Quartz Crystal Microbalance Measurement of Histidine-Rich Glycoprotein and Stanniocalcin-2 Binding to Each Other and to Inflammatory Cells

por Persson Skare, Tor, Kaito, Hiroshi, Durall, Claudia, Aastrup, Teodor, Claesson-Welsh, Lena
Publicado 2022

Alport syndrome caused by a COL4A5 deletion and exonization of an adjacent AluY

por Nozu, Kandai, Iijima, Kazumoto, Ohtsuka, Yasufumi, Fu, Xue Jun, Kaito, Hiroshi, Nakanishi, Koichi, Vorechovsky, Igor
Publicado 2014

Autosomal dominant pseudohypoaldosteronism type 1 with a novel splice site mutation in MR gene

por Kanda, Kyoko, Nozu, Kandai, Yokoyama, Naoki, Morioka, Ichiro, Miwa, Akihiro, Hashimura, Yuya, Kaito, Hiroshi, Iijima, Kazumoto, Matsuo, Masafumi
Publicado 2009

Three Severe Cases of Viral Infections with Post-Kidney Transplantation Successfully Confirmed by Polymerase Chain Reaction and Flow Cytometry

por Nakanishi, Keita, Kaito, Hiroshi, Ogi, Miki, Takai, Denshi, Fujimura, Junya, Horinouchi, Tomoko, Yamamura, Tomohiko, Minamikawa, Shogo, Ninchoji, Takeshi, Nozu, Kandai, Imadome, Ken-Ichi, Iijima, Kazumoto
Publicado 2018

A birth of bipartite exon by intragenic deletion

por Nozu, Kandai, Iijima, Kazumoto, Igarashi, Toru, Yamada, Shiro, Kralovicova, Jana, Nozu, Yoshimi, Yamamura, Tomohiko, Minamikawa, Shogo, Morioka, Ichiro, Ninchoji, Takeshi, Kaito, Hiroshi, Nakanishi, Koichi, Vorechovsky, Igor
Publicado 2017

A patient with autosomal recessive Alport syndrome due to segmental maternal isodisomy

por Fu, Xue J, Morisada, Naoya, Hashimoto, Fusako, Taniguchi-Ikeda, Mariko, Hashimura, Yuya, Ohtsubo, Hiromi, Ninchoji, Takeshi, Kaito, Hiroshi, Nozu, Kandai, Takahashi, Eihiko, Nakanishi, Koichi, Kurahashi, Hiroki, Iijima, Kazumoto
Publicado 2014

The utility of urinary CD80 as a diagnostic marker in patients with renal diseases

por Minamikawa, Shogo, Nozu, Kandai, Maeta, Shingo, Yamamura, Tomohiko, Nakanishi, Keita, Fujimura, Junya, Horinouchi, Tomoko, Nagano, China, Sakakibara, Nana, Nagase, Hiroaki, Shima, Hideaki, Noda, Kenta, Ninchoji, Takeshi, Kaito, Hiroshi, Iijima, Kazumoto
Publicado 2018

An in vitro splicing assay reveals the pathogenicity of a novel intronic variant in ATP6V0A4 for autosomal recessive distal renal tubular acidosis

por Yamamura, Tomohiko, Nozu, Kandai, Miyoshi, Yuya, Nakanishi, Keita, Fujimura, Junya, Horinouchi, Tomoko, Minamikawa, Shogo, Mori, Nobuo, Fujimaru, Rika, Nakanishi, Koichi, Ninchoji, Takeshi, Kaito, Hiroshi, Mariko, Taniguchi-Ikeda, Morioka, Ichiro, Matsuo, Masafumi, Iijima, Kazumoto
Publicado 2017

A multicenter randomized trial indicates initial prednisolone treatment for childhood nephrotic syndrome for two months is not inferior to six-month treatment

por Yoshikawa, Norishige, Nakanishi, Koichi, Sako, Mayumi, Oba, Mari S, Mori, Rintaro, Ota, Erika, Ishikura, Kenji, Hataya, Hiroshi, Honda, Masataka, Ito, Shuichi, Shima, Yuko, Kaito, Hiroshi, Nozu, Kandai, Nakamura, Hidefumi, Igarashi, Takashi, Ohashi, Yasuo, Iijima, Kazumoto
Publicado 2015

Natural History and Genotype–Phenotype Correlation in Female X-Linked Alport Syndrome

por Yamamura, Tomohiko, Nozu, Kandai, Fu, Xue Jun, Nozu, Yoshimi, Ye, Ming Juan, Shono, Akemi, Yamanouchi, Satoko, Minamikawa, Shogo, Morisada, Naoya, Nakanishi, Koichi, Shima, Yuko, Yoshikawa, Norishige, Ninchoji, Takeshi, Morioka, Ichiro, Kaito, Hiroshi, Iijima, Kazumoto
Publicado 2017

Clinical and Genetic Characteristics in Patients With Gitelman Syndrome

por Fujimura, Junya, Nozu, Kandai, Yamamura, Tomohiko, Minamikawa, Shogo, Nakanishi, Keita, Horinouchi, Tomoko, Nagano, China, Sakakibara, Nana, Nakanishi, Koichi, Shima, Yuko, Miyako, Kenichi, Nozu, Yoshimi, Morisada, Naoya, Nagase, Hiroaki, Ninchoji, Takeshi, Kaito, Hiroshi, Iijima, Kazumoto
Publicado 2018

Determination of the pathogenicity of known COL4A5 intronic variants by in vitro splicing assay

por Horinouchi, Tomoko, Nozu, Kandai, Yamamura, Tomohiko, Minamikawa, Shogo, Nagano, China, Sakakibara, Nana, Nakanishi, Koichi, Shima, Yuko, Morisada, Naoya, Ishiko, Shinya, Aoto, Yuya, Nagase, Hiroaki, Takeda, Hiroki, Rossanti, Rini, Kaito, Hiroshi, Matsuo, Masafumi, Iijima, Kazumoto
Publicado 2019

