Detalhe da pesquisa
1.
[Digital twin hospitals: transforming the future of healthcare].
Sheng Wu Yi Xue Gong Cheng Xue Za Zhi
; 41(2): 376-382, 2024 Apr 25.
Artigo
em Zh
| MEDLINE | ID: mdl-38686420
2.
Shotgun metagenomics reveals both taxonomic and tryptophan pathway differences of gut microbiota in major depressive disorder patients.
Psychol Med
; 51(1): 90-101, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31685046
3.
Shotgun metagenomics reveals an enrichment of potentially cross-reactive bacterial epitopes in ankylosing spondylitis patients, as well as the effects of TNFi therapy upon microbiome composition.
Ann Rheum Dis
; 79(1): 132-140, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31662318
4.
Frequent mutation of hypoxia-related genes in persistent pulmonary hypertension of the newborn.
Respir Res
; 21(1): 53, 2020 Feb 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-32054482
5.
Altered gut microbiota and mucosal immunity in patients with schizophrenia.
Brain Behav Immun
; 85: 120-127, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31255682
6.
Alteration of gut microbiota-associated epitopes in children with autism spectrum disorders.
Brain Behav Immun
; 75: 192-199, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30394313
7.
Comprehensive investigating of cytokine and receptor related genes variants in patients with chronic hepatitis B virus infection.
Cytokine
; 103: 10-14, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29287219
8.
High prevalence of serum folate receptor autoantibodies in children with autism spectrum disorders.
Biomarkers
; 23(7): 622-624, 2018 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-29578363
9.
A metagenome-wide association study of gut microbiota in type 2 diabetes.
Nature
; 490(7418): 55-60, 2012 Oct 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-23023125
10.
Whole genome sequencing identifies a novel ALMS1 gene mutation in two Chinese siblings with Alström syndrome.
BMC Med Genet
; 18(1): 75, 2017 07 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-28724398
11.
Upregulation of Circulating miR-195-3p in Heart Failure.
Cardiology
; 138(2): 107-114, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28618405
12.
Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing.
Am J Hum Genet
; 93(2): 249-63, 2013 Aug 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-23849776
13.
Analysis of the Repertoire Features of TCR Beta Chain CDR3 in Human by High-Throughput Sequencing.
Cell Physiol Biochem
; 39(2): 651-67, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27442436
14.
Abnormalities in Clostridioides and related metabolites before ACTH treatment may be associated with its efficacy in patients with infantile epileptic spasm syndrome.
CNS Neurosci Ther
; 30(1): e14398, 2024 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37553527
15.
Human-derived fecal microbiota transplantation alleviates social deficits of the BTBR mouse model of autism through a potential mechanism involving vitamin B6 metabolism.
mSystems
; : e0025724, 2024 May 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-38780265
16.
PCDHA9 as a candidate gene for amyotrophic lateral sclerosis.
Nat Commun
; 15(1): 2189, 2024 Mar 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-38467605
17.
High-throughput sequencing of autism spectrum disorders comes of age.
Genet Res (Camb)
; 95(4): 121-9, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24074369
18.
Whole-Exome Sequencing Revealing De Novo Heterozygous Variant OF KCNT1 in a Twin Discordant for Benign Epilepsy with Centrotemporal Spikes.
J Paediatr Child Health
; 54(6): 709-710, 2018 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-29870100
19.
Lower serum branched-chain amino acid catabolic intermediates are predictive signatures specific to patients with diabetic foot.
Nutr Res
; 119: 33-42, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37716292
20.
Comprehensive systematic review and meta-analysis of the association between common genetic variants and autism spectrum disorder.
Gene
; 887: 147723, 2023 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-37598788