Roles for c-Myc in Self-renewal of Hematopoietic Stem Cells von Satoh, Yusuke, Matsumura, Itaru, Tanaka, Hirokazu, Ezoe, Sachiko, Sugahara, Hiroyuki, Mizuki, Masao, Shibayama, Hirohiko, Ishiko, Eri, Ishiko, Jun, Nakajima, Koichi, Kanakura, Yuzuru

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Notch Signals Inhibit the Development of Erythroid/Megakaryocytic Cells by Suppressing GATA-1 Activity through the Induction of HES1 von Ishiko, Eri, Matsumura, Itaru, Ezoe, Sachiko, Gale, Karin, Ishiko, Jun, Satoh, Yusuke, Tanaka, Hirokazu, Shibayama, Hirohiko, Mizuki, Masao, Era, Takumi, Enver, Tariq, Kanakura, Yuzuru

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Examination of the predicted prevalence of Gitelman syndrome by ethnicity based on genome databases von Kondo, Atsushi, Nagano, China, Ishiko, Shinya, Omori, Takashi, Aoto, Yuya, Rossanti, Rini, Sakakibara, Nana, Horinouchi, Tomoko, Yamamura, Tomohiko, Nagai, Sadayuki, Okada, Eri, Shima, Yuko, Nakanishi, Koichi, Ninchoji, Takeshi, Kaito, Hiroshi, Takeda, Hiroki, Nagase, Hiroaki, Morisada, Naoya, Iijima, Kazumoto, Nozu, Kandai

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Blister fluid is a useful diagnostic tool for diagnosis of vancomycin‐induced linear IgA bullous dermatosis von Yoshida, Kenji, Yoshihama, Eri, Morii, Kaya, Ishiko, Akira

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X-chromosome inactivation patterns in females with Fabry disease examined by both ultra-deep RNA sequencing and methylation-dependent assay von Rossanti, Rini, Nozu, Kandai, Fukunaga, Atsushi, Nagano, China, Horinouchi, Tomoko, Yamamura, Tomohiko, Sakakibara, Nana, Minamikawa, Shogo, Ishiko, Shinya, Aoto, Yuya, Okada, Eri, Ninchoji, Takeshi, Kato, Noritoshi, Maruyama, Shoichi, Kono, Keiji, Nishi, Shinichi, Iijima, Kazumoto, Fujii, Hideki

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Clinical features of autosomal recessive polycystic kidney disease in the Japanese population and analysis of splicing in PKHD1 gene for determination of phenotypes von Ishiko, Shinya, Morisada, Naoya, Kondo, Atsushi, Nagai, Sadayuki, Aoto, Yuya, Okada, Eri, Rossanti, Rini, Sakakibara, Nana, Nagano, China, Horinouchi, Tomoko, Yamamura, Tomohiko, Ninchoji, Takeshi, Kaito, Hiroshi, Hamada, Riku, Shima, Yuko, Nakanishi, Koichi, Matsuo, Masafumi, Iijima, Kazumoto, Nozu, Kandai

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Genotype and X-chromosome inactivation are associated with disease severity in females with X-linked Alport syndrome von Suzuki, Ryota, Sakakibara, Nana, Murakami, Sae, Ichikawa, Yuta, Kitakado, Hideaki, Ueda, Chika, Tanaka, Yu, Okada, Eri, Kondo, Atsushi, Aoto, Yuya, Ishiko, Shinya, Ishimori, Shingo, Nagano, China, Yamamura, Tomohiko, Horinouchi, Tomoko, Okamoto, Takayuki, Nozu, Kandai

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All reported non-canonical splice site variants in GLA cause aberrant splicing von Okada, Eri, Horinouchi, Tomoko, Yamamura, Tomohiko, Aoto, Yuya, Suzuki, Ryota, Ichikawa, Yuta, Tanaka, Yu, Masuda, Chika, Kitakado, Hideaki, Kondo, Atsushi, Sakakibara, Nana, Ishiko, Shinya, Nagano, China, Ishimori, Shingo, Usui, Joichi, Yamagata, Kunihiro, Matsuo, Masafumi, Nozu, Kandai

