Kagawa Reiko 香川礼子

Researcher Number	40806634
Other IDs	https://orcid.org/0000-0001-7155-0673
Affiliation (Current)	2024: 広島大学, 病院(医), 助教
Affiliation (based on the past Project Information) *help	2021 – 2023: 広島大学, 病院(医), 助教 2019 – 2020: 広島大学, 病院(医), 医科診療医
Review Section/Research Field	Principal Investigator Basic Section 52050:Embryonic medicine and pediatrics-related
Keywords	Principal Investigator 真菌感染症 / 原発性免疫不全症 / CARD7欠損症 / TNF-α / CXCL1 / IL8 / IL6 / IL1B / CARD9 / 機能解析 … More / NF-kB / TNF / IL-8 / IL-6 / CARD7 / 機能獲得型変異 / 慢性皮膚粘膜カンジダ症(CMCD) / STAT1GOF変異 / R274Q / T385M / STAT1 GOF変異 / 脱リン酸化障害 / STAT1 / ISG / 脱リン酸化酵素 / 複合型免疫不全症 / CMCD / STAT1-GOF Less

Establishment of a method for functional analysis of CARD9 mutationsPrincipal Investigator
- Principal Investigator
  
  Kagawa Reiko
- Project Period (FY)
  2021 – 2023
- Research Category
  
  Grant-in-Aid for Early-Career Scientists
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Hiroshima University
Study of molecular pathology in which STAT1 gain-of-function mutations cause autoimmune endocrine disordersPrincipal Investigator
- Principal Investigator
  
  Kagawa Reiko
- Project Period (FY)
  2019 – 2021
- Research Category
  
  Grant-in-Aid for Early-Career Scientists
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Hiroshima University

All 2024 2023 2022 2021 2020

All Journal Article

[Journal Article] Using the C14:1/Medium-Chain Acylcarnitine Ratio Instead of C14:1 to Reduce False-Positive Results for Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency in Newborn Screening in Japan2024
- Author(s)
  Tajima Go、Aisaki Junko、Hara Keiichi、Tsumura Miyuki、Kagawa Reiko、Sakura Fumiaki、Sasai Hideo、Yuasa Miori、Shigematsu Yosuke、Okada Satoshi
- Journal Title
  
  International Journal of Neonatal Screening
  
  Volume: 10 Issue: 1 Pages: 15-15
- DOI
  10.3390/ijns10010015
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23K14943, KAKENHI-PROJECT-22K07889, KAKENHI-PROJECT-21K15904
[Journal Article] Blood glucose trends in glycogen storage disease type Ia: A cross‐sectional study2023
- Author(s)
  Fukuda Tokiko、Ito Tetsuya、Hamazaki Takashi、Inui Ayano、Ishige Mika、Kagawa Reiko、Sakai Norio、Watanabe Yoriko、Kobayashi Hironori、Wasaki Yosuke、Taura Junki、Imamura Yuki、Tsukiuda Tsutomu、Nakamura Kimitoshi
- Journal Title
  
  Journal of Inherited Metabolic Disease
  
  Volume: 46 Issue: 4 Pages: 618-633
- DOI
  10.1002/jimd.12610
- Data Source
  KAKENHI-PROJECT-21K15904
[Journal Article] Growth Hormone Injection Log Analysis with Electronic Injection Device for Qualifying Adherence to Low-Irritant Formulation and Exploring Influential Factors on Adherence2023
- Author(s)
  Takasawa Kei、Mabe Hiroyo、Nagamatsu Fusa、Amano Naoko、Miyakawa Yuichi、Sutani Akito、Kagawa Reiko、Okada Satoshi、Tanahashi Yusuke、Suzuki Shigeru、Hiroshima Shota、Nagasaki Keisuke、Dateki Sumito、Takishima Shigeru、Takahashi Ikuko、Kashimada Kenichi
- Journal Title
  
  Patient Preference and Adherence
  
  Volume: Volume 17 Pages: 1885-1894
- DOI
  10.2147/ppa.s417142
- Data Source
  KAKENHI-PROJECT-21K15904
[Journal Article] Newborn Screening with (C16 + C18:1)/C2 and C14/C3 for Carnitine Palmitoyltransferase II Deficiency throughout Japan Has Revealed C12/C0 as an Index of Higher Sensitivity and Specificity2023
- Author(s)
  Tajima Go、Hara Keiichi、Tsumura Miyuki、Kagawa Reiko、Sakura Fumiaki、Sasai Hideo、Yuasa Miori、Shigematsu Yosuke、Okada Satoshi
- Journal Title
  
