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1.
Upregulation of GBP1 in thyroid primordium is required for developmental thyroid morphogenesis.
Genet Med
; 23(10): 1944-1951, 2021 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-34194003
2.
Correlation of DUOX2 residual enzymatic activity with phenotype in congenital hypothyroidism caused by biallelic DUOX2 defects.
Clin Genet
; 100(6): 713-721, 2021 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-34564849
3.
A five-gene panel refines differential diagnosis of thyroid nodules.
J Clin Lab Anal
; 35(9): e23920, 2021 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-34318534
4.
A dense mapping study of six European AITD susceptibility regions in a large Chinese Han Cohort of Graves' disease.
Clin Endocrinol (Oxf)
; 89(6): 840-848, 2018 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-30176063
5.
Genome-wide association study identifies a novel susceptibility gene for serum TSH levels in Chinese populations.
Hum Mol Genet
; 23(20): 5505-17, 2014 Oct 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-24852370
6.
Identification of BACH2 as a susceptibility gene for Graves' disease in the Chinese Han population based on a three-stage genome-wide association study.
Hum Genet
; 133(5): 661-71, 2014 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-24346624
7.
Hyperglycemia magnifies bupivacaine-induced cell apoptosis triggered by mitochondria dysfunction and endoplasmic reticulum stress.
J Neurosci Res
; 91(6): 786-98, 2013 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-23553889
8.
Spleen stiffness and splenoportal venous flow: assessment before and after transjugular intrahepatic portosystemic shunt placement.
J Ultrasound Med
; 32(2): 221-8, 2013 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-23341376
9.
Comparison and development of machine learning for thalidomide-induced peripheral neuropathy prediction of refractory Crohn's disease in Chinese population.
World J Gastroenterol
; 29(24): 3855-3870, 2023 Jun 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-37426324
10.
The isl2a transcription factor regulates pituitary development in zebrafish.
Front Endocrinol (Lausanne)
; 14: 920548, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-36824359
11.
Liver and spleen stiffness measured by acoustic radiation force impulse elastography for noninvasive assessment of liver fibrosis and esophageal varices in patients with chronic hepatitis B.
J Ultrasound Med
; 31(8): 1245-53, 2012 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-22837289
12.
Lymphocyte infiltration and thyrocyte destruction are driven by stromal and immune cell components in Hashimoto's thyroiditis.
Nat Commun
; 13(1): 775, 2022 02 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-35140214
13.
Detection of BRAF V600E in Fine-Needle Aspiration Samples of Thyroid Nodules by Droplet Digital PCR.
Int J Endocrinol
; 2022: 6243696, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-35392249
14.
Three-dimensional microscopy and image fusion reconstruction analysis of the thyroid gland during morphogenesis.
FEBS Open Bio
; 11(5): 1417-1427, 2021 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-33735512
15.
Compelling Evidence Linking CD40 Gene With Graves' Disease in the Chinese Han Population.
Front Endocrinol (Lausanne)
; 12: 759597, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34867801
16.
Genetic Study in a Large Cohort Supported Different Pathogenesis of Graves' Disease and Hashimoto's Hypothyroidism.
J Clin Endocrinol Metab
; 105(7)2020 07 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-32246145
17.
Uterus globulin associated protein 1 (UGRP1) is a potential marker of progression of Graves' disease into hypothyroidism.
Mol Cell Endocrinol
; 494: 110492, 2019 08 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-31255731
18.
A Weighted Genetic Risk Score Using Known Susceptibility Variants to Predict Graves Disease Risk.
J Clin Endocrinol Metab
; 104(6): 2121-2130, 2019 06 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-30649410
19.
Assessment of Molecular Subtypes in Thyrotoxic Periodic Paralysis and Graves Disease Among Chinese Han Adults: A Population-Based Genome-Wide Association Study.
JAMA Netw Open
; 2(5): e193348, 2019 05 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-31050781
20.
The genetic characteristics of congenital hypothyroidism in China by comprehensive screening of 21 candidate genes.
Eur J Endocrinol
; 178(6): 623-633, 2018 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-29650690