Detalhe da pesquisa
1.
High triiodothyronine levels induce myocardial hypertrophy via BAFF overexpression.
J Cell Mol Med
; 26(16): 4453-4462, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35808902
2.
Paternal origin of Tungusic-speaking populations: Insights from the updated phylogenetic tree of Y-chromosome haplogroup C2a-M86.
Am J Hum Biol
; 33(2): e23462, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32657006
3.
Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis.
Hum Mol Genet
; 22(16): 3347-62, 2013 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-23612905
4.
Single-Cell RNA Sequencing Analysis of Steroidogenesis and Spermatogenesis Impairment in the Testis of db/db Mice.
Int J Endocrinol
; 2024: 8797972, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38817616
5.
Dense mapping of IL2RA shows no association with Graves' disease in Chinese Han population.
Clin Endocrinol (Oxf)
; 79(2): 267-74, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23170961
6.
[The association between vitamin D deficiency and diabetic nephropathy in type 2 diabetic patients].
Zhonghua Nei Ke Za Zhi
; 52(11): 970-4, 2013 Nov.
Artigo
em Chinês
| MEDLINE | ID: mdl-24439194
7.
Toxic effects of perfluorocaproic acid (PFHxA) on crucian carp (Carassius auratus) and the response of the intestinal microbial community.
Comp Biochem Physiol C Toxicol Pharmacol
; 271: 109683, 2023 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-37328133
8.
Functional study of an aberrant splicing variant of the human luteinizing hormone (LH) receptor.
Mol Hum Reprod
; 18(3): 129-35, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22002533
9.
Real-Time Flash Glucose Monitoring Had Better Effects on Daily Glycemic Control Compared With Retrospective Flash Glucose Monitoring in Patients With Type 2 Diabetes on Premix Insulin Therapy.
Front Endocrinol (Lausanne)
; 13: 832102, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35222287
10.
Functional study on a novel missense mutation of the transcription factor FOXL2 causes blepharophimosis-ptosis-epicanthus inversus syndrome (BPES).
Mutagenesis
; 26(2): 283-9, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21068205
11.
Effects of Dapagliflozin Adjunct to Insulin on Glycemic Variations in Patients with Newly Diagnosed Type 2 Diabetes: A Randomized, Controlled, Open-Labeled Trial.
Biomed Res Int
; 2021: 6618257, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34497852
12.
High Levels of Thyroid Hormone Impair Regulatory T Cell Function Via Reduced PD-1 Expression.
J Clin Endocrinol Metab
; 106(9): 2738-2753, 2021 08 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-33758937
13.
Identification of steroid biosynthetic defects in genotype-proven heterozygous individuals for 17alpha-hydroxylase/17,20-lyase deficiency.
Clin Endocrinol (Oxf)
; 72(3): 312-9, 2010 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-19508587
14.
GATA4 mutations in Chinese patients with congenital cardiac septal defects.
Pediatr Cardiol
; 31(1): 85-9, 2010 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-19915893
15.
Osteonecrosis in patients after severe acute respiratory syndrome (SARS): possible role of anticardiolipin antibodies.
J Clin Rheumatol
; 16(2): 61-3, 2010 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-20216125
16.
Intrathyroid injection of dexamethasone inhibits Th2 cells in Graves' disease.
Arch Endocrinol Metab
; 64(3): 243-250, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32555990
17.
Sexual Differences in response to Mid- or Low-Premixed Insulin Analogue in Patients with Type 2 Diabetes.
J Diabetes Res
; 2020: 8152640, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32090123
18.
A splice site mutation combined with a novel missense mutation of LHCGR cause male pseudohermaphroditism.
Hum Mutat
; 30(9): E855-65, 2009 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-19551906
19.
[Preliminary functional analysis of a novel mutation in GATA-4 gene in Chinese patients with congenital cardiac septal defects].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 26(3): 277-81, 2009 Jun.
Artigo
em Chinês
| MEDLINE | ID: mdl-19504439
20.
[Clinical and molecular genetic analysis for 7 patients from 5 pedigrees with 17a-hydroxylase/17, 20 lyase deficiency].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 26(3): 282-7, 2009 Jun.
Artigo
em Chinês
| MEDLINE | ID: mdl-19504440