Nivedita Singh
Bengaluru, KA, India
Last Updated: 09/26/2026
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Found 12 publications
Real-time heterogeneity of supramolecular assembly of amyloid precursor protein is modulated by an endocytic risk factor PICALM.
Journal: Cellular and molecular life sciences : CMLS
Published: April 05, 2023
Neuronal PET tracers for Alzheimer's disease.
Journal: Biochemical and biophysical research communications
Published: November 23, 2021
Achieving nanoscale precision using neuromorphic localization microscopy.
Journal: Nature nanotechnology
Published: November 11, 2021
Nanoscale regulation of Ca2+ dependent phase transitions and real-time dynamics of SAP97/hDLG.
Journal: Nature communications
Published: September 17, 2021
Exome sequencing and functional studies in zebrafish identify WDR8 as the causative gene for isolated Microspherophakia in Indian families.
Journal: Human molecular genetics
Published: January 07, 2021
Genetic analysis of ATP7B in 102 south Indian families with Wilson disease.
Journal: PloS one
Published: February 11, 2019
A homozygous mutation in TRIM36 causes autosomal recessive anencephaly in an Indian family.
Journal: Human molecular genetics
Published: September 09, 2016
Genetic Analysis of PLA2G6 in 22 Indian Families with Infantile Neuroaxonal Dystrophy, Atypical Late-Onset Neuroaxonal Dystrophy and Dystonia Parkinsonism Complex.
Journal: PloS one
Published: October 29, 2015
Non-Wilsonian hepatolenticular degeneration: Clinical and MRI observations in four families from south India.
Journal: Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia
Published: May 01, 2015
Showing 1-12 of 12
Last Updated: 09/26/2026