Detalhe da pesquisa
1.
Cell-Extrinsic MHC Class I Molecule Engagement Augments Human NK Cell Education Programmed by Cell-Intrinsic MHC Class I.
Immunity
; 45(2): 280-91, 2016 08 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-27496730
2.
ZFHX3 variants cause childhood partial epilepsy and infantile spasms with favourable outcomes.
J Med Genet
; 2024 Mar 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-38508705
3.
CCDC88C variants are associated with focal epilepsy and genotype-phenotype correlation.
Clin Genet
; 105(4): 397-405, 2024 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-38173219
4.
Variants in BSN gene associated with epilepsy with favourable outcome.
J Med Genet
; 60(8): 776-783, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-36600631
5.
[Research progress on Rhododendron molle in treatment of rheumatoid arthritis].
Zhongguo Zhong Yao Za Zhi
; 48(21): 5690-5700, 2023 Nov.
Artigo
em Chinês
| MEDLINE | ID: mdl-38114165
6.
Optimization of in silico tools for predicting genetic variants: individualizing for genes with molecular sub-regional stratification.
Brief Bioinform
; 21(5): 1776-1786, 2020 09 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-31686106
7.
TMEM151A Variants Cause Paroxysmal Kinesigenic Dyskinesia: A Large-Sample Study.
Mov Disord
; 37(3): 545-552, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34820915
8.
UNC13B variants associated with partial epilepsy with favourable outcome.
Brain
; 144(10): 3050-3060, 2021 11 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-33876820
9.
[Relationship between Blood Glucose and Lipid Levels and Intestinal Bifidobacteriumin Middle-Aged and Older Adults in Chengdu].
Sichuan Da Xue Xue Bao Yi Xue Ban
; 53(2): 297-302, 2022 Mar.
Artigo
em Chinês
| MEDLINE | ID: mdl-35332733
10.
CELSR1 variants are associated with partial epilepsy of childhood.
Am J Med Genet B Neuropsychiatr Genet
; 189(7-8): 247-256, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36453712
11.
Construction and Application of YOLOv3-Based Diatom Identification Model of Scanning Electron Microscope Images.
Fa Yi Xue Za Zhi
; 38(1): 46-52, 2022 Feb 25.
Artigo
em Inglês, Chinês
| MEDLINE | ID: mdl-35725703
12.
The Phenotypic and Genetic Spectrum of Paroxysmal Kinesigenic Dyskinesia in China.
Mov Disord
; 35(8): 1428-1437, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32392383
13.
The Effect of Auricular Acupressure on Sleep Disturbance Among Patients With Leukemia: A Feasibility Study.
Holist Nurs Pract
; 34(2): 103-112, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32049696
14.
Evaluating the pathogenic potential of genes with de novo variants in epileptic encephalopathies.
Genet Med
; 21(1): 17-27, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29895856
15.
Immunological features and functional analysis of anti-CFH autoantibodies in patients with atypical hemolytic uremic syndrome.
Pediatr Nephrol
; 34(2): 269-281, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30315407
16.
ARHGEF9 mutations in epileptic encephalopathy/intellectual disability: toward understanding the mechanism underlying phenotypic variation.
Neurogenetics
; 19(1): 9-16, 2018 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29130122
17.
Proline-rich transmembrane protein 2-negative paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 163 patients.
Mov Disord
; 33(3): 459-467, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29356177
18.
[An assessment of nutritional status in children on maintenance hemodialysis due to stage 5 chronic kidney disease].
Zhongguo Dang Dai Er Ke Za Zhi
; 20(3): 189-194, 2018 Mar.
Artigo
em Chinês
| MEDLINE | ID: mdl-29530117
19.
CS2164, a novel multi-target inhibitor against tumor angiogenesis, mitosis and chronic inflammation with anti-tumor potency.
Cancer Sci
; 108(3): 469-477, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-28004478
20.
The clinical and laboratory features of Chinese Han anti-factor H autoantibody-associated hemolytic uremic syndrome.
Pediatr Nephrol
; 32(5): 811-822, 2017 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28035470