Arama Sonuçları - Chakrabarti, Subhabrata
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Variations in TIMP3 are associated with age-related macular degeneration Yazar: Kaur, Inderjeet, Rathi, Sonika, Chakrabarti, Subhabrata
Baskı/Yayın Bilgisi 2010Metin -
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Complex genetic mechanisms in glaucoma: An overview Yazar: Rao, Kollu N, Nagireddy, Srujana, Chakrabarti, Subhabrata
Baskı/Yayın Bilgisi 2011Metin -
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Primary Congenital Glaucoma and the Involvement of CYP1B1 Yazar: Kaur, Kiranpreet, Mandal, Anil K, Chakrabarti, Subhabrata
Baskı/Yayın Bilgisi 2011Metin -
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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 Yazar: Khanna, Rohit C, Marmamula, Srinivas, Krishnaiah, Sannapaneni, Giridhar, Pyda, Chakrabarti, Subhabrata, Rao, Gullapalli N
Baskı/Yayın Bilgisi 2012Metin -
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Exfoliation syndrome and exfoliation glaucoma-associated LOXL1 variations are not involved in pigment dispersion syndrome and pigmentary glaucoma Yazar: Rao, Kollu Nageswara, Ritch, Robert, Dorairaj, Syril K., Kaur, Inderjeet, Liebmann, Jeffrey M., Thomas, Ravi, Chakrabarti, Subhabrata
Baskı/Yayın Bilgisi 2008Metin -
10
Mutation spectrum of the Norrie disease pseudoglioma (NDP) gene in Indian patients with FEVR Yazar: Musada, Ganeswara Rao, Jalali, Subhadra, Hussain, Anjli, Chururu, Anupama Reddy, Gaddam, Pramod Reddy, Chakrabarti, Subhabrata, Kaur, Inderjeet
Baskı/Yayın Bilgisi 2016Metin -
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A Systematic Investigation on Complement Pathway Activation in Diabetic Retinopathy Yazar: Shahulhameed, Shahna, Vishwakarma, Sushma, Chhablani, Jay, Tyagi, Mudit, Pappuru, Rajeev R., Jakati, Saumya, Chakrabarti, Subhabrata, Kaur, Inderjeet
Baskı/Yayın Bilgisi 2020Metin -
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Evaluation of the OPTC gene in primary open angle glaucoma: functional significance of a silent change Yazar: Acharya, Moulinath, Mookherjee, Suddhasil, Bhattacharjee, Ashima, Thakur, Sanjay KD, Bandyopadhyay, Arun K, Sen, Abhijit, Chakrabarti, Subhabrata, Ray, Kunal
Baskı/Yayın Bilgisi 2007Metin -
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Disease-Causing Mutations in Proteins: Structural Analysis of the CYP1b1 Mutations Causing Primary Congenital Glaucoma in Humans Yazar: 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.
Baskı/Yayın Bilgisi 2006Metin -
14
Cataract, Visual Impairment and Long-Term Mortality in a Rural Cohort in India: The Andhra Pradesh Eye Disease Study Yazar: 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.
Baskı/Yayın Bilgisi 2013Metin -
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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 Yazar: Singh, Nakul, Eeda, Shiva Shankar, Gudapati, Bala Krishna, Reddy, Srinivasa, Kanade, Pushkar, Shantha, Ghanshyam Palamaner Subash, Rani, Padmaja Kumari, Chakrabarti, Subhabrata, Khanna, Rohit C
Baskı/Yayın Bilgisi 2014Metin -
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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 Yazar: 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
Baskı/Yayın Bilgisi 2020Metin -
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Population Based Outcomes of Cataract Surgery in Three Tribal Areas of Andhra Pradesh, India: Risk Factors for Poor Outcomes Yazar: 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.
Baskı/Yayın Bilgisi 2012Metin -
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An interplay of microglia and matrix metalloproteinase MMP9 under hypoxic stress regulates the opticin expression in retina Yazar: 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
Baskı/Yayın Bilgisi 2021Metin -
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Abnormal Complement Activation and Inflammation in the Pathogenesis of Retinopathy of Prematurity Yazar: 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
Baskı/Yayın Bilgisi 2017Metin -
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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 Yazar: 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
Baskı/Yayın Bilgisi 2021Metin