These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

147 related articles for article (PubMed ID: 18379122)

  • 1. Thyrotropin receptor and thyroid transcription factor-1 genes variant in Chinese children with congenital hypothyroidism.
    Yuan ZF; Mao HQ; Luo YF; Wu YD; Shen Z; Zhao ZY
    Endocr J; 2008 May; 55(2):415-23. PubMed ID: 18379122
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Thyrotropin receptor gene inactivating mutation in Chinese children with congenital hypothyroidism].
    Yuan ZF; Luo YF; Wu YD; Shen Z; Zhao ZY
    Zhonghua Er Ke Za Zhi; 2007 Jul; 45(7):508-12. PubMed ID: 17953807
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The R450H mutation and D727E polymorphism of the thyrotropin receptor gene in a Chinese child with congenital hypothyroidism.
    Ma SG; Fang PH; Hong B; Yu WN
    J Pediatr Endocrinol Metab; 2010 Dec; 23(12):1339-44. PubMed ID: 21714469
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Next-generation sequencing of NKX2.1, FOXE1, PAX8, NKX2.5, and TSHR in 100 Chinese patients with congenital hypothyroidism and athyreosis.
    Wang F; Liu C; Jia X; Liu X; Xu Y; Yan S; Jia X; Huang Z; Liu S; Gu M
    Clin Chim Acta; 2017 Jul; 470():36-41. PubMed ID: 28455095
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. The genetic characteristics of congenital hypothyroidism in China by comprehensive screening of 21 candidate genes.
    Sun F; Zhang JX; Yang CY; Gao GQ; Zhu WB; Han B; Zhang LL; Wan YY; Ye XP; Ma YR; Zhang MM; Yang L; Zhang QY; Liu W; Guo CC; Chen G; Zhao SX; Song KY; Song HD
    Eur J Endocrinol; 2018 Jun; 178(6):623-633. PubMed ID: 29650690
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Pathogenic
    Shreder EV; Vadina TA; Solodovnikova EN; Zakharova VV; Degtyarev MV; Konyukhova MB; Sergeeva NV; Bezlepkina OB
    Probl Endokrinol (Mosk); 2023 Feb; 69(1):76-85. PubMed ID: 36842079
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. Targeted next-generation sequencing of thirteen causative genes in Chinese patients with congenital hypothyroidism.
    Long W; Lu G; Zhou W; Yang Y; Zhang B; Zhou H; Jiang L; Yu B
    Endocr J; 2018 Oct; 65(10):1019-1028. PubMed ID: 30022773
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Evaluation of the tshr gene reveals polymorphisms associated with typical symptoms in primary congenital hypothyroidism.
    Cortinhas Alves EA; Andrade RC; de Melo Amaral CE; Fernandes Caldato MC; Rocha Bastos AM; da Silva LC
    J Pediatr Endocrinol Metab; 2016 Jan; 29(1):71-6. PubMed ID: 26356361
    [TBL] [Abstract][Full Text] [Related]  

  • 14.
    Zhang HY; Wu FY; Li XS; Tu PH; Zhang CX; Yang RM; Cui RJ; Wu CY; Fang Y; Yang L; Song HD; Zhao SX
    Ann Lab Med; 2024 Jul; 44(4):343-353. PubMed ID: 38433572
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification of a novel pax8 gene sequence variant in four members of the same family: from congenital hypothyroidism with thyroid hypoplasia to mild subclinical hypothyroidism.
    Vincenzi M; Camilot M; Ferrarini E; Teofoli F; Venturi G; Gaudino R; Cavarzere P; De Marco G; Agretti P; Dimida A; Tonacchera M; Boner A; Antoniazzi F
    BMC Endocr Disord; 2014 Aug; 14():69. PubMed ID: 25146893
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. High frequency of D727E polymorphisms in exon 10 of the TSHR gene in Brazilian patients with congenital hypothyroidism.
    Alves EA; Cruz CM; Pimentel CP; Ribeiro RC; Santos AK; Caldato MC; Santana-da-silva LC
    J Pediatr Endocrinol Metab; 2010 Dec; 23(12):1321-8. PubMed ID: 21714466
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Congenital Hypothyroidism Patients With Thyroid Hormone Receptor Variants Are Not Rare: A Systematic Review.
    Da DZ; Wang Y; Wang M; Long Z; Wang Q; Liu J
    Inquiry; 2021; 58():469580211067943. PubMed ID: 34919466
    [TBL] [Abstract][Full Text] [Related]  

  • 19. R450H TSH receptor mutation in congenital hypothyroidism in Taiwanese children.
    Chang WC; Liao CY; Chen WC; Fan YC; Chiu SJ; Kuo HC; Woon PY; Chao MC
    Clin Chim Acta; 2012 Jun; 413(11-12):1004-7. PubMed ID: 22405933
    [TBL] [Abstract][Full Text] [Related]  

  • 20. TSH receptor and Gs(alpha) genetic analysis in children with Down's syndrome and subclinical hypothyroidism.
    Tonacchera M; Perri A; De Marco G; Agretti P; Montanelli L; Banco ME; Corrias A; Bellone J; Tosi MT; Vitti P; Martino E; Pinchera A; Chiovato L
    J Endocrinol Invest; 2003 Oct; 26(10):997-1000. PubMed ID: 14759073
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.