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Monogenic causes of pigmentary mosaicism von Saida, Ken, Chong, Pin Fee, Yamaguchi, Asuka, Saito, Naka, Ikehara, Hajime, Koshimizu, Eriko, Miyata, Rie, Ishiko, Akira, Nakamura, Kazuyuki, Ohnishi, Hidenori, Fujioka, Kei, Sakakibara, Takafumi, Asada, Hideo, Ogawa, Kohei, Kudo, Kyoko, Ohashi, Eri, Kawai, Michiko, Abe, Yuichi, Tsuchida, Naomi, Uchiyama, Yuri, Hamanaka, Kohei, Fujita, Atsushi, Mizuguchi, Takeshi, Miyatake, Satoko, Miyake, Noriko, Kato, Mitsuhiro, Kira, Ryutaro, Matsumoto, Naomichi

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Hepatic hemangioma in a simple liver cyst mimicking biliary cystic neoplasm von Karashima, Ryuichi, Yamamura, Kensuke, Oda, Eri, Ozaki, Nobuyuki, Ishiko, Takatoshi, Nagayama, Yasunori, Yamada, Rin, Komohara, Yoshihiko, Koba, Ikuro, Beppu, Toru

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Corrigendum to “Detecting MUC1 Variants in Patients Clinicopathologically Diagnosed With Having Autosomal Dominant Tubulointerstitial Kidney Disease”Kidney International Reports, V... von Okada, Eri, Morisada, Naoya, Horinouchi, Tomoko, Fujii, Hideki, Tsuji, Takayuki, Miura, Masayoshi, Katori, Hideyuki, Kitagawa, Masashi, Morozumi, Kunio, Toriyama, Takanobu, Nakamura, Yuki, Nishikomori, Ryuta, Nagai, Sadayuki, Kondo, Atsushi, Aoto, Yuya, Ishiko, Shinya, Rossanti, Rini, Sakakibara, Nana, Nagano, China, Yamamura, Tomohiko, Ishimori, Shingo, Usui, Joichi, Yamagata, Kunihiro, Iijima, Kazumoto, Imasawa, Toshiyuki, Nozu, Kandai

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Identification of novel OCRL isoforms associated with phenotypic differences between Dent disease-2 and Lowe syndrome von Sakakibara, Nana, Ijuin, Takeshi, Horinouchi, Tomoko, Yamamura, Tomohiko, Nagano, China, Okada, Eri, Ishiko, Shinya, Aoto, Yuya, Rossanti, Rini, Ninchoji, Takeshi, Awano, Hiroyuki, Nagase, Hiroaki, Minamikawa, Shogo, Tanaka, Ryojiro, Matsuyama, Takeshi, Nagatani, Koji, Kamei, Koichi, Jinnouchi, Kumiko, Ohtsuka, Yasufumi, Oka, Masafumi, Araki, Yoshinori, Tanaka, Toju, Harada, Mari S, Igarashi, Toru, Kitahara, Hikaru, Morisada, Naoya, Nakamura, Shun-ichi, Okada, Taro, Iijima, Kazumoto, Nozu, Kandai

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Last Nucleotide Substitutions of COL4A5 Exons Cause Aberrant Splicing von Aoto, Yuya, Horinouchi, Tomoko, Yamamura, Tomohiko, Kondo, Atsushi, Nagai, Sadayuki, Ishiko, Shinya, Okada, Eri, Rossanti, Rini, Sakakibara, Nana, Nagano, China, Awano, Hiroyuki, Nagase, Hiroaki, Shima, Yuko, Nakanishi, Koichi, Matsuo, Masafumi, Iijima, Kazumoto, Nozu, Kandai

