Resultados da busca - Chakrabarti, Subhabrata
- Mostrando 1 - 20 resultados de 28
- Ir para a próxima página
-
1
-
2
-
3
-
4
-
5
-
6
-
7
-
8
Changing trends in the prevalence of blindness and visual impairment in a rural district of India: Systematic observations over a decade por Khanna, Rohit C, Marmamula, Srinivas, Krishnaiah, Sannapaneni, Giridhar, Pyda, Chakrabarti, Subhabrata, Rao, Gullapalli N
Publicado em 2012Texto -
9
Exfoliation syndrome and exfoliation glaucoma-associated LOXL1 variations are not involved in pigment dispersion syndrome and pigmentary glaucoma por Rao, Kollu Nageswara, Ritch, Robert, Dorairaj, Syril K., Kaur, Inderjeet, Liebmann, Jeffrey M., Thomas, Ravi, Chakrabarti, Subhabrata
Publicado em 2008Texto -
10
Mutation spectrum of the Norrie disease pseudoglioma (NDP) gene in Indian patients with FEVR por Musada, Ganeswara Rao, Jalali, Subhadra, Hussain, Anjli, Chururu, Anupama Reddy, Gaddam, Pramod Reddy, Chakrabarti, Subhabrata, Kaur, Inderjeet
Publicado em 2016Texto -
11
A Systematic Investigation on Complement Pathway Activation in Diabetic Retinopathy por Shahulhameed, Shahna, Vishwakarma, Sushma, Chhablani, Jay, Tyagi, Mudit, Pappuru, Rajeev R., Jakati, Saumya, Chakrabarti, Subhabrata, Kaur, Inderjeet
Publicado em 2020Texto -
12
Evaluation of the OPTC gene in primary open angle glaucoma: functional significance of a silent change por Acharya, Moulinath, Mookherjee, Suddhasil, Bhattacharjee, Ashima, Thakur, Sanjay KD, Bandyopadhyay, Arun K, Sen, Abhijit, Chakrabarti, Subhabrata, Ray, Kunal
Publicado em 2007Texto -
13
Disease-Causing Mutations in Proteins: Structural Analysis of the CYP1b1 Mutations Causing Primary Congenital Glaucoma in Humans por 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.
Publicado em 2006Texto -
14
Cataract, Visual Impairment and Long-Term Mortality in a Rural Cohort in India: The Andhra Pradesh Eye Disease Study por 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.
Publicado em 2013Texto -
15
Prevalence and Causes of Blindness and Visual Impairment and Their Associated Risk Factors, in Three Tribal Areas of Andhra Pradesh, India por Singh, Nakul, Eeda, Shiva Shankar, Gudapati, Bala Krishna, Reddy, Srinivasa, Kanade, Pushkar, Shantha, Ghanshyam Palamaner Subash, Rani, Padmaja Kumari, Chakrabarti, Subhabrata, Khanna, Rohit C
Publicado em 2014Texto -
16
A Robust Model System for Retinal Hypoxia: Live Imaging of Calcium Dynamics and Gene Expression Studies in Primary Human Mixed Retinal Culture por 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
Publicado em 2020Texto -
17
Population Based Outcomes of Cataract Surgery in Three Tribal Areas of Andhra Pradesh, India: Risk Factors for Poor Outcomes por 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.
Publicado em 2012Texto -
18
An interplay of microglia and matrix metalloproteinase MMP9 under hypoxic stress regulates the opticin expression in retina por 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
Publicado em 2021Texto -
19
Abnormal Complement Activation and Inflammation in the Pathogenesis of Retinopathy of Prematurity por 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
Publicado em 2017Texto -
20
Binding of Gtf2i-β/δ transcription factors to the ARMS2 gene leads to increased circulating HTRA1 in AMD patients and in vitro por 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
Publicado em 2021Texto