Novel nonsense mutation in the Na+/HCO3- cotransporter gene (SLC4A4) in a patient with permanent isolated proximal renal tubular acidosis and bilateral glaucoma von IGARASHI, Takashi, INATOMI, Jun, NAKAMURA, Hajime, ENDOU, Hitoshi, SEKINE, Takashi, SEKI, George, SHIMADZU, Mitsunobu, TOZAWA, Fumiko, TAKESHIMA, Yasuhiro, TAKUMI, Toru, TAKAHASHI, Toshikazu, YOSHIKAWA, Norishige

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Molecular basis of ocular abnormalities associated with proximal renal tubular acidosis von Usui, T, Hara, M, Satoh, H, Moriyama, N, Kagaya, H, Amano, S, Oshika, T, Ishii, Y, Ibaraki, N, Hara, C, Kunimi, M, Noiri, E, Tsukamoto, K, Inatomi, J, Kawakami, H, Endou, H, Igarashi, T, Goto, A, Fujita, T, Araie, M, Seki, G

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Effect of Mechanical Strain on Electric Conductance of Molecular Junctions von Inatomi, Junichi, Fujii, Shintaro, Marqués-González, Santiago, Masai, Hiroshi, Tsuji, Yasushi, Terao, Jun, Kiguchi, Manabu

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Human L-type amino acid transporter 1 (LAT1): characterization of function and expression in tumor cell lines von Yanagida, Osamu, Kanai, Yoshikatsu, Chairoungdua, Arthit, Kim, Do Kyung, Segawa, Hiroko, Nii, Tomoko, Cha, Seok Ho, Matsuo, Hirotaka, Fukushima, Jun-ichi, Fukasawa, Yoshiki, Tani, Yoshiko, Taketani, Yutaka, Uchino, Hiroshi, Kim, Ju Young, Inatomi, Jun, Okayasu, Isao, Miyamoto, Ken-ichi, Takeda, Eiji, Goya, Tomoyuki, Endou, Hitoshi

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Unraveling the molecular pathogenesis of isolated proximal renal tubular acidosis von IGARASHI, Takashi, SEKINE, Takashi, INATOMI, Jun, SEKI, George

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Functional analysis of NBC1 mutants associated with proximal renal tubular acidosis and ocular abnormalities von HORITA, Shoko, YAMADA, Hideomi, SHIMADZU, Mitsunobu, SEKI, George, FUJITA, Toshiro, INATOMI, Jun, MORIYAMA, Nobuo, SEKINE, Takashi, IGARASHI, Takashi, ENDO, Yoko, DASOUKI, Majed, EKIM, Mesiha, AL-GAZALI, Lihadh

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Chronic active Epstein-Barr virus infection successfully treated with allogeneic peripheral blood stem cell transplantation von Taketani, T, Kikuchi, A, Inatomi, J, Hanada, R, Kawaguchi, H, Ida, K, Oh-ishi, T, Arai, T, Kishimoto, H, Yamamoto, K

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Cyclosporine C2 Monitoring for the Treatment of Frequently Relapsing Nephrotic Syndrome in Children: A Multicenter Randomized Phase II Trial von Iijima, Kazumoto, Sako, Mayumi, Oba, Mari Saito, Ito, Shuichi, Hataya, Hiroshi, Tanaka, Ryojiro, Ohwada, Yoko, Kamei, Koichi, Ishikura, Kenji, Yata, Nahoko, Nozu, Kandai, Honda, Masataka, Nakamura, Hidefumi, Nagata, Michio, Ohashi, Yasuo, Nakanishi, Koichi, Yoshikawa, Norishige

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Mutations in SLC4A4 cause permanent isolated proximal renal tubular acidosis with ocular abnormalities von Igarashi, Takashi, Inatomi, Jun, Sekine, Takashi, Cha, Seok Ho, Kanai, Yoshikatsu, Kunimi, Motoei, Tsukamoto, Kazuhisa, Satoh, Hiroaki, Shimadzu, Mitsunobu, Tozawa, Fumiko, Mori, Tetsuo, Shiobara, Masaaki, Seki, George, Endou, Hitoshi

