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Kunal Ray

Showing results (51-60 of 113) with videos related to

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Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 15, 2004
A Line 1 insertion in the Factor IX gene segregates with mild hemophilia B in dogsMarjory B Brooks, Weikuan Gu, Jennifer L Barnas, et al.
Neurobiology of Aging|December 7, 2010
Role of tau kinases (CDK5R1 and GSK3B) in Parkinson's disease: a study from IndiaGautami Das, Amar K Misra, Shyamal K Das, et al.
Disease Markers|September 11, 2012
Genetic association and gene-gene interaction of HAS2, HABP1 and HYAL3 implicate hyaluronan metabolic genes in glaucomatous neurodegenerationKaustuv Basu, Abhijit Sen, Kunal Ray, et al.
Molecular Vision|August 2, 2005
Higher prevalence of OCA1 in an ethnic group of eastern India is due to a founder mutation in the tyrosinase geneMoumita Chaki, Arijit Mukhopadhyay, Shamba Chatterjee, et al.
Molecular Vision|October 26, 2011
WDR36 variants in East Indian primary open-angle glaucoma patientsSuddhasil Mookherjee, Subhadip Chakraborty, Mansi Vishal, et al.
Journal of Genetics|June 29, 2016
TBK1 duplication is found in normal tension and not in high tension glaucoma patients of Indian originLalit Kaurani, Mansi Vishal, Jharna Ray, et al.
Genetic Testing and Molecular Biomarkers|August 18, 2016
Evaluation of the IL1 Gene Cluster Single Nucleotide Polymorphisms in Primary Open-Angle Glaucoma PathogenesisSuddhasil Mookherjee, Deblina Banerjee, Subhadip Chakraborty, et al.
Behavioral and Brain Functions : BBF|June 17, 2010
A novel COMMD1 mutation Thr174Met associated with elevated urinary copper and signs of enhanced apoptotic cell death in a Wilson Disease patientArnab Gupta, Ishita Chattopadhyay, Shashwata Mukherjee, et al.
International Journal of Hematology|December 2, 2015
Hemophagocytic syndrome following haploidentical peripheral blood stem cell transplantation with post-transplant cyclophosphamideSarita Rani Jaiswal, Aditi Chakrabarti, Sumita Chatterjee, et al.
The Journal of Investigative Dermatology|September 24, 2010
Molecular and functional studies of tyrosinase variants among Indian oculocutaneous albinism type 1 patientsMoumita Chaki, Mainak Sengupta, Maitreyee Mondal, et al.
Pageof 12

Showing results (51-60 of 113) with videos related to

Sort By:
Pageof 12
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 15, 2004
A Line 1 insertion in the Factor IX gene segregates with mild hemophilia B in dogsMarjory B Brooks, Weikuan Gu, Jennifer L Barnas, et al.
Neurobiology of Aging|December 7, 2010
Role of tau kinases (CDK5R1 and GSK3B) in Parkinson's disease: a study from IndiaGautami Das, Amar K Misra, Shyamal K Das, et al.
Disease Markers|September 11, 2012
Genetic association and gene-gene interaction of HAS2, HABP1 and HYAL3 implicate hyaluronan metabolic genes in glaucomatous neurodegenerationKaustuv Basu, Abhijit Sen, Kunal Ray, et al.
Molecular Vision|August 2, 2005
Higher prevalence of OCA1 in an ethnic group of eastern India is due to a founder mutation in the tyrosinase geneMoumita Chaki, Arijit Mukhopadhyay, Shamba Chatterjee, et al.
Molecular Vision|October 26, 2011
WDR36 variants in East Indian primary open-angle glaucoma patientsSuddhasil Mookherjee, Subhadip Chakraborty, Mansi Vishal, et al.
Journal of Genetics|June 29, 2016
TBK1 duplication is found in normal tension and not in high tension glaucoma patients of Indian originLalit Kaurani, Mansi Vishal, Jharna Ray, et al.
Genetic Testing and Molecular Biomarkers|August 18, 2016
Evaluation of the IL1 Gene Cluster Single Nucleotide Polymorphisms in Primary Open-Angle Glaucoma PathogenesisSuddhasil Mookherjee, Deblina Banerjee, Subhadip Chakraborty, et al.
Behavioral and Brain Functions : BBF|June 17, 2010
A novel COMMD1 mutation Thr174Met associated with elevated urinary copper and signs of enhanced apoptotic cell death in a Wilson Disease patientArnab Gupta, Ishita Chattopadhyay, Shashwata Mukherjee, et al.
International Journal of Hematology|December 2, 2015
Hemophagocytic syndrome following haploidentical peripheral blood stem cell transplantation with post-transplant cyclophosphamideSarita Rani Jaiswal, Aditi Chakrabarti, Sumita Chatterjee, et al.
The Journal of Investigative Dermatology|September 24, 2010
Molecular and functional studies of tyrosinase variants among Indian oculocutaneous albinism type 1 patientsMoumita Chaki, Mainak Sengupta, Maitreyee Mondal, et al.
Pageof 12