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Molecular Vision|February 11, 2009
Immunophenotypes of macular corneal dystrophy in India and correlation with mutations in CHST6Afia Sultana, Gordon K Klintworth, Eugene J-M A Thonar, et al.Archives of Pathology & Laboratory Medicine|July 31, 2010
Hypomethylation of the DNMT3L promoter in ocular surface squamous neoplasiaGuru Prasad Manderwad, Gopinathan Gokul, Chitra Kannabiran, et al.Progress in Retinal and Eye Research|March 16, 2007
Tyrosinase and ocular diseases: some novel thoughts on the molecular basis of oculocutaneous albinism type 1Kunal Ray, Moumita Chaki, Mainak SenguptaBiomed Research International|July 9, 2014
Structure-function correlation analysis of connexin50 missense mutations causing congenital cataract: electrostatic potential alteration could determine intracellular trafficking fate of mutantsDevroop Sarkar, Kunal Ray, Mainak SenguptaMolecular and Cellular Biochemistry|November 19, 2003
Recent advances in molecular genetics of glaucomaKunal Ray, Arijit Mukhopadhyay, Moulinath AcharyaHuman Mutation|May 17, 2005
Determination of variants in the 3'-region of the tyrosinase gene requires locus specific amplificationMoumita Chaki, Arijit Mukhopadhyay, Kunal RayMetallomics : Integrated Biometal Science|February 24, 2018
A glimpse into the regulation of the Wilson disease protein, ATP7B, sheds light on the complexity of mammalian apical trafficking pathwaysArnab Gupta, Santanu Das, Kunal RayStem Cell Research|June 13, 2024
Generation and characterization of a Stargardt's disease-specific induced pluripotent stem cell line (LVPEIi008-A) with a homozygous nonsense mutation in exon 44 of ABCA4Divya Pidishetty, Savitri Maddileti, Sudipta Mahato, et al.Stem Cell Research|April 6, 2025
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 iPSC line (LVPEIi006-B-1)Sudipta Mahato, Savitri Maddileti, Trupti Agrawal, et al.Ophthalmic Genetics|August 21, 2002
Mutational analysis of the RB1 gene in Indian patients with retinoblastomaM Ata-ur-Rasheed, Geeta k Vemuganti, Santosh g Honavar, et al.Pageof 14