Himanshi Kapoor

About

Post-Doctoral Fellow at NCMBM, Oslo, Norway. Always interested in the science of cells and organelles. A microscopy enthusiast, an experimental biologist.

Employment

• Universitetet i Oslo Post Doctoral Fellow
  2025 - Present
• Institute of Genomics and Integrative Biology Post Doctoral Fellow
  2024 - 2025
• Institute of Genomics and Integrative Biology Senior Research Associate
  2021 - 2023
• Institute of Genomics and Integrative Biology SERB-National Post Doctoral Fellow
  2018 - 2020
• University of Delhi DST-PURSE Research Associate
  2017 - 2018

Education

• University of Delhi Ph.D.
  2011 - 2017

Projects & Funding

Projects & funding information is unavailable.

Publications (15)

• Generation and characterization of human-derived induced pluripotent stem cell line (IGIBi010-A) from a patient with neurodegenerative disease phenotype carrying mutation in SQSTM1/p62 gene
  Stem Cell Research 2024 DOI: 10.1016/j.scr.2024.103520
  +Save
• Generation and characterization of iPSC lines from Friedreich’s ataxia patient (FRDA) with GAA.TTC repeat expansion in the Frataxin (FXN) gene’s first intron (IGIBi016-A) and a non-FRDA healthy control individual (IGIBi017-A)
  Stem Cell Research 2024 DOI: 10.1016/j.scr.2024.103382
  +Save
• Molecular clues unveiling spinocerebellar ataxia type-12 pathogenesis
  iScience 2024 DOI: 10.1016/j.isci.2024.109768
  +Save
• Generation of an Induced pluripotent stem cell (iPSC) line (IGIBi011-A) from a Spinocerebellar ataxia type 12 gait dominant patient
  Stem Cell Research 2024 DOI: 10.1016/j.scr.2024.103319
  +Save
• Generation of two human induced pluripotent stem cell lines, IGIBi012-A and IGIBi013-A from Friedreich’s ataxia (FRDA) patients with homozygous GAA repeat expansion in FXN gene
  Stem Cell Research 2024 DOI: 10.1016/j.scr.2024.103340
  +Save
• Cognitive Impairment, Ataxia, Dystonia, and Gaze Palsy Due to a Novel Variant in <scp>SQSTM1</scp>: New Lessons
  Movement Disorders 2024 DOI: 10.1002/mds.29684
  +Save
• Generation and characterization of two human iPSC lines, IGIBi014-A and IGIBi015-A, from Friedreich's ataxia (FRDA) patients with pathogenic (GAA/TTC)n repeat expansion in first intron of the Frataxin (FXN) gene
  Stem Cell Research 2024 DOI: 10.1016/j.scr.2023.103289
  +Save
• Childhood onset myoclonus-dystonia associated with a novel KCTD17 variant in an Indian patient
  Parkinsonism & Related Disorders 2023 DOI: 10.1016/j.parkreldis.2023.105925
  +Save
• Resveratrol mitigates miR-212-3p mediated progression of diesel exhaust-induced pulmonary fibrosis by regulating SIRT1/FoxO3
  Science of The Total Environment 2023 DOI: 10.1016/j.scitotenv.2023.166063
  +Save
• Generation of two induced pluripotent stem cell (iPSC) lines from patients with Duchenne muscular dystrophy (IGIBi006-A and IGIBi008-A) carrying exonic deletions in the dystrophin gene
  Stem Cell Research 2022 DOI: 10.1016/j.scr.2022.102927
  +Save