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Kunal Ray

Showing results (11-20 of 113) with videos related to

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Journal of Genetics|September 24, 2010
Analysis of single nucleotide polymorphisms of PRNP gene in twenty-four ethnic groups of IndiaMainak Sengupta, Amrita Chakraborty, , 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 Sengupta
Human Genetics|June 29, 2007
Gene symbol: CYP1B1Kunal Ray, Moulinath Acharya, Suddhasil Mookherjee
Human Genetics|June 29, 2007
Gene symbol: SLC45A2Kunal Ray, Moumita Chaki, Mainak Sengupta
Biomed 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 Sengupta
Human Genetics|April 3, 2008
Novel human pathological mutations. Gene symbol: TYR. Disease: tyrosinase deficiencyKunal Ray, Moumita Chaki, Mainak Sengupta
Molecular and Cellular Biochemistry|November 19, 2003
Recent advances in molecular genetics of glaucomaKunal Ray, Arijit Mukhopadhyay, Moulinath Acharya
Human Mutation|May 17, 2005
Determination of variants in the 3'-region of the tyrosinase gene requires locus specific amplificationMoumita Chaki, Arijit Mukhopadhyay, Kunal Ray
Human Genetics|April 3, 2008
Novel human pathological mutations. Gene symbol: TYR. Disease: tyrosinase deficiencyKunal Ray, Moumita Chaki, Mainak Sengupta
Metallomics : 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 Ray
Pageof 12

Showing results (11-20 of 113) with videos related to

Sort By:
Pageof 12
Journal of Genetics|September 24, 2010
Analysis of single nucleotide polymorphisms of PRNP gene in twenty-four ethnic groups of IndiaMainak Sengupta, Amrita Chakraborty, , 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 Sengupta
Human Genetics|June 29, 2007
Gene symbol: CYP1B1Kunal Ray, Moulinath Acharya, Suddhasil Mookherjee
Human Genetics|June 29, 2007
Gene symbol: SLC45A2Kunal Ray, Moumita Chaki, Mainak Sengupta
Biomed 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 Sengupta
Human Genetics|April 3, 2008
Novel human pathological mutations. Gene symbol: TYR. Disease: tyrosinase deficiencyKunal Ray, Moumita Chaki, Mainak Sengupta
Molecular and Cellular Biochemistry|November 19, 2003
Recent advances in molecular genetics of glaucomaKunal Ray, Arijit Mukhopadhyay, Moulinath Acharya
Human Mutation|May 17, 2005
Determination of variants in the 3'-region of the tyrosinase gene requires locus specific amplificationMoumita Chaki, Arijit Mukhopadhyay, Kunal Ray
Human Genetics|April 3, 2008
Novel human pathological mutations. Gene symbol: TYR. Disease: tyrosinase deficiencyKunal Ray, Moumita Chaki, Mainak Sengupta
Metallomics : 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 Ray
Pageof 12