Detalhe da pesquisa
1.
Comparative Flavivirus-Host Protein Interaction Mapping Reveals Mechanisms of Dengue and Zika Virus Pathogenesis.
Cell
; 175(7): 1931-1945.e18, 2018 12 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-30550790
2.
The Psychiatric Cell Map Initiative: A Convergent Systems Biological Approach to Illuminating Key Molecular Pathways in Neuropsychiatric Disorders.
Cell
; 174(3): 505-520, 2018 07 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-30053424
3.
Integrating non-mammalian model organisms in the diagnosis of rare genetic diseases in humans.
Nat Rev Genet
; 25(1): 46-60, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37491400
4.
Morgan's legacy: fruit flies and the functional annotation of conserved genes.
Cell
; 163(1): 12-4, 2015 Sep 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-26406362
5.
Glial lipid droplets and ROS induced by mitochondrial defects promote neurodegeneration.
Cell
; 160(1-2): 177-90, 2015 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25594180
6.
Control of Synaptic Connectivity by a Network of Drosophila IgSF Cell Surface Proteins.
Cell
; 163(7): 1770-1782, 2015 Dec 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-26687361
7.
Ig Superfamily Ligand and Receptor Pairs Expressed in Synaptic Partners in Drosophila.
Cell
; 163(7): 1756-69, 2015 Dec 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-26687360
8.
A drosophila genetic resource of mutants to study mechanisms underlying human genetic diseases.
Cell
; 159(1): 200-214, 2014 Sep 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-25259927
9.
miR-9a minimizes the phenotypic impact of genomic diversity by buffering a transcription factor.
Cell
; 155(7): 1556-67, 2013 Dec 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-24360277
10.
The Daam2-VHL-Nedd4 axis governs developmental and regenerative oligodendrocyte differentiation.
Genes Dev
; 34(17-18): 1177-1189, 2020 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32792353
11.
De novo variants in FRYL are associated with developmental delay, intellectual disability, and dysmorphic features.
Am J Hum Genet
; 111(4): 742-760, 2024 Apr 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-38479391
12.
Loss of the endoplasmic reticulum protein Tmem208 affects cell polarity, development, and viability.
Proc Natl Acad Sci U S A
; 121(9): e2322582121, 2024 Feb 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-38381787
13.
Rare de novo gain-of-function missense variants in DOT1L are associated with developmental delay and congenital anomalies.
Am J Hum Genet
; 110(11): 1919-1937, 2023 11 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-37827158
14.
Bi-allelic variants in INTS11 are associated with a complex neurological disorder.
Am J Hum Genet
; 110(5): 774-789, 2023 05 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-37054711
15.
Dueling Ca2+ sensors in neurotransmitter release.
Cell
; 147(3): 491-3, 2011 Oct 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-22036557
16.
Daam2 phosphorylation by CK2α negatively regulates Wnt activity during white matter development and injury.
Proc Natl Acad Sci U S A
; 120(35): e2304112120, 2023 08 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-37607236
17.
The fly homolog of SUPT16H, a gene associated with neurodevelopmental disorders, is required in a cell-autonomous fashion for cell survival.
Hum Mol Genet
; 32(6): 984-997, 2023 03 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36255738
18.
'Fly-ing' from rare to common neurodegenerative disease mechanisms.
Trends Genet
; 38(9): 972-984, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35484057
19.
The recurrent de novo c.2011C>T missense variant in MTSS2 causes syndromic intellectual disability.
Am J Hum Genet
; 109(10): 1923-1931, 2022 10 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36067766
20.
De novo variants in FRMD5 are associated with developmental delay, intellectual disability, ataxia, and abnormalities of eye movement.
Am J Hum Genet
; 109(10): 1932-1943, 2022 10 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36206744