Zobrazeno 1 - 10
of 651
pro vyhledávání: '"Lee Chien-Nan"'
Autor:
Yen, I-Weng, Kuo, Chun-Heng, Lin, Ming-Wei, Tai, Yi-Yun, Chen, Kuan-Yu, Chen, Szu-Chieh, Lin, Chia-Hung, Hsu, Chih-Yao, Lee, Chien-Nan, Lin, Shin-Yu, Li, Hung-Yuan, Fan, Kang-Chih
Publikováno v:
In Journal of the Formosan Medical Association March 2024 123(3):325-330
Autor:
Yen, I-Weng, Lin, Shin-Yu, Lin, Ming-Wei, Lee, Chien-Nan, Kuo, Chun-Heng, Chen, Szu-Chieh, Tai, Yi-Yun, Kuo, Ching-Hua, Kuo, Han-Chun, Lin, Heng-Huei, Juan, Hsien-Chia, Lin, Chia-Hung, Fan, Kang-Chih, Wang, Chih-Yuan, Li, Hung-Yuan
Publikováno v:
In Clinica Chimica Acta 1 February 2024 554
Akademický článek
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Autor:
Lin Shuan-Pei, Chen Chih-Ping, Lee Chien-Nan, Lin Shin-Yu, Hung Chia-Cheng, Chao Mei-Chyn, Chiou Shyh-Shin, Su Yi-Ning
Publikováno v:
BMC Medical Genetics, Vol 12, Iss 1, p 76 (2011)
Abstract Background Retinoblastoma is caused by compound heterozygosity or homozygosity of retinoblastoma gene (RB1) mutations. In germline retinoblastoma, mutations in the RB1 gene predispose individuals to increased cancer risks during development.
Externí odkaz:
https://doaj.org/article/2dc7c29ce71c4a679524112835bdb07d
Autor:
Hwang, Yaw-Huei, Wu, Hui-Chu, Shyu, Ming-Kwang, Lee, Chien-Nan, Lin, Shin-Yu, Chen, Pau-Chung, Chuang, Hung-Yi, Lin, Pei-Wen, Wu, Tso-Hsien, Chen, Yen-Tzu
Publikováno v:
In Environmental Pollution 1 September 2023 332
Autor:
Cheng Wen-Fang, Chang Chien-Hui, Chang Yin-Fei, Lin Chia-Yun, Su Yi-Ning, Hung Chia-Cheng, Chen Chi-An, Lee Chien-Nan, Lin Win-Li
Publikováno v:
BMC Biotechnology, Vol 8, Iss 1, p 62 (2008)
Abstract Background Beta-thalassemia is a common autosomal recessive hereditary disease in the Meditertanean, Asia and African areas. Over 600 mutations have been described in the beta-globin (HBB), of which more than 200 are associated with a beta-t
Externí odkaz:
https://doaj.org/article/783be171cce44c3b98e28c99e211906f
Autor:
Chang Chieh-Ting, Chiou Shyh-Shin, Tsay Woei, Hung Chia-Cheng, Su Yi-Ning, Lin Shin-Yu, Ho Hong-Nerng, Lee Chien-Nan
Publikováno v:
BMC Medical Genetics, Vol 9, Iss 1, p 53 (2008)
Abstract Background Hemophilia A represents the most common and severe inherited hemorrhagic disorder. It is caused by mutations in the F8 gene, which leads to a deficiency or dysfunctional factor VIII protein, an essential cofactor in the factor X a
Externí odkaz:
https://doaj.org/article/2d357c3b53454e4f8518f93ccf1c075b
Autor:
Hsieh Chia-Jung, Chen Pau-Chung, Chen Chih-Chuan, Liou Horng-Huei, Chien Shu-Chin, Su Yi-Ning, Hung Chia-Cheng, Chen Chih-Ping, Lee Wang-Tso, Lin Win-Li, Lee Chien-Nan
Publikováno v:
BMC Medical Genetics, Vol 7, Iss 1, p 72 (2006)
Abstract Background Tuberous sclerosis complex (TSC) is an autosomal dominant disease characterized by the development of multiple hamartomas in many internal organs. Mutations in either one of 2 genes, TSC1 and TSC2, have been attributed to the deve
Externí odkaz:
https://doaj.org/article/cfa378b064e842c780636572b7e284c7
Publikováno v:
In Journal of the Formosan Medical Association August 2023 122(8):785-789
Autor:
Hu, Ya-Li, Lin, Shin-Yu, Lee, Chien-Nan, Shih, Jin-Chung, Cheng, Ai-Ling, Chen, Shun-Hua, Chang, Luan-Yin, Fang, Chi-Tai
Publikováno v:
In Journal of Microbiology, Immunology and Infection August 2023 56(4):766-771