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 | 75 | 2019 |
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 | 26 | 2016 |
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 | 24 | 2019 |
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 | 5 | 2022 |
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 | 2 | 2022 |
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 | 1 | 2023 |
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 | 1 | 2022 |
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 | | |