Identification and Functional Characterization of a Novel Mutation in theNKX2-1Gene: Comparison with the Data in the Literature-Reference-Cited by-同舟云学术

Identification and Functional Characterization of a Novel Mutation in theNKX2-1Gene: Comparison with the Data in the Literature

Published:2013-06 Issue:6 Volume:23 Page:675-682
ISSN:1050-7256
Container-title:Thyroid
language:en
Short-container-title:Thyroid

Author:

Nettore Immacolata Cristina¹,Mirra Paola²,Ferrara Alfonso Massimiliano¹,Sibilio Annarita¹,Pagliara Valentina¹,Kay Claudia Suemi Kamoi³,Lorenzoni Paulo Josè³,Werneck Lineu Cesar³,Bruck Isac⁴,dos Santos Lucia Helena Coutinho⁴,Beguinot Francesco²,Salvatore Domenico¹,Ungaro Paola²,Fenzi Gianfranco¹,Scola Rosana Herminia³,Macchia Paolo Emidio¹

Affiliation:

1. Department of Molecular and Clinical Endocrinology and Oncology, University of Naples “Federico II”, Naples, Italy.

2. Department of Cellular Biology and Pathology & Institute of Endocrinology and Molecular Oncology of CNR, University of Naples “Federico II”, Naples, Italy.

3. Neuromuscular Division, Clinical Hospital, Parana Federal University, Curitiba, Parana, Brazil.

4. Neurology Pediatrics Division, Clinical Hospital, Parana Federal University, Curitiba, Parana, Brazil.

Publisher

Mary Ann Liebert Inc

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

https://www.liebertpub.com/doi/pdf/10.1089/thy.2012.0267

Reference41 articles.

1. A thyroid-specific nuclear protein essential for tissue-specific expression of the thyroglobulin promoter.

2. Thyroid Development and Its Disorders: Genetics and Molecular Mechanisms

3. PAX8,TITF1, andFOXE1Gene Expression Patterns during Human Development: New Insights into Human Thyroid Development and Thyroid Dysgenesis-Associated Malformations