Developmental iodine deficiency resulting in hypothyroidism reduces hippocampal ERK1/2 and CREB in lactational and adolescent rats

por Dong, Jing, Liu, Wanyang, Wang, Yi, Hou, Yi, Xi, Qi, Chen, Jie
Publicado 2009

Developmental iodine deficiency and hypothyroidism impair neural development in rat hippocampus: involvement of doublecortin and NCAM-180

por Gong, Jian, Liu, Wanyang, Dong, Jing, Wang, Yi, Xu, Hongde, Wei, Wei, Zhong, Jiapeng, Xi, Qi, Chen, Jie
Publicado 2010

The Play of Genes and Non-genetic Factors on Type 2 Diabetes

por Mambiya, Michael, Shang, Mengke, Wang, Yue, Li, Qian, Liu, Shan, Yang, Luping, Zhang, Qian, Zhang, Kaili, Liu, Mengwei, Nie, Fangfang, Zeng, Fanxin, Liu, Wanyang
Publicado 2019

Predictive role of modifiable factors in stroke: an umbrella review

por Wang, Xiaotong, Liang, Man, Zeng, Fanxin, Wang, Yue, Yang, Yuetian, Nie, Fangfang, Shang, Mengke, Ta, Na, Wen, Lu, Ou, Lanxin, Yang, Zhibin, Liu, Wanyang
Publicado 2022

Association between ADIPOQ G276T and C11377G polymorphisms and the risk of non‐alcoholic fatty liver disease: An updated meta‐analysis

por Liu, Mengwei, Liu, Shan, Shang, Mengke, Liu, Xiuping, Wang, Yue, Li, Qian, Mambiya, Michael, Yang, Luping, Zhang, Qian, Zhang, Kaili, Nie, Fangfang, Zeng, Fanxin, Liu, Wanyang
Publicado 2019

Association of single nucleotide polymorphisms of MTHFR, TCN2, RNF213 with susceptibility to hypertension and blood pressure

por Liu, Shan, Liu, Mengwei, Li, Qian, Liu, Xiuping, Wang, Yue, Mambiya, Michael, Zhang, Kaili, Yang, Luping, Zhang, Qian, Shang, Mengke, Zeng, Fanxin, Nie, Fangfang, Liu, Wanyang
Publicado 2019

Rare variants in RNF213, a susceptibility gene for moyamoya disease, are found in patients with pulmonary hypertension and aggravate hypoxia-induced pulmonary hypertension in mice

por Kobayashi, Hatasu, Kabata, Risako, Kinoshita, Hideyuki, Morimoto, Takaaki, Ono, Koh, Takeda, Midori, Choi, Jungmi, Okuda, Hiroko, Liu, Wanyang, Harada, Kouji H., Kimura, Takeshi, Youssefian, Shohab, Koizumi, Akio
Publicado 2018

Predictive role of heterozygous p.R4810K of RNF213 in the phenotype of Chinese moyamoya disease

por Wang, Yue, Zhang, Zhengshan, Wei, Ling, Zhang, Qian, Zou, Zhengxing, Yang, Luping, Li, Desheng, Shang, Mengke, Han, Cong, Mambiya, Michael, Li, Qian, Hao, Fangbin, Zhang, Kaili, Wang, Hui, Liu, Shan, Liu, Mengwei, Zeng, Fanxin, Nie, Fangfang, Wang, Kai, Liu, Wanyang, Duan, Lian
Publicado 2020

Identification of RNF213 as a Susceptibility Gene for Moyamoya Disease and Its Possible Role in Vascular Development

por Liu, Wanyang, Morito, Daisuke, Takashima, Seiji, Mineharu, Yohei, Kobayashi, Hatasu, Hitomi, Toshiaki, Hashikata, Hirokuni, Matsuura, Norio, Yamazaki, Satoru, Toyoda, Atsushi, Kikuta, Ken-ichiro, Takagi, Yasushi, Harada, Kouji H., Fujiyama, Asao, Herzig, Roman, Krischek, Boris, Zou, Liping, Kim, Jeong Eun, Kitakaze, Masafumi, Miyamoto, Susumu, Nagata, Kazuhiro, Hashimoto, Nobuo, Koizumi, Akio
Publicado 2011