Nagano China

ナガノチナ | Nagano China

Affiliation and department：
Job title： Assistant Professor

Research field (1)： Other

Research theme for competitive and other funds (5)：

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
2020 - 2022 WT1遺伝子異常症に対する病態解明と新規治療法の開発
2018 - 2021 小児ネフローゼ症候群疾患感受性遺伝子及び薬剤感受性遺伝子同定のための国際共同研究
2018 - 2020 WT1遺伝子変異によるFrasier症候群の病態解明および新規治療法の開発

Papers (116)：

花房宏昭, 森貞直哉, 長坂美和子, 叶明娟, 野口裕子, 長野智那, 野津寛大, 粟野宏之. MSL3領域のヌリソミーで生じたBasilicata-Akhtar症候群の日本人男児例(Basilicata-Akhtar syndrome derived from a nullisomy of the MSL3 region in a Japanese boy). 脳と発達. 2023. 55. 4. 279-282
花房宏昭, 森貞直哉, 長坂美和子, 叶明娟, 野口裕子, 長野智那, 野津寛大, 粟野宏之. MSL3領域のヌリソミーで生じたBasilicata-Akhtar症候群の日本人男児例(Basilicata-Akhtar syndrome derived from a nullisomy of the MSL3 region in a Japanese boy). 脳と発達. 2023. 55. 4. 279-282
Ryota Suzuki, Nana Sakakibara, Yuta Ichikawa, Hideaki Kitakado, Chika Ueda, Yu Tanaka, Eri Okada, Atsushi Kondo, Shinya Ishiko, Shingo Ishimori, et al. Systematic Review of Clinical Characteristics and Genotype-Phenotype Correlation in LAMB2-Associated Disease. Kidney International Reports. 2023
Eri Okada, Tomoko Horinouchi, Tomohiko Yamamura, Yuya Aoto, Ryota Suzuki, Yuta Ichikawa, Yu Tanaka, Chika Masuda, Hideaki Kitakado, Atsushi Kondo, et al. All reported non-canonical splice site variants in GLA cause aberrant splicing. Clinical and experimental nephrology. 2023
Eri Okada, Naoya Morisada, Tomoko Horinouchi, Hideki Fujii, Takayuki Tsuji, Masayoshi Miura, Hideyuki Katori, Masashi Kitagawa, Kunio Morozumi, Takanobu Toriyama, et al. Corrigendum to "Detecting MUC1 Variants in Patients Clinicopathologically Diagnosed With Having Autosomal Dominant Tubulointerstitial Kidney Disease"Kidney International Reports, Volume 7, Issue 4, April 2022, Pages 857-866. Kidney international reports. 2023. 8. 5. 1127-1129

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MISC (25)：

榊原菜々, 野津寛大, 青砥悠哉, 長野智那, 堀之内智子, 忍頂寺毅史, 岡田絵里, 川口武彦, 今澤俊之, 稲垣徹史, et al. CLCN5遺伝子を含むX染色体微細欠失により発症したDent disease-1女性の2例. 日本腎臓学会誌(Web). 2021. 63. 4
森貞直哉, 森貞直哉, 洪本加奈, 近藤淳, ROSSANTI Rini, 石河慎也, 青砥裕哉, 岡田絵里, 榊原奈々, 長野智那, et al. 嚢胞性腎疾患の包括的遺伝子解析. 日本人類遺伝学会大会プログラム・抄録集. 2021. 66th (CD-ROM)
榊原菜々, 岡本孝之, 野津寛大, 佐藤泰征, 林麻子, 高橋俊行, 上田泰弘, 近藤淳, 永井貞之, 青砥悠哉, et al. Dent disease-2の女児例に関する初めての報告およびその発症機序の解明. 日本小児腎臓病学会雑誌(Web). 2020. 33. 1
長野智那, 野津寛大, 飯島一誠. Genetic disease of the kidney and the urinary tract. 腎臓内科・泌尿器科 = Nephrology & urology. 2019. 9. 5. 425-429
堀之内智子, 山村智彦, 榊原菜々, 長野智那, 藤村順也, 中西啓太, 南川将吾, 貝藤裕史, 野津寛大, 飯島一誠. In vitro実験系を用いたCOL4A5 intron変異の病原性の検討. 日本小児腎臓病学会雑誌. 2018. 31. 1Suppl. 99-99

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Lectures and oral presentations (27)：

OFD1に変異を有するシリオパチーの生存男児3例
(第40回日本小児腎不全学会学術集会 2018)
The utility of urinary CD80 as a diagnostic maker in patients with renal diseases
(51th Annual Scientific Meeting of the European Society for Paediatric Nephrology 2018)
Splicing assay with hybrid minigene: assessing pathogenicities in COL4A5 intronic mutations
(52st Annual Meeting of the American Society of Nephrology 2018)
Factors regulating the severity in male X-linked Alport syndrome: study of 367 cases
(52st Annual Meeting of the American Society of Nephrology 2018)
Comprehensive genetic analysis of nephronophthisis-related ciliopathies (NPHP-RC) using next generation sequencing
(51th Annual Scientific Meeting of the European Society for Paediatric Nephrology 2018)

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Education (1)：

2017 - 2020 Kobe University Graduate School of Medicine

Professional career (1)：

学士(医学) (岐阜大学)

Awards (3)：

2021/02 - 第55回日本小児腎臓病学会学術集会優秀演題奨励賞臨床研究部門
2019/06 - Japanese Society of Nephrology Excellent Presentation Award
2018/06 - Japanese Society for Pediatric Nephrology Excellent Presentation Award

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