196 related articles for article (PubMed ID: 29507327)
1. Generation and characterization of a hypothyroidism rat model with truncated thyroid stimulating hormone receptor.
Yang J; Yi N; Zhang J; He W; He D; Wu W; Xu S; Li F; Fan G; Zhu X; Xue Z; Zhou W
Sci Rep; 2018 Mar; 8(1):4004. PubMed ID: 29507327
[TBL] [Abstract][Full Text] [Related]
2. [The thyroid as a model for molecular mechanisms in genetic diseases].
Rivolta CM; Moya CM; Esperante SA; Gutnisky VJ; Varela V; Targovnik HM
Medicina (B Aires); 2005; 65(3):257-67. PubMed ID: 16042141
[TBL] [Abstract][Full Text] [Related]
3. Functional characterization of the novel sequence variant p.S304R in the hinge region of TSHR in a congenital hypothyroidism patients and analogy with other formerly known mutations of this gene portion.
Cerqueira TL; Carré A; Chevrier L; Szinnai G; Tron E; Léger J; Cabrol S; Queinnec C; De Roux N; Castanet M; Polak M; Ramos HE
J Pediatr Endocrinol Metab; 2015 Jul; 28(7-8):777-84. PubMed ID: 25153578
[TBL] [Abstract][Full Text] [Related]
4. A novel mutation in the thyrotropin (thyroid-stimulating hormone) receptor gene in a case of congenital hypothyroidism.
Jeziorowska A; Pniewska-Siark B; Brzeziańska E; Pastuszak-Lewandoska D; Lewiński A
Thyroid; 2006 Dec; 16(12):1303-9. PubMed ID: 17199441
[TBL] [Abstract][Full Text] [Related]
5. Molecular screening of the TSH receptor (TSHR) and thyroid peroxidase (TPO) genes in Korean patients with nonsyndromic congenital hypothyroidism.
Lee ST; Lee DH; Kim JY; Kwon MJ; Kim JW; Hong YH; Lee YW; Ki CS
Clin Endocrinol (Oxf); 2011 Nov; 75(5):715-21. PubMed ID: 21707688
[TBL] [Abstract][Full Text] [Related]
6. A family with congenital hypothyroidism caused by a combination of loss-of-function mutations in the thyrotropin receptor and adenylate cyclase-stimulating G alpha-protein subunit genes.
Lado-Abeal J; Castro-Piedras I; Palos-Paz F; Labarta-Aizpún JI; Albero-Gamboa R
Thyroid; 2011 Feb; 21(2):103-9. PubMed ID: 21186955
[TBL] [Abstract][Full Text] [Related]
7. Moderate doses of iodide in vivo inhibit cell proliferation and the expression of thyroperoxidase and Na+/I- symporter mRNAs in dog thyroid.
Uyttersprot N; Pelgrims N; Carrasco N; Gervy C; Maenhaut C; Dumont JE; Miot F
Mol Cell Endocrinol; 1997 Aug; 131(2):195-203. PubMed ID: 9296378
[TBL] [Abstract][Full Text] [Related]
8. Inactivation of a Frameshift TSH Receptor Variant Val711Phefs*18 is Due to Acquisition of a Hydrophobic Degron.
Sugisawa C; Ono M; Kashimada K; Hasegawa T; Narumi S
J Clin Endocrinol Metab; 2021 Jan; 106(1):e265-e272. PubMed ID: 33108452
[TBL] [Abstract][Full Text] [Related]
9. Defining thyrotropin-dependent and -independent steps of thyroid hormone synthesis by using thyrotropin receptor-null mice.
Marians RC; Ng L; Blair HC; Unger P; Graves PN; Davies TF
Proc Natl Acad Sci U S A; 2002 Nov; 99(24):15776-81. PubMed ID: 12432094
[TBL] [Abstract][Full Text] [Related]
10. Mutations of the human thyrotropin receptor gene causing thyroid hypoplasia and persistent congenital hypothyroidism.
Biebermann H; Schöneberg T; Krude H; Schultz G; Gudermann T; Grüters A
J Clin Endocrinol Metab; 1997 Oct; 82(10):3471-80. PubMed ID: 9329388
[TBL] [Abstract][Full Text] [Related]
11. Newborn screening and single nucleotide variation profiling of TSHR, TPO, TG and DUOX2 candidate genes for congenital hypothyroidism.
