Minamikawa Shogo 南川将吾

… Alternative Names

Researcher Number	10772634
Other IDs	https://orcid.org/0000-0001-9652-6266
Affiliation (Current)	2021: 神戸大学, 医学研究科, 医学研究員
Affiliation (based on the past Project Information) *help	2019 – 2020: 神戸大学, 医学研究科, 医学研究員 2017 – 2018: 神戸大学, 医学部附属病院, 特定助教 2017: 神戸大学, 医学部付属病院, 特定助教
Review Section/Research Field	Principal Investigator Kidney internal medicine / Basic Section 52050:Embryonic medicine and pediatrics-related Except Principal Investigator Pediatrics
Keywords	Principal Investigator Lowe syndrome / Dent disease 2 / urine-derived cell / OCRL activity / Lowe症候群 / 尿中落下細胞 / 次世代シークエンサー / ナンセンスリードスルー / Dent病 / OCRL … More Except Principal Investigator Alport症候群 / 次世代シークエンサー / 網羅的遺伝子解析 / 体細胞モザイク / 高い診断能力 / 修飾遺伝子 / 診断 Less

気管切開児における下気道細菌感染症の臨床的・血液学的特徴の解明Principal InvestigatorOngoing
- Principal Investigator
  
  南川将吾
- Project Period (FY)
  2020 – 2021
- Research Category
  
  Grant-in-Aid for Early-Career Scientists
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Kobe University
Clarification of pathophysiology and development of new treatment for lowe syndrome using patient-derived proximal tubular cellsPrincipal Investigator
- Principal Investigator
  
  Minamikawa Shogo
- Project Period (FY)
  2017 – 2019
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Kidney internal medicine
- Research Institution
  Kobe University
Establishment of a comprehensive diagnostic method using next generation sequencer for Alport syndrome
- Principal Investigator
  
  Yamamura Tomohiko
- Project Period (FY)
  2016 – 2017
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Pediatrics
- Research Institution
  Kobe University

All 2020 2019 2018 2017

All Journal Article Presentation

[Journal Article] Molecular mechanisms determining severity in patients with Pierson syndrome2020
- Author(s)
  Minamikawa S、Miwa S、Inagaki T、Nishiyama K、Kaito H、Ninchoji T、Yamamura T、Nagano C、Sakakibara N、Ishimori S、Hara S、Yoshikawa No、Hirano D、Harada R、Hamada R、Matsunoshita N、Nagata M、Shima Y、Nakanishi K、Nagase H、Takeda H、Morisada N、Iijima K、Nozu K
- Journal Title
  
  Journal of Human Genetics
  
  Volume: 65 Pages: 355-362
- DOI
  10.1038/s10038-019-0715-0
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18K08243, KAKENHI-PROJECT-19K08726, KAKENHI-PROJECT-19K17297, KAKENHI-PROJECT-17K16087
[Journal Article] Detection of copy number variations by pair analysis using next-generation sequencing data in inherited kidney diseases.2018
- Author(s)
  Nagano C, Nozu K, Morisada N, Yazawa M, Ichikawa D, Numasawa K, Kourakata H, Matsumura C, Tazoe S, Tanaka R, Yamamura T, Minamikawa S, Horinouchi T, Nakanishi K, Fujimura J, Sakakibara N, Nozu Y, Ye MJ, Kaito H, Iijima K
- Journal Title
  
  Clin Exp Nephrol.
  