Pathogenic evaluation of synonymous COL4A5 variants in X‐linked Alport syndrome using a minigene assay

por Horinouchi, Tomoko, Yamamura, Tomohiko, Minamikawa, Shogo, Nagano, China, Sakakibara, Nana, Nakanishi, Koichi, Shima, Yuko, Morisada, Naoya, Ishiko, Shinya, Aoto, Yuya, Nagase, Hiroaki, Takeda, Hiroki, Rossanti, Rini, Ishimori, Shingo, Kaito, Hiroshi, Matsuo, Masafumi, Iijima, Kazumoto, Nozu, Kandai
Publicado 2020

Comparison between conventional and comprehensive sequencing approaches for genetic diagnosis of Alport syndrome

por Yamamura, Tomohiko, Nozu, Kandai, Minamikawa, Shogo, Horinouchi, Tomoko, Sakakibara, Nana, Nagano, China, Aoto, Yuya, Ishiko, Shinya, Nakanishi, Koichi, Shima, Yuko, Nagase, Hiroaki, Rossanti, Rini, Ye, Ming J., Nozu, Yoshimi, Ishimori, Shingo, Morisada, Naoya, Kaito, Hiroshi, Iijima, Kazumoto
Publicado 2019

Clinical features of autosomal recessive polycystic kidney disease in the Japanese population and analysis of splicing in PKHD1 gene for determination of phenotypes

por 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
Publicado 2021

A review of clinical characteristics and genetic backgrounds in Alport syndrome

por Nozu, Kandai, Nakanishi, Koichi, Abe, Yoshifusa, Udagawa, Tomohiro, Okada, Shinichi, Okamoto, Takayuki, Kaito, Hiroshi, Kanemoto, Katsuyoshi, Kobayashi, Anna, Tanaka, Eriko, Tanaka, Kazuki, Hama, Taketsugu, Fujimaru, Rika, Miwa, Saori, Yamamura, Tomohiko, Yamamura, Natsusmi, Horinouchi, Tomoko, Minamikawa, Shogo, Nagata, Michio, Iijima, Kazumoto
Publicado 2018

Examination of the predicted prevalence of Gitelman syndrome by ethnicity based on genome databases

por 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
Publicado 2021

Glomerular galactose-deficient IgA1 expression analysis in pediatric patients with glomerular diseases

por Ishiko, Shinya, Horinouchi, Tomoko, Fujimaru, Rika, Shima, Yuko, Kaito, Hiroshi, Tanaka, Ryojiro, Ishimori, Shingo, Kondo, Atsushi, Nagai, Sadayuki, Aoto, Yuya, Sakakibara, Nana, Nagano, China, Yamamura, Tomohiko, Yoshimura, Momoka, Nakanishi, Koichi, Fujimura, Junya, Kamiyoshi, Naohiro, Nagase, Hiroaki, Yoshikawa, Norishige, Iijima, Kazumoto, Nozu, Kandai
Publicado 2020

Female mice lacking Pald1 exhibit endothelial cell apoptosis and emphysema

por Egaña, Isabel, Kaito, Hiroshi, Nitzsche, Anja, Becker, Lore, Ballester-Lopez, Carolina, Niaudet, Colin, Petkova, Milena, Liu, Wei, Vanlandewijck, Michael, Vernaleken, Alexandra, Klopstock, Thomas, Fuchs, Helmut, Gailus-Durner, Valerie, Hrabe de Angelis, Martin, Rask-Andersen, Helge, Johansson, Henrik J., Lehtiö, Janne, He, Liqun, Yildirim, Ali Ö., Hellström, Mats
Publicado 2017

Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment

por Ashraf, Shazia, Kudo, Hiroki, Rao, Jia, Kikuchi, Atsuo, Widmeier, Eugen, Lawson, Jennifer A., Tan, Weizhen, Hermle, Tobias, Warejko, Jillian K., Shril, Shirlee, Airik, Merlin, Jobst-Schwan, Tilman, Lovric, Svjetlana, Braun, Daniela A., Gee, Heon Yung, Schapiro, David, Majmundar, Amar J., Sadowski, Carolin E., Pabst, Werner L., Daga, Ankana, van der Ven, Amelie T., Schmidt, Johanna M., Low, Boon Chuan, Gupta, Anjali Bansal, Tripathi, Brajendra K., Wong, Jenny, Campbell, Kirk, Metcalfe, Kay, Schanze, Denny, Niihori, Tetsuya, Kaito, Hiroshi, Nozu, Kandai, Tsukaguchi, Hiroyasu, Tanaka, Ryojiro, Hamahira, Kiyoshi, Kobayashi, Yasuko, Takizawa, Takumi, Funayama, Ryo, Nakayama, Keiko, Aoki, Yoko, Kumagai, Naonori, Iijima, Kazumoto, Fehrenbach, Henry, Kari, Jameela A., El Desoky, Sherif, Jalalah, Sawsan, Bogdanovic, Radovan, Stajić, Nataša, Zappel, Hildegard, Rakhmetova, Assel, Wassmer, Sharon-Rose, Jungraithmayr, Therese, Strehlau, Juergen, Kumar, Aravind Selvin, Bagga, Arvind, Soliman, Neveen A., Mane, Shrikant M., Kaufman, Lewis, Lowy, Douglas R., Jairajpuri, Mohamad A., Lifton, Richard P., Pei, York, Zenker, Martin, Kure, Shigeo, Hildebrandt, Friedhelm
Publicado 2018