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 *

219 related articles for article (PubMed ID: 25153580)

  • 41. 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]  

  • 42. High frequency of mutations in 'dyshormonogenesis genes' in severe congenital hypothyroidism.
    Makretskaya N; Bezlepkina O; Kolodkina A; Kiyaev A; Vasilyev EV; Petrov V; Kalinenkova S; Malievsky O; Dedov II; Tiulpakov A
    PLoS One; 2018; 13(9):e0204323. PubMed ID: 30240412
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Genetics of normal and abnormal thyroid development in humans.
    Szinnai G
    Best Pract Res Clin Endocrinol Metab; 2014 Mar; 28(2):133-50. PubMed ID: 24629857
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Biochemical, radiological, and genetic characterization of congenital hypothyroidism in Abu Dhabi, United Arab Emirates.
    Deeb A; Elkadry I; Attia S; Al Suwaidi H; Obaid L; Schoenmakers NA
    J Pediatr Endocrinol Metab; 2016 Jul; 29(7):801-6. PubMed ID: 27060741
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Implementation of a congenital hypothyroidism newborn screening procedure with mutation detection on genomic DNA extracted from blood spots: the experience of the Italian northeastern reference center.
    Camilot M; Teofoli F; Vincenzi M; Federici F; Perlini S; Tatò L
    Genet Test; 2007; 11(4):387-90. PubMed ID: 18294054
    [TBL] [Abstract][Full Text] [Related]  

  • 46.
    Wang F; Zang Y; Li M; Liu W; Wang Y; Yu X; Li H; Wang F; Liu S
    Front Endocrinol (Lausanne); 2020; 11():237. PubMed ID: 32425884
    [No Abstract]   [Full Text] [Related]  

  • 47. 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]  

  • 48. Thyroid developmental anomalies among first-degree relatives of children with thyroid dysgenesis and congenital hypothyroidism.
    Kumorowicz-Czoch M; Tylek-Lemanskaz D; Wyrobek L; Grodzicka T; Starzyk J
    J Pediatr Endocrinol Metab; 2012; 25(5-6):413-8. PubMed ID: 22876532
    [TBL] [Abstract][Full Text] [Related]  

  • 49. The mutation screening in candidate genes related to thyroid dysgenesis by targeted next-generation sequencing panel in the Chinese congenital hypothyroidism.
    Zhang RJ; Yang GL; Cheng F; Sun F; Fang Y; Zhang CX; Wang Z; Wu FY; Zhang JX; Zhao SX; Liang J; Song HD
    Clin Endocrinol (Oxf); 2022 Apr; 96(4):617-626. PubMed ID: 34374102
    [TBL] [Abstract][Full Text] [Related]  

  • 50. New genetics in congenital hypothyroidism.
    Stoupa A; Kariyawasam D; Muzza M; de Filippis T; Fugazzola L; Polak M; Persani L; Carré A
    Endocrine; 2021 Mar; 71(3):696-705. PubMed ID: 33650047
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Targeted Next-Generation Sequencing for Congenital Hypothyroidism With Positive Neonatal TSH Screening.
    Yamaguchi T; Nakamura A; Nakayama K; Hishimura N; Morikawa S; Ishizu K; Tajima T
    J Clin Endocrinol Metab; 2020 Aug; 105(8):. PubMed ID: 32459320
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Update of Thyroid Developmental Genes.
    Stoupa A; Kariyawasam D; Carré A; Polak M
    Endocrinol Metab Clin North Am; 2016 Jun; 45(2):243-54. PubMed ID: 27241962
    [TBL] [Abstract][Full Text] [Related]  

  • 53. An essential splice site mutation (c.317+1G>A) in the TSHR gene leads to severe thyroid dysgenesis.
    Cangul H; Saglam H; Saglam Y; Eren E; Dogan D; Kendall M; Tarim O; Maher ER; Barrett TG
    J Pediatr Endocrinol Metab; 2014 Sep; 27(9-10):1021-5. PubMed ID: 24859513
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Screening of 23 candidate genes by next-generation sequencing of patients with permanent congenital hypothyroidism: novel variants in TG, TSHR, DUOX2, FOXE1, and SLC26A7.
    Acar S; Gürsoy S; Arslan G; Nalbantoğlu Ö; Hazan F; Köprülü Ö; Özkaya B; Özkan B
    J Endocrinol Invest; 2022 Apr; 45(4):773-786. PubMed ID: 34780050
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Screening of HHEX Mutations in Chinese Children with Thyroid Dysgenesis.
    Liu S; Chai J; Zheng G; Li H; Lu D; Ge Y
    J Clin Res Pediatr Endocrinol; 2016 Mar; 8(1):21-5. PubMed ID: 26757609
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Nineteen years of national screening for congenital hypothyroidism: familial cases with thyroid dysgenesis suggest the involvement of genetic factors.
    Castanet M; Polak M; Bonaïti-Pellié C; Lyonnet S; Czernichow P; Léger J;
    J Clin Endocrinol Metab; 2001 May; 86(5):2009-14. PubMed ID: 11344199
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Linkage and mutational analysis of familial thyroid dysgenesis demonstrate genetic heterogeneity implicating novel genes.
    Castanet M; Sura-Trueba S; Chauty A; Carré A; de Roux N; Heath S; Léger J; Lyonnet S; Czernichow P; Polak M
    Eur J Hum Genet; 2005 Feb; 13(2):232-9. PubMed ID: 15547625
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Novel THRB mutation analysis in congenital hypothyroidism with thyroid dysgenesis.
    Zhou Z; Yang C; Lv F; Liu W; Yan S; Zang H; Li M; Wang F; Zang Y; Liu S
    J Cell Biochem; 2018 Nov; 119(11):9474-9482. PubMed ID: 30074255
    [TBL] [Abstract][Full Text] [Related]  

  • 59. PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis.
    Macchia PE; Lapi P; Krude H; Pirro MT; Missero C; Chiovato L; Souabni A; Baserga M; Tassi V; Pinchera A; Fenzi G; Grüters A; Busslinger M; Di Lauro R
    Nat Genet; 1998 May; 19(1):83-6. PubMed ID: 9590296
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Screening of PAX8 mutations in Chinese patients with congenital hypothyroidism.
    Liu SG; Zhang SS; Zhang LQ; Li WJ; Zhang AQ; Lu KN; Wang MJ; Yan SL; Ma X
    J Endocrinol Invest; 2012 Nov; 35(10):889-92. PubMed ID: 22293317
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.