Detalhe da pesquisa
1.
iPSC-derived healthy human astrocytes selectively load miRNAs targeting neuronal genes into extracellular vesicles.
Mol Cell Neurosci
; 129: 103933, 2024 Apr 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-38663691
2.
Regulation, diversity and function of MECP2 exon and 3'UTR isoforms.
Hum Mol Genet
; 29(R1): R89-R99, 2020 09 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-32681172
3.
Identification of TIA1 mRNA targets during human neuronal development.
Mol Biol Rep
; 48(9): 6349-6361, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-34410578
4.
Transcriptional buffering and 3'UTR lengthening are shaped during human neurodevelopment by shifts in mRNA stability and microRNA load.
bioRxiv
; 2023 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36909614
5.
Buffering of transcription rate by mRNA half-life is a conserved feature of Rett syndrome models.
Nat Commun
; 14(1): 1896, 2023 04 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-37019888
6.
Wide spectrum of neuronal and network phenotypes in human stem cell-derived excitatory neurons with Rett syndrome-associated MECP2 mutations.
Transl Psychiatry
; 12(1): 450, 2022 10 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-36253345
7.
Quantification of mRNA ribosomal engagement in human neurons using parallel translating ribosome affinity purification (TRAP) and RNA sequencing.
STAR Protoc
; 2(1): 100229, 2021 03 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-33364619
8.
Alternative polyadenylation is a determinant of oncogenic Ras function.
Sci Adv
; 7(51): eabh0562, 2021 Dec 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-34919436
9.
Modeling neuronal consequences of autism-associated gene regulatory variants with human induced pluripotent stem cells.
Mol Autism
; 11(1): 33, 2020 05 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32398033
10.
Shifts in Ribosome Engagement Impact Key Gene Sets in Neurodevelopment and Ubiquitination in Rett Syndrome.
Cell Rep
; 30(12): 4179-4196.e11, 2020 03 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-32209477
11.
Synaptic Dysfunction in Human Neurons With Autism-Associated Deletions in PTCHD1-AS.
Biol Psychiatry
; 87(2): 139-149, 2020 01 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31540669
12.
SHANK2 mutations associated with autism spectrum disorder cause hyperconnectivity of human neurons.
Nat Neurosci
; 22(4): 556-564, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30911184