Detalhe da pesquisa
1.
Firing of Replication Origins Is Disturbed by a CDK4/6 Inhibitor in a pRb-Independent Manner.
Int J Mol Sci
; 24(13)2023 Jun 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-37445805
2.
Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia.
Mol Psychiatry
; 26(7): 3004-3017, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33057169
3.
Genetic and Environmental Influences on the Visual Word Form and Fusiform Face Areas.
Cereb Cortex
; 25(9): 2478-93, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-24825786
4.
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders.
Nat Genet
; 39(1): 25-7, 2007 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-17173049
5.
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders.
PLoS Genet
; 8(2): e1002521, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-22346768
6.
Genetic variants of FOXP2 and KIAA0319/TTRAP/THEM2 locus are associated with altered brain activation in distinct language-related regions.
J Neurosci
; 32(3): 817-25, 2012 Jan 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-22262880
7.
Key role for gene dosage and synaptic homeostasis in autism spectrum disorders.
Trends Genet
; 26(8): 363-72, 2010 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-20609491
8.
Production of soluble, active acetyl serotonin methyl transferase in Leishmania tarentolae.
Protein Expr Purif
; 75(1): 114-8, 2011 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-20688166
9.
Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disorders.
J Pineal Res
; 51(4): 394-9, 2011 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-21615493
10.
Efficient, quick and easy-to-use DNA replication timing analysis with START-R suite.
NAR Genom Bioinform
; 2(2): lqaa045, 2020 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-33575597
11.
An investigation of ribosomal protein L10 gene in autism spectrum disorders.
BMC Med Genet
; 10: 7, 2009 Jan 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-19166581
12.
Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia.
Transl Psychiatry
; 9(1): 77, 2019 02 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30741946
13.
Analysis of X chromosome inactivation in autism spectrum disorders.
Am J Med Genet B Neuropsychiatr Genet
; 147B(6): 830-5, 2008 Sep 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-18361425
14.
A hypothesis-driven approach identifies CDK4 and CDK6 inhibitors as candidate drugs for treatments of adrenocortical carcinomas.
Aging (Albany NY)
; 9(12): 2695-2716, 2017 12 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-29283884
15.
Disruption of melatonin synthesis is associated with impaired 14-3-3 and miR-451 levels in patients with autism spectrum disorders.
Sci Rep
; 7(1): 2096, 2017 05 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-28522826
16.
Characterization of the replication timing program of 6 human model cell lines.
Genom Data
; 9: 113-7, 2016 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-27508120
17.
Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort.
Eur J Hum Genet
; 22(5): 675-80, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24022301
18.
[Alterations in synapsis formation and function in autism disorders]. / Identification d'une voie synaptique associée à l'autisme.
Med Sci (Paris)
; 24(1): 25-8, 2008 Jan.
Artigo
em Francês
| MEDLINE | ID: mdl-18198104
19.
Variations of the candidate SEZ6L2 gene on Chromosome 16p11.2 in patients with autism spectrum disorders and in human populations.
PLoS One
; 6(3): e17289, 2011 Mar 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-21394203
20.
Doublecortin interacts with the ubiquitin protease DFFRX, which associates with microtubules in neuronal processes.
Mol Cell Neurosci
; 28(1): 153-64, 2005 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-15607950