Back to search

Article

Associationj of TSHR Gene Single Neucleotide Intronic Polymorphism with the Risk of Hypothyroid and Hyperthyroid Disorders in Yazd Province.

2022-01-07

Abstract excerpt

The present study was carried, for the first time, out to evaluate the association of rs2268458 polymorphism, biochemical and environmental factors on hypothyroid and hyperthyroid disorders in thyroid patients and healthy individuals in Yazd province, Iran. In this study, blood samples were collected from a total of 100 cases, including 60 hypothyroid, 20 hyperthyroidism individual cases and 20 normal individuals....

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
7fe37e96-00b1-5378-aaef-e074b1a52703
DOI
10.21203/rs.3.rs-1229601/v1
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Associationj of TSHR Gene Single Neucleotide Intronic Polymorphism with the Risk of Hypothyroid and Hyperthyroid Disorders in Yazd Province.DOI 10.21203/rs.3.rs-1229601/v1
Association of TSHR gene single nucleotide intronic polymorphism with the risk of hypothyroid and hyperthyroid disorders in Yazd province.Semantic proximity
Is the TSHR D727E polymorphism a genetic predisposition for multinodular goiter in the Turkish population?Semantic proximity
SNP Genes Effect on Thyroid Disorders in a Chinese DemographicSemantic proximity
Association between thyroid stimulating hormone receptor gene intron polymorphisms and autoimmune thyroid disease in a Chinese Han population.Semantic proximity
Genetic associations of the thyroid stimulating hormone receptor gene with Graves diseases and Graves ophthalmopathy: A meta-analysis.Semantic proximity
Central dogma in thyroid dysfunction: a review on structure modification of TSHR as a cornerstone for thyroid abnormalities.Semantic proximity
Association of polymorphisms of rs179247 and rs12101255 in thyroid stimulating hormone receptor intron 1 with an increased risk of Graves' disease: A meta-analysis.Semantic proximity
Association of single-nucleotide polymorphisms in the STAT3 gene with autoimmune thyroid disease in Chinese individuals.Semantic proximity
Association analysis of clinical phenotype and exon gene mutation locus in children with hyperthyroidismSemantic proximity
Association of Thyroid Peroxidase Gene Polymorphisms and Serum Anti- TPO Levels in Egyptian Patients with Autoimmune Hypothyroidism.Semantic proximity
Congenital Hypothyroidism Patients With Thyroid Hormone Receptor Variants Are Not Rare: A Systematic Review.Semantic proximity
Vitamin D status in Hashimoto's thyroiditis and its association with vitamin D receptor genetic variants.Semantic proximity
Select a neighboring publication to make it the new centre.