Detalhe da pesquisa
1.
Programmable RNA-Guided RNA Effector Proteins Built from Human Parts.
Cell
; 178(1): 122-134.e12, 2019 06 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-31230714
2.
Identification of the regulatory circuit governing corneal epithelial fate determination and disease.
PLoS Biol
; 21(10): e3002336, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37856539
3.
Measuring thermodynamic preferences to form non-native conformations in nucleic acids using ultraviolet melting.
Proc Natl Acad Sci U S A
; 119(24): e2112496119, 2022 06 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-35671421
4.
Dysregulated mitochondrial and cytosolic tRNA m1A methylation in Alzheimer's disease.
Hum Mol Genet
; 31(10): 1673-1680, 2022 05 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-34897434
5.
Effects of enhanced recovery after surgery plus pulmonary rehabilitation on complications after video-assisted lung cancer surgery: a multicentre randomised controlled trial.
Thorax
; 78(6): 574-586, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35835552
6.
A high neutrophil-to-platelet ratio is associated with hematoma expansion in patients with spontaneous intracerebral hemorrhage: a retrospective study.
BMC Neurol
; 23(1): 27, 2023 Jan 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-36653741
7.
ANANSE: an enhancer network-based computational approach for predicting key transcription factors in cell fate determination.
Nucleic Acids Res
; 49(14): 7966-7985, 2021 08 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-34244796
8.
Evolution of a reverse transcriptase to map N1-methyladenosine in human messenger RNA.
Nat Methods
; 16(12): 1281-1288, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31548705
9.
Measuring healthy female nulliparous pubovisceral muscle from diffusion kurtosis imaging.
NMR Biomed
; 35(9): e4753, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35485163
10.
Single-cell RNA-seq identifies a reversible mesodermal activation in abnormally specified epithelia of p63 EEC syndrome.
Proc Natl Acad Sci U S A
; 116(35): 17361-17370, 2019 08 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-31413199
11.
Mutations in the Epithelial Cadherin-p120-Catenin Complex Cause Mendelian Non-Syndromic Cleft Lip with or without Cleft Palate.
Am J Hum Genet
; 102(6): 1143-1157, 2018 06 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29805042
12.
Terminal keratinocyte differentiation in vitro is associated with a stable DNA methylome.
Exp Dermatol
; 30(8): 1023-1032, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32681572
13.
An FEVR-associated mutation in ZNF408 alters the expression of genes involved in the development of vasculature.
Hum Mol Genet
; 27(20): 3519-3527, 2018 10 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29982478
14.
Duplicated Enhancer Region Increases Expression of CTSB and Segregates with Keratolytic Winter Erythema in South African and Norwegian Families.
Am J Hum Genet
; 100(5): 737-750, 2017 May 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-28457472
15.
Why are Hoogsteen base pairs energetically disfavored in A-RNA compared to B-DNA?
Nucleic Acids Res
; 46(20): 11099-11114, 2018 11 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-30285154
16.
Increased H3K9 methylation and impaired expression of Protocadherins are associated with the cognitive dysfunctions of the Kleefstra syndrome.
Nucleic Acids Res
; 46(10): 4950-4965, 2018 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29554304
17.
Does a pulmonary rehabilitation based ERAS program (PREP) affect pulmonary complication incidence, pulmonary function and quality of life after lung cancer surgery? Study protocol for a multicenter randomized controlled trial.
BMC Pulm Med
; 20(1): 44, 2020 Feb 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-32070326
18.
ΔNp63-mediated regulation of hyaluronic acid metabolism and signaling supports HNSCC tumorigenesis.
Proc Natl Acad Sci U S A
; 114(50): 13254-13259, 2017 12 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-29162693
19.
p63 exerts spatio-temporal control of palatal epithelial cell fate to prevent cleft palate.
PLoS Genet
; 13(6): e1006828, 2017 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-28604778
20.
Functional convergence of histone methyltransferases EHMT1 and KMT2C involved in intellectual disability and autism spectrum disorder.
PLoS Genet
; 13(10): e1006864, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-29069077