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Systematic Review of Genotype-Phenotype Correlations in Frasier Syndrome von Tsuji, Yurika, Yamamura, Tomohiko, Nagano, China, Horinouchi, Tomoko, Sakakibara, Nana, Ishiko, Shinya, Aoto, Yuya, Rossanti, Rini, Okada, Eri, Tanaka, Eriko, Tsugawa, Koji, Okamoto, Takayuki, Sawai, Toshihiro, Araki, Yoshinori, Shima, Yuko, Nakanishi, Koichi, Nagase, Hiroaki, Matsuo, Masafumi, Iijima, Kazumoto, Nozu, Kandai

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Systematic Review of Clinical Characteristics and Genotype-Phenotype Correlation in LAMB2-Associated Disease von Suzuki, Ryota, Sakakibara, Nana, Ichikawa, Yuta, Kitakado, Hideaki, Ueda, Chika, Tanaka, Yu, Okada, Eri, Kondo, Atsushi, Ishiko, Shinya, Ishimori, Shingo, Nagano, China, Yamamura, Tomohiko, Horinouchi, Tomoko, Okamoto, Takayuki, Nozu, Kandai

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Detecting MUC1 Variants in Patients Clinicopathologically Diagnosed With Having Autosomal Dominant Tubulointerstitial Kidney Disease von Okada, Eri, Morisada, Naoya, Horinouchi, Tomoko, Fujii, Hideki, Tsuji, Takayuki, Miura, Masayoshi, Katori, Hideyuki, Kitagawa, Masashi, Morozumi, Kunio, Toriyama, Takanobu, Nakamura, Yuki, Nishikomori, Ryuta, Nagai, Sadayuki, Kondo, Atsushi, Aoto, Yuya, Ishiko, Shinya, Rossanti, Rini, Sakakibara, Nana, Nagano, China, Yamamura, Tomohiko, Ishimori, Shingo, Usui, Joichi, Yamagata, Kunihiro, Iijima, Kazumoto, Imasawa, Toshiyuki, Nozu, Kandai

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Evaluation of Suspected Autosomal Alport Syndrome Synonymous Variants von Rossanti, Rini, Horinouchi, Tomoko, Yamamura, Tomohiko, Nagano, China, Sakakibara, Nana, Ishiko, Shinya, Aoto, Yuya, Kondo, Atsushi, Nagai, Sadayuki, Okada, Eri, Ishimori, Shingo, Nagase, Hiroaki, Matsui, Satoshi, Tamagaki, Keiichi, Ubara, Yoshifumi, Nagahama, Masahiko, Shima, Yuko, Nakanishi, Koichi, Ninchoji, Takeshi, Matsuo, Masafumi, Iijima, Kazumoto, Nozu, Kandai

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Genotype-Phenotype Correlation in WT1 Exon 8 to 9 Missense Variants von Nagano, China, Takaoka, Yutaka, Kamei, Koichi, Hamada, Riku, Ichikawa, Daisuke, Tanaka, Kazuki, Aoto, Yuya, Ishiko, Shinya, Rossanti, Rini, Sakakibara, Nana, Okada, Eri, Horinouchi, Tomoko, Yamamura, Tomohiko, Tsuji, Yurika, Noguchi, Yuko, Ishimori, Shingo, Nagase, Hiroaki, Ninchoji, Takeshi, Iijima, Kazumoto, Nozu, Kandai

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Detection of antibodies against human metapneumovirus by western blot using recombinant nucleocapsid and matrix proteins von Ishiguro, Nobuhisa, Ebihara, Takashi, Endo, Rika, Ma, Xiaoming, Kawai, Eri, Ishiko, Hiroaki, Kikuta, Hideaki

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Clinical Evaluation of the Q-Tip Test in Normal Pregnant Women von Nakamura, Tetsuo, Ishiko, Osamu, Hirai, Kouzo, Sumi, Toshiyuki, Nakagawa, Eri, Nakai, Yuichiro, Tomoda, Shoji, Ogita, Sachio

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