NAGANO CHINA 長野智那

… Alternative Names

Nagano China 長野智那

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Researcher Number	60814316
Other IDs
Affiliation (Current)	2025: 神戸大学, 医学部附属病院, 助教
Affiliation (based on the past Project Information) *help	2025: 神戸大学, 医学部附属病院, 助教 2023: 神戸大学, 医学研究科, 助教 2020 – 2022: 神戸大学, 医学研究科, 医学研究員 2020: 神戸大学, 医学研究科, 助教 2018 – 2019: 神戸大学, 医学研究科, 特命助教
Review Section/Research Field	Principal Investigator Basic Section 52050:Embryonic medicine and pediatrics-related Except Principal Investigator Medium-sized Section 53:Organ-based internal medicine and related fields / Basic Section 53040:Nephrology-related
Keywords	Principal Investigator WT1 / Frasier症候群 / Denys-Drash症候群 / 転写因子 / WT1遺伝子 / アンチセンス治療薬 / スプライシング Except Principal Investigator 小児ネフローゼ症候群 / ネフリン / 疾患感受性遺伝子 … More / GWASメタ解析 / ネフローゼ症候群 / 抗ネフリン抗体 / 腎臓オルガノイド / iPS細胞 / 器官システム内科学 / 腎臓学 / フィンランド型先天性ネフローゼ症候群 / ゲノムワイド関連解析 / ステロイド感受性ネフローゼ症候群 Less

WT1関連異常症の病態解明と治療法開発Principal Investigator
- Principal Investigator
  
  長野智那
- Project Period (FY)
  2025 – 2027
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Kobe University
WT1遺伝子異常症に対する病態解明と新規治療法の開発Principal Investigator
- Principal Investigator
  
  長野智那
- Project Period (FY)
  2022 – 2024
- Research Category
  
  Grant-in-Aid for Early-Career Scientists
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Kobe University
Joint international Research Project for International GWAS Meta-Analysis and Anti-Nephrin Autoantibodies in Childhood Nephrotic Syndrome
- Principal Investigator
  
  Iijima Kazumoto
- Project Period (FY)
  2021 – 2023
- Research Category
  
  Fund for the Promotion of Joint International Research (Fostering Joint International Research (B))
- Review Section
  
  Medium-sized Section 53:Organ-based internal medicine and related fields
- Research Institution
  Kobe University
Clarification of the pathogenesis of childhood nephrotic syndrome using iPS cell-derived kidney organoids
- Principal Investigator
  
  Iijima Kazumoto
- Project Period (FY)
  2020 – 2022
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 53040:Nephrology-related
- Research Institution
  Kobe University
Elucidation of pathogenicity and development of new treatment for Frasier syndromePrincipal Investigator
- Principal Investigator
  
  Nagano China
- Project Period (FY)
  2018 – 2019
- Research Category
  
  Grant-in-Aid for Early-Career Scientists
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Kobe University
Joint International Research for identification of disease-susceptible genes and drug-sensitive genes in childhood nephrotic syndrome
- Principal Investigator
  
  IIJIMA KAZUMOTO
- Project Period (FY)
  2018 – 2020
- Research Category
  
  Fund for the Promotion of Joint International Research (Fostering Joint International Research (B))
- Review Section
  
  Medium-sized Section 53:Organ-based internal medicine and related fields
- Research Institution
  Kobe University

All 2024 2023 2022 2021 2020 2019 2018

All Journal Article Presentation

[Journal Article] WT1 exon 10 missense variant in a pediatric patient with focal segmental glomerulosclerosis with embryonal hyperplasia2024
- Author(s)
  Kurokawa Mari、Nishimura Manao、Nishiyama Kei、Matsuoka Kentaro、Nagano China、Kaku Yoshitsugu
- Journal Title
  
  Pediatric Nephrology
  
  Volume: - Issue: 7 Pages: 2083-2085
- DOI
  10.1007/s00467-024-06293-w
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20K16926
[Journal Article] 【腎臓学この1年の進歩】ネフリンとネフローゼ症候群2024
- Author(s)
  飯島一誠, 堀之内智子, 長野智那, 野津寛大
- Journal Title
  
  日本腎臓学会誌
  
  Volume: 66巻 Pages: 303-309
- Data Source
  KAKENHI-PROJECT-21KK0147
[Journal Article] Anti-nephrin antibodies in steroid-sensitive nephrotic syndrome in Japanese children2023
- Author(s)
  Horinouchi Tomoko、Nagano China、Watts Andrew J. B.
- Journal Title
  
