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Moumita Chaki

Showing results (11-20 of 42) with videos related to

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Human Genetics|September 13, 2005
Gene symbol: TYR. Disease: Albinism, oculocutaneous 1K Ray, Moumita Chaki, Arijit Mukhopadhyay
Human Genetics|June 29, 2007
Gene symbol: SLC45A2Kunal Ray, Moumita Chaki, Mainak Sengupta
Human Genetics|June 29, 2007
Gene symbol: SLC45A2Kunal Ray, Moumita Chaki, Mainak Sengupta
Human Genetics|November 28, 2006
Gene symbol: TYR. Disease: albinism, oculocutaneous 1K Ray, Moumita Chaki, Mainak Sengupta
Human Genetics|July 2, 2005
Gene symbol: TYR. Disease: Albinism, oculocutaneous 1K Ray, Moumita Chaki, Arijit Mukhopadhyay
Human Genetics|April 3, 2008
Novel human pathological mutations. Gene symbol: TYR. Disease: albinism, oculocutaneous 1Kunal Ray, Moumita Chaki, Mainak Sengupta
Molecular Vision|September 5, 2007
SLC45A2 variations in Indian oculocutaneous albinism patientsMainak Sengupta, Moumita Chaki, N Arti, et al.
Journal of Genetics|June 19, 2008
SNPs in genes with copy number variation: a question of specificityMainak Sengupta, Ananya Ray, Moumita Chaki, et al.
Expert Review of Molecular Diagnostics|November 4, 2025
<i>ESR1</i> ctDNA testing: literature review and comparison of assays for <i>ESR1</i> mutation detection in advanced hormone receptor-positive breast cancerAlexander Yarunin, Hanna Ahlgren, Moumita Chaki, et al.
Molecular Vision|August 2, 2005
Higher prevalence of OCA1 in an ethnic group of eastern India is due to a founder mutation in the tyrosinase geneMoumita Chaki, Arijit Mukhopadhyay, Shamba Chatterjee, et al.
Pageof 5

Showing results (11-20 of 42) with videos related to

Sort By:
Pageof 5
Human Genetics|September 13, 2005
Gene symbol: TYR. Disease: Albinism, oculocutaneous 1K Ray, Moumita Chaki, Arijit Mukhopadhyay
Human Genetics|June 29, 2007
Gene symbol: SLC45A2Kunal Ray, Moumita Chaki, Mainak Sengupta
Human Genetics|June 29, 2007
Gene symbol: SLC45A2Kunal Ray, Moumita Chaki, Mainak Sengupta
Human Genetics|November 28, 2006
Gene symbol: TYR. Disease: albinism, oculocutaneous 1K Ray, Moumita Chaki, Mainak Sengupta
Human Genetics|July 2, 2005
Gene symbol: TYR. Disease: Albinism, oculocutaneous 1K Ray, Moumita Chaki, Arijit Mukhopadhyay
Human Genetics|April 3, 2008
Novel human pathological mutations. Gene symbol: TYR. Disease: albinism, oculocutaneous 1Kunal Ray, Moumita Chaki, Mainak Sengupta
Molecular Vision|September 5, 2007
SLC45A2 variations in Indian oculocutaneous albinism patientsMainak Sengupta, Moumita Chaki, N Arti, et al.
Journal of Genetics|June 19, 2008
SNPs in genes with copy number variation: a question of specificityMainak Sengupta, Ananya Ray, Moumita Chaki, et al.
Expert Review of Molecular Diagnostics|November 4, 2025
<i>ESR1</i> ctDNA testing: literature review and comparison of assays for <i>ESR1</i> mutation detection in advanced hormone receptor-positive breast cancerAlexander Yarunin, Hanna Ahlgren, Moumita Chaki, et al.
Molecular Vision|August 2, 2005
Higher prevalence of OCA1 in an ethnic group of eastern India is due to a founder mutation in the tyrosinase geneMoumita Chaki, Arijit Mukhopadhyay, Shamba Chatterjee, et al.
Pageof 5