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- Publications
- Influence
Cytogenetic damage and genetic variants in the individuals susceptible to arsenic‐induced cancer through drinking water
In West Bengal, India, more than 300,000 arsenic‐exposed people are showing symptoms of arsenic toxicity, which include cancers of skin and different internal organs. Since only 15–20% of the exposed… Expand
Tyrosinase and ocular diseases: Some novel thoughts on the molecular basis of oculocutaneous albinism type 1
- K. Ray, M. Chaki, M. Sengupta
- Biology, Medicine
- Progress in Retinal and Eye Research
- 1 July 2007
Tyrosinase (TYR) is a multifunctional copper-containing glycoenzyme (approximately 80 kDa), which plays a key role in the rate-limiting steps of the melanin biosynthetic pathway. This membrane-bound… Expand
Indian genetic disease database
- S. Pradhan, M. Sengupta, +4 authors K. Ray
- Biology, Medicine
- Nucleic Acids Res.
- 30 October 2010
TLDR
Genetic landscape of the people of India: a canvas for disease gene exploration
- S. Brahmachari, P. Majumder, +148 authors A. Mukhopadhyay
- Biology, Medicine
- Journal of Genetics
- 1 April 2008
Analyses of frequency profiles of markers on disease or drug-response related genes in diverse populations are important for the dissection of common diseases. We report the results of analyses of… Expand
A novel COMMD1 mutation Thr174Met associated with elevated urinary copper and signs of enhanced apoptotic cell death in a Wilson Disease patient
- A. Gupta, I. Chattopadhyay, S. Mukherjee, M. Sengupta, S. Das, K. Ray
- Biology, Medicine
- Behavioral and Brain Functions
- 15 June 2010
Wilson disease (WD) results from accumulation of copper and caused due to mutations in ATP7B, a copper transporting ATPase. Besides regular hepatic and neurological symptoms, WD patients occasionally… Expand
Molecular and functional studies of tyrosinase variants among Indian oculocutaneous albinism type 1 patients.
- M. Chaki, M. Sengupta, +4 authors K. Ray
- Medicine
- The Journal of investigative dermatology
- 2011
OCA1 in Different Ethnic Groups of India is Primarily Due to Founder Mutations in the Tyrosinase Gene
- M. Chaki, M. Sengupta, +5 authors K. Ray
- Biology, Medicine
- Annals of human genetics
- 1 September 2006
Oculocutaneous albinism (OCA) is a heterogeneous group of autosomal recessive disorders characterized by an abnormally low amount of melanin in the eyes, skin and hair, and associated with common… Expand
Meta-Analysis of Polymorphic Variants Conferring Genetic Risk to Cervical Cancer in Indian Women Supports CYP1A1 as an Important Associated Locus
- D. Sengupta, Udayan Guha, Sagnik Mitra, Sampurna Ghosh, Samsiddhi Bhattacharjee, M. Sengupta
- Medicine
- Asian Pacific journal of cancer prevention…
- 1 August 2018
Objective: Association of multiple polymorphic variants with cervical cancer has been elucidated by several candidate gene based as well as genome-wide association studies. However, contradictory… Expand
Closed loop speed control of a laboratory fabricated brush-less DC motor drive prototype using position sensor
- P. Mukherjee, M. Sengupta
- Computer Science
- National Power Electronics Conference (NPEC)
- 1 December 2017
TLDR
Design and implementation of sensorless vector control of surface mounted PMSM using back-EMF estimation and PLL based technique
- S. Paitandi, M. Sengupta
- Computer Science
- National Power Electronics Conference (NPEC)
- 1 December 2017
TLDR