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Showing results 1 to 5 of 5

1
CYFIP2 p.Arg87Cys Causes Neurological Defects and Degradation of CYFIP2

Kang, Muwon; Zhang, Yinhua; Kang, Hyae Rim; Kim, Seoyeong; Ma, Ruiying; Yi, Yunho; Lee, Seungjoon; et al, ANNALS OF NEUROLOGY, v.93, no.1, pp.155 - 163, 2023-01

2
Genetic Analysis of CLCN7 in an Old Female Patient with Type II Autosomal Dominant Osteopetrosis

Kim, Seon Young; Lee, Younghak; Kang, Yea Eun; Kim, Ji Min; Joung, Kyong Hye; Lee, Ju Hee; Kim, Koon Soon; et al, ENDOCRINOLOGY AND METABOLISM, v.33, no.3, pp.380 - 386, 2018-09

3
Mutations in FAM50A suggest that Armfield XLID syndrome is a spliceosomopathy

Lee, Yu-Ri; Khan, Kamal; Armfield-Uhas, Kim; Srikanth, Sujata; Thompson, Nicola A.; Pardo, Mercedes; Yu, Lu; et al, NATURE COMMUNICATIONS, v.11, no.1, 2020-07

4
Non-Cell Autonomous Epileptogenesis in Focal Cortical Dysplasia

Koh, Hyun Yong; Jang, Jaeson; Ju, Sang Hyeon; Kim, Ryunhee; Cho, Gyu-Bon; Kim, Dong Seok; Sohn, Jong-Woo; et al, ANNALS OF NEUROLOGY, v.90, no.2, pp.285 - 299, 2021-08

5
NQO1-Knockout Mice Are Highly Sensitive to Clostridium Difficile Toxin A-Induced Enteritis

Nam, Seung Taek; Hwang, Jung Hwan; Kim, Dae Hong; Lu, Li Fang; Hong, Ji; Zhang, Peng; Yoon, I. Na; et al, JOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY, v.26, no.8, pp.1446 - 1451, 2016-08

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