Search research articles
Contact Us
Filters
Showing results (21-30 of 52) with videos related to
Page
of 6
Sort By:
Molecular Vision
|
September 5, 2007
SLC45A2 variations in Indian oculocutaneous albinism patients
Mainak Sengupta, Moumita Chaki, N Arti, et al.
Protoplasma
|
December 24, 2014
Molecular phylogenetic studies based on rDNA ITS, cpDNA trnL intron sequence and cladode characteristics in nine Protasparagus taxa
Partha Sarathi Saha, Sudipta Ray, Mainak Sengupta, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
December 3, 2022
Missing heritability of Wilson disease: a search for the uncharacterized mutations
Shubhrajit Roy, Sampurna Ghosh, Jharna Ray, et al.
Journal of Genetics
|
June 19, 2008
SNPs in genes with copy number variation: a question of specificity
Mainak Sengupta, Ananya Ray, Moumita Chaki, et al.
Asian Pacific Journal of Cancer Prevention : APJCP
|
August 25, 2018
Meta-Analysis of Polymorphic Variants Conferring Genetic Risk to Cervical Cancer in Indian Women Supports CYP1A1 as an Important Associated Locus
Debmalya Sengupta, Udayan Guha, Sagnik Mitra, et al.
Scientific Reports
|
August 25, 2022
A comprehensive meta-analysis and prioritization study to identify vitiligo associated coding and non-coding SNV candidates using web-based bioinformatics tools
Tithi Dutta, Sayantan Mitra, Arpan Saha, et al.
Journal of Genetics
|
August 24, 2013
Analysis of MC1R variants in Indian oculocutaneous albinism patients: highlighting the risk of skin cancer among albinos
Mainak Sengupta, Devroop Sarkar, Maitreye Mondal, et al.
Molecular Biology Reports
|
July 16, 2024
Identifying genetic defects in oculocutaneous albinism patients of West Bengal, Eastern India
Tithi Dutta, Kausik Ganguly, Arpan Saha, 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 patient
Arnab Gupta, Ishita Chattopadhyay, Shashwata Mukherjee, et al.
Molecular Biology Reports
|
March 27, 2026
Exploratory associations of candidate modifier variants with disease severity, age at onset, and drug response in three Wilson disease patients sharing the same ATP7B mutation
Arpan Saha, Preyangsee Dutta, Aratrika Dutta, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 52) with videos related to
Sort By:
Page
of 6
Molecular Vision
|
September 5, 2007
SLC45A2 variations in Indian oculocutaneous albinism patients
Mainak Sengupta, Moumita Chaki, N Arti, et al.
Protoplasma
|
December 24, 2014
Molecular phylogenetic studies based on rDNA ITS, cpDNA trnL intron sequence and cladode characteristics in nine Protasparagus taxa
Partha Sarathi Saha, Sudipta Ray, Mainak Sengupta, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
December 3, 2022
Missing heritability of Wilson disease: a search for the uncharacterized mutations
Shubhrajit Roy, Sampurna Ghosh, Jharna Ray, et al.
Journal of Genetics
|
June 19, 2008
SNPs in genes with copy number variation: a question of specificity
Mainak Sengupta, Ananya Ray, Moumita Chaki, et al.
Asian Pacific Journal of Cancer Prevention : APJCP
|
August 25, 2018
Meta-Analysis of Polymorphic Variants Conferring Genetic Risk to Cervical Cancer in Indian Women Supports CYP1A1 as an Important Associated Locus
Debmalya Sengupta, Udayan Guha, Sagnik Mitra, et al.
Scientific Reports
|
August 25, 2022
A comprehensive meta-analysis and prioritization study to identify vitiligo associated coding and non-coding SNV candidates using web-based bioinformatics tools
Tithi Dutta, Sayantan Mitra, Arpan Saha, et al.
Journal of Genetics
|
August 24, 2013
Analysis of MC1R variants in Indian oculocutaneous albinism patients: highlighting the risk of skin cancer among albinos
Mainak Sengupta, Devroop Sarkar, Maitreye Mondal, et al.
Molecular Biology Reports
|
July 16, 2024
Identifying genetic defects in oculocutaneous albinism patients of West Bengal, Eastern India
Tithi Dutta, Kausik Ganguly, Arpan Saha, 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 patient
Arnab Gupta, Ishita Chattopadhyay, Shashwata Mukherjee, et al.
Molecular Biology Reports
|
March 27, 2026
Exploratory associations of candidate modifier variants with disease severity, age at onset, and drug response in three Wilson disease patients sharing the same ATP7B mutation
Arpan Saha, Preyangsee Dutta, Aratrika Dutta, et al.
Page
of 6