Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Yung-Tsai Liou"'
Autor:
Ya-Yun Cheng, Ying-Tsen Chou, Feng-Jie Lai, Ming-Shiou Jan, Tsung-Hao Chang, I-Ming Jou, Pei-Shiuan Chen, Jui-Yen Lo, Shiang-Suo Huang, Nan-Shan Chang, Yung-Tsai Liou, Po-Chih Hsu, Hui-Ching Cheng, Yee-Shin Lin, Li-Jin Hsu
Publikováno v:
Acta Neuropathologica Communications, Vol 8, Iss 1, Pp 1-16 (2020)
Abstract Human WWOX gene resides in the chromosomal common fragile site FRA16D and encodes a tumor suppressor WW domain-containing oxidoreductase. Loss-of-function mutations in both alleles of WWOX gene lead to autosomal recessive abnormalities in pe
Externí odkaz:
https://doaj.org/article/eb7e53c62cb94d12a058fc878897c937
Autor:
Feng-Jie Lai, Yee Shin Lin, Ya Yun Cheng, Pei-Shiuan Chen, Jui-Yen Lo, Hui-Ching Cheng, Tsung-Hao Chang, I-Ming Jou, Shiang-Suo Huang, Ying-Tsen Chou, Li Jin Hsu, Nan-Shan Chang, Po-Chih Hsu, Yung-Tsai Liou, Ming-Shiou Jan
Publikováno v:
Acta Neuropathologica Communications, Vol 8, Iss 1, Pp 1-16 (2020)
Acta Neuropathologica Communications
Acta Neuropathologica Communications
Human WWOX gene resides in the chromosomal common fragile site FRA16D and encodes a tumor suppressor WW domain-containing oxidoreductase. Loss-of-function mutations in both alleles of WWOX gene lead to autosomal recessive abnormalities in pediatric p
Autor:
Cheng, Ya-Yun, Ying-Tsen Chou, Feng-Jie Lai, Ming-Shiou Jan, Tsung-Hao Chang, I-Ming Jou, Pei-Shiuan Chen, Jui-Yen Lo, Shiang-Suo Huang, Nan-Shan Chang, Yung-Tsai Liou, Po-Chih Hsu, Hui-Ching Cheng, Yee-Shin Lin, Hsu, Li-Jin
Additional file 1: Supplementary Methods. Figure S1. Wwox gene deletion causes microcephaly and abnormal brain morphology in mice. Figure S2. Immunofluorescence staining of sagittal cerebellar tissue sections from Wwox+/+ and Wwox-/- mice using an an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76ed3b99c529b74e0557179004dea174