Výsledky vyhledávání - "Chien Chih-Cheng"

Akademický článek

A predicted protein, KIAA0247, is a cell cycle modulator in colorectal cancer cells under 5-FU treatment

Autor: Chen Yan-Chu, Chien Chih-Cheng, Lin Chih-Ming, Yang Shung-Haur, Huang Shih-Ming, Huang Chi-Jung, Lee Chia-Long, Wu Hao-Han, Chang Chun-Chao

Publikováno v: Journal of Translational Medicine, Vol 9, Iss 1, p 82 (2011)

Abstract Background Colorectal cancer (CRC) is the predominant gastrointestinal malignancy and the leading cause of cancer death. The identification of genes related to CRC is important for the development of successful therapies and earlier diagnosi

Externí odkaz: https://doaj.org/article/b1367d8f97b647a18857e2e05d694610

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Akademický článek

Increased spinal prodynorphin gene expression in reinflammation-associated hyperalgesia after neonatal inflammatory insult

Autor: Wen Yeong-Ray, Lin Shih-Chang, Chien Chih-Cheng, Chen Julia, Cheng Yu-Che, Lin Jack, Tsou Tsung-Shan, Ling Qing-Dong

Publikováno v: BMC Neuroscience, Vol 11, Iss 1, p 139 (2010)

Abstract Background Neuroplasticity induced by neonatal inflammation is the consequence of a combination of activity-dependent changes in neurons. We investigated neuronal sensitivity to a noxious stimulus in a rat model of neonatal hind-paw peripher

Externí odkaz: https://doaj.org/article/111d69eef3cf4257adf51ea37b3dfc72

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Akademický článek

Clinical meaning of age-related expression of fecal cytokeratin 19 in colorectal malignancy

Autor: Sun Hsiao-Lun, Lin Chih-Ming, Lee Chia-Long, Pan Shiann, Chen Shu-Hung, Chien Chih-Cheng, Yang Shung-Haur, Chang Chun-Chao, Huang Chi-Cheng, Wu Yih-Yiing, Yang Ruey-Neng, Huang Chi-Jung

Publikováno v: BMC Cancer, Vol 9, Iss 1, p 376 (2009)

Abstract Background Colorectal cancer (CRC) is one of the leading causes of malignant death worldwide. Because young age of onset is often considered a poor prognostic factor for CRC, it is important to identify the poor outcomes of CRC in a younger

Externí odkaz: https://doaj.org/article/d1e105d31dd7452dba1bf2d85cdf6374

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Akademický článek

Unambiguous molecular detections with multiple genetic approach for the complicated chromosome 22q11 deletion syndrome

Autor: Lin Lung-Huang, Hung Kun-Long, Cheong Mei-Leng, Huang Cheng-Hung, Yang Chen, Yu Yeong-Seng, Chien Chih-Cheng, Huang Huei-Chen, Chen Chan-Wei, Huang Chi-Jung

Publikováno v: BMC Medical Genetics, Vol 10, Iss 1, p 16 (2009)

Abstract Background Chromosome 22q11 deletion syndrome (22q11DS) causes a developmental disorder during the embryonic stage, usually because of hemizygous deletions. The clinical pictures of patients with 22q11DS vary because of polymorphisms: on ave

Externí odkaz: https://doaj.org/article/21a45069833b486da601ab68d49931eb

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