Detalhe da pesquisa
1.
Large-scale analysis of Drosophila core promoter function using synthetic promoters.
Mol Syst Biol
; 18(2): e9816, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35156763
2.
Different Clinical Features of Pediatric Generalized Pustular Psoriasis in Patients with or without IL36RN Variants.
Dermatology
; 239(2): 217-226, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36577391
3.
Identification of discriminative neuroimaging markers for patients on hemodialysis with insomnia: a fractional amplitude of low frequency fluctuation-based machine learning analysis.
BMC Psychiatry
; 23(1): 9, 2023 01 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36600230
4.
Effects of home medication review on drug-related problems and health-related quality of life among community-dwelling older adults in China.
J Am Pharm Assoc (2003)
; 62(2): 481-486, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-34776338
5.
Exome sequencing as the first-tier test for pediatric respiratory diseases: A single-center study.
Hum Mutat
; 42(7): 891-900, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33942430
6.
Case Report : Li-Fraumeni Syndrome with Central Nervous System Tumors in Two Siblings.
BMC Pediatr
; 21(1): 588, 2021 12 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-34961499
7.
Duplications involving the long range HMX1 enhancer are associated with human isolated bilateral concha-type microtia.
J Transl Med
; 18(1): 244, 2020 06 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-32552830
8.
[Clinical practice guidelines for albinism].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 37(3): 252-257, 2020 Mar 10.
Artigo
em Chinês
| MEDLINE | ID: mdl-32128740
9.
Simpson-Golabi-Behmel syndrome with 46,XY disorders of sex development: A case report.
Am J Med Genet A
; 179(2): 285-289, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30667571
10.
Congenital hyperinsulinism in Chinese patients: 5-yr treatment outcome of 95 clinical cases with genetic analysis of 55 cases.
Pediatr Diabetes
; 17(3): 227-34, 2016 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25639667
11.
[Patterns of recurrence in patients with stage pT3N0M0 thoracic esophageal squamous cell carcinoma after two-field esophagectomy].
Zhonghua Zhong Liu Za Zhi
; 38(1): 48-54, 2016 Jan.
Artigo
em Chinês
| MEDLINE | ID: mdl-26796807
12.
[Therapeutic effects and mechanisms of Opuntia dillenii Haw on atherosclerosis of rats].
Yao Xue Xue Bao
; 50(4): 453-8, 2015 Apr.
Artigo
em Chinês
| MEDLINE | ID: mdl-26223127
13.
[Identification of three novel frameshift mutations in the RUNX2 gene in three sporadic Chinese cases with cleidocranial dysplasia].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 31(4): 415-9, 2014 Aug.
Artigo
em Chinês
| MEDLINE | ID: mdl-25119901
14.
Research on plasma modified fly ash denitration.
Sci Rep
; 14(1): 4390, 2024 Feb 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-38388827
15.
The first Chinese intellectual developmental disorder, autosomal recessive 57 patient with two novel MBOAT7 variants.
Mol Genet Genomic Med
; 12(2): e2391, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38407511
16.
Genetic screening reveals hotspot variants and prevalence rates of Hermansky-Pudlak syndrome in the Chinese population.
Clin Chim Acta
; 561: 119813, 2024 Jun 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-38876249
17.
Data mining and analysis of adverse event signals associated with teprotumumab using the Food and Drug Administration adverse event reporting system database.
Int J Clin Pharm
; 46(2): 471-479, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38245664
18.
HIF1α/ATF3 partake PGK1 K191/K192 succinylation by modulating P4HA1/succinate signaling in glioblastoma.
Neuro Oncol
; 2024 Mar 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38441561
19.
Mutations in PRRT2 result in paroxysmal dyskinesias with marked variability in clinical expression.
J Med Genet
; 49(2): 79-82, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-22209761
20.
Neonates are armed with deviated immune cell proportion and cytokine reduction but higher T cell proliferation potentiality.
Acta Biochim Biophys Sin (Shanghai)
; 50(9): 934-937, 2018 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30052714