Genetic association of PRKCD and CARD9 polymorphisms with Vogt-Koyanagi-Harada disease in the Chinese Han population.

Zhou, Chunya; Cai, Shiya; Xie, Yuhong; Zeng, Zhen; Zhang, Jun; Su, Guannan; Wu, Qiuying; Ye, Xingsheng; Cao, Qingfeng; Yang, Peizeng; Hu, Jianmin

Zhou, Chunya; Cai, Shiya; Xie, Yuhong; Zeng, Zhen; Zhang, Jun; Su, Guannan; Wu, Qiuying; Ye, Xingsheng; Cao, Qingfeng; Yang, Peizeng; Hu, Jianmin.

Afiliación

Zhou C; Department of Ophthalmology, The Second Affiliated Hospital of Fujian Medical University, Engineering Research Center of Assistive Technology for Visual Impairment, Fujian Province University, Quanzhou, 362000, People's Republic of China.
Cai S; Department of Ophthalmology and Optometry, The School of Medical Technology and Engineering, Fujian Medical University, Jiaotong Road 88, Fuzhou, 350004, People's Republic of China.
Xie Y; Department of Ophthalmology, The Second Affiliated Hospital of Fujian Medical University, Engineering Research Center of Assistive Technology for Visual Impairment, Fujian Province University, Quanzhou, 362000, People's Republic of China.
Zeng Z; Department of Ophthalmology and Optometry, The School of Medical Technology and Engineering, Fujian Medical University, Jiaotong Road 88, Fuzhou, 350004, People's Republic of China.
Zhang J; Department of Ophthalmology, The Second Affiliated Hospital of Fujian Medical University, Engineering Research Center of Assistive Technology for Visual Impairment, Fujian Province University, Quanzhou, 362000, People's Republic of China.
Su G; Department of Ophthalmology and Optometry, The School of Medical Technology and Engineering, Fujian Medical University, Jiaotong Road 88, Fuzhou, 350004, People's Republic of China.
Wu Q; Department of Ophthalmology, The Second Affiliated Hospital of Fujian Medical University, Engineering Research Center of Assistive Technology for Visual Impairment, Fujian Province University, Quanzhou, 362000, People's Republic of China.
Ye X; Department of Ophthalmology and Optometry, The School of Medical Technology and Engineering, Fujian Medical University, Jiaotong Road 88, Fuzhou, 350004, People's Republic of China.
Cao Q; The First Affiliated Hospital of Chongqing Medical University, Chongqing Key Laboratory of Ophthalmology and Chongqing Eye Institute, Youyi Road 1, Chongqing, 400016, China.
Yang P; The First Affiliated Hospital of Chongqing Medical University, Chongqing Key Laboratory of Ophthalmology and Chongqing Eye Institute, Youyi Road 1, Chongqing, 400016, China.
Hu J; The First Affiliated Hospital of Chongqing Medical University, Chongqing Key Laboratory of Ophthalmology and Chongqing Eye Institute, Youyi Road 1, Chongqing, 400016, China.

Hum Genomics ; 17(1): 9, 2023 02 13.

Article en En | MEDLINE | ID: mdl-36782298

Asunto(s)

Proteína Quinasa C-delta; Síndrome Uveomeningoencefálico; Humanos; Proteína Quinasa C-delta/genética; Proteína Quinasa C-delta/metabolismo; Frecuencia de los Genes; Síndrome Uveomeningoencefálico/genética; Síndrome Uveomeningoencefálico/metabolismo; Estudios de Casos y Controles; Pueblos del Este de Asia; Predisposición Genética a la Enfermedad; Polimorfismo de Nucleótido Simple/genética; Citocinas/genética; Citocinas/metabolismo; ARN Mensajero; Proteínas Adaptadoras de Señalización CARD/genética; Proteínas Adaptadoras de Señalización CARD/metabolismo

Palabras clave

Caspase recruitment domain family member 9; Genetic susceptibility; Protein kinase C delta; Single-nucleotide polymorphism; VogtKoyanagiHarada disease

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome Uveomeningoencefálico / Proteína Quinasa C-delta Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Hum Genomics Asunto de la revista: GENETICA Año: 2023 Tipo del documento: Article Pais de publicación: Reino Unido

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