Detalhe da pesquisa
1.
Pathogenic variations in MAML2 and MAMLD1 contribute to congenital hypothyroidism due to dyshormonogenesis by regulating the Notch signalling pathway.
J Med Genet
; 60(9): 874-884, 2023 09.
Artigo
Inglês
| MEDLINE | ID: mdl-36898841
2.
Large-scale forward genetic screening of zebrafish affecting thyroid development.
Biochem Biophys Res Commun
; 642: 21-26, 2023 01 29.
Artigo
Inglês
| MEDLINE | ID: mdl-36543020
3.
Deficiency of the HGF/Met pathway leads to thyroid dysgenesis by impeding late thyroid expansion.
Nat Commun
; 15(1): 3165, 2024 Apr 11.
Artigo
Inglês
| MEDLINE | ID: mdl-38605010
4.
The isl2a transcription factor regulates pituitary development in zebrafish.
Front Endocrinol (Lausanne)
; 14: 920548, 2023.
Artigo
Inglês
| MEDLINE | ID: mdl-36824359
5.
Mutation Screening and Functional Study of SLC26A4 in Chinese Patients with Congenital Hypothyroidism
J Clin Res Pediatr Endocrinol
; 14(1): 46-55, 2022 03 03.
Artigo
Inglês
| MEDLINE | ID: mdl-34545167
6.
NUCB2 polymorphisms are associated with an increased risk for type 2 diabetes in the Chinese population.
Ann Transl Med
; 8(6): 290, 2020 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-32355734
7.
Candidate gene associations reveal sex-specific Graves' disease risk alleles among Chinese Han populations.
Mol Genet Genomic Med
; 8(7): e1249, 2020 07.
Artigo
Inglês
| MEDLINE | ID: mdl-32342657
8.
The TPO mutation screening and genotype-phenotype analysis in 230 Chinese patients with congenital hypothyroidism.
Mol Cell Endocrinol
; 506: 110761, 2020 04 15.
Artigo
Inglês
| MEDLINE | ID: mdl-32088313
9.
Mutation screening of the TSHR gene in 220 Chinese patients with congenital hypothyroidism.
Clin Chim Acta
; 497: 147-152, 2019 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-31356790
10.
Fine mapping of thyroglobulin gene identifies two independent risk loci for Graves' disease in Chinese Han population.
Ann Transl Med
; 7(18): 434, 2019 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-31700870