Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Josiah A. Quinn"'
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 12 (2024)
Introduction: Astrocytic GLT-1 glutamate transporters ensure the fidelity of glutamic neurotransmission by spatially and temporally limiting glutamate signals. The ability to limit neuronal hyperactivity relies on the localization and diffusion of GL
Externí odkaz:
https://doaj.org/article/0de1109ea4534bfca3859670132e4890
Autor:
Lauren C, Panzera, Ben, Johnson, Josiah A, Quinn, In Ha, Cho, Michael M, Tamkun, Michael B, Hoppa
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 119(30)
The endoplasmic reticulum (ER) forms a continuous and dynamic network throughout a neuron, extending from dendrites to axon terminals, and axonal ER dysfunction is implicated in several neurological disorders. In addition, tight junctions between the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e420db0ba8c6374b14e13dc765b47407
https://pubmed.ncbi.nlm.nih.gov/35862456
https://pubmed.ncbi.nlm.nih.gov/35862456
Autor:
Casandra L, Larrivee, Huijie, Feng, Josiah A, Quinn, Vincent S, Shaw, Jeffrey R, Leipprandt, Elena Y, Demireva, Huirong, Xie, Richard R, Neubig
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 373(1)
Neurodevelopmental disorder with involuntary movements (Online Mendelian Inheritance in Man: 617493) is a severe, early onset neurologic condition characterized by a delay in psychomotor development, hypotonia, and hyperkinetic involuntary movements.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f662aa559ddd06470d8001891ef06614
https://pubmed.ncbi.nlm.nih.gov/31907305
https://pubmed.ncbi.nlm.nih.gov/31907305
Autor:
Jeffrey R. Leipprandt, Vincent Shaw, Huirong Xie, Josiah A Quinn, Huijie Feng, Casandra L Larrivee, Richard R. Neubig, Elena Y. Demireva
Neurodevelopmental disorder with involuntary movements (NEDIM, OMIM: 617493) is a severe, early onset neurological condition characterized by a delay in psychomotor development, hypotonia, and hyperkinetic involuntary movements. Heterozygous de novo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::857b1e76e14e57978deb85cb81843576
Publikováno v:
Mol Pharmacol
Regulators of G-protein signaling (RGS) proteins modulate receptor signaling by binding to activated G-protein α-subunits, accelerating GTP hydrolysis. Selective inhibition of RGS proteins increases G-protein activity and may provide unique tissue s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68bf54ab88861a058125bf22358d126f
https://pubmed.ncbi.nlm.nih.gov/31543506
https://pubmed.ncbi.nlm.nih.gov/31543506
Publikováno v:
The FASEB Journal. 33
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::30065c6b79b294519a3d4cd53b1c73b4
https://doi.org/10.1096/fasebj.2019.33.1_supplement.784.16
https://doi.org/10.1096/fasebj.2019.33.1_supplement.784.16