Translocation of the ABC transporter ABCD4 from the endoplasmic reticulum to lysosomes requires the escort protein LMBD1

Por Kawaguchi, Kosuke, Okamoto, Takumi, Morita, Masashi, Imanaka, Tsuneo
Publicado no Sci Rep (2016)

Structural basis for docking of peroxisomal membrane protein carrier Pex19p onto its receptor Pex3p

Por Sato, Yasuhiko, Shibata, Hiroyuki, Nakatsu, Toru, Nakano, Hiroaki, Kashiwayama, Yoshinori, Imanaka, Tsuneo, Kato, Hiroaki
Publicado em 2010

Acyl-CoA thioesterase activity of peroxisomal ABC protein ABCD1 is required for the transport of very long-chain acyl-CoA into peroxisomes

Por Kawaguchi, Kosuke, Mukai, Emi, Watanabe, Shiro, Yamashita, Atsushi, Morita, Masashi, So, Takanori, Imanaka, Tsuneo
Publicado no Sci Rep (2021)

Generation of an immortalized astrocytic cell line from Abcd1-deficient H-2K(b)tsA58 mice to facilitate the study of the role of astrocytes in X-linked adrenoleukodystrophy

Por Morita, Masashi, Toida, Ai, Horiuchi, Yuki, Watanabe, Shiro, Sasahara, Masakiyo, Kawaguchi, Kosuke, So, Takanori, Imanaka, Tsuneo
Publicado no Heliyon (2021)

The regulation of DNAse activities in subcellular compartments of activated thymocytes

Por Nagata, Takuya, Kishi, Hiroyuki, Liu, Qin Li, Matsuda, Tadashi, Imanaka, Tsuneo, Tsukada, Kazuhiro, Kang, Dongchon, Muraguchi, Atsushi
Publicado em 2002

Peroxisomes Are Formed from Complex Membrane Structures in PEX6-deficient CHO Cells upon Genetic Complementation

Por Hashiguchi, Noriyo, Kojidani, Tomoko, Imanaka, Tsuneo, Haraguchi, Tokuko, Hiraoka, Yasushi, Baumgart, Eveline, Yokota, Sadaki, Tsukamoto, Toshiro, Osumi, Takashi
Publicado em 2002

A Novel Double Mutation in the ABCD1 Gene in a Patient with X-linked Adrenoleukodystrophy: Analysis of the Stability and Function of the Mutant ABCD1 Protein

Por Morita, Masashi, Kobayashi, Junpei, Yamazaki, Kozue, Kawaguchi, Kosuke, Honda, Ayako, Sugai, Kenji, Shimozawa, Nobuyuki, Koide, Reiji, Imanaka, Tsuneo
Publicado em 2013

Effect of Lorenzo’s Oil on Hepatic Gene Expression and the Serum Fatty Acid Level in abcd1-Deficient Mice

Por Morita, Masashi, Honda, Ayako, Kobayashi, Akira, Watanabe, Yuichi, Watanabe, Shiro, Kawaguchi, Kosuke, Takashima, Shigeo, Shimozawa, Nobuyuki, Imanaka, Tsuneo
Publicado no JIMD Rep (2017)

An HTRF based high-throughput screening for discovering chemical compounds that inhibit the interaction between Trypanosoma brucei Pex5p and Pex14p

Por Watanabe, Yuichi, Kawaguchi, Kosuke, Saito, Syuken, Okabe, Takayoshi, Yonesu, Kiyoaki, Egashira, Shinichiro, Kameya, Masafumi, Morita, Masashi, Kashiwayama, Yoshinori, Imanaka, Tsuneo
Publicado no Biochem Biophys Rep (2016)

Identification of a Substrate-binding Site in a Peroxisomal β-Oxidation Enzyme by Photoaffinity Labeling with a Novel Palmitoyl Derivative

Por Kashiwayama, Yoshinori, Tomohiro, Takenori, Narita, Kotomi, Suzumura, Miyuki, Glumoff, Tuomo, Hiltunen, J. Kalervo, Van Veldhoven, Paul P., Hatanaka, Yasumaru, Imanaka, Tsuneo
Publicado em 2010

Stability of the ABCD1 Protein with a Missense Mutation: A Novel Approach to Finding Therapeutic Compounds for X-Linked Adrenoleukodystrophy

Por Morita, Masashi, Matsumoto, Shun, Sato, Airi, Inoue, Kengo, Kostsin, Dzmitry G., Yamazaki, Kozue, Kawaguchi, Kosuke, Shimozawa, Nobuyuki, Kemp, Stephan, Wanders, Ronald J., Kojima, Hirotatsu, Okabe, Takayoshi, Imanaka, Tsuneo
Publicado no JIMD Rep (2018)

Tissue-specific expression and subcellular localization of ALADIN, the absence of which causes human triple A syndrome

Por Cho, A-Ri, Yang, Keum-Jin, Bae, Yoonsun, Bahk, Young Yil, Kim, Eunmin, Lee, Hyungnam, Kim, Jeong Ki, Park, Wonsang, Rhim, Hyanshuk, Choi, Soo Young, Imanaka, Tsuneo, Moon, Sungdae, Yoon, Jongbok, Yoon, Sungjoo Kim
Publicado em 2009