  International Journal of Neonatal Screening
  
  Volume: 9 Issue: 4 Pages: 62-62
- DOI
  10.3390/ijns9040062
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23K14943, KAKENHI-PROJECT-22K07889, KAKENHI-PROJECT-21K15904
[Journal Article] Enhanced osteoclastogenesis in patients with MSMD due to impaired response to IFN-γ2022
- Author(s)
  Tsumura Miyuki、Miki Mizuka、Mizoguchi Yoko、Hirata Osamu、Nishimura Shiho、Tamaura Moe、Kagawa Reiko、Hayakawa Seiichi、Kobayashi Masao、Okada Satoshi
- Journal Title
  
  Journal of Allergy and Clinical Immunology
  
  Volume: 149 Issue: 1 Pages: 252-261
- DOI
  10.1016/j.jaci.2021.05.018
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K17301, KAKENHI-PROJECT-19H03620, KAKENHI-PROJECT-20K08158, KAKENHI-PROJECT-21K15905, KAKENHI-PROJECT-21K15904, KAKENHI-PROJECT-22K15921, KAKENHI-PROJECT-20K22780
[Journal Article] Inborn errors of immunity with loss- and gain-of-function germline mutations in STAT12022
- Author(s)
  Asano Takaki、Utsumi Takanori、Kagawa Reiko、Karakawa Shuhei、Okada Satoshi
- Journal Title
  
  Clinical and Experimental Immunology
  
  Volume: 149 Issue: 2 Pages: 252-261
- DOI
  10.1093/cei/uxac106
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21K15904, KAKENHI-PROJECT-22K20772
[Journal Article] Current Perspectives on Neonatal Screening for Propionic Acidemia in Japan: An Unexpectedly High Incidence of Patients with Mild Disease Caused by a Common PCCB Variant2021
- Author(s)
  Tajima Go、Kagawa Reiko、Sakura Fumiaki、Nakamura-Utsunomiya Akari、Hara Keiichi、Yuasa Miori、Hasegawa Yuki、Sasai Hideo、Okada Satoshi
- Journal Title
  
  International Journal of Neonatal Screening
  
  Volume: 7 Issue: 3 Pages: 35-35
- DOI
  10.3390/ijns7030035
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K17301, KAKENHI-PROJECT-21K15904
[Journal Article] Inherited CARD9 Deficiency in a Child with Invasive Disease Due to Exophiala dermatitidis and Two Older but Asymptomatic Siblings2021
- Author(s)
  Imanaka Yusuke、Taniguchi Maki、Doi Takehiko、Tsumura Miyuki、Nagaoka Rie、Shimomura Maiko、Asano Takaki、Kagawa Reiko、Mizoguchi Yoko、Karakawa Shuhei、Arihiro Koji、Imai Kohsuke、Morio Tomohiro、Casanova Jean-Laurent、Puel Anne、Ohara Osamu、Kamei Katsuhiko、Kobayashi Masao、Okada Satoshi
- Journal Title
  
  Journal of Clinical Immunology
  
  Volume: - Issue: 5 Pages: 975-986
- DOI
  10.1007/s10875-021-00988-7
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19H03620, KAKENHI-PROJECT-18K07814, KAKENHI-PROJECT-18KK0228, KAKENHI-PROJECT-19K17301, KAKENHI-PROJECT-21K15904, KAKENHI-PROJECT-21K15905
[Journal Article] Pilot Study on Neonatal Screening for Methylmalonic Acidemia Caused by Defects in the Adenosylcobalamin Synthesis Pathway and Homocystinuria Caused by Defects in Homocysteine Remethylation2021
- Author(s)
  Kagawa Reiko、Tajima Go、Maeda Takako、Sakura Fumiaki、Nakamura-Utsunomiya Akari、Hara Keiichi、Nishimura Yutaka、Yuasa Miori、Shigematsu Yosuke、Tanaka Hiromi、Fujihara Saki、Yoshii Chiyoko、Okada Satoshi
- Journal Title
  
  International Journal of Neonatal Screening
  
  Volume: 7 Issue: 3 Pages: 39-39
- DOI
  10.3390/ijns7030039
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K17301, KAKENHI-PROJECT-21K15904
[Journal Article] Autosomal recessive complete STAT1 deficiency caused by compound heterozygous intronic mutations2020
- Author(s)
  Sakata Sonoko、Tsumura Miyuki、Matsubayashi Tadashi、Karakawa Shuhei、Kimura Shunsuke、Tamaura Moe、Okano Tsubasa、Naruto Takuya、Mizoguchi Yoko、Kagawa Reiko、Nishimura Shiho、Imai Kohsuke、Le Voyer Tom、Casanova Jean-Laurent、Bustamante Jacinta、Morio Tomohiro、Ohara Osamu、Kobayashi Masao、Okada Satoshi
- Journal Title
  
  International Immunology
  
  Volume: 32 Issue: 10 Pages: 663-671
- DOI
  10.1093/intimm/dxaa043
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K08158, KAKENHI-PROJECT-19K17301, KAKENHI-PROJECT-20K22780, KAKENHI-PROJECT-19H03620, KAKENHI-PROJECT-18K07814, KAKENHI-PROJECT-18