Detalhe da pesquisa
1.
Human iPSC 4R tauopathy model uncovers modifiers of tau propagation.
Cell
; 187(10): 2446-2464.e22, 2024 May 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-38582079
2.
CA10 regulates neurexin heparan sulfate addition via a direct binding in the secretory pathway.
EMBO Rep
; 22(4): e51349, 2021 04 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33586859
3.
Calsyntenin-3 interacts with both α- and ß-neurexins in the regulation of excitatory synaptic innervation in specific Schaffer collateral pathways.
J Biol Chem
; 295(27): 9244-9262, 2020 07 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32434929
4.
Carbonic anhydrase-related protein CA10 is an evolutionarily conserved pan-neurexin ligand.
Proc Natl Acad Sci U S A
; 114(7): E1253-E1262, 2017 02 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-28154140
5.
TANGO2 deficiency as a cause of neurodevelopmental delay with indirect effects on mitochondrial energy metabolism.
J Inherit Metab Dis
; 42(5): 898-908, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31276219
6.
Presynaptic Neuronal Pentraxin Receptor Organizes Excitatory and Inhibitory Synapses.
J Neurosci
; 37(5): 1062-1080, 2017 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27986928
7.
Mitofusin 2 is necessary for striatal axonal projections of midbrain dopamine neurons.
Hum Mol Genet
; 21(22): 4827-35, 2012 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22914740
8.
Altered dopamine metabolism and increased vulnerability to MPTP in mice with partial deficiency of mitochondrial complex I in dopamine neurons.
Hum Mol Genet
; 21(5): 1078-89, 2012 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22090423
9.
Impaired mitochondrial transport and Parkin-independent degeneration of respiratory chain-deficient dopamine neurons in vivo.
Proc Natl Acad Sci U S A
; 108(31): 12937-42, 2011 Aug 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-21768369
10.
Liprin-α proteins are master regulators of human presynapse assembly.
Nat Neurosci
; 27(4): 629-642, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38472649
11.
Role of neurexin heparan sulfate in the molecular assembly of synapses - expanding the neurexin code?
FEBS J
; 290(2): 252-265, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34699130
12.
Ribonuclease inhibitor 1 (RNH1) deficiency cause congenital cataracts and global developmental delay with infection-induced psychomotor regression and anemia.
Eur J Hum Genet
; 31(8): 887-894, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-36935417
13.
AGC1 deficiency associated with global cerebral hypomyelination.
N Engl J Med
; 361(5): 489-95, 2009 Jul 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-19641205
14.
Bi-allelic VPS16 variants limit HOPS/CORVET levels and cause a mucopolysaccharidosis-like disease.
EMBO Mol Med
; 13(5): e13376, 2021 05 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33938619
15.
LRPPRC is a mitochondrial matrix protein that is conserved in metazoans.
Biochem Biophys Res Commun
; 398(4): 759-64, 2010 Aug 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-20633537
16.
Deorphanizing FAM19A proteins as pan-neurexin ligands with an unusual biosynthetic binding mechanism.
J Cell Biol
; 219(9)2020 09 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32706374
17.
Lrrk2 and alpha-synuclein are co-regulated in rodent striatum.
Mol Cell Neurosci
; 39(4): 586-91, 2008 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-18790059
18.
Glial cell line-derived neurotrophic factor partially ameliorates motor symptoms without slowing neurodegeneration in mice with respiratory chain-deficient dopamine neurons.
Cell Transplant
; 22(9): 1529-39, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23051605