Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Fang-Chi Kao"'
Autor:
Ya-Wen Chou, Fu-Hsin Hung, Hsiao-Lin Lee, Meng-Lun Hsieh, Chu-Hsuan Chiu, Chi-Ming Tai, Yi-Cheng Chang, Jing-Yong Huang, Fang-Chi Kao, Chih-Neng Hsu, Teng-Kuang Yeh, Shih-Yi Chen, Lee-Ming Chuang, Bi-Yu Liu, Juey-Jen Hwang, Tzu-Yu Chen, Yvonne Shih, Ting-Jen Cheng, Fu-An Li, Yi-Yu Ke, Yu-Hua Tseng, Ming-Shiu Hung, Jamie Cheng, Shih-Yao Lin, Lun Tsou, Jiun-Yi Nong, Wei-Shun Yang, Yet-Ran Chen, Siow-Wey Hee
Insulin resistance and obesity are pivotal features of type 2 diabetes mellitus. Peroxisome proliferator-activated receptor γ (PPARγ) is a master transcriptional regulator of systemic insulin sensitivity and energy balance. The anti-diabetic drug t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2411d76f38c514201c45ebedddb1efc6
https://doi.org/10.21203/rs.3.rs-490889/v1
https://doi.org/10.21203/rs.3.rs-490889/v1
Methyl-CpG binding protein 2 (MeCP2) is a chromatin regulator highly expressed in mature neurons. Mutations ofMECP2gene cause >90% cases of Rett syndrome, a neurodevelopmental disorder featured by striking psychomotor dysfunction. InMecp2-null mice,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::caa65dab4a7bb6b6e18cacf46d4b2b4f
https://europepmc.org/articles/PMC6605173/
https://europepmc.org/articles/PMC6605173/
Publikováno v:
Brain structurefunction. 220(1)
Rett Syndrome (RTT) is a neurodevelopmental disorder caused by mutations in the methyl-CpG-binding protein 2 (MECP2) gene. Affected individuals develop motor deficits including stereotypic hand movements, impaired motor learning and difficulties with