Detalhe da pesquisa
1.
A Next Generation Connectivity Map: L1000 Platform and the First 1,000,000 Profiles.
Cell
; 171(6): 1437-1452.e17, 2017 Nov 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-29195078
2.
Intronic elements associated with insomnia and restless legs syndrome exhibit cell-type-specific epigenetic features contributing to MEIS1 regulation.
Hum Mol Genet
; 31(11): 1733-1746, 2022 06 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34888668
3.
Collagen VI Regulates Motor Circuit Plasticity and Motor Performance by Cannabinoid Modulation.
J Neurosci
; 42(8): 1557-1573, 2022 02 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-34965974
4.
Discovery of mobocertinib, a new irreversible tyrosine kinase inhibitor indicated for the treatment of non-small-cell lung cancer harboring EGFR exon 20 insertion mutations.
Med Chem Res
; 31(10): 1647-1662, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36065226
5.
Investigation of dopaminergic signalling in Meis homeobox 1 (Meis1) deficient mice as an animal model of restless legs syndrome.
J Sleep Res
; 30(5): e13311, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34008292
6.
Code Words.
N Engl J Med
; 387(5): 393-395, 2022 08 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35904485
7.
Muscle-induced loading as an important source of variation in craniofacial skeletal shape.
Genesis
; 57(1): e23263, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30418689
8.
Recessive variants in ZNF142 cause a complex neurodevelopmental disorder with intellectual disability, speech impairment, seizures, and dystonia.
Genet Med
; 21(11): 2532-2542, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31036918
9.
Update on KMT2B-Related Dystonia.
Curr Neurol Neurosci Rep
; 19(11): 92, 2019 11 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-31768667
10.
Recessive mutations in the α3 (VI) collagen gene COL6A3 cause early-onset isolated dystonia.
Am J Hum Genet
; 96(6): 883-93, 2015 Jun 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-26004199
11.
Reduced-representation Phosphosignatures Measured by Quantitative Targeted MS Capture Cellular States and Enable Large-scale Comparison of Drug-induced Phenotypes.
Mol Cell Proteomics
; 15(5): 1622-41, 2016 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-26912667
12.
Partially redundant enhancers cooperatively maintain Mammalian pomc expression above a critical functional threshold.
PLoS Genet
; 11(2): e1004935, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25671638
13.
CT Imaging Findings after Craniosynostosis Reconstructive Surgery.
Pediatr Neurosurg
; 53(4): 215-221, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29874675
14.
Association of AHSG with alopecia and mental retardation (APMR) syndrome.
Hum Genet
; 136(3): 287-296, 2017 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28054173
15.
Renal ApoA-1 amyloidosis with Glu34Lys mutation and intra-amyloid lipid accumulation.
J Am Soc Nephrol
; 25(12): 2703-5, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24925720
16.
Spatial enhancer activation influences inhibitory neuron identity during mouse embryonic development.
Nat Neurosci
; 27(5): 862-872, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38528203
17.
A patient-enriched MEIS1 coding variant causes a restless legs syndrome-like phenotype in mice.
Sleep
; 47(5)2024 May 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-38314840
18.
Digital broadband linearization of optical links.
Opt Lett
; 38(4): 446-8, 2013 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-23455097
19.
Timing of dialysis initiation in the geriatric population: toward a patient-centered approach.
Semin Dial
; 26(6): 682-9, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-24112631
20.
Serotonin 2C receptor agonists improve type 2 diabetes via melanocortin-4 receptor signaling pathways.
Cell Metab
; 6(5): 398-405, 2007 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-17983585