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Mainak Sengupta

Showing results (11-20 of 52) 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: SLC45A2Kunal Ray, Moumita Chaki, Mainak Sengupta
Journal of Ophthalmology|April 17, 2015
The aging eyeSuddhasil Mookherjee, Ashima Bhattacharjee, 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
Environmental and Molecular Mutagenesis|October 28, 2017
Association of 12 polymorphic variants conferring genetic risk to lung cancer in Indian population: An extensive meta-analysisDebmalya Sengupta, Udayan Guha, Samsiddhi Bhattacharjee, et al.
Plant Direct|July 1, 2022
The <i>rolB</i>-transgenic <i>Nicotiana tabacum</i> plants exhibit upregulated <i>ARF7</i> and <i>ARF19</i> gene expressionRahul Bose, Mainak Sengupta, Debabrata Basu, et al.
Scientific Reports|December 15, 2020
Structural insights and evaluation of the potential impact of missense variants on the interactions of SLIT2 with ROBO1/4 in cancer progressionDebmalya Sengupta, Gairika Bhattacharya, Sayak Ganguli, et al.
Mutation Research. Reviews in Mutation Research|November 23, 2025
Non-coding RNAs in Wilson's Disease: Plausible drivers of hepatic symptom heterogeneityNeelanjana Sarkar, Arpan Saha, Shubhrajit Roy, et al.
Pageof 6

Showing results (11-20 of 52) with videos related to

Sort By:
Pageof 6
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: SLC45A2Kunal Ray, Moumita Chaki, Mainak Sengupta
Journal of Ophthalmology|April 17, 2015
The aging eyeSuddhasil Mookherjee, Ashima Bhattacharjee, 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
Environmental and Molecular Mutagenesis|October 28, 2017
Association of 12 polymorphic variants conferring genetic risk to lung cancer in Indian population: An extensive meta-analysisDebmalya Sengupta, Udayan Guha, Samsiddhi Bhattacharjee, et al.
Plant Direct|July 1, 2022
The <i>rolB</i>-transgenic <i>Nicotiana tabacum</i> plants exhibit upregulated <i>ARF7</i> and <i>ARF19</i> gene expressionRahul Bose, Mainak Sengupta, Debabrata Basu, et al.
Scientific Reports|December 15, 2020
Structural insights and evaluation of the potential impact of missense variants on the interactions of SLIT2 with ROBO1/4 in cancer progressionDebmalya Sengupta, Gairika Bhattacharya, Sayak Ganguli, et al.
Mutation Research. Reviews in Mutation Research|November 23, 2025
Non-coding RNAs in Wilson's Disease: Plausible drivers of hepatic symptom heterogeneityNeelanjana Sarkar, Arpan Saha, Shubhrajit Roy, et al.
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