Kollati Y; Akella RRD; Naushad SM; Borkar D; Thalla M; Nagalingam S; Lingappa L; Patel RK; Reddy GB; Dirisala VR
Mol Biol Rep; 2020 Oct; 47(10):7467-7475. PubMed ID: 32930933
[TBL] [Abstract][Full Text] [Related]
12. Thyroid hormone deprival and TSH/TSHR signaling deficiency lead to central hypothyroidism-associated intestinal dysplasia.
Peng L; Luan S; Shen X; Zhan H; Ge Y; Liang Y; Wang J; Xu Y; Wu S; Zhong X; Zhang H; Gao L; Zhao J; He Z
Life Sci; 2024 May; 345():122577. PubMed ID: 38521387
[TBL] [Abstract][Full Text] [Related]
13. Long-term outcome of loss-of-function mutations in thyrotropin receptor gene.
Tenenbaum-Rakover Y; Almashanu S; Hess O; Admoni O; Hag-Dahood Mahameed A; Schwartz N; Allon-Shalev S; Bercovich D; Refetoff S
Thyroid; 2015 Mar; 25(3):292-9. PubMed ID: 25557138
[TBL] [Abstract][Full Text] [Related]
14. Congenital hypothyroidism and apparent athyreosis with compound heterozygosity or compensated hypothyroidism with probable hemizygosity for inactivating mutations of the TSH receptor.
Park SM; Clifton-Bligh RJ; Betts P; Chatterjee VK
Clin Endocrinol (Oxf); 2004 Feb; 60(2):220-7. PubMed ID: 14725684
[TBL] [Abstract][Full Text] [Related]
15. Next-generation sequencing analysis of TSHR in 384 Chinese subclinical congenital hypothyroidism (CH) and CH patients.
Fu C; Wang J; Luo S; Yang Q; Li Q; Zheng H; Hu X; Su J; Zhang S; Chen R; Luo J; Zhang Y; Shen Y; Wei H; Meng D; Gui B; Zeng Z; Fan X; Chen S
Clin Chim Acta; 2016 Nov; 462():127-132. PubMed ID: 27637299
[TBL] [Abstract][Full Text] [Related]
16. Mild congenital primary hypothyroidism in a Turkish family caused by a homozygous missense thyrotropin receptor (TSHR) gene mutation (A593 V).
Fricke-Otto S; Pfarr N; Mühlenberg R; Pohlenz J
Exp Clin Endocrinol Diabetes; 2005 Dec; 113(10):582-5. PubMed ID: 16320156
[TBL] [Abstract][Full Text] [Related]
17. Double variants in TSHR and DUOX2 in a patient with hypothyroidism: case report.
Sasivari Z; Szinnai G; Seebauer B; Konrad D; Lang-Muritano M
J Pediatr Endocrinol Metab; 2019 Nov; 32(11):1299-1303. PubMed ID: 31541602
[TBL] [Abstract][Full Text] [Related]
18. Mutation screening of the TSHR gene in 220 Chinese patients with congenital hypothyroidism.
Fang Y; Sun F; Zhang RJ; Zhang CR; Yan CY; Zhou Z; Zhang QY; Li L; Ying YX; Zhao SX; Liang J; Song HD
Clin Chim Acta; 2019 Oct; 497():147-152. PubMed ID: 31356790
[TBL] [Abstract][Full Text] [Related]
19. Thyrotropin and Insulin-Like Growth Factor 1 Receptor Crosstalk Upregulates Sodium-Iodide Symporter Expression in Primary Cultures of Human Thyrocytes.
Morgan SJ; Neumann S; Marcus-Samuels B; Gershengorn MC
Thyroid; 2016 Dec; 26(12):1794-1803. PubMed ID: 27638195
[TBL] [Abstract][Full Text] [Related]
20. Duox expression and related H2O2 measurement in mouse thyroid: onset in embryonic development and regulation by TSH in adult.
Milenkovic M; De Deken X; Jin L; De Felice M; Di Lauro R; Dumont JE; Corvilain B; Miot F
J Endocrinol; 2007 Mar; 192(3):615-26. PubMed ID: 17332529
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
