DDHD1, but Not DDHD2, Suppresses Neurite Outgrowth in SH-SY5Y and PC12 Cells by Regulating Protein Transport From Recycling Endosomes

por Maemoto, Yuki, Maruyama, Tomohiro, Nemoto, Kazuaki, Baba, Takashi, Motohashi, Manae, Ito, Akihiro, Tagaya, Mitsuo, Tani, Katsuko
Publicado 2020

The NESH/Abi-3-based WAVE2 complex is functionally distinct from the Abi-1-based WAVE2 complex

por Sekino, Saki, Kashiwagi, Yuriko, Kanazawa, Hitoshi, Takada, Kazuki, Baba, Takashi, Sato, Seiichi, Inoue, Hiroki, Kojima, Masaki, Tani, Katsuko
Publicado 2015

Late-onset spastic ataxia phenotype in a patient with a homozygous DDHD2 mutation

por Doi, Hiroshi, Ushiyama, Masao, Baba, Takashi, Tani, Katsuko, Shiina, Masaaki, Ogata, Kazuhiro, Miyatake, Satoko, Fukuda-Yuzawa, Yoko, Tsuji, Shoji, Nakashima, Mitsuko, Tsurusaki, Yoshinori, Miyake, Noriko, Saitsu, Hirotomo, Ikeda, Shu-ichi, Tanaka, Fumiaki, Matsumoto, Naomichi, Yoshida, Kunihiro
Publicado 2014

Loss of DDHD2, whose mutation causes spastic paraplegia, promotes reactive oxygen species generation and apoptosis

por Maruyama, Tomohiro, Baba, Takashi, Maemoto, Yuki, Hara-Miyauchi, Chikako, Hasegawa-Ogawa, Minami, Okano, Hirotaka James, Enda, Yuki, Matsumoto, Kei, Arimitsu, Nagisa, Nakao, Kazuki, Hamamoto, Hiroshi, Sekimizu, Kazuhisa, Ohto-Nakanishi, Takayo, Nakanishi, Hiroki, Tokuyama, Takeshi, Yanagi, Shigeru, Tagaya, Mitsuo, Tani, Katsuko
Publicado 2018