Nozu Kandai

ノヅカンダイ | Nozu Kandai

Affiliation and department：
Job title：特命教授

Research field (1)： Fetal medicine/Pediatrics

Research keywords (4)： Tubulopathies , Inherited Kidney Diseases , Pediatric Nephrology , Pediatrics

Research theme for competitive and other funds (17)：

2023 - 2026 Elucidation of the mechanism of rituximab-induced long-term remission in childhood nephrotic syndrome
2021 - 2024 Joint international Research Project for International GWAS Meta-Analysis and Anti-Nephrin Autoantibodies in Childhood Nephrotic Syndrome
2020 - 2023 iPS細胞由来腎臓オルガノイドを用いた小児ネフローゼ症候群の発症機序の解明
2019 - 2022 Contribution of aberrant splicing to the onset mechanisms in inherited kidney diseases
2020 - 2022 Alport症候群に対するエクソンスキッピング療法の開発

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Papers (569)：

Yuimi Koyama, Mary Ann Suico, Aimi Owaki, Ryoichi Sato, Jun Kuwazuru, Shota Kaseda, Yuya Sannomiya, Jun Horizono, Kohei Omachi, Tomoko Horinouchi, et al. Trimerization profile of type IV collagen COL4A5 exon deletion in X-linked Alport syndrome. Clinical and Experimental Nephrology. 2024
Naoko Nakatani, Akihiro Tamura, Hiroaki Hanafusa, Nanako Nino, Nobuyuki Yamamoto, Hiroyuki Awano, Yasuhiro Tanaka, Naoya Morisada, Suguru Uemura, Atsuro Saito, et al. A novel NFKB1 variant in a Japanese pedigree with common variable immunodeficiency. Human genome variation. 2024. 11. 1. 15-15
Toshiki Hyodo, Shigeo Hara, Shunsuke Goto, Hideki Fujii, Shinichi Nishi, Tomoko Horinouchi, Kandai Nozu, Norishige Yoshikawa, Akihiro Yoshimoto, Tomoo Itoh. Immunohistological analysis reveals IgG1-dominant immunophenotype of tubulointerstitial nephritis unassociated with IgG4-related diseases. International urology and nephrology. 2024
Tomohiro Sameshima, Mariko Ashina, Takuya Fukuda, Takumi Kido, Shinya Abe, Yuko Watanabe, Itsuko Sato, Yoshihiko Yano, Kenji Tanimura, Hiroaki Nagase, et al. Range of protein induced by vitamin K absence or antagonist-II levels in neonates at birth. Scientific reports. 2024. 14. 1. 921-921
Yoshinori Nambu, Taku Shirakawa, Kayo Osawa, Hisahide Nishio, Kandai Nozu, Masafumi Matsuo, Hiroyuki Awano. Brothers with Becker muscular dystrophy show discordance in skeletal muscle computed tomography findings: A case report. SAGE Open Medical Case Reports. 2024. 12

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MISC (332)：

森貞直哉, 森貞直哉, 洪本加奈, 藤代瞳, 親里嘉展, 野津寛大, 小崎健次郎, 角谷真知子, 和田芳直, 岡本伸彦, et al. 当院で経験した希少先天性グリコシル化異常症(CDG)の2女児例. 日本先天代謝異常学会雑誌. 2023. 39
森貞直哉, 森貞直哉, 森貞直哉, 洪本加奈, 坂田亮介, 小川禎治, 横田聡, 前川嵩太, 苅田典生, 野津寛大. こどもたちへの遺伝カウンセリング後に診断を確定したOptic atrophy plus症候群の親子例. 日本小児遺伝学会学術集会プログラム・抄録集. 2023. 46th
野津寛大. 電解質異常から発見する小児遺伝性腎疾患バーター症候群・ギッテルマン症候群. 日本小児科学会雑誌. 2022. 126. 2. 215-215
洪本加奈, 森貞直哉, 森貞直哉, 森貞直哉, 平久進也, 大西徳子, 大西徳子, 船越徹, 野津寛大, 飯島一誠, et al. Genetic autopsyで17q12欠失症候群と診断したPotter sequenceの1男児例. 日本人類遺伝学会大会プログラム・抄録集. 2022. 67th (CD-ROM)
大西徳子, 大西徳子, 洪本加奈, 森貞直哉, 森貞直哉, 森貞直哉, 佐伯啓介, 野津寛大. 周期的な不機嫌を呈したBosch-Boonstra-Schoaf optic atrophy syndromeの1例. 日本人類遺伝学会大会プログラム・抄録集. 2022. 67th (CD-ROM)

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Lectures and oral presentations (267)：

遺伝性腎疾患における遺伝子診断の現状とこれからの課題
(第47回日本腎臓学会東部学術集会 2017)
シクロスポリンの効果は一時的であったACTN4新規遺伝子変異を伴うFSGS男児例
(第47回日本腎臓学会東部学術集会 2017)
The comprehensive gene screening for congenital, infantile, and steroid resistant nephrotic syndrome in Japan
(ASN Kidney Week 2017 2017)
TGFBI関連眼腎症候群の1例:顆粒状角膜ジストロフィII型と腎症の合併例
(第47回日本腎臓学会東部学術集会 2017)
治療方針の決定に疾患パネル解析を用いたステロイド抵抗性ネフローゼ症候群の1例
(・第38回日本小児腎不全学会 2017)

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Education (1)：

Professional career (1)：

Work history (10)：

2021/06 - 現在 Kobe University Graduate School of Medicine Department of Pediatrics Professor
2018/08 - 現在 Kobe University Graduate School of Medicine Pediatrics Professor
2016/04 - 2018/07 Kobe University Graduate School of Medicine Pediatrics Associated Professor
2014/07 - 2016/03 Kobe University Graduate School of Medicine Pediatrics Lecturer
2013/04 - 2014/06 Kobe University Graduate School of Medicine Pediatrics Assistant Professor

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Awards (12)：

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