Identification of FOXP3-negative regulatory T-like (CD4+ CD25+ CD127low ) cells in patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome von Otsubo, Keisuke, Kanegane, Hirokazu, Kamachi, Yoshiro, Kobayashi, Ichiro, Tsuge, Ikuya, Imaizumi, Masue, Sasahara, Yoji, Hayakawa, Akira, Nozu, Kandai, Iijima, Kazumoto, Ito, Shuichi, Horikawa, Reiko, Nagai, Yoshinori, Takatsu, Kiyoshi, Mori, Hisashi, Ochs, Hans D, Miyawaki, Toshio

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Right hypoplastic kidney von Ogawa, Ayu, Kitamura, Shinji, Nakayama, Kazunori, Sugiyama, Hitoshi, Morisada, Naoya, Iijima, Kazumoto, Makino, Hirofumi

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Predisposition to relapsing nephrotic syndrome by a nephrin mutation that interferes with assembly of functioning microdomains von Shono, Akemi, Tsukaguchi, Hiroyasu, Kitamura, Akiko, Hiramoto, Ryugo, Qin, Xiao-Song, Doi, Toshio, Iijima, Kazumoto

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Steroid-resistant nephrotic syndrome von Kitamura, Akiko, Tsukaguchi, Hiroyasu, Maruyama, Kenichi, Shono, Akemi, Iijima, Kazumoto, Kagami, Shoji, Doi, Toshio

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Group A streptococcal antigen in the glomeruli of children with henoch-schönlein nephritis von Masuda, Miwa, Nakanishi, Koichi, Yoshizawa, Nobuyuki, Iijima, Kazumoto, Yoshikawa, Norishige

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DP-E3. Detecting Pathogenic deep intronic variant in Gitelman Syndrome von Rini Rossanti, Kandai Nozu, Tomoko Horinouchi, Tomohiko Yamamura, China Nagano, Nana Sakakibara, Shinya Ishiko, Yuya Aoto, Atsushi Kondo, Sadayuki Nagai, Kazumoto lijima

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Somatic mosaicism for a mutation of the COL4A5 gene is a cause of mild phenotype male Alport syndrome von Krol, Rafal Przybyslaw, Nozu, Kandai, Nakanishi, Koichi, Iijima, Kazumoto, Takeshima, Yasuhiro, Fu, Xue Jun, Nozu, Yoshimi, Kaito, Hiroshi, Kanda, Kyoko, Matsuo, Masafumi, Yoshikawa, Norishige

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Detection of mutations in the COL4A5 gene in over 90% of male patients with x-linked Alport's syndrome by RT-PCR and direct sequencing von Inoue, Yuji, Nishio, Hisahide, Shirakawa, Taku, Nakanishi, Koichi, Nakamura, Hajime, Sumino, Kimiaki, Nishiyama, Kaoru, Iijima, Kazumoto, Yoshikawa, Norishige

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Role of platelet-activating factor acetylhydrolase gene mutation in Japanese childhood IgA nephropathy von Tanaka, Ryojiro, Iijima, Kazumoto, Xu, Hong, Inoue, Yuji, Murakami, Ryusuke, Shirakawa, Taku, Nishiyama, Kaoru, Miwa, Masao, Shiozawa, Shunichi, Nakamura, Hajime, Yoshikawa, Norishige

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