Detalhe da pesquisa
1.
Perturbations of genes essential for Müllerian duct and Wölffian duct development in Mayer-Rokitansky-Küster-Hauser syndrome.
Am J Hum Genet;
108(2): 337-345, 2021 02 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33434492
2.
Clover: tree structure-based efficient DNA clustering for DNA-based data storage.
Brief Bioinform;
23(5)2022 09 20.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35975958
3.
Rational Design of a Highly Sensitive Carboxylesterase Probe and Its Application in High-Throughput Screening for Uncovering Carboxylesterase Inhibitors.
J Org Chem;
2024 May 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38720168
4.
Factors associated with oral health service utilization among young people in southern China.
BMC Oral Health;
24(1): 289, 2024 Feb 28.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38418980
5.
JianPi-QingHua formula attenuates nonalcoholic fatty liver disease by regulating the AMPK/SIRT1/NF-κB pathway in high-fat-diet-fed C57BL/6 mice.
Pharm Biol;
61(1): 647-656, 2023 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37038833
6.
A genotype-first analysis in a cohort of Mullerian anomaly.
J Hum Genet;
67(6): 347-352, 2022 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35022528
7.
Diagnostic yield and clinical impact of exome sequencing in early-onset scoliosis (EOS).
J Med Genet;
58(1): 41-47, 2021 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32381727
8.
A hypothetical role for autophagy during the day/night rhythm-regulated melatonin synthesis in the rat pineal gland.
J Pineal Res;
71(1): e12742, 2021 Aug.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33960014
9.
Inflammatory cytokines as key players of apoptosis induced by environmental estrogens in the ovary.
Environ Res;
198: 111225, 2021 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33971129
10.
TBX6 missense variants expand the mutational spectrum in a non-Mendelian inheritance disease.
Hum Mutat;
41(1): 182-195, 2020 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31471994
11.
A novel COMP mutation in a Chinese family with multiple epiphyseal dysplasia.
BMC Med Genet;
21(1): 115, 2020 05 27.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32460719
12.
Identification of novel FBN1 variations implicated in congenital scoliosis.
J Hum Genet;
65(3): 221-230, 2020 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31827250
13.
Estrogen Receptors (ESRs) Mutations in Adolescent Idiopathic Scoliosis: A Cross-Sectional Study.
Med Sci Monit;
26: e921611, 2020 Mar 16.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32218412
14.
TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model.
Genet Med;
21(7): 1548-1558, 2019 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30636772
15.
Perturbations of BMP/TGF-ß and VEGF/VEGFR signalling pathways in non-syndromic sporadic brain arteriovenous malformations (BAVM).
J Med Genet;
55(10): 675-684, 2018 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30120215
16.
The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.
Hum Genet;
137(6-7): 553-567, 2018 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30019117
17.
Whole-exome sequencing reveals known and novel variants in a cohort of intracranial vertebral-basilar artery dissection (IVAD).
J Hum Genet;
63(11): 1119-1128, 2018 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30115950
18.
[A review of mixed gas detection system based on infrared spectroscopic technique].
Guang Pu Xue Yu Guang Pu Fen Xi;
34(10): 2851-7, 2014 Oct.
Artigo
em Zh
| MEDLINE
| ID: mdl-25739237
19.
Immune rebalancing at the maternal-fetal interface of maternal SARS-CoV-2 infection during early pregnancy.
Protein Cell;
15(6): 460-473, 2024 May 28.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38441496
20.
The Interaction Between Age and Risk Factors for Diabetes and Prediabetes: A Community-Based Cross-Sectional Study.
Diabetes Metab Syndr Obes;
16: 85-93, 2023.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36760587