Detalhe da pesquisa
1.
Disassembly and Mislocalization of AQP4 in Incipient Scar Formation after Experimental Stroke.
Int J Mol Sci
; 23(3)2022 Jan 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-35163040
2.
Targeted deletion of ß1-syntrophin causes a loss of Kir 4.1 from Müller cell endfeet in mouse retina.
Glia
; 67(6): 1138-1149, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30803043
3.
Role of aquaporin-4 polarization in extracellular solute clearance.
Fluids Barriers CNS
; 21(1): 28, 2024 Mar 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-38532513
4.
Aquaporin-9 in the Brain Inflammatory Response: Evidence from Mice Injected with the Parkinsonogenic Toxin MPP.
Biomolecules
; 13(4)2023 03 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-37189335
5.
Canonical Bone Morphogenetic Protein Signaling Regulates Expression of Aquaporin-4 and Its Anchoring Complex in Mouse Astrocytes.
Front Cell Neurosci
; 16: 878154, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35518645
6.
Orchestrating aquaporin-4 and connexin-43 expression in brain: Differential roles of α1- and ß1-syntrophin.
Biochim Biophys Acta Biomembr
; 1863(8): 183616, 2021 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33872576
7.
Pro-Inflammatory Role of AQP4 in Mice Subjected to Intrastriatal Injections of the Parkinsonogenic Toxin MPP.
Cells
; 9(11)2020 11 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33167342
8.
Functional specialization of retinal Müller cell endfeet depends on an interplay between two syntrophin isoforms.
Mol Brain
; 13(1): 40, 2020 03 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-32178707
9.
Uncoupling of the Astrocyte Syncytium Differentially Affects AQP4 Isoforms.
Cells
; 9(2)2020 02 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32046059
10.
Targeted deletion of the aquaglyceroporin AQP9 is protective in a mouse model of Parkinson's disease.
PLoS One
; 13(3): e0194896, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29566083
11.
Targeted deletion of Aqp4 promotes the formation of astrocytic gap junctions.
Brain Struct Funct
; 222(9): 3959-3972, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-28551776
12.
Novel PIGT Variant in Two Brothers: Expansion of the Multiple Congenital Anomalies-Hypotonia Seizures Syndrome 3 Phenotype.
Genes (Basel)
; 7(12)2016 Nov 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-27916860