Zobrazeno 1 - 10
of 291
pro vyhledávání: '"Subhadra Jalali"'
Autor:
Sunita Chaurasia, Sushma Sri, Kandibanda Srinivas, Joveeta Joseph, Mudit Tyagi, Vivek Pravin Dave, Subhadra Jalali
Publikováno v:
Indian Journal of Ophthalmology, Vol 72, Iss 9, Pp 1254-1260 (2024)
Purpose: To report the clinical profile and donor characteristics of post-optical keratoplasty adverse events notified at an eye bank. Methods: Between January 2013 and December 2022, 37,041 donor corneas were utilized for keratoplasty, of which 16,5
Externí odkaz:
https://doaj.org/article/4d1ccbd3b9c344a0840432117d20aea4
Autor:
Sundaram Acharya, Asgar Hussain Ansari, Prosad Kumar 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
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-23 (2024)
Abstract The clinical success of CRISPR therapies hinges on the safety and efficacy of Cas proteins. The Cas9 from Francisella novicida (FnCas9) is highly precise, with a negligible affinity for mismatched substrates, but its low cellular targeting e
Externí odkaz:
https://doaj.org/article/967b3513bca24917a4d3b9306cf6ba0f
Autor:
Divya Pidishetty, Savitri Maddileti, Sudipta Mahato, Trupti Agrawal, Milind Naik, Chitra Kannabiran, Subhadra Jalali, Indumathi Mariappan
Publikováno v:
Stem Cell Research, Vol 78, Iss , Pp 103458- (2024)
The Stargardt’s Disease, Type 1 (STGD1) is associated with the loss of function mutations in ABCA4. This gene codes for a retina-specific, ATP-binding cassette (ABC) family transporter, involved in the transport of the key visual cycle intermediate
Externí odkaz:
https://doaj.org/article/0cf2fa3c348b48f59d11241addbe9cd5
Publikováno v:
Indian Journal of Ophthalmology, Vol 72, Iss 7, Pp 956-961 (2024)
This study aims to investigate the relationship between pachychoroid spectrum disorders and retinitis pigmentosa (RP) or rod-cone dystrophy through a comprehensive literature review. The purpose is to explore the association between these disorders,
Externí odkaz:
https://doaj.org/article/ece2574bc3904dc992a218d8395e2c90
Autor:
Tapas R Padhi, Souvik Bhunia, Taraprasad Das, Sameer Nayak, Manav Jalan, Suryasnata Rath, Biswajeet Barik, Hasnat Ali, Padmaja Kumari Rani, Dipanwita Routray, Subhadra Jalali
Publikováno v:
Indian Journal of Ophthalmology, Vol 72, Iss 5, Pp 697-703 (2024)
Purpose: To evaluate the feasibility and outcome of a real-time retinopathy of prematurity (ROP) telescreening strategy using videoconferencing in a community setting in India. Method: In a prospective study, trained allied ophthalmic personnel obtai
Externí odkaz:
https://doaj.org/article/20a14f2fb84d40ffab2fb7c90689a092
Autor:
Divya Pidishetty, Savitri Maddileti, Sudipta Mahato, Trupti Agrawal, Vinay Kumar Pulimamidi, Milind Naik, Chitra Kannabiran, Subhadra Jalali, Indumathi Mariappan
Publikováno v:
Stem Cell Research, Vol 77, Iss , Pp 103418- (2024)
Mutations in ABCA4 gene leads to the most common form of an inherited retinal disease namely, the Stargardt disease, type 1. Here, we report the generation of two different patient-specific induced pluripotent stem cell lines (LVPEIi007-B and LVPEIi0
Externí odkaz:
https://doaj.org/article/7726dd4ff35945f0abb9827ce50ed60f
Autor:
Savitri Maddileti, Sudipta Mahato, Trupti Agrawal, Vivek Pravin Dave, Milind Naik, Mohammad Javed Ali, Chitra Kannabiran, Subhadra Jalali, Giridhara R. Jayandharan, Indumathi Mariappan
Publikováno v:
Stem Cell Research, Vol 77, Iss , Pp 103413- (2024)
Leber Congenital Amaurosis 2 is an early onset retinal dystrophy that occurs due to mutation in RPE65 gene. Here, we report the generation of two patient specific induced pluripotent stem cell lines harboring nonsense mutations in exon 7 (c.646A > T)
Externí odkaz:
https://doaj.org/article/8dfb0c33d4d541bdb48c5748200716a6
Autor:
Sudipta Mahato, Savitri Maddileti, Milind Naik, Chitra Kannabiran, Subhadra Jalali, Indumathi Mariappan
Publikováno v:
Stem Cell Research, Vol 77, Iss , Pp 103380- (2024)
Leber congenital amaurosis (LCA) is a congenital, early onset, autosomal recessive inherited retinal disease (IRD). This report describes an LCA12 patient-specific iPSC line (LVPEIi006-A), generated by the reprogramming of dermal fibroblasts using in
Externí odkaz:
https://doaj.org/article/de3db48639284adab08feed674805637
Autor:
Anand Singh Brar, Deepika C. Parameswarappa, Brijesh Takkar, Raja Narayanan, Subhadra Jalali, Sohini Mandal, Kaoru Fujinami, Srikanta Kumar Padhy
Publikováno v:
Ophthalmology and Therapy, Vol 13, Iss 1, Pp 21-50 (2023)
Abstract This comprehensive review provides a thorough examination of inherited retinal diseases (IRDs), encompassing their classification, genetic underpinnings, and the promising landscape of gene therapy trials. IRDs, a diverse group of genetic co
Externí odkaz:
https://doaj.org/article/adc88959d8544dac8e5ff5e88e49deff
Autor:
Şengül Özdek, Ece Özdemir Zeydanlı, Caroline Baumal, Sandra Hoyek, Nimesh Patel, Audina Berrocal, Ashley Lopez-Cañizares, Hasenin Al-Khersan, Shunji Kusaka, Fukutaro Mano, Subhadra Jalali, Domenico Lepore, Solmaz Akar
Publikováno v:
Türk Oftalmoloji Dergisi, Vol 53, Iss 1, Pp 44-57 (2023)
Avascular peripheral retina in an infant is a common characteristic of numerous pediatric retinal vascular disorders and often presents a diagnostic challenge to the clinician. In this review, key features of each disease in the differential diagnosi
Externí odkaz:
https://doaj.org/article/e34fe9325ef44aa3aafbd00b9fd0c6c0