  Pediatric Nephrology
  
  Volume: 39 Issue: 1 Pages: 337-337
- DOI
  10.1007/s00467-023-06107-5
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21KK0147, KAKENHI-PROJECT-23K27617
[Journal Article] Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome2023
- Author(s)
  Barry A, McNulty MT, Jia X, Nagano C, Horinouchi T, Nozu K, Tokunaga K, Ronco P, Iijima K, Sampson MG, et al.
- Journal Title
  
  Nature Communications
  
  Volume: 14 Issue: 1 Pages: 2481-2481
- DOI
  10.1038/s41467-023-37985-w
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21KK0147, KAKENHI-PROJECT-23K27617
[Journal Article] A multicenter retrospective study of calcineurin inhibitors in nephrotic syndrome secondary to podocyte gene variants2023
- Author(s)
  Malakasioti G, Iancu D, Milovanova A, Tsygin A, Horinouchi T, Nagano C, Nozu K, Kamei K, Fujinaga S, Iijima K, et al. ; CNI in Monogenic SRNS Study Investigators
- Journal Title
  
  Kidney International
  
  Volume: 103 Issue: 5 Pages: 962-972
- DOI
  10.1016/j.kint.2023.02.022
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21KK0147, KAKENHI-PROJECT-20H03698
[Journal Article] Clinical, Pathological, and Genetic Characteristics in Patients with Focal Segmental Glomerulosclerosis2022
- Author(s)
  Nagano C, Hara S, Yoshikawa N, Takeda A, Gotoh Y, Hamada R, Matsuoka K, Yamamoto M, Fujinaga S, Sakuraya K, Kamei K, Hamasaki Y, Oguchi H, Araki Y, Ogawa Y, Okamoto T, Ito S, Tanaka S, Kaito H, Aoto Y, Ishiko S, Rossanti R, Sakakibara N, Horinouchi T, Yamamura T, Nagase H, Iijima K, Nozu K
- Journal Title
  
  Kidney360
  
  Volume: 3 Issue: 8 Pages: 1384-1393
- DOI
  10.34067/kid.0000812022
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21KK0147, KAKENHI-PROJECT-20H03698
[Journal Article] FAT1 biallelic truncating mutation causes a non-syndromic proteinuria in a child.2021
- Author(s)
  Rossanti R, Watanabe T, Nagano C, Hara S, Horinouchi T, Yamamura T, Sakakibara N, Ninchoji T, Iijima K, Nozu K.
- Journal Title
  
  CEN Case Reports
  
  Volume: 10(1) Issue: 1 Pages: 100-105
- DOI
  10.1007/s13730-020-00529-y
- Open Access
- Data Source
  KAKENHI-PROJECT-18KK0244
[Journal Article] Genotype-phenotype correlation in WT1 exon 8 to 9 missense variants2021
- Author(s)
  China Nagano, Yutaka Takaoka, Koichi Kamei, Riku Hamada, Daisuke Ichikawa, Kazuki Tanaka, Yuya Aoto, Shinya Ishiko, Rini Rossanti, Nana Sakakibara, Eri Okada, Tomoko Horinouchi, Tomohiko Yamamura, Yurika Tsuji, Yuko Noguchi, Shingo Ishimori, Hiroaki Nagase, Takeshi Ninchoji, Kazumoto Iijima, Kandai Nozu
- Journal Title
  
  Kidney International Reports
  
  Volume: - Issue: 8 Pages: 2114-2121
- DOI
  10.1016/j.ekir.2021.05.009
- NAID
  120007140164
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-20K16926, KAKENHI-PROJECT-21K12110
[Journal Article] An extremely mild clinical course in a case with LAMB2-associated nephritis diagnosed with next-generation sequencing.2021
- Author(s)
  Sakuraya K, Nozu K, Murakami H, Nagano C, Horinouchi T, Fujinaga S, Iijima K, Ohtomo Y.
- Journal Title
  
  CEN Case Reports
  
  Volume: - Issue: 3 Pages: 359-363
- DOI
  10.1007/s13730-021-00574-1
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18KK0244, KAKENHI-PROJECT-19K08726
[Journal Article] Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome2020
- Author(s)
  Jia Xiaoyuan、Yamamura Tomohiko、et al.
- Journal Title
  
  Kidney International
  
  Volume: 98 Issue: 5 Pages: 1308-1322
- DOI
  10.1016/j.kint.2020.05.029
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07799, KAKENHI-PROJECT-19K08726, KAKENHI-PROJECT-20K08370, KAKENHI-PROJECT-20K16892, KAKENHI-PROJECT-18KK0244, KAKENHI-PROJECT-20H03698
[Journal Article] Molecular mechanisms determining severity in patients with Pierson syndrome2020
- Author(s)
  Minamikawa Shogo、Miwa Saori、Inagaki Tetsuji、Nishiyama Kei、Kaito Hiroshi、Ninchoji Takeshi、Yamamura Tomohiko、Nagano China、Sakakibara Nana、Ishimori Shingo、Hara Shigeo、Yoshikawa Norishige、Hirano Daishi、Harada Ryoko、Hamada Riku、Matsunoshita Natsuki、Nagata Michio、Shima Yuko、Nozu Kandai
- Journal Title
  
