Medha Sengupta
Overview
Explore the profile of Medha Sengupta including associated specialties, affiliations and a list of published articles.
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Articles
5
Citations
110
Followers
0
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Recent Articles
1.
Henderson M, Sengupta M, Trojanowski J, Lee V
Acta Neuropathol Commun
. 2024 Jun;
12(1):110.
PMID: 38943188
No abstract available.
2.
Richardson K, Sengupta M, Sujkowski A, Libohova K, Harris A, Wessells R, et al.
J Neurosci Res
. 2024 Jan;
102(1):e25278.
PMID: 38284836
Spinal and bulbar muscular atrophy (SBMA) is an X-linked disorder that affects males who inherit the androgen receptor (AR) gene with an abnormal CAG triplet repeat expansion. The resulting protein...
3.
Sengupta M, Pluciennik A, Merry D
Front Mol Neurosci
. 2022 Oct;
15:1020143.
PMID: 36277484
Spinal and bulbar muscular atrophy (SBMA) is a neurodegenerative and neuromuscular genetic disease caused by the expansion of a polyglutamine-encoding CAG tract in the androgen receptor (AR) gene. The AR...
4.
Henderson M, Sengupta M, Trojanowski J, Lee V
Acta Neuropathol Commun
. 2019 Nov;
7(1):183.
PMID: 31733655
Mutations in leucine-rich repeat kinase 2 (LRRK2) are the most common cause of familial Parkinson's disease (PD). While the clinical presentation of LRRK2 mutation carriers is similar to that of...
5.
Henderson M, Sengupta M, McGeary I, Zhang B, Olufemi M, Brown H, et al.
Acta Neuropathol Commun
. 2019 Feb;
7(1):28.
PMID: 30808409
Mutations in leucine-rich repeat kinase 2 (LRRK2) are one of the most common causes of familial Parkinson's disease (PD). The most common mutations in the LRRK2 gene induce elevated kinase...