Follow
Prashant Phulpagar
Title
Cited by
Cited by
Year
Effective visualization and easy tracking of extracellular vesicles in glioma cells
A Mondal, KA Ashiq, P Phulpagar, DK Singh, A Shiras
Biological procedures online 21, 1-12, 2019
752019
Capsicum annuum proteinase inhibitor ingestion negatively impacts the growth of sorghum pest Chilo partellus and promotes differential protease expression
AR Jadhav, AR War, AN Nikam, AS Adhav, VS Gupta, HC Sharma, ...
Biochemistry and biophysics reports 8, 302-309, 2016
262016
Hydroxyapatite nanorods loaded with parathyroid hormone (PTH) synergistically enhance the net formative effect of PTH anabolic therapy
JR Dave, AM Dewle, ST Mhaske, PT Phulpagar, VL Mathe, SE More, ...
Nanomedicine: Nanotechnology, Biology and Medicine 15 (1), 218-230, 2019
242019
A splice altering variant in NDRG1 gene causes Charcot-Marie-Tooth disease, type 4D
P Pravinbabu, VV Holla, P Phulpagar, N Kamble, M Netravathi, R Yadav, ...
Neurological Sciences 43 (7), 4463-4472, 2022
52022
Spinocerebellar ataxia recessive type 7 due to novel compound heterozygous variants in TPP1: First report from India
VV Holla, S Jha, PK Pal, R Yadav, P Phulpagar, B Muthusamy, ...
Parkinsonism & Related Disorders 94, 117-119, 2022
22022
A rare case of ophthalmoplegia with ataxia in genetically proven abetalipoproteinemia
S Gurram, VV Holla, N Sriram, P Phulpagar, S Jha, P Sharma, ...
Movement Disorders Clinical Practice 10 (3), 514, 2023
12023
Whole exome sequencing and transcript analysis discover a novel pathogenic splice site mutation in DCAF17 gene underlying Woodhouse‐Sakati syndrome.
R Kumari, VV Holla, P Phulpagar, N Sriram, AG Hegde, S Vengalil, ...
Journal of Neuroendocrinology 34 (10), e13185, 2022
12022
Clinicogenetic Characterization of Patients with PD and Heterozygous GBA1 Variants in an Indian Cohort
SD Kamath, VV Holla, P Phulpagar, N Kamble, R Yadav, B Muthusamy, ...
Movement Disorders, 2023
2023
Novel CWF19L1 mutations in patients with spinocerebellar ataxia, autosomal recessive 17
P Phulpagar, VV Holla, D Tomar, N Kamble, R Yadav, PK Pal, ...
Journal of Human Genetics 68 (12), 859-866, 2023
2023
CLCN2‐Related Leukoencephalopathy in Two Unrelated Patients Due to Novel Variants
VV Holla, P Phulpagar, J Saini, N Kamble, PK Pal, R Yadav, ...
Movement Disorders Clinical Practice 10 (7), 1155-1158, 2023
2023
Molecular Insight of Exosomes Mediated Angiogenesis in Glioblastoma
A Mondal, A Sharma, P Phulpagar, A Shiras
The system can't perform the operation now. Try again later.
Articles 1–11