Home > LILACS - Literatura Latinoamericana y del Caribe de Ciencias de la Salud > Search result

Results: 3

Efecto combinado de la interacción genética sobre el desarrollo del bocio nodular con tiroiditis autoinmune y adenoma tiroideo en los habitantes de Bucovina del Norte
Combined effect of gene-gene interaction on the development of nodular goiter with autoimmune thyroiditis and thyroid adenoma in the inhabitants of Northern Bukovyna

Sheremet, M. I; Sydorchuk, L. P; Shidlovskyi, V. O; Bedenyuk, A. D; Sydorchuk, R. I; Shidlovskyi, O. V; Batig, V. M; Maksymyuk, V. V; Bezruk, V. V; Bezruk, T. O; Chympoi, K. A; Gresko, M. D.
Rev. argent. endocrinol. metab; 55 (1), 2018
ABSTRAC This article presents the results of a comprehensive analysis of the combined influence of genetic polymorphisms associated with various links of apoptosis regulation (BCL-2, CTLA-4 and APO-1/Fas) on the development of nodular goiter with autoimmune thyroiditis and thyroid adenoma in the studied ...
Bocio Nodular/etiología, Apoptosis/fisiología, Bocio Nodular/fisiopatología, Neoplasias de la Tiroides/genética, Polimorfismo Genético/fisiología, Reducción de Dimensionalidad Multifactorial/métodos, Tiroiditis Autoinmune/genética, Bocio Nodular/genética, Abatacept/análisis, Receptor fas/análisis, Genes bcl-2/genética
Fulltext

Mutation screening of the SLC26A4 gene in a cohort of 192 Chinese patients with congenital hypothyroidism

Fu, Chunyun; Zheng, Haiyang; Zhang, Shujie; Chen, Yun; Su, Jiasun; Wang, Jin; Xie, Bobo; Hu, Xuyun; Fan, Xin; Luo, Jingsi; Li, Chuan; Chen, Rongyu; Shen, Yiping; Chen, Shaoke.
Arch. endocrinol. metab. (Online); 60 (4), 2016
ABSTRACT Objective Pendred syndrome (PS) is an autosomal recessive disorder characterised by sensorineural hearing loss and thyroid dyshormonogenesis. It is caused by biallelic mutations in the SLC26A4 gene encoding for pendrin. Hypothyroidism in PS can be present from birth and therefore diagnosed by ...
China/epidemiología, Estudios de Cohortes, Pruebas Genéticas/métodos, Bocio Nodular/epidemiología, Bocio Nodular/genética, Pérdida Auditiva Sensorineural/epidemiología, Pérdida Auditiva Sensorineural/genética, Proteínas de Transporte de Membrana/genética, Mutación, Tamizaje Neonatal/métodos, Prevalencia, Transportadores de Sulfato, Tirotropina/sangre, Tiroxina/sangre, Acueducto Vestibular/anomalías
Fulltext