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Mainak Sengupta

Showing results (31-40 of 52) with videos related to

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Annals of Human Genetics|March 3, 2020
Mapping the TYR gene reveals novel and previously reported variants in Eastern Indian patients highlighting preponderance of the same changes in multiple unrelated ethnicitiesKausik Ganguly, Tithi Dutta, Arpan Saha, et al.
Pediatric Neurology|March 29, 2024
An Effort to Identify Genetic Determinants in Siblings With Wilson Disease Manifesting Striking Clinical Heterogeneity: An Exome Profiling Study of Two Indian FamiliesArpan Saha, Shristi Das, Samragni De, 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.
Future Oncology (London, England)|August 4, 2020
A meta-analysis and <i>in silico</i> analysis of polymorphic variants conferring breast cancer risk in the Indian subcontinentDebmalya Sengupta, Souradeep Banerjee, Pramiti Mukhopadhyay, et al.
Annals of Indian Academy of Neurology|February 7, 2025
Motor and Non-motor Neurologic Symptoms of Wilson's Disease: Exploring the AssociationsArka Prava Chakraborty, Adreesh Mukherjee, Uma Sinharoy, et al.
Nucleic Acids Research|November 2, 2010
Indian genetic disease databaseSanchari Pradhan, Mainak Sengupta, Anirban Dutta, et al.
Bioscience Reports|November 17, 2022
Analysis of DNMT1 gene variants in progression of neural tube defects-an in silico to in vitro approachSusanta Sadhukhan, Nirvika Paul, Sudakshina Ghosh, et al.
Journal of Psychiatric Research|December 9, 2021
Prioritization of human well-being spectrum related GWAS-SNVs using ENCODE-based web-tools predict interplay between PSMC3, ITIH4, and SERPINC1 genes in modulating well-beingTushar Pyne, Poulomi Ghosh, Mrinmay Dhauria, et al.
Neurology India|April 27, 2021
Mitochondrial DNA Haplogroups and Three Independent Polymorphisms have no Association with the Risk of Parkinson's Disease in East Indian PopulationTania Saha, Somrita Roy, Rajashree Chakraborty, et al.
Archives of Dermatological Research|February 14, 2019
Meta-analysis and prioritization of human skin pigmentation-associated GWAS-SNPs using ENCODE data-based web-toolsKausik Ganguly, Tania Saha, Arpan Saha, et al.
Pageof 6

Showing results (31-40 of 52) with videos related to

Sort By:
Pageof 6
Annals of Human Genetics|March 3, 2020
Mapping the TYR gene reveals novel and previously reported variants in Eastern Indian patients highlighting preponderance of the same changes in multiple unrelated ethnicitiesKausik Ganguly, Tithi Dutta, Arpan Saha, et al.
Pediatric Neurology|March 29, 2024
An Effort to Identify Genetic Determinants in Siblings With Wilson Disease Manifesting Striking Clinical Heterogeneity: An Exome Profiling Study of Two Indian FamiliesArpan Saha, Shristi Das, Samragni De, 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.
Future Oncology (London, England)|August 4, 2020
A meta-analysis and <i>in silico</i> analysis of polymorphic variants conferring breast cancer risk in the Indian subcontinentDebmalya Sengupta, Souradeep Banerjee, Pramiti Mukhopadhyay, et al.
Annals of Indian Academy of Neurology|February 7, 2025
Motor and Non-motor Neurologic Symptoms of Wilson's Disease: Exploring the AssociationsArka Prava Chakraborty, Adreesh Mukherjee, Uma Sinharoy, et al.
Nucleic Acids Research|November 2, 2010
Indian genetic disease databaseSanchari Pradhan, Mainak Sengupta, Anirban Dutta, et al.
Bioscience Reports|November 17, 2022
Analysis of DNMT1 gene variants in progression of neural tube defects-an in silico to in vitro approachSusanta Sadhukhan, Nirvika Paul, Sudakshina Ghosh, et al.
Journal of Psychiatric Research|December 9, 2021
Prioritization of human well-being spectrum related GWAS-SNVs using ENCODE-based web-tools predict interplay between PSMC3, ITIH4, and SERPINC1 genes in modulating well-beingTushar Pyne, Poulomi Ghosh, Mrinmay Dhauria, et al.
Neurology India|April 27, 2021
Mitochondrial DNA Haplogroups and Three Independent Polymorphisms have no Association with the Risk of Parkinson's Disease in East Indian PopulationTania Saha, Somrita Roy, Rajashree Chakraborty, et al.
Archives of Dermatological Research|February 14, 2019
Meta-analysis and prioritization of human skin pigmentation-associated GWAS-SNPs using ENCODE data-based web-toolsKausik Ganguly, Tania Saha, Arpan Saha, et al.
Pageof 6