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Journal of Genetics
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September 24, 2010
Analysis of single nucleotide polymorphisms of PRNP gene in twenty-four ethnic groups of India
Mainak 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 1
Kunal Ray, Moumita Chaki, Mainak Sengupta
Human Genetics
|
June 29, 2007
Gene symbol: CYP1B1
Kunal Ray, Moulinath Acharya, Suddhasil Mookherjee
Human Genetics
|
June 29, 2007
Gene symbol: SLC45A2
Kunal 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 mutants
Devroop Sarkar, Kunal Ray, Mainak Sengupta
Human Genetics
|
April 3, 2008
Novel human pathological mutations. Gene symbol: TYR. Disease: tyrosinase deficiency
Kunal Ray, Moumita Chaki, Mainak Sengupta
Molecular and Cellular Biochemistry
|
November 19, 2003
Recent advances in molecular genetics of glaucoma
Kunal Ray, Arijit Mukhopadhyay, Moulinath Acharya
Human Mutation
|
May 17, 2005
Determination of variants in the 3'-region of the tyrosinase gene requires locus specific amplification
Moumita Chaki, Arijit Mukhopadhyay, Kunal Ray
Human Genetics
|
April 3, 2008
Novel human pathological mutations. Gene symbol: TYR. Disease: tyrosinase deficiency
Kunal 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 pathways
Arnab Gupta, Santanu Das, Kunal Ray
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of 12
Search research articles
Search
Showing results (11-20 of 113) with videos related to
Sort By:
Page
of 12
Journal of Genetics
|
September 24, 2010
Analysis of single nucleotide polymorphisms of PRNP gene in twenty-four ethnic groups of India
Mainak 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 1
Kunal Ray, Moumita Chaki, Mainak Sengupta
Human Genetics
|
June 29, 2007
Gene symbol: CYP1B1
Kunal Ray, Moulinath Acharya, Suddhasil Mookherjee
Human Genetics
|
June 29, 2007
Gene symbol: SLC45A2
Kunal 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 mutants
Devroop Sarkar, Kunal Ray, Mainak Sengupta
Human Genetics
|
April 3, 2008
Novel human pathological mutations. Gene symbol: TYR. Disease: tyrosinase deficiency
Kunal Ray, Moumita Chaki, Mainak Sengupta
Molecular and Cellular Biochemistry
|
November 19, 2003
Recent advances in molecular genetics of glaucoma
Kunal Ray, Arijit Mukhopadhyay, Moulinath Acharya
Human Mutation
|
May 17, 2005
Determination of variants in the 3'-region of the tyrosinase gene requires locus specific amplification
Moumita Chaki, Arijit Mukhopadhyay, Kunal Ray
Human Genetics
|
April 3, 2008
Novel human pathological mutations. Gene symbol: TYR. Disease: tyrosinase deficiency
Kunal 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 pathways
Arnab Gupta, Santanu Das, Kunal Ray
Page
of 12