Work

Deletion of exons encoding carboxypeptidase domain of Nna1 results in Purkinje cell degeneration (pcd) phenotype

Year: 2018

Type: article

Source: Journal of Neurochemistry

DOI: 10.1111/jnc.14591

Authors: Li Zhou, M. Ibrahim Hossain, Maya Yamazaki, Manabu Abe, Rie Natsume, Kohtaro Konno, Shun Kageyama, Masaaki Komatsu, Masahiko Watanabe, Kenji Sakimura, Hirohide Takebayashi

Institutions: Brain Research Institute, Niigata University, Niigata University, Hokkaido University

Language: English

Topic: Genetic Neurodegenerative Diseases

Subfield: Cellular and Molecular Neuroscience

Field: Neuroscience

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: Ministry of Education, Culture, Sports, Science and Technology, Japan Society for the Promotion of Science

Awards: G1180075368, Elucidation of the mechanism of dystonia development using animal model and attempts to restore the symptoms, G2185810054, Development of a comprehensive tag-insertion method that enables dynamic in vivo analysis, G2883883149, G4046918617, G4210344234, Functional analysis of Alfy, a selective autophagy related molecule involved in brain formation, G4852455942, Development of a new generation method of transgenic common marmoset, a potential resource for various researches, G6163398366, G7682237518, Advanced Animal Model Support, Functional analysis of genes responsible for neurological diseases by conditional mutagenesis in a single generation

OpenAlex ID: W2889869191

FWCI: 1.075

Cites: 55

Cited by: 29

Related to: 10