Extranodal natural killer/T‐cell lymphoma in an 11‐year‐old child

le Ninchoji, Takeshi, Fujimura, Junya, Uemura, Suguru, Yamamoto, Nobuyuki, Nozu, Kandai, Iijima, Kazumoto
Foilsithe in Clin Case Rep (2020)

eNOS-induced vascular barrier disruption in retinopathy by c-Src activation and tyrosine phosphorylation of VE-cadherin

le Ninchoji, Takeshi, Love, Dominic T, Smith, Ross O, Hedlund, Marie, Vestweber, Dietmar, Sessa, William C, Claesson-Welsh, Lena
Foilsithe in eLife (2021)

Vascular permeability in retinopathy is regulated by VEGFR2 Y949 signaling to VE-cadherin

le Smith, Ross O, Ninchoji, Takeshi, Gordon, Emma, André, Helder, Dejana, Elisabetta, Vestweber, Dietmar, Kvanta, Anders, Claesson-Welsh, Lena
Foilsithe in eLife (2020)

FAT1 biallelic truncating mutation causes a non-syndromic proteinuria in a child

le Rossanti, Rini, Watanabe, Toshio, Nagano, China, Hara, Shigeo, Horinouchi, Tomoko, Yamamura, Tomohiko, Sakakibara, Nana, Ninchoji, Takeshi, Iijima, Kazumoto, Nozu, Kandai
Foilsithe in CEN Case Rep (2020)

Genetic background, recent advances in molecular biology, and development of novel therapy in Alport syndrome

le Nozu, Kandai, Takaoka, Yutaka, Kai, Hirofumi, Takasato, Minoru, Yabuuchi, Kensuke, Yamamura, Tomohiko, Horinouchi, Tomoko, Sakakibara, Nana, Ninchoji, Takeshi, Nagano, China, Iijima, Kazumoto
Foilsithe in Kidney Res Clin Pract (2020)

Axon Guidance-Related Factor FLRT3 Regulates VEGF-Signaling and Endothelial Cell Function

le Jauhiainen, Suvi, Laakkonen, Johanna P., Ketola, Kirsi, Toivanen, Pyry I., Nieminen, Tiina, Ninchoji, Takeshi, Levonen, Anna-Liisa, Kaikkonen, Minna U., Ylä-Herttuala, Seppo
Foilsithe in Front Physiol (2019)

Multivariate analysis of the impact of weather and air pollution on emergency department visits for night-time headaches among children: retrospective, clinical observational study

le Yamaguchi, Hiroshi, Nozu, Kandai, Ishiko, Shinya, Nagase, Hiroaki, Ninchoji, Takeshi, Nagano, China, Takeda, Hiroki, Unzaki, Ai, Ishibashi, Kazuto, Morioka, Ichiro, Iijima, Kazumoto, Ishida, Akihito
Foilsithe in BMJ Open (2021)

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

le 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
Foilsithe in Case Rep Nephrol Dial (2018)

A birth of bipartite exon by intragenic deletion

le 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
Foilsithe in Mol Genet Genomic Med (2017)

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

le 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
Foilsithe in Hum Genome Var (2014)

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

le 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
Foilsithe in Sci Rep (2018)

Paladin is a phosphoinositide phosphatase regulating endosomal VEGFR2 signalling and angiogenesis

le Nitzsche, Anja, Pietilä, Riikka, Love, Dominic T, Testini, Chiara, Ninchoji, Takeshi, Smith, Ross O, Ekvärn, Elisabet, Larsson, Jimmy, Roche, Francis P, Egaña, Isabel, Jauhiainen, Suvi, Berger, Philipp, Claesson‐Welsh, Lena, Hellström, Mats
Foilsithe in EMBO Rep (2020)

Somatic mosaicism and variant frequency detected by next-generation sequencing in X-linked Alport syndrome

le Fu, Xue Jun, Nozu, Kandai, Kaito, Hiroshi, Ninchoji, Takeshi, Morisada, Naoya, Nakanishi, Koichi, Yoshikawa, Norishige, Ohtsubo, Hiromi, Matsunoshita, Natsuki, Kamiyoshi, Naohiro, Matsumura, Chieko, Takagi, Nobuaki, Maekawa, Kohei, Taniguchi-Ikeda, Mariko, Iijima, Kazumoto
Foilsithe in Eur J Hum Genet (2016)

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

le 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
Foilsithe in BMC Nephrol (2017)

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

le 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
Foilsithe in Kidney Int Rep (2017)

Clinical and Genetic Characteristics in Patients With Gitelman Syndrome

le 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
Foilsithe in Kidney Int Rep (2018)

Genetic, Clinical, and Pathologic Backgrounds of Patients with Autosomal Dominant Alport Syndrome

le Kamiyoshi, Naohiro, Nozu, Kandai, Fu, Xue Jun, Morisada, Naoya, Nozu, Yoshimi, Ye, Ming Juan, Imafuku, Aya, Miura, Kenichiro, Yamamura, Tomohiko, Minamikawa, Shogo, Shono, Akemi, Ninchoji, Takeshi, Morioka, Ichiro, Nakanishi, Koichi, Yoshikawa, Norishige, Kaito, Hiroshi, Iijima, Kazumoto
Foilsithe in Clin J Am Soc Nephrol (2016)