Showing results (31-40 of 139) with videos related to
Sort By:
Pageof 14
Nature Clinical Practice. Neurology|August 26, 2006
Wilson's disease: an updateShyamal K Das, Kunal RayJournal of Biosciences|June 10, 2011
Splicing aberrations caused by constitutional RB1 gene mutations in retinoblastomaVidya Latha Parsam, Mohammed Javed Ali, Santosh G Honavar, et al.Biochimica Et Biophysica Acta|February 7, 2016
Human βA3/A1-crystallin splicing mutation causes cataracts by activating the unfolded protein response and inducing apoptosis in differentiating lens fiber cellsZhiwei Ma, Wenliang Yao, Chi-Chao Chan, et al.Orphanet Journal of Rare Diseases|September 17, 2022
Identification and in silico analysis of a spectrum of SLC4A11 variations in Indian familial and sporadic cases of congenital hereditary endothelial dystrophyMohd Salman, Anshuman Verma, Sunita Chaurasia, et al.Scientific Reports|November 23, 2017
Association of Human Leukocyte Antigen Class 1 genes with Stevens Johnson Syndrome with severe ocular complications in an Indian populationChitra Kannabiran, Mayumi Ueta, Virender Sangwan, et al.Investigative Ophthalmology & Visual Science|November 26, 2008
Phenotypic characterization of retinoblastoma for the presence of putative cancer stem-like cell markers by flow cytometryMurali M S Balla, Geeta K Vemuganti, Chitra Kannabiran, et al.Molecular Vision|June 5, 2013
Mutational screening of Indian families with hereditary congenital cataractSurya Prakash Goud Ponnam, Kekkunaya Ramesha, Jyoti Matalia, et al.FEBS Open Bio|June 18, 2013
A cataract-causing connexin 50 mutant is mislocalized to the ER due to loss of the fourth transmembrane domain and cytoplasmic domainMadhavi Latha Somaraju Chalasani, Madhavi Muppirala, Surya Prakash G Ponnam, et al.Molecular Vision|January 22, 2004
Novel mutations of the carbohydrate sulfotransferase-6 (CHST6) gene causing macular corneal dystrophy in IndiaAfia Sultana, Mittanamalli S Sridhar, Aparna Jagannathan, et al.Frontiers in Genetics|January 29, 2021
Genetic Markers for Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis in the Asian Indian Population: Implications on PreventionSwapna S Shanbhag, Madhuri A Koduri, Chitra Kannabiran, et al.Pageof 14