Year |
Citation |
Score |
2022 |
Chalkiadaki K, Hooshmandi M, Lach G, Statoulla E, Simbriger K, Amorim IS, Kouloulia S, Zafeiri M, Pothos P, Bonneil É, Gantois I, Popic J, Kim SH, Wong C, Cao R, et al. Mnk1/2 kinases regulate memory and autism-related behaviours via Syngap1. Brain : a Journal of Neurology. PMID 36315645 DOI: 10.1093/brain/awac398 |
0.623 |
|
2020 |
Simbriger K, Amorim IS, Lach G, Chalkiadaki K, Kouloulia S, Jafarnejad SM, Khoutorsky A, Gkogkas CG. Uncovering memory-related gene expression in contextual fear conditioning using ribosome profiling. Progress in Neurobiology. 101903. PMID 32860876 DOI: 10.1016/J.Pneurobio.2020.101903 |
0.592 |
|
2019 |
Kouloulia S, Hallin EI, Simbriger K, Amorim IS, Lach G, Amvrosiadis T, Chalkiadaki K, Kampaite A, Truong VT, Hooshmandi M, Jafarnejad SM, Skehel P, Kursula P, Khoutorsky A, Gkogkas CG. Raptor-Mediated Proteasomal Degradation of Deamidated 4E-BP2 Regulates Postnatal Neuronal Translation and NF-κB Activity. Cell Reports. 29: 3620-3635.e7. PMID 31825840 DOI: 10.1016/J.Celrep.2019.11.023 |
0.583 |
|
2018 |
Silva Amorim I, Kedia S, Kouloulia S, Simbriger K, Gantois I, Jafarnejad SM, Li Y, Kampaite A, Pooters T, Romanò N, Gkogkas CG. Loss of eIF4E phosphorylation engenders depression-like behaviors via selective mRNA translation. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 29367404 DOI: 10.1523/Jneurosci.2673-17.2018 |
0.712 |
|
Low-probability matches (unlikely to be authored by this person) |
2017 |
Kouloulia S, Lazaridou M, Christopoulos TK, Ioannou PC. Multi-allele dipstick assay for visual genotyping of four novel SIRT1 gene variant alleles as candidate biomarkers for sporadic Parkinson disease Microchimica Acta. 184: 2845-2853. DOI: 10.1007/S00604-017-2252-X |
0.055 |
|
2020 |
Emmanouilidou E, Papagiannakis N, Kouloulia S, Galaziou A, Antonellou R, Papadimitriou D, Athanasiadou A, Bozi M, Koros C, Maniati M, Vekrellis K, Ioannou PC, Stefanis L. Peripheral alpha-synuclein levels in patients with genetic and non-genetic forms of Parkinson's disease. Parkinsonism & Related Disorders. 73: 35-40. PMID 32234683 DOI: 10.1016/j.parkreldis.2020.03.014 |
0.025 |
|
Hide low-probability matches. |