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Decreased expression of A20 is associated with ocular Behcet's disease (BD) but not with Vogt-Koyanagi-Harada (VKH) disease.
He, Yue; Wang, Chaokui; Su, Guannan; Deng, Bolin; Ye, Zi; Huang, Yang; Yuan, Gangxiang; Aize, Kijlstra; Li, Hong; Yang, Peizeng.
Afiliación
  • He Y; The First Affiliated Hospital of Chongqing Medical University, Chongqing Key Laboratory of Ophthalmology and Chongqing Eye Institute, Chongqing, China.
  • Wang C; The First Affiliated Hospital of Chongqing Medical University, Chongqing Key Laboratory of Ophthalmology and Chongqing Eye Institute, Chongqing, China.
  • Su G; The First Affiliated Hospital of Chongqing Medical University, Chongqing Key Laboratory of Ophthalmology and Chongqing Eye Institute, Chongqing, China.
  • Deng B; The First Affiliated Hospital of Chongqing Medical University, Chongqing Key Laboratory of Ophthalmology and Chongqing Eye Institute, Chongqing, China.
  • Ye Z; The First Affiliated Hospital of Chongqing Medical University, Chongqing Key Laboratory of Ophthalmology and Chongqing Eye Institute, Chongqing, China.
  • Huang Y; The First Affiliated Hospital of Chongqing Medical University, Chongqing Key Laboratory of Ophthalmology and Chongqing Eye Institute, Chongqing, China.
  • Yuan G; The First Affiliated Hospital of Chongqing Medical University, Chongqing Key Laboratory of Ophthalmology and Chongqing Eye Institute, Chongqing, China.
  • Aize K; University Eye Clinic Maastricht, Maastricht, The Netherlands.
  • Li H; The First Affiliated Hospital of Chongqing Medical University, Chongqing Key Laboratory of Ophthalmology and Chongqing Eye Institute, Chongqing, China peizengycmu@126.com lihongcqmu@163.com.
  • Yang P; The First Affiliated Hospital of Chongqing Medical University, Chongqing Key Laboratory of Ophthalmology and Chongqing Eye Institute, Chongqing, China peizengycmu@126.com lihongcqmu@163.com.
Br J Ophthalmol ; 102(8): 1167-1172, 2018 08.
Article en En | MEDLINE | ID: mdl-29699987
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome Uveomeningoencefálico / Regulación de la Expresión Génica / Síndrome de Behçet / Proteína 3 Inducida por el Factor de Necrosis Tumoral alfa Tipo de estudio: Diagnostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Br J Ophthalmol Año: 2018 Tipo del documento: Article País de afiliación: China Pais de publicación: Reino Unido
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome Uveomeningoencefálico / Regulación de la Expresión Génica / Síndrome de Behçet / Proteína 3 Inducida por el Factor de Necrosis Tumoral alfa Tipo de estudio: Diagnostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Br J Ophthalmol Año: 2018 Tipo del documento: Article País de afiliación: China Pais de publicación: Reino Unido