Detalhe da pesquisa
1.
A highly conserved program of neuronal microexons is misregulated in autistic brains.
Cell
; 159(7): 1511-23, 2014 Dec 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-25525873
2.
Autism-Misregulated eIF4G Microexons Control Synaptic Translation and Higher Order Cognitive Functions.
Mol Cell
; 77(6): 1176-1192.e16, 2020 03 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-31999954
3.
Autism spectrum disorder: insights into convergent mechanisms from transcriptomics.
Nat Rev Genet
; 20(1): 51-63, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30390048
4.
A vertebrate Polycomb response element governs segmentation of the posterior hindbrain.
Cell
; 138(5): 885-97, 2009 Sep 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-19737517
5.
Misregulation of an Activity-Dependent Splicing Network as a Common Mechanism Underlying Autism Spectrum Disorders.
Mol Cell
; 64(6): 1023-1034, 2016 12 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27984743
6.
Essential roles for the splicing regulator nSR100/SRRM4 during nervous system development.
Genes Dev
; 29(7): 746-59, 2015 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25838543
7.
The linear ubiquitin-specific deubiquitinase gumby regulates angiogenesis.
Nature
; 498(7454): 318-24, 2013 Jun 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-23708998
8.
Cdx1 refines positional identity of the vertebrate hindbrain by directly repressing Mafb expression.
Development
; 138(1): 65-74, 2011 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-21098558
9.
An interaction between OTULIN and SCRIB uncovers roles for linear ubiquitination in planar cell polarity.
Dis Model Mech
; 16(8)2023 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37589075
10.
Disc1 point mutations in mice affect development of the cerebral cortex.
J Neurosci
; 31(9): 3197-206, 2011 Mar 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-21368031
11.
A tryptophan hydroxlyase 1 reporter that directs Cre recombinase extinguishable placental alkaline phosphatase expression in serotonergic (5-HT) neurons and peripheral tissues.
Genesis
; 49(11): 851-61, 2011 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-21438125
12.
N-ethyl-N-nitrosourea mutagenesis: boarding the mouse mutant express.
Microbiol Mol Biol Rev
; 69(3): 426-39, 2005 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-16148305
13.
Generation of a transgenic mouse line expressing GFP-Cre protein from a Hoxb4 neural enhancer.
Genesis
; 46(2): 119-24, 2008 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-18257073
14.
The tyrosine kinase receptor Tyro3 enhances lifespan and neuropeptide Y (Npy) neuron survival in the mouse anorexia (anx) mutation.
Dis Model Mech
; 10(5): 581-595, 2017 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28093506
15.
A genetic screen for mutations that affect cranial nerve development in the mouse.
J Neurosci
; 25(50): 11787-95, 2005 Dec 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-16354937
16.
The vHNF1 homeodomain protein establishes early rhombomere identity by direct regulation of Kreisler expression.
Mech Dev
; 122(12): 1300-9, 2005 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-16274963
17.
A genetic screen for mouse mutations with defects in serotonin responsiveness.
Brain Res Mol Brain Res
; 115(2): 162-72, 2003 Jul 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-12877987
18.
Abnormal interneuron development in disrupted-in-schizophrenia-1 L100P mutant mice.
Mol Brain
; 6: 20, 2013 Apr 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-23631734
19.
Analysis of hindbrain patterning defects caused by the kreisler(enu) mutation reveals multiple roles of Kreisler in hindbrain segmentation.
Dev Dyn
; 227(1): 134-42, 2003 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-12701106