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Plos One|June 1, 2016
Functional and Structural Analyses of CYP1B1 Variants Linked to Congenital and Adult-Onset Glaucoma to Investigate the Molecular Basis of These DiseasesAntara Banerjee, Subhadip Chakraborty, Abhijit Chakraborty, et al.Plos One|October 3, 2012
Molecular basis for involvement of CYP1B1 in MYOC upregulation and its potential implication in glaucoma pathogenesisSuddhasil Mookherjee, Moulinath Acharya, Deblina Banerjee, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 3, 2022
Missing heritability of Wilson disease: a search for the uncharacterized mutationsShubhrajit Roy, Sampurna Ghosh, Jharna Ray, et al.Molecular Vision|July 27, 2002
Did myocilin evolve from two different primordial proteins?Arijit Mukhopadhyay, Arnab Gupta, Saibal Mukherjee, et al.FEBS Letters|June 11, 2005
Upregulation of human mitochondrial NADH dehydrogenase subunit 5 in intestinal epithelial cells is modulated by Vibrio cholerae pathogenesisMadhubanti Sarkar, Soumita Das, Arunava Bandyopadhaya, et al.Molecular Vision|June 28, 2012
Comprehensive analysis of myocilin variants in east Indian POAG patientsDeblina Banerjee, Ashima Bhattacharjee, Archisman Ponda, et al.Taiwan Journal of Ophthalmology|January 22, 2024
Updates on congenital hereditary endothelial dystrophyNeet Mehta, Anshuman Verma, Divya Sree Achanta, et al.Haematologica|December 7, 2007
Evaluation of genetic markers linked to hemophilia A locus: an Indian experienceAtreyee Saha, Saibal Mukherjee, Mahua Maulik, et al.Pediatric Transplantation|May 25, 2016
Haploidentical transplantation in children with unmanipulated peripheral blood stem cell graft: The need to look beyond post-transplantation cyclophosphamide in younger childrenSarita Rani Jaiswal, Aditi Chakrabarti, Sumita Chatterjee, et al.Disease Markers|September 11, 2012
DJ-1 variants in Indian Parkinson's disease patientsTamal Sadhukhan, Arindam Biswas, Shyamal K Das, et al.Pageof 14