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Anna O Kulinich

Explore the profile of Anna O Kulinich including associated specialties, affiliations and a list of published articles. Areas
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Articles 5
Citations 19
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Recent Articles
1.
Prentiss A, Baggio C, Pagett J, Kulinich A, Ethell I, Muzzarelli K, et al.
J Med Chem . 2024 Dec; 67(24):22245-22253. PMID: 39656022
The activity of the receptor tyrosine kinase EphA4 has been implicated in several pathologies including oncology (gastric and pancreatic cancers) and neurodegenerative diseases (amyotrophic lateral sclerosis and Alzheimer's disease). However,...
2.
Sutley-Koury S, Anderson A, Taitano-Johnson C, Ajayi M, Kulinich A, Contreras K, et al.
ASN Neuro . 2024 Oct; 16(1):2401753. PMID: 39437409
Astrocytes have been implicated in oligodendrocyte development and myelination, however, the mechanisms by which astrocytes regulate oligodendrocytes remain unclear. Our findings suggest a new mechanism that regulates astrocyte-mediated oligodendrocyte development...
3.
Sutley-Koury S, Taitano-Johnson C, Kulinich A, Farooq N, Wagner V, Robles M, et al.
J Neurosci . 2024 Sep; 44(45). PMID: 39327008
Impaired inhibitory synapse development is suggested to drive neuronal hyperactivity in autism spectrum disorders (ASD) and epilepsy. We propose a novel mechanism by which astrocytes control the development of parvalbumin...
4.
Talvio K, Wagner V, Minkeviciene R, Kirkwood J, Kulinich A, Umemori J, et al.
Commun Biol . 2023 Jul; 6(1):789. PMID: 37516746
Cholesterol is an essential membrane structural component and steroid hormone precursor, and is involved in numerous signaling processes. Astrocytes regulate brain cholesterol homeostasis and they supply cholesterol to the needs...
5.
Kulinich A, Reinhard S, Rais M, Lovelace J, Scott V, Binder D, et al.
Neurobiol Dis . 2019 Nov; 134:104622. PMID: 31698054
Background: Fragile X syndrome (FXS) is the most common genetic cause of autism and intellectual disability. Fragile X mental retardation gene (Fmr1) knock-out (KO) mice display core deficits of FXS,...