Detalhe da pesquisa
1.
Pediatric brain tumor cell lines exhibit miRNA-depleted, Y RNA-enriched extracellular vesicles.
J Neurooncol
; 156(2): 269-279, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34984645
2.
Natural underlying mtDNA heteroplasmy as a potential source of intra-person hiPSC variability.
EMBO J
; 35(18): 1979-90, 2016 09 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27436875
3.
Short non-coding RNA sequencing of glioblastoma extracellular vesicles.
J Neurooncol
; 146(2): 253-263, 2020 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-31912278
4.
Long-lived particles at the energy frontier: the MATHUSLA physics case.
Rep Prog Phys
; 82(11): 116201, 2019 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-31185458
5.
Recessive TAF1A mutations reveal ribosomopathy in siblings with end-stage pediatric dilated cardiomyopathy.
Hum Mol Genet
; 26(15): 2874-2881, 2017 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28472305
6.
Noncardiac genetic predisposition in sudden infant death syndrome.
Genet Med
; 21(3): 641-649, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30139991
7.
A Comprehensive Approach to Sequence-oriented IsomiR annotation (CASMIR): demonstration with IsomiR profiling in colorectal neoplasia.
BMC Genomics
; 19(1): 401, 2018 May 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-29801434
8.
Exome-Wide Rare Variant Analyses in Sudden Infant Death Syndrome.
J Pediatr
; 203: 423-428.e11, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30268395
9.
Enhancer of Zeste Homolog 2 Inhibition Stimulates Bone Formation and Mitigates Bone Loss Caused by Ovariectomy in Skeletally Mature Mice.
J Biol Chem
; 291(47): 24594-24606, 2016 Nov 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-27758858
10.
Homozygous/Compound Heterozygous Triadin Mutations Associated With Autosomal-Recessive Long-QT Syndrome and Pediatric Sudden Cardiac Arrest: Elucidation of the Triadin Knockout Syndrome.
Circulation
; 131(23): 2051-60, 2015 Jun 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-25922419
11.
TNNI3K mutation in familial syndrome of conduction system disease, atrial tachyarrhythmia and dilated cardiomyopathy.
Hum Mol Genet
; 23(21): 5793-804, 2014 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24925317
12.
De novo RRAGC mutation activates mTORC1 signaling in syndromic fetal dilated cardiomyopathy.
Hum Genet
; 135(8): 909-917, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27234373
13.
Compound heterozygous NOTCH1 mutations underlie impaired cardiogenesis in a patient with hypoplastic left heart syndrome.
Hum Genet
; 134(9): 1003-11, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-26164125
14.
PatternCNV: a versatile tool for detecting copy number changes from exome sequencing data.
Bioinformatics
; 30(18): 2678-80, 2014 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24876377
15.
Exome sequencing establishes diagnosis of Alström syndrome in an infant presenting with non-syndromic dilated cardiomyopathy.
Am J Med Genet A
; 167A(4): 886-90, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25706677
16.
Association between magnitude of the virus-specific plasmablast response and disease severity in dengue patients.
J Immunol
; 190(1): 80-7, 2013 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23203929
17.
Integrated analysis of genome-wide DNA methylation and gene expression profiles in molecular subtypes of breast cancer.
Nucleic Acids Res
; 41(18): 8464-74, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23887935
18.
HiChIP: a high-throughput pipeline for integrative analysis of ChIP-Seq data.
BMC Bioinformatics
; 15: 280, 2014 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25128017
19.
Histone deacetylase inhibition promotes osteoblast maturation by altering the histone H4 epigenome and reduces Akt phosphorylation.
J Biol Chem
; 288(40): 28783-91, 2013 Oct 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-23940046
20.
CAP-miRSeq: a comprehensive analysis pipeline for microRNA sequencing data.
BMC Genomics
; 15: 423, 2014 Jun 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-24894665