  Volume: 印刷中 Pages: 881-888
- DOI
  10.1007/s10157-018-1534-x
- NAID
  120006624236
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-17H04189, KAKENHI-PROJECT-15K09261, KAKENHI-PROJECT-15K09691, KAKENHI-PROJECT-16K19642, KAKENHI-PROJECT-18K08243
[Journal Article] Natural History and Genotype-Phenotype Correlation in Female X-Linked Alport Syndrome2017
- Author(s)
  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
- Journal Title
  
  Kidney Int Rep
  
  Volume: 2 Pages: 850-855
- DOI
  10.1016/j.ekir.2017.04.011
- NAID
  120006373817
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15K09694, KAKENHI-PROJECT-16K10066, KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-17H04189, KAKENHI-PROJECT-15K09695, KAKENHI-PROJECT-16K19642
[Journal Article] Female X-linked Alport syndrome with somatic mosaicism.2017
- Author(s)
  Yokota K, Nozu K, Minamikawa S, Yamamura T, Nakanishi K, Kaneda H, Hamada R, Nozu Y, Shono A, Ninchoji T, Morisada N, Ishimori S, Fujimura J, Horinouchi T, Kaito H, Nakanishi K, Morioka I, Taniguchi-Ikeda M, Iijima K.
- Journal Title
  
  Clinical and Experimental Nephrology
  
  Volume: 印刷中 Pages: 877-883
- DOI
  10.1007/s10157-016-1352-y
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15K09261, KAKENHI-PROJECT-16K10066, KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-17H04189, KAKENHI-PROJECT-16K19642
[Presentation] Lowe症候群とDent disease-2の2疾患における分子生物学的発症機序の解明2020
- Author(s)
  榊原菜々、南川将吾、野津寛大、飯島一誠
- Organizer
  第55回日本小児腎臓病学会学術集会
- Data Source
  KAKENHI-PROJECT-17K16087
[Presentation] Comparison of clinical and genetic characteristics between Dent disease-1 and Dent disease-22019
- Author(s)
  榊原菜々、南川将吾、野津寛大、飯島一誠
- Organizer
  IPNA Congress 2019
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K16087
[Presentation] Clinical and genetic characteristics in Dent disease 2 and Lowe syndrome.2019
- Author(s)
  榊原菜々、南川将吾、野津寛大、飯島一誠
- Organizer
  ASN Kidney Week 2019
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K16087

1. Yamamura Tomohiko (30770242)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
2. IIJIMA Kazumoto (00240854)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
3. NOZU Kandai (70362796)

# of Collaborated Projects: 1 results

# of Collaborated Products: 4 results
4. MORISADA Naoya

# of Collaborated Projects: 0 results

# of Collaborated Products: 3 results
5. YOSHIKAWA Norishige

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
6. NAKANISHI Koichi

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
7. SHIMA Yuko

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
8. 庄野朱美

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results

Minamikawa Shogo 南川 将吾

MINAMIKAWA Shogo 南川 将吾

Research Projects

Research Products

Co-Researchers

気管切開児における下気道細菌感染症の臨床的・血液学的特徴の解明Principal InvestigatorOngoing

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Clarification of pathophysiology and development of new treatment for lowe syndrome using patient-derived proximal tubular cellsPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Establishment of a comprehensive diagnostic method using next generation sequencer for Alport syndrome

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] Molecular mechanisms determining severity in patients with Pierson syndrome2020

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Detection of copy number variations by pair analysis using next-generation sequencing data in inherited kidney diseases.2018

Author(s)

Journal Title

DOI

NAID

Data Source

[Journal Article] Natural History and Genotype-Phenotype Correlation in Female X-Linked Alport Syndrome2017

Author(s)

Journal Title

DOI

NAID

Data Source

[Journal Article] Female X-linked Alport syndrome with somatic mosaicism.2017

Author(s)

Journal Title

DOI

Data Source

[Presentation] Lowe症候群とDent disease-2の2疾患における分子生物学的発症機序の解明2020

Author(s)

Organizer

Data Source

[Presentation] Comparison of clinical and genetic characteristics between Dent disease-1 and Dent disease-22019

Author(s)

Organizer

Data Source

[Presentation] Clinical and genetic characteristics in Dent disease 2 and Lowe syndrome.2019

Author(s)

Organizer

Data Source

Minamikawa Shogo 南川将吾

MINAMIKAWA Shogo 南川将吾