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Journal Abstract Search

160 related items for PubMed ID: 25328990

  • 1. A truncating TPO mutation (Y55X) in patients with hypothyroidism and total iodide organification defect.
    Cangul H, Darendeliler F, Saglam Y, Kucukemre B, Kendall M, Boelaert K, Barrett TG, Maher ER.
    Endocr Res; 2015; 40(3):146-50. PubMed ID: 25328990
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  • 2. One Base Deletion (c.2422delT) in the TPO Gene Causes Severe Congenital Hypothyroidism.
    Cangül H, Doğan M, Sağlam Y, Kendall M, Boelaert K, Barrett TG, Maher ER.
    J Clin Res Pediatr Endocrinol; 2014 Sep; 6(3):169-73. PubMed ID: 25241611
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  • 9. Screening and Functional Analysis of TPO Gene Mutations in a Cohort of Chinese Patients With Congenital Hypothyroidism.
    Wang H, Wang W, Chen X, Shi H, Shi Y, Ding G.
    Front Endocrinol (Lausanne); 2021 Sep; 12():774941. PubMed ID: 35002963
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  • 10. Analysis of TPO gene in Turkish children with iodide organification defect: identification of a novel mutation.
    Turkkahraman D, Alper OM, Pehlivanoglu S, Aydin F, Yildiz A, Luleci G, Akcurin S, Bircan I.
    Endocrine; 2010 Feb; 37(1):124-8. PubMed ID: 20963560
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  • 12. Case Report: Functional Analysis and Neuropsychological Evaluation of Dyshormonogenetic Fetal Goiter in Siblings Caused by Novel Compound Hyterozygous TPO Gene Mutations.
    Rodrigues TMB, Silva MMDC, Freitas MM, Duarte ZMC, Frutuoso VS, Rodrigues MT, Rubio IGS.
    Front Endocrinol (Lausanne); 2021 Feb; 12():671659. PubMed ID: 34220711
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  • 13. Novel genetic variants in the TPO gene cause congenital hypothyroidism.
    Ma SG, Qiu YL, Zhu H, Liu H, Li Q, Ji CM.
    Scand J Clin Lab Invest; 2015 Feb; 75(8):633-7. PubMed ID: 26174974
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  • 15. Frequency of Mutations in the TPO Gene in Patients with Congenital Hypothyroidism Due to Dyshormonogenesis in Chile.
    Arteaga-Jacobo MC, Roco-Videla Á, Villota Arcos C, González-Hormazábal P, Gonzalo-Castro V, Pérez-Flores MV.
    Medicina (Kaunas); 2024 Jul 16; 60(7):. PubMed ID: 39064575
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  • 19. The Missense Alteration A5T of the Thyroid Peroxidase Gene is Pathogenic and Associated with Mild Congenital Hypothyroidism.
    Cangül H, Demir K, Babayiğit HÖ, Abacı A, Böber E.
    J Clin Res Pediatr Endocrinol; 2015 Sep 16; 7(3):238-41. PubMed ID: 26831560
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  • 20. Mutation Spectrum in TPO Gene of Bangladeshi Patients with Thyroid Dyshormonogenesis and Analysis of the Effects of Different Mutations on the Structural Features and Functions of TPO Protein through In Silico Approach.
    Begum MN, Islam MT, Hossain SR, Bhuyan GS, Halim MA, Shahriar I, Sarker SK, Haque S, Konika TK, Islam MS, Rahat A, Qadri SK, Sultana R, Begum S, Sultana S, Saha N, Hasan M, Hasanat MA, Banu H, Shekhar HU, Chowdhury EK, Sajib AA, Islam ABMMK, Qadri SS, Qadri F, Akhteruzzaman S, Mannoor K.
    Biomed Res Int; 2019 Sep 16; 2019():9218903. PubMed ID: 30915365
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