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Human cystine/glutamate transporter: cDNA cloning and upregulation by oxidative stress in glioma cells von Kim, Ju Young, Kanai, Yoshikatsu, Chairoungdua, Arthit, Cha, Seok Ho, Matsuo, Hirotaka, Kim, Do Kyung, Inatomi, Jun, Sawa, Hiroki, Ida, Yoshiteru, Endou, Hitoshi

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Expression of Human Organic Anion Transporters in the Choroid Plexus and Their Interactions With Neurotransmitter Metabolites von Alebouyeh, Mahmoud, Takeda, Michio, Onozato, Maristela Lika, Tojo, Akihiro, Noshiro, Rie, Hasannejad, Habib, Inatomi, Jun, Narikawa, Shinichi, Huang, Xiu-Lin, Khamdang, Suparat, Anzai, Naohiko, Endou, Hitoshi

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Expression of a system L neutral amino acid transporter at the blood–brain barrier von Matsuo, Hirotaka, Tsukada, Shingo, Nakata, Takahiro, Chairoungdua, Arthit, Kim, Do Kyung, Cha, Seok Ho, Inatomi, Jun, Yorifuji, Hiroshi, Fukuda, Jun, Endou, Hitoshi, Kanai, Yoshikatsu

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Mutational and functional analysis of SLC4A4 in a patient with proximal renal tubular acidosis von Inatomi, Jun, Horita, Shoko, Braverman, Nancy, Sekine, Takashi, Yamada, Hideomi, Suzuki, Yoshiro, Kawahara, Katsumasa, Moriyama, Nobuo, Kudo, Akihiko, Kawakami, Hayato, Shimadzu, Mitsunobu, Endou, Hitoshi, Fujita, Toshiro, Seki, George, Igarashi, Takashi

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The W258X mutation in SLC22A12 is the predominant cause of Japanese renal hypouricemia von Komoda, Fusako, Sekine, Takashi, Inatomi, Jun, Enomoto, Atsushi, Endou, Hitoshi, Ota, Toshiyuki, Matsuyama, Takeshi, Ogata, Tsutomu, Ikeda, Masahiro, Awazu, Midori, Muroya, Koji, Kamimaki, Isamu, Igarashi, Takashi

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Identification and Characterization of a Novel Member of the Heterodimeric Amino Acid Transporter Family Presumed to be Associated with an Unknown Heavy Chain von Chairoungdua, Arthit, Kanai, Yoshikatsu, Matsuo, Hirotaka, Inatomi, Jun, Kim, Do Kyung, Endou, Hitoshi

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Growth factor mRNA and protein in preserved human amniotic membrane von Koizumi, Noriko, Inatomi, Tsutomu, Sotozono, Chie, Fullwood, Nigel J., Quantock, Andrew J., Kinoshita, Shigeru

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Identification of a Novel Na+-independent Acidic Amino Acid Transporter with Structural Similarity to the Member of a Heterodimeric Amino Acid Transporter Family Associated with Un... von Matsuo, Hirotaka, Kanai, Yoshikatsu, Kim, Ju Young, Chairoungdua, Arthit, Kim, Do Kyung, Inatomi, Jun, Shigeta, Yasuhiro, Ishimine, Hisako, Chaekuntode, Sophapun, Tachampa, Kittipong, Choi, Hye Won, Babu, Ellappan, Fukuda, Jun, Endou, Hitoshi

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Cloning and characterization of a human brain Na+-independent transporter for small neutral amino acids that transports D-serine with high affinity von NAKAUCHI, J, MATSUO, H, ENDOU, H, KANAI, Y, DO KYUNG KIM, GOTO, A, CHAIROUNGDUA, A, SEOK HO CHA, INATOMI, J, SHIOKAWA, Y, YAMAGUCHI, K, SAITO, I

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Renovascular hypertension complicated with VATER association von Inatomi, Jun, Miyazaki, Osamu, Fujimaru, Rika, Iijima, Kazumoto

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Functional characterization of renal chloride channel, CLCN5, mutations associated with Dent's disease

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