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akaturk Akademik ölçüm

Akademisyen profili · PROFESÖR

ARZU KARABAY KORKMAZ

İSTANBUL TEKNİK ÜNİVERSİTESİ

  • Ana Dal Sağlık Bilimleri Temel Alanı
  • Yan Dal Tıbbi Biyoloji
  • FEN-EDEBİYAT FAKÜLTESİ
  • MOLEKÜLER BİYOLOJİ VE GENETİK BÖLÜMÜ
Makale YÖKSİS 36
Proje 1
Kitap 0
Bildiri 10
Patent 1
Sanatsal 1
Scopus (SJR)
Q1 25 Q2 5 Q3 4 Q4 0
WoS (JCR)
Q1 13 Q2 12 Q3 5 Q4 4
TR Index 1 makale

Scopus (SJR)

Q1 25 Q2 5 Q3 4 Q4 0

WoS (JCR)

Q1 13 Q2 12 Q3 5 Q4 4

TR Index

1 makale

Toplam 36 yayın

Makaleler

  1. 2026 Spastin Is Required to Prevent SPAST ‐Related Demyelination Journal of Neurochemistry DOI 10.1111/jnc.70407
  2. 2025 A Comprehensive Overview of the Clinical, Electrophysiological, and Neuroimaging Features of BPAN: Insights From a New Case Series Annals of Clinical and Translational Neurology DOI 10.1002/acn3.70220
  3. 2025 Quantitative Iron Measurements in the Basal Ganglia of NBIA Patients Using QSM : Insights From a Tertiary Center Annals of Clinical and Translational Neurology DOI 10.1002/acn3.70161
  4. 2025 Meteorin Is a Novel Interaction Partner of p60‐Katanin During Mitosis in HCT ‐116 Colorectal Cancer Cells Cytoskeleton DOI 10.1002/cm.70059
  5. 2025 C-Myc Indirectly Controls ATP13A2 Levels via HIF-1α Activation JOURNAL OF NEUROCHEMISTRY DOI 10.1111/jnc.70296
  6. 2025 A novel MAP7D1 mutation causes mitotic defects and RPS14 accumulation in Shwachman−Diamond syndrome patient cells Disease Models & Mechanisms DOI 10.1242/dmm.052409
  7. 2023 Spastin Promotes the Migration and Invasion Capability of T98G Glioblastoma Cells by Interacting with Pin1 through Its Microtubule-Binding Domain CELLS DOI 10.3390/cells12030427
  8. 2023 miR96- and miR182-driven regulation of cytoskeleton results in inhibition of glioblastoma motility Cytoskeleton DOI 10.1002/cm.21754
  9. 2022 MYO1H is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia Molecular Genetics and Genomics DOI 10.1007/s00438-022-01910-5
  10. 2022 Modeling gain-of-function and loss-of-function components of SPAST-based hereditary spastic paraplegia using transgenic mice Human Molecular Genetics DOI 10.1093/hmg/ddab367
  11. 2020 Novel mutations in ATP13A2 associated with mixed neurological presentations and iron toxicity due to nonsense-mediated decay BRAIN RESEARCH DOI 10.1016/j.brainres.202067
  12. 2019 Elk1 affects katanin and spastin proteins via differential transcriptional and post-transcriptional regulations PLOS ONE DOI 10.1371/journal.pone.0212518
  13. 2019 p53 regulates katanin-p60 promoter in HCT 116 cells Gene DOI 10.1016/j.gene.2019.144241
  14. 2018 Efficacy of Exome-Targeted Capture Sequencing to Detect Mutations in Known Cerebellar Ataxia Genes JAMA Neurology DOI 10.1001/jamaneurol.2017.5121
  15. 2018 Exploring the role of miRNAs in the diagnosis of MODY3 Turkish Journal Of Medical Sciences DOI 10.3906/sag-1711-98
  16. 2018 Okadaic acid-induced tau hyperphosphorylation and the downregulation of Pin1 expression in primary cortical neurons JOURNAL OF CHEMICAL NEUROANATOMY DOI 10.1016/j.jchemneu.2018.05.006
  17. 2016 Expression of cell cycle proteins in cortical neurons Correlation with glutamate induced neurotoxicity BioFactors DOI 10.1002/biof.1282
  18. 2015 Knockdown of Pin1 leads to reduced angiogenic potential and tumorigenicity in glioblastoma cells Oncology Letters DOI 10.3892/ol.2015.3512
  19. 2015 Neuroprotective strategies against calpain mediated neurodegeneration Neuropsychiatric Disease and Treatment DOI 10.2147/NDT.S78226
  20. 2015 Novel POC1A mutation in Primordial Dwarfism reveals new insights for centriole biogenesis Human Molecular Genetics DOI 10.1093/hmg/ddv261

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