Associated Papers
Thyroid peroxidase gene variants and autoimmunity in subclinical hypothyroidism: molecular mechanisms and clinical implications.
Adam LN et al.
Molecular Biology Reports, 2025
A novel pathogenic DICER1 gene variant is associated with hereditary multinodular goiter in an Argentine family as evidenced by clinical, biochemical and molecular genetic analysis.
Targovnik HM et al.
Endocrine, 2025
Frequency of Mutations in the TPO Gene in Patients with Congenital Hypothyroidism Due to Dyshormonogenesis in Chile.
Arteaga-Jacobo MC et al.
Medicina (kaunas, Lithuania), 2024
High-resolution melt curve analysis: An approach for variant detection in the TPO gene of congenital hypothyroid patients in Bangladesh.
Begum MN et al.
Plos One, 2024
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 et al.
Biomed Research International, 2019
Association between TPO Asn698Thr and Thr725Pro gene polymorphisms and serum anti-TPO levels in Iranian patients with subclinical hypothyroidism.
Khoshi A et al.
Hormones (athens, Greece), 2017
Genetic analysis of thyroid peroxidase (TPO) gene in patients whose hypothyroidism was found in adulthood in West Bengal, India.
Balmiki N et al.
Endocrine Journal, 2014
Functional analysis of thyroid peroxidase gene mutations detected in patients with thyroid dyshormonogenesis.
Guria S et al.
International Journal of Endocrinology, 2014
A Novel, Homozygous c.1502T>G (p.Val501Gly) Mutation in the Thyroid peroxidase Gene in Malaysian Sisters with Congenital Hypothyroidism and Multinodular Goiter.
Lee CC et al.
International Journal of Endocrinology, 2013
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