Detalhe da pesquisa
1.
Tet3 CXXC domain and dioxygenase activity cooperatively regulate key genes for Xenopus eye and neural development.
Cell
; 151(6): 1200-13, 2012 Dec 07.
Artigo
Inglês
| MEDLINE | ID: mdl-23217707
2.
Loss of 5-hydroxymethylcytosine is an epigenetic hallmark of melanoma.
Cell
; 150(6): 1135-46, 2012 Sep 14.
Artigo
Inglês
| MEDLINE | ID: mdl-22980977
3.
Glucose-regulated phosphorylation of TET2 by AMPK reveals a pathway linking diabetes to cancer.
Nature
; 559(7715): 637-641, 2018 07.
Artigo
Inglês
| MEDLINE | ID: mdl-30022161
4.
Sex-specific difference in phenotype of Kabuki syndrome type 2 patients: a matched case-control study.
BMC Pediatr
; 24(1): 133, 2024 Feb 19.
Artigo
Inglês
| MEDLINE | ID: mdl-38373926
5.
Mechanism of downward migration of quinolone antibiotics in antibiotics polluted natural soil replenishment water and its effect on soil microorganisms.
Environ Res
; 218: 115032, 2023 02 01.
Artigo
Inglês
| MEDLINE | ID: mdl-36502909
6.
ACCURACY OF NEW INTRAOCULAR LENS CALCULATION FORMULAE IN EYES UNDERGOING SILICONE OIL REMOVAL/PARS PLANA VITRECTOMY-CATARACT SURGERY.
Retina
; 43(9): 1579-1589, 2023 09 01.
Artigo
Inglês
| MEDLINE | ID: mdl-37307580
7.
Bedside nurses' antimicrobial stewardship practice scope and competencies in acute hospital settings: A scoping review.
J Clin Nurs
; 32(17-18): 6061-6088, 2023 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-37186422
8.
Novel compound heterozygous variant of TOE1 results in a mild type of pontocerebellar hypoplasia type 7: an expansion of the clinical phenotype.
Neurogenetics
; 23(1): 11-17, 2022 01.
Artigo
Inglês
| MEDLINE | ID: mdl-34716526
9.
Identification of QTLs and joint QTL segments of leaflet traits at different canopy layers in an interspecific RIL population of soybean.
Theor Appl Genet
; 135(12): 4261-4275, 2022 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-36203035
10.
Mass transfer characteristics and effect of flue gas used in microalgae culture.
Appl Microbiol Biotechnol
; 106(21): 7013-7025, 2022 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-36173453
11.
RETINAL AND CHOROIDAL BLOOD PERFUSION IN PATIENTS WITH BIETTI CRYSTALLINE DYSTROPHY.
Retina
; 41(11): 2351-2360, 2021 Nov 01.
Artigo
Inglês
| MEDLINE | ID: mdl-33840785
12.
Further delineation of primary B cell immunodeficiency caused by novel variants of the BLNK gene in two Chinese patients.
Clin Immunol
; 214: 108387, 2020 05.
Artigo
Inglês
| MEDLINE | ID: mdl-32194234
13.
The phenotypic spectrum of Kabuki syndrome in patients of Chinese descent: A case series.
Am J Med Genet A
; 182(4): 640-651, 2020 04.
Artigo
Inglês
| MEDLINE | ID: mdl-31883305
14.
Genome-wide regulation of 5hmC, 5mC, and gene expression by Tet1 hydroxylase in mouse embryonic stem cells.
Mol Cell
; 42(4): 451-64, 2011 May 20.
Artigo
Inglês
| MEDLINE | ID: mdl-21514197
15.
[Analysis of SATB2 gene mutation in a child with Glass syndrome].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 36(7): 712-715, 2019 Jul 10.
Artigo
Chinês
| MEDLINE | ID: mdl-31302918
16.
Proband-only medical exome sequencing as a cost-effective first-tier genetic diagnostic test for patients without prior molecular tests and clinical diagnosis in a developing country: the China experience.
Genet Med
; 20(9): 1045-1053, 2018 09.
Artigo
Inglês
| MEDLINE | ID: mdl-29095814
17.
Human LSD2/KDM1b/AOF1 regulates gene transcription by modulating intragenic H3K4me2 methylation.
Mol Cell
; 39(2): 222-33, 2010 Jul 30.
Artigo
Inglês
| MEDLINE | ID: mdl-20670891
18.
[Genetic analysis of two children patients affected with CHARGE syndrome].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 35(2): 244-247, 2018 Apr 10.
Artigo
Chinês
| MEDLINE | ID: mdl-29653002
19.
Biallelic mutations in GPD1 gene in a Chinese boy mainly presented with obesity, insulin resistance, fatty liver, and short stature.
Am J Med Genet A
; 173(12): 3189-3194, 2017 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-28944580
20.
Clinical and Molecular Characterization of Patients with Fructose 1,6-Bisphosphatase Deficiency.
Int J Mol Sci
; 18(4)2017 Apr 18.
Artigo
Inglês
| MEDLINE | ID: mdl-28420223