Detalhe da pesquisa
1.
Regulation of alternative polyadenylation by the C2H2-zinc-finger protein Sp1.
Mol Cell
; 82(17): 3135-3150.e9, 2022 09 01.
Artigo
Inglês
| MEDLINE | ID: mdl-35914531
2.
Efficient and Accurate Quantitative Profiling of Alternative Splicing Patterns of Any Complexity on a Laptop.
Mol Cell
; 72(1): 187-200.e6, 2018 10 04.
Artigo
Inglês
| MEDLINE | ID: mdl-30220560
3.
Identifying human pre-mRNA cleavage and polyadenylation factors by genome-wide CRISPR screens using a dual fluorescence readthrough reporter.
Nucleic Acids Res
; 52(8): 4483-4501, 2024 May 08.
Artigo
Inglês
| MEDLINE | ID: mdl-38587191
4.
Multilayered Control of Alternative Splicing Regulatory Networks by Transcription Factors.
Mol Cell
; 65(3): 539-553.e7, 2017 Feb 02.
Artigo
Inglês
| MEDLINE | ID: mdl-28157508
5.
An atlas of alternative splicing profiles and functional associations reveals new regulatory programs and genes that simultaneously express multiple major isoforms.
Genome Res
; 27(10): 1759-1768, 2017 10.
Artigo
Inglês
| MEDLINE | ID: mdl-28855263
6.
RNAcompete methodology and application to determine sequence preferences of unconventional RNA-binding proteins.
Methods
; 118-119: 3-15, 2017 04 15.
Artigo
Inglês
| MEDLINE | ID: mdl-27956239
7.
RNAcompete-S: Combined RNA sequence/structure preferences for RNA binding proteins derived from a single-step in vitro selection.
Methods
; 126: 18-28, 2017 08 15.
Artigo
Inglês
| MEDLINE | ID: mdl-28651966
8.
RNA sequencing reveals the role of splicing polymorphisms in regulating human gene expression.
Genome Res
; 21(4): 545-54, 2011 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-21173033
9.
ARHGDIA: a novel gene implicated in nephrotic syndrome.
J Med Genet
; 50(5): 330-8, 2013 May.
Artigo
Inglês
| MEDLINE | ID: mdl-23434736
10.
Novel mutations in SCO1 as a cause of fatal infantile encephalopathy and lactic acidosis.
Hum Mutat
; 34(10): 1366-70, 2013 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-23878101
11.
Mutations in SCARF2 are responsible for Van Den Ende-Gupta syndrome.
Am J Hum Genet
; 87(4): 553-9, 2010 Oct 08.
Artigo
Inglês
| MEDLINE | ID: mdl-20887961
12.
Combined malonic and methylmalonic aciduria: exome sequencing reveals mutations in the ACSF3 gene in patients with a non-classic phenotype.
J Med Genet
; 48(9): 602-5, 2011 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-21785126
13.
Differential contribution of transcriptomic regulatory layers in the definition of neuronal identity.
Nat Commun
; 12(1): 335, 2021 01 12.
Artigo
Inglês
| MEDLINE | ID: mdl-33436550
14.
Unexpected allelic heterogeneity and spectrum of mutations in Fowler syndrome revealed by next-generation exome sequencing.
Hum Mutat
; 31(8): 918-23, 2010 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-20518025
15.
Genetic interaction mapping and exon-resolution functional genomics with a hybrid Cas9-Cas12a platform.
Nat Biotechnol
; 38(5): 638-648, 2020 05.
Artigo
Inglês
| MEDLINE | ID: mdl-32249828
16.
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
Inglês
| MEDLINE | ID: mdl-32209477
17.
QAPA: a new method for the systematic analysis of alternative polyadenylation from RNA-seq data.
Genome Biol
; 19(1): 45, 2018 03 28.
Artigo
Inglês
| MEDLINE | ID: mdl-29592814
18.
Comparative genomics of elastin: Sequence analysis of a highly repetitive protein.
Matrix Biol
; 26(7): 524-40, 2007 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-17628459
19.
Oncogenic Activation of the RNA Binding Protein NELFE and MYC Signaling in Hepatocellular Carcinoma.
Cancer Cell
; 32(1): 101-114.e8, 2017 07 10.
Artigo
Inglês
| MEDLINE | ID: mdl-28697339
20.
MECP2 Is Post-transcriptionally Regulated during Human Neurodevelopment by Combinatorial Action of RNA-Binding Proteins and miRNAs.
Cell Rep
; 17(3): 720-734, 2016 10 11.
Artigo
Inglês
| MEDLINE | ID: mdl-27732849