Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Kunal Ray

Showing results (71-80 of 113) with videos related to

Pageof 12
Sort By:
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|November 28, 2015
Haploidentical Peripheral Blood Stem Cell Transplantation with Post-Transplantation Cyclophosphamide in Children with Advanced Acute Leukemia with Fludarabine-, Busulfan-, and Melphalan-Based ConditioningSarita Rani Jaiswal, Aditi Chakrabarti, Sumita Chatterjee, et al.
Indian Journal of Ophthalmology|November 7, 2003
Myocilin mutation 1109 C>T (Pro 370 Leu) is the most common gene defect causing early onset primary open angle glaucomaArijit Mukhopadhyay, Moulinath Acharya, Jharna Ray, et al.
Neuroscience Letters|April 1, 2018
Evaluation of FGF 20 variants for susceptibility to Parkinson's disease in Eastern IndiansDipanwita Sadhukhan, Gautami Das, Arindam Biswas, et al.
Scientific Reports|August 12, 2020
Analysis of Wilson disease mutations revealed that interactions between different ATP7B mutants modify their propertiesShubhrajit Roy, Courtney J McCann, Martina Ralle, et al.
Clinical Chemistry|July 20, 2007
Molecular diagnosis of Wilson disease using prevalent mutations and informative single-nucleotide polymorphism markersArnab Gupta, Mahua Maulik, Poonam Nasipuri, et al.
Cellular and Molecular Neurobiology|September 8, 2007
Molecular pathogenesis of Wilson disease among Indians: a perspective on mutation spectrum in ATP7B gene, prevalent defects, clinical heterogeneity and implication towards diagnosisArnab Gupta, Ishita Chattopadhyay, Sumit Dey, et al.
Molecular Vision|May 17, 2008
Leu432Val polymorphism in CYP1B1 as a susceptible factor towards predisposition to primary open-angle glaucomaAshima Bhattacharjee, Deblina Banerjee, Suddhasil Mookherjee, et al.
Scientific Reports|May 31, 2014
Evaluation of genetic association of the INK4 locus with primary open angle glaucoma in East Indian populationMansi Vishal, Anchal Sharma, Lalit Kaurani, et al.
Neuroscience Letters|December 4, 2016
Genetic screening of THAP1 in primary dystonia patients of IndiaSubhajit Giri, Tufan Naiya, Zaffar Equbal, et al.
Plos One|August 14, 2013
Mitochondrial genome analysis of primary open angle glaucoma patientsDeblina Banerjee, Antara Banerjee, Suddhasil Mookherjee, et al.
Pageof 12

Showing results (71-80 of 113) with videos related to

Sort By:
Pageof 12
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|November 28, 2015
Haploidentical Peripheral Blood Stem Cell Transplantation with Post-Transplantation Cyclophosphamide in Children with Advanced Acute Leukemia with Fludarabine-, Busulfan-, and Melphalan-Based ConditioningSarita Rani Jaiswal, Aditi Chakrabarti, Sumita Chatterjee, et al.
Indian Journal of Ophthalmology|November 7, 2003
Myocilin mutation 1109 C>T (Pro 370 Leu) is the most common gene defect causing early onset primary open angle glaucomaArijit Mukhopadhyay, Moulinath Acharya, Jharna Ray, et al.
Neuroscience Letters|April 1, 2018
Evaluation of FGF 20 variants for susceptibility to Parkinson's disease in Eastern IndiansDipanwita Sadhukhan, Gautami Das, Arindam Biswas, et al.
Scientific Reports|August 12, 2020
Analysis of Wilson disease mutations revealed that interactions between different ATP7B mutants modify their propertiesShubhrajit Roy, Courtney J McCann, Martina Ralle, et al.
Clinical Chemistry|July 20, 2007
Molecular diagnosis of Wilson disease using prevalent mutations and informative single-nucleotide polymorphism markersArnab Gupta, Mahua Maulik, Poonam Nasipuri, et al.
Cellular and Molecular Neurobiology|September 8, 2007
Molecular pathogenesis of Wilson disease among Indians: a perspective on mutation spectrum in ATP7B gene, prevalent defects, clinical heterogeneity and implication towards diagnosisArnab Gupta, Ishita Chattopadhyay, Sumit Dey, et al.
Molecular Vision|May 17, 2008
Leu432Val polymorphism in CYP1B1 as a susceptible factor towards predisposition to primary open-angle glaucomaAshima Bhattacharjee, Deblina Banerjee, Suddhasil Mookherjee, et al.
Scientific Reports|May 31, 2014
Evaluation of genetic association of the INK4 locus with primary open angle glaucoma in East Indian populationMansi Vishal, Anchal Sharma, Lalit Kaurani, et al.
Neuroscience Letters|December 4, 2016
Genetic screening of THAP1 in primary dystonia patients of IndiaSubhajit Giri, Tufan Naiya, Zaffar Equbal, et al.
Plos One|August 14, 2013
Mitochondrial genome analysis of primary open angle glaucoma patientsDeblina Banerjee, Antara Banerjee, Suddhasil Mookherjee, et al.
Pageof 12