Detalhe da pesquisa
1.
Upregulation of CALD1 predicted a poor prognosis for platinum-treated ovarian cancer and revealed it as a potential therapeutic resistance target.
BMC Genomics
; 25(1): 183, 2024 Feb 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-38365611
2.
Haplotype-specific MAPK3 expression in 16p11.2 deletion contributes to variable neurodevelopment.
Brain
; 146(8): 3347-3363, 2023 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36869767
3.
Phenotypic Spectrum of Trisomy 18 Mosaicism: a New Patient and Literature Review.
Clin Lab
; 69(3)2023 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36912299
4.
Genome sequencing demonstrates high diagnostic yield in children with undiagnosed global developmental delay/intellectual disability: A prospective study.
Hum Mutat
; 43(5): 568-581, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35143101
5.
Phase Separation of Epstein-Barr Virus EBNA2 and Its Coactivator EBNALP Controls Gene Expression.
J Virol
; 94(7)2020 03 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-31941785
6.
Eph receptors: the bridge linking host and virus.
Cell Mol Life Sci
; 77(12): 2355-2365, 2020 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-31893311
7.
[Analysis of genetic variants in four children with congenital hyperinsulinemia].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 38(7): 635-638, 2021 Jul 10.
Artigo
em Chinês
| MEDLINE | ID: mdl-34247366
8.
Epstein-Barr virus miR-BART3-3p promotes tumorigenesis by regulating the senescence pathway in gastric cancer.
J Biol Chem
; 294(13): 4854-4866, 2019 03 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-30674552
9.
A novel pathogenic frameshift variant unmasked by a large de novo deletion at 13q21.33-q31.1 in a Chinese patient with neuronal ceroid lipofuscinosis type 5.
BMC Med Genet
; 21(1): 100, 2020 05 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32393339
10.
Epstein-Barr Virus MicroRNA miR-BART5-3p Inhibits p53 Expression.
J Virol
; 92(23)2018 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30209170
11.
Genetic analyses of oculocutaneous albinism types 1 and 2 with four novel mutations.
BMC Med Genet
; 20(1): 106, 2019 06 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-31196117
12.
MicroRNAs Provide Feedback Regulation of Epithelial-Mesenchymal Transition Induced by Growth Factors.
J Cell Physiol
; 231(1): 120-9, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26032086
13.
Inflammation-induced S100A8 activates Id3 and promotes colorectal tumorigenesis.
Int J Cancer
; 137(12): 2803-14, 2015 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26135667
14.
Lactoferrin suppresses the Epstein-Barr virus-induced inflammatory response by interfering with pattern recognition of TLR2 and TLR9.
Lab Invest
; 94(11): 1188-99, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25068657
15.
A novel variant in NSUN2 causes intellectual disability in a Chinese family.
BMC Med Genomics
; 17(1): 95, 2024 Apr 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-38643142
16.
Phenotypic and genotypic characterization of NPRL3-related epilepsy: Two case reports and literature review.
Epilepsia Open
; 9(1): 33-40, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37902097
17.
Compound heterozygous WDR19 variants associated with nephronophthisis, Caroli disease, refractory epilepsy and congenital bilateral central blindness: Case report.
Heliyon
; 10(1): e23257, 2024 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38163131
18.
Clinical features and molecular genetic investigation of infantile-onset ascending hereditary spastic paralysis (IAHSP) in two Chinese siblings caused by a novel splice site ALS2 variation.
BMC Med Genomics
; 17(1): 44, 2024 Jan 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-38297306
19.
Single Cell Map of Human Azoospermia Testis Caused by Cyclophosphamide Chemotherapy.
Sci Data
; 11(1): 163, 2024 Feb 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38307907
20.
Clinical and genetic analysis of trichohepatoneurodevelopmental syndrome caused by a CCDC47 variant.
Heliyon
; 10(6): e27955, 2024 Mar 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-38524542