  Journal of Human Genetics
  
  Volume: 65 Issue: 4 Pages: 355-362
- DOI
  10.1038/s10038-019-0715-0
- NAID
  120006811107
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K08726, KAKENHI-PROJECT-17K16087, KAKENHI-PROJECT-18K07799, KAKENHI-PROJECT-18K08243, KAKENHI-PROJECT-19K17297, KAKENHI-PROJECT-18KK0244
[Journal Article] Comprehensive genetic diagnosis of Japanese patients with severe proteinuria.2020
- Author(s)
  Nagano C, Yamamura T, Horinouchi T, Aoto Y, Ishiko S, Sakakibara N, Shima Y, Nakanishi K, Nagase H, Iijima K, Nozu K.
- Journal Title
  
  Sci Rep.
  
  Volume: 10(1) Issue: 1 Pages: 428-437
- DOI
  10.1038/s41598-019-57149-5
- NAID
  120006884200
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07799, KAKENHI-PROJECT-19K08726, KAKENHI-PROJECT-18KK0244, KAKENHI-PROJECT-18K15713
[Journal Article] Molecular assay for an intronic variant in NUP93 that causes steroid resistant nephrotic syndrome2019
- Author(s)
  Rossanti Rini、Shono Akemi、Miura Kenichiro、Hattori Motoshi、Yamamura Tomohiko、Nakanishi Keita、Minamikawa Shogo、Fujimura Junya、Horinouchi Tomoko、Nagano China、Sakakibara Nana、Kaito Hiroshi、Nagase Hiroaki、Morisada Naoya、Asanuma Katsuhiko、Matsuo Masafumi、Nozu Kandai、Iijima Kazumoto
- Journal Title
  
  Journal of Human Genetics
  
  Volume: 64 Issue: 7 Pages: 673-679
- DOI
  10.1038/s10038-019-0606-4
- NAID
  120006653286
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K08243, KAKENHI-PROJECT-19K09921, KAKENHI-PROJECT-18KK0244, KAKENHI-PROJECT-18K15712, KAKENHI-PROJECT-18H02823
[Journal Article] The utility of urinary CD80 as a diagnostic marker in patients with renal diseases2018
- Author(s)
  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
- Journal Title
  
  Scientific Reports
  
  Volume: 8 Issue: 1 Pages: 17322-17322
- DOI
  10.1038/s41598-018-35798-2
- NAID
  120006543320
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18KK0244
[Journal Article] Pair analysis and custom array CGH can detect a small copy number variation in COQ6 gene2018
- Author(s)
  Nakanishi Keita、Okamoto Takayuki、Nozu Kandai、Hara Shigeo、Sato Yasuyuki、Hayashi Asako、Takahashi Toshiyuki、Nagano China、Sakakibara Nana、Horinouchi Tomoko、Fujimura Junya、Minamikawa Shogo、Yamamura Tomohiko、Rossanti Rini、Nagase Hiroaki、Kaito Hiroshi、Ariga Tadashi、Iijima Kazumoto
- Journal Title
  
  Clinical and Experimental Nephrology
  
  Volume: 23 Issue: 5 Pages: 669-675
- DOI
  10.1007/s10157-018-1682-z
- NAID
  120006644119
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18KK0244, KAKENHI-PROJECT-17K16262, KAKENHI-PROJECT-18K15712
[Presentation] WT1遺伝子exon8-9ミスセンス変異における遺伝子型－臨床型の相関に関する検討2020
- Author(s)
  長野　智那
- Organizer
  第63回　日本腎臓学会学術総会
- Data Source
  KAKENHI-PROJECT-20K16926
[Presentation] WT1遺伝子exon8-9ミスセンス変異における遺伝型－臨床型の相関に関する研究2020
- Author(s)
  長野　智那
- Organizer
  第55回　日本小児腎臓病学会学術集会
- Data Source
  KAKENHI-PROJECT-20K16926
[Presentation] NPHS1は小児ステロイド感受性ネフローゼ症候群の疾患感受性遺伝子である2019
- Author(s)
  山村智彦、長野智那、堀之内智子、野津寛大、飯島一誠
- Organizer
  第62回日本腎臓学会学術集会
- Data Source
  KAKENHI-PROJECT-18KK0244
[Presentation] 遺伝性ネフローゼ症候群における臨床的特徴の検討2019
- Author(s)
  長野　智那
- Organizer
  第54回日本小児腎臓病学会学術集会
- Data Source
  KAKENHI-PROJECT-18K15713
[Presentation] Comprehensive genetic diagnosis system for steroid-resistant nephrotic syndrome in Japanese population2019
- Author(s)
  長野　智那
- Organizer
  International Pediartic Nephrology Association 2019
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K15713
[Presentation] 先天性/乳児およびステロイド抵抗性ネフローゼ症候群における網羅的遺伝子診断2019
- Author(s)
  長野智那、野津寛大、青砥悠哉、石河慎也、榊原菜々、南川将吾、山村智彦、飯島一誠
- Organizer
  第122回日本小児科学会学術集会
- Data Source
  KAKENHI-PROJECT-18KK0244
[Presentation] Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome2019
- Author(s)
  Tomoko Horinouchi, Tomohiko Yamamura, Rasheed A. Gbadegesin, Matthew G. Sampson, China Nagano, Kandai Nozu, Kenji Ishikura, Pierre M. Ronco, Hae Il Cheong, Kazumoto Iijima
- Organizer
  American Society of Nephrology Kidney week 2019
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18KK0244
[Presentation] 遺伝性ネフローゼ症候群における臨床的特徴の検討2019
- Author(s)
  長野智那、野津寛大、青砥悠哉、石河慎也、榊原菜々、南川将吾、山村智彦、飯島一誠
- Organizer
  第54回日本小児腎臓病学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-18KK0244
[Presentation] 遺伝性ネフローゼ症候群における臨床的特徴の検討2019
- Author(s)
  長野　智那
- Organizer
  第62回日本腎臓学会学術集会
- Data Source
  KAKENHI-PROJECT-18K15713
[Presentation] 遺伝性腎疾患に対するプレシジョンメデイスン　小児ステロイド感受性ネフローゼ症候群の疾患感受性遺伝子2019
- Author(s)
  飯島一誠、 Jia Xiaoyuan,、山村智彦、人見祐基、長野智那、堀之内智子、野津寛大、徳永勝士
- Organizer
  第54回日本小児腎臓病学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-18KK0244

1. IIJIMA KAZUMOTO (00240854)

# of Collaborated Projects: 3 results

# of Collaborated Products: 13 results
2. 堀之内智子 (30754593)

# of Collaborated Projects: 3 results

# of Collaborated Products: 12 results
3. 野津寛大 (70362796)

# of Collaborated Projects: 3 results

# of Collaborated Products: 14 results
4. 人見祐基 (10525819)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
5. 高里実 (40788676)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
6. 賈暁媛 (20914328)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
7. 中山真紀子 (80469999)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
8. MORISADA Naoya

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
9. NAKANISHI Koichi

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
10. SHIMA Yuko

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

NAGANO CHINA 長野 智那

Nagano China 長野 智那

Research Projects

Research Products

Co-Researchers

WT1関連異常症の病態解明と治療法開発Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

WT1遺伝子異常症に対する病態解明と新規治療法の開発Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Joint international Research Project for International GWAS Meta-Analysis and Anti-Nephrin Autoantibodies in Childhood Nephrotic Syndrome

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Clarification of the pathogenesis of childhood nephrotic syndrome using iPS cell-derived kidney organoids

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Elucidation of pathogenicity and development of new treatment for Frasier syndromePrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Joint International Research for identification of disease-susceptible genes and drug-sensitive genes in childhood nephrotic syndrome

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

[Journal Article] WT1 exon 10 missense variant in a pediatric patient with focal segmental glomerulosclerosis with embryonal hyperplasia2024

Author(s)

Journal Title

DOI

Data Source

[Journal Article] 【腎臓学この1年の進歩】ネフリンとネフローゼ症候群2024

Author(s)

Journal Title

Data Source

[Journal Article] Anti-nephrin antibodies in steroid-sensitive nephrotic syndrome in Japanese children2023

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome2023

Author(s)

Journal Title

DOI

Data Source

[Journal Article] A multicenter retrospective study of calcineurin inhibitors in nephrotic syndrome secondary to podocyte gene variants2023

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Clinical, Pathological, and Genetic Characteristics in Patients with Focal Segmental Glomerulosclerosis2022

Author(s)

Journal Title

DOI

Data Source

[Journal Article] FAT1 biallelic truncating mutation causes a non-syndromic proteinuria in a child.2021

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Genotype-phenotype correlation in WT1 exon 8 to 9 missense variants2021

Author(s)

Journal Title

DOI

NAID

NAGANO CHINA 長野智那

Nagano China 長野智那

[Presentation] 先天性/乳児およびステロイド抵抗性ネフローゼ症候群における網羅的遺伝子診断2019