Detalhe da pesquisa
1.
Gastrointestinal Dysfunction in Genetically Defined Neurodevelopmental Disorders.
Semin Neurol
; 43(4): 645-660, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37586397
2.
Cryptic Amyloidogenic Elements in the 3' UTRs of Neurofilament Genes Trigger Axonal Neuropathy.
Am J Hum Genet
; 98(4): 597-614, 2016 Apr 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27040688
3.
Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis.
Hum Mol Genet
; 24(14): 4006-23, 2015 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25882707
4.
Knock-down DHDDS expression induces photoreceptor degeneration in zebrafish.
Adv Exp Med Biol
; 801: 543-50, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24664742
5.
Distinct phenotypes in zebrafish models of human startle disease.
Neurobiol Dis
; 60: 139-51, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24029548
6.
Drugs prescribed for Phelan-McDermid syndrome differentially impact sensory behaviors in shank3 zebrafish models.
F1000Res
; 12: 84, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37868296
7.
Context-dependent hyperactivity in syngap1a and syngap1b zebrafish autism models.
bioRxiv
; 2023 Sep 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-37786701
8.
The Gut-Brain-Microbiome Axis and Its Link to Autism: Emerging Insights and the Potential of Zebrafish Models.
Front Cell Dev Biol
; 9: 662916, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33937265
9.
Restoring Shank3 in the rostral brainstem of shank3ab-/- zebrafish autism models rescues sensory deficits.
Commun Biol
; 4(1): 1411, 2021 12 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-34921227
10.
Elevated preoptic brain activity in zebrafish glial glycine transporter mutants is linked to lethargy-like behaviors and delayed emergence from anesthesia.
Sci Rep
; 11(1): 3148, 2021 02 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33542258
11.
Genetic compensation in a stable slc25a46 mutant zebrafish: A case for using F0 CRISPR mutagenesis to study phenotypes caused by inherited disease.
PLoS One
; 15(3): e0230566, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32208444
12.
Intestinal dysmotility in a zebrafish (Danio rerio) shank3a;shank3b mutant model of autism.
Mol Autism
; 10: 3, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30733854
13.
Zebrafish: A Pharmacogenetic Model for Anesthesia.
Methods Enzymol
; 602: 189-209, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29588029
14.
Spatial patterning of excitatory and inhibitory neuropil territories during spinal circuit development.
J Comp Neurol
; 525(7): 1649-1667, 2017 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27997694
15.
A defect in the inner kinetochore protein CENPT causes a new syndrome of severe growth failure.
PLoS One
; 12(12): e0189324, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-29228025
16.
Function Over Form: Modeling Groups of Inherited Neurological Conditions in Zebrafish.
Front Mol Neurosci
; 9: 55, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27458342
17.
A conserved role but different partners for the transcriptional corepressor CoREST in fly and mammalian nervous system formation.
J Neurosci
; 24(32): 7186-93, 2004 Aug 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-15306652
18.
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder.
Nat Genet
; 47(8): 926-32, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26168012
19.
Glycinergic synapse development, plasticity, and homeostasis in zebrafish.
Front Mol Neurosci
; 2: 30, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-20126315
20.
Synaptic homeostasis in a zebrafish glial glycine transporter mutant.
J Neurophysiol
; 100(4): 1716-23, 2008 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-18715895