Associated Papers
Molecular analysis of the evolutionary history of endometrial and ovarian carcinoma in Lynch syndrome.
Kauppinen AK et al.
International Journal of Cancer, 2025
Thyroid Peroxidase and its Gene Variants as Diagnostic Markers in Subclinical Hypothyroidism: Evidence from a Duhok Case-Control Study.
Adam LN et al.
Biochemical Genetics, 2025
Thyroid peroxidase gene variants and autoimmunity in subclinical hypothyroidism: molecular mechanisms and clinical implications.
Adam LN et al.
Molecular Biology Reports, 2025
Functional Domain Mapping of TPO: Insights from Six Variants in Sudanese Kindreds with Congenital Hypothyroidism.
Islam MS et al.
The Journal of Clinical Endocrinology and Metabolism, 2025
Exon 11 Polymorphism (rs1126797) in the Thyroid Peroxidase (TPO) Gene Among Caucasian Polish Patients with Autoimmune Thyroiditis: A Short Communication.
Lacka K et al.
International Journal of Molecular Sciences, 2025
Altered carnitine-acylcarnitine profiles in levothyroxine-treated congenital hypothyroid patients with fatigue: An LC-MS/MS-based study from Bangladesh.
Begum MN et al.
Plos One, 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
Novel NARS2 variants in a patient with early-onset status epilepticus: case study and literature review.
Yang N et al.
Bmc Pediatrics, 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
Longitudinal Associations Between TPO Gene Variants and Thyroid Peroxidase Antibody Seroconversion in a Population-Based Study: Tehran Thyroid Study.
Ghanooni AH et al.
Genetic Testing and Molecular Biomarkers, 2023
Investigation of the impact of nonsynonymous mutations on thyroid peroxidase dimer.
Begum MN et al.
Plos One, 2023
Molecular insights into the role of genetic determinants of congenital hypothyroidism.
Kollati Y et al.
Genomics & Informatics, 2021
Graves' disease: introducing new genetic and epigenetic contributors.
Razmara E et al.
Journal of Molecular Endocrinology, 2021
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
A Comprehensive Meta-analysis of Case-Control Association Studies to Evaluate Polymorphisms Associated with the Risk of Differentiated Thyroid Carcinoma.
Figlioli G et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology, 2016
Serum Anti-TPO and TPO Gene Polymorphism as a Predictive Factor for Hidden Autoimmune Thyroiditis in Patient with Bronchial Asthma and Allergic Rhinitis.
El Shabrawy RM et al.
The Egyptian Journal of Immunology, 2016
Segregation of S292F TPO gene mutation in three large Tunisian families with thyroid dyshormonogenesis: evidence of a founder effect.
Bougacha-Elleuch N et al.
European Journal of Pediatrics, 2015
Evaluation of Hybridization Capture Versus Amplicon-Based Methods for Whole-Exome Sequencing.
Samorodnitsky E et al.
Human Mutation, 2015
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
Monoallelic thyroid peroxidase gene mutation in a patient with congenital hypothyroidism with total iodide organification defect.
Neves SC et al.
Arquivos Brasileiros De Endocrinologia E Metabologia, 2010
Final diagnosis in children with subclinical hypothyroidism and mutation analysis of the thyroid peroxidase gene (TPO).
Turkkahraman D et al.
Journal of Pediatric Endocrinology & Metabolism : Jpem, 2009
High prevalence of thyroid peroxidase gene mutations in patients with thyroid dyshormonogenesis.
Avbelj M et al.
European Journal of Endocrinology, 2007
[DIO2, TPO, CYP1A1 AND CYP1A2 gene polymorphism in women with thyroid disease].
Kochetova OV et al.
Gigiena I Sanitariia, 0
RGS3 and IL1RAPL1 missense variants implicate defective neurotransmission in early-onset inherited schizophrenias.
Kanwal A et al.
Journal of Psychiatry & Neuroscience : Jpn, 0