LONRF2 is a protein quality control ubiquitin ligase whose deficiency causes late-onset neurological deficits
Dan Li(Guangzhou University of Chinese Medicine), Makoto Nakanishi(The Cancer Institute Hospital), Kiyoshi Yamaguchi(Tokyo Medical University), Hiroya Naruse(The University of Tokyo), Yoichi Furukawa(The University of Tokyo), Yoshikazu Johmura(Kanazawa University), Naoki Suzuki(Tohoku University), Ayumi Nishiyama(Tohoku University), Hideyuki Okano(Keio University), Manabu Ozawa(Systems Biology Institute), Tatsushi Toda(National Center of Neurology and Psychiatry), Shoichi Shimada(The University of Osaka), Kenta Nakai(The University of Tokyo), Satoshi Yamazaki(Institute for Stem Cell Biology and Regenerative Medicine), Shoji Tsuji(The University of Tokyo), Akane Inoue‐Yamauchi(Memorial Sloan Kettering Cancer Center), Satoru Morimoto(Mie University), Takashi Okada(The University of Tokyo), Masashi Aoki(Tohoku University), Miyuki Doi(The University of Osaka), Narumi Suzuki(Tokyo University of Science), Chieko Konishi, Atsuya Nishiyama(The University of Tokyo), Yuji Tsunekawa(Tokyo Medical University), Yukio Takeshita(Yamaguchi University), Takashi Matsukawa(The University of Tokyo), Keiko Nakanishi(Aichi Human Service Center), Xin Zeng(Capital Medical University), Alexander S. Harris(Tokyo University of Science), Masato Morita, Yuji Yamanashi(The University of Tokyo)
Cited by 14
Related Papers
Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease
|Nature Genetics|2009|1.3k
Navigating the DNA methylation landscape of cancer
|Trends in Genetics|2021|1k
AXIN1 mutations in hepatocellular carcinomas, and growth suppression in cancer cells by virus-mediated transfer of AXIN1
|Nature Genetics|2000|950
An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy
|Nature|1998|804
The Movement Disorder Society Criteria for the Diagnosis of Multiple System Atrophy
|Movement Disorders|2022|788