Monoallelic Deletion in the 5' Gene as a Cause of Sporadic Nonendemic Simple Goiter Region of the Thyroglobulin-Reference-Cited by-同舟云学术

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Monoallelic Deletion in the 5' Gene as a Cause of Sporadic Nonendemic Simple Goiter Region of the Thyroglobulin

Published:2001-08 Issue:8 Volume:11 Page:789-793
ISSN:1050-7256
Container-title:Thyroid
language:en
Short-container-title:Thyroid

Author:

González-Sarmiento Rogelio,Corral Javier,Mories María Teresa,Corrales Juan J.,Miguel-Velado Eduardo,Miralles-García José M.

Publisher

Mary Ann Liebert Inc

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

https://www.liebertpub.com/doi/pdf/10.1089/10507250152484655

Reference26 articles.

1. Mapping of human thyroglobulin gene on the long arm of chromosome 8 by in situ hybridization

2. The human thyroglobulin gene is over 300 kb long and contains introns of up to 64 kb

3. Primary structure of human thyroglobulin deduced from the sequence of its 8448-base complementary DNA

4. Structure-function relationship in thyroglobulin: amino acid sequence of two different thyroxine-containing peptides from porcine thyroglobulin.

5. Thyroglobulin structure-function. The amino acid sequence surrounding thyroxine.

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2. Curating the gnomAD database: Report of novel variants in the thyrogobulin gene using in silico bioinformatics algorithms;Molecular and Cellular Endocrinology;2021-08

3. Structure and genetic variants of thyroglobulin: Pathophysiological implications;Molecular and Cellular Endocrinology;2021-05

4. A novel mutation in intron 11 donor splice site, responsible of a rare genotype in thyroglobulin gene by altering the pre-mRNA splincing process. Cell expression and bioinformatic analysis;Molecular and Cellular Endocrinology;2021-02

5. Molecular analysis of thyroglobulin mutations found in patients with goiter and hypothyroidism;Molecular and Cellular Endocrinology;2018-09

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