery in Three Tribal Areas of Andhra Pradesh, India: Risk Factors for Poor Outcomes gan 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.
Cyhoeddwyd 2012Text -
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An interplay of microglia and matrix metalloproteinase MMP9 under hypoxic stress regulates the opticin expression in retina gan 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
Cyhoeddwyd 2021Text -
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Abnormal Complement Activation and Inflammation in the Pathogenesis of Retinopathy of Prematurity gan 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
Cyhoeddwyd 2017Text -
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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 gan 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
Cyhoeddwyd 2021Text