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.
The mutation screening in candidate genes related to thyroid dysgenesis by targeted next-generation sequencing panel in the Chinese congenital hypothyroidism.
Clin Endocrinol (Oxf)
; 96(4): 617-626, 2022 04.
Artigo
Inglês
| MEDLINE | ID: mdl-34374102
4.
Upregulation of GBP1 in thyroid primordium is required for developmental thyroid morphogenesis.
Genet Med
; 23(10): 1944-1951, 2021 10.
Artigo
Inglês
| MEDLINE | ID: mdl-34194003
5.
Involvement of LeMDR, an ATP-binding cassette protein gene, in shikonin transport and biosynthesis in Lithospermum erythrorhizon.
BMC Plant Biol
; 17(1): 198, 2017 Nov 13.
Artigo
Inglês
| MEDLINE | ID: mdl-29132307
6.
A Classic Near-Infrared Probe Indocyanine Green for Detecting Singlet Oxygen.
Int J Mol Sci
; 17(2): 219, 2016 Feb 06.
Artigo
Inglês
| MEDLINE | ID: mdl-26861313
7.
Identification and functional analysis of the cathepsin D gene promoter of Bombyx mori.
Mol Biol Rep
; 41(3): 1623-30, 2014 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-24398552
8.
TSHR Variant Screening and Phenotype Analysis in 367 Chinese Patients With Congenital Hypothyroidism.
Ann Lab Med
; 44(4): 343-353, 2024 Jul 01.
Artigo
Inglês
| MEDLINE | ID: mdl-38433572
9.
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
10.
Identification of Eukaryotic Translation Initiation Factor 4B as a Novel Candidate Gene for Congenital Hypothyroidism.
J Clin Endocrinol Metab
; 2024 Apr 24.
Artigo
Inglês
| MEDLINE | ID: mdl-38654471
11.
Contactin 6, A Novel Causative Gene for Congenital Hypothyroidism, Mediates Thyroid Hormone Biosynthesis Through Notch Signaling.
Thyroid
; 34(3): 324-335, 2024 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-38183624
12.
The isl2a transcription factor regulates pituitary development in zebrafish.
Front Endocrinol (Lausanne)
; 14: 920548, 2023.
Artigo
Inglês
| MEDLINE | ID: mdl-36824359
13.
Myeloid cells interact with a subset of thyrocytes to promote their migration and follicle formation through NF-κB.
Nat Commun
; 14(1): 8082, 2023 Dec 06.
Artigo
Inglês
| MEDLINE | ID: mdl-38057310
14.
Genetic screening and functional analysis of TPO variants in Chinese patients with congenital hypothyroidism.
Horm Res Paediatr
; 2023 Sep 13.
Artigo
Inglês
| MEDLINE | ID: mdl-37703865
15.
Identification of ecdysone response elements (EcREs) in the Bombyx mori cathepsin D promoter.
Biochem Biophys Res Commun
; 425(1): 113-8, 2012 Aug 17.
Artigo
Inglês
| MEDLINE | ID: mdl-22828514
16.
Recent progress in epigenetics of obesity.
Diabetol Metab Syndr
; 14(1): 171, 2022 Nov 17.
Artigo
Inglês
| MEDLINE | ID: mdl-36397166
17.
T Cell Receptor Repertoire Analysis Reveals Signatures of T Cell Responses to Human Mycobacterium tuberculosis.
Front Microbiol
; 13: 829694, 2022.
Artigo
Inglês
| MEDLINE | ID: mdl-35197957
18.
CCL5-Secreting Virtual Memory CD8+ T Cells Inversely Associate With Viral Reservoir Size in HIV-1-Infected Individuals on Antiretroviral Therapy.
Front Immunol
; 13: 897569, 2022.
Artigo
Inglês
| MEDLINE | ID: mdl-35720272
19.
Single-cell analysis of diverse immune phenotypes in malignant pleural effusion.
Nat Commun
; 12(1): 6690, 2021 11 18.
Artigo
Inglês
| MEDLINE | ID: mdl-34795282
20.
Genetic Manipulation on Zebrafish duox Recapitulate the Clinical Manifestations of Congenital Hypothyroidism.
Endocrinology
; 162(8)2021 08 01.
Artigo
Inglês
| MEDLINE | ID: mdl-34019632