檢索結果 - Subhadra Jalali
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Chorioretinal coloboma in a paediatric population 由 O M Uhumwangho, Subhadra Jalali
出版 2014Artigo -
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Generation and validation of a Leber Congenital Amaurosis, Type 12 patient-specific iPSC line (LVPEIi006-B) with a splice-site mutation in RD3 and an isogenic mutation-corrected iP... 由 Sudipta Mahato, Savitri Maddileti, Trupti Agrawal, Sundaram Acharya, Chitra Kannabiran, Subhadra Jalali, Debojyoti Chakraborty, Indumathi Mariappan
出版 2025Artigo -
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Endophthalmitis after open globe injuries: changes in microbiological spectrum and isolate susceptibility patterns over 14 years 由 Animesh Jindal, Avinash Pathengay, Kopal Mithal, Subhadra Jalali, Annie Mathai, Rajeev Reddy Pappuru, Raja Narayanan, Jay Chhablani, Swapna Reddy Motukupally, Savitri Sharma, Taraprasad Das, Harry W. Flynn
出版 2014Artigo -
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Abnormal Complement Activation and Inflammation in the Pathogenesis of Retinopathy of Prematurity 由 Sonika Rathi, Subhadra Jalali, Satish Patnaik, Shahna Shahulhameed, Ganeswara Rao Musada, Divya Balakrishnan, Padmaja Kumari Rani, Ramesh Kekunnaya, Preeti Patil Chhablani, Sarpras Swain, Lopamudra Giri, Subhabrata Chakrabarti, Inderjeet Kaur
出版 2017Artigo -
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Premature Truncation of a Novel Protein, RD3, Exhibiting Subnuclear Localization Is Associated with Retinal Degeneration 由 James S. Friedman, Bo Chang, Chitra Kannabiran, Christina Chakarova, Hardeep Singh, Subhadra Jalali, Norman L. Hawes, Kari Branham, Mohammad Othman, Elena V. Filippova, Debra A. Thompson, Andrew R. Webster, Sten Andréasson, Samuel G. Jacobson, Shomi S. Bhattacharya, John R. Heckenlively, Anand Swaroop
出版 2006Artigo -
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PAM-flexible Engineered FnCas9 variants for robust and ultra-precise genome editing and diagnostics 由 Sundaram Acharya, Asgar Hussain Ansari, P.K. Das, Seiichi Hirano, Meghali Aich, Riya Rauthan, Sudipta Mahato, Savitri Maddileti, Sajal Sarkar, Manoj Kumar, Rhythm Phutela, Sneha Gulati, Abdul Rahman, Arushi Goel, C. Afzal, Deepanjan Paul, Trupti Agrawal, Vinay Kumar Pulimamidi, Subhadra Jalali, Hiroshi Nishimasu, Indumathi Mariappan, Osamu Nureki, Souvik Maiti, Debojyoti Chakraborty
出版 2024Artigo -
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NMNAT1 mutations cause Leber congenital amaurosis 由 Marni J. Falk, Qi Zhang, Eiko Nakamaru‐Ogiso, Chitra Kannabiran, Zoë Fonseca-Kelly, Christina Chakarova, Isabelle Audo, Donna S. Mackay, Christina Zeitz, Arundhati Dev Borman, Magdalena Staniszewska, Rachna Shukla, Lakshmi Palavalli, Saddek Mohand‐Saïd, Naushin Waseem, Subhadra Jalali, Juan C. Perín, Emily Place, Julian Ostrovsky, Rui Xiao, Shomi S. Bhattacharya, Mark Consugar, Andrew R. Webster, José‐Alain Sahel, Anthony T. Moore, Eliot L. Berson, Qin Liu, Xiaowu Gai, Eric A. Pierce
出版 2012Artigo
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