Detalhe da pesquisa
1.
The complement system in neurodegenerative diseases.
Clin Sci (Lond)
; 138(6): 387-412, 2024 03 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-38505993
2.
Complement receptor 1 is expressed on brain cells and in the human brain.
Glia
; 71(6): 1522-1535, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36825534
3.
Alzheimer's disease-associated complement gene variants influence plasma complement protein levels.
J Neuroinflammation
; 20(1): 169, 2023 Jul 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-37480051
4.
Sideroflexin 3 is an α-synuclein-dependent mitochondrial protein that regulates synaptic morphology.
J Cell Sci
; 130(2): 325-331, 2017 01 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28049716
5.
Analysis of gene expression in the nervous system identifies key genes and novel candidates for health and disease.
Neurogenetics
; 18(2): 81-95, 2017 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-28190221
6.
Loss-of-function mutations in TBC1D20 cause cataracts and male infertility in blind sterile mice and Warburg micro syndrome in humans.
Am J Hum Genet
; 93(6): 1001-14, 2013 Dec 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-24239381
7.
Quantitative imaging of tissue sections using infrared scanning technology.
J Anat
; 228(1): 203-13, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26510706
8.
Mutation spectrum in RAB3GAP1, RAB3GAP2, and RAB18 and genotype-phenotype correlations in warburg micro syndrome and Martsolf syndrome.
Hum Mutat
; 34(5): 686-96, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23420520
9.
The role of RPGR in cilia formation and actin stability.
Hum Mol Genet
; 20(24): 4840-50, 2011 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21933838
10.
Terminal complement pathway activation drives synaptic loss in Alzheimer's disease models.
Acta Neuropathol Commun
; 10(1): 99, 2022 07 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35794654
11.
Novel Monoclonal Antibodies Against Mouse C1q: Characterisation and Development of a Quantitative ELISA for Mouse C1q.
Mol Neurobiol
; 58(9): 4323-4336, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-34002346
12.
The Impact of Complement Genes on the Risk of Late-Onset Alzheimer's Disease.
Genes (Basel)
; 12(3)2021 03 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-33804666
13.
Genetic Insights into the Impact of Complement in Alzheimer's Disease.
Genes (Basel)
; 12(12)2021 12 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-34946939
14.
27th International Mammalian Genome Conference meeting report.
Mamm Genome
; 25(5-6): 195-201, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24752582
15.
Therapeutic Inhibition of the Complement System in Diseases of the Central Nervous System.
Front Immunol
; 10: 362, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30886620
16.
Pro-death NMDA receptor signaling is promoted by the GluN2B C-terminus independently of Dapk1.
Elife
; 62017 07 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-28731405
17.
Warburg Micro syndrome is caused by RAB18 deficiency or dysregulation.
Open Biol
; 5(6): 150047, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-26063829
18.
Rab18 and a Rab18 GEF complex are required for normal ER structure.
J Cell Biol
; 205(5): 707-20, 2014 Jun 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-24891604
19.
A novel mouse model of Warburg Micro syndrome reveals roles for RAB18 in eye development and organisation of the neuronal cytoskeleton.
Dis Model Mech
; 7(6): 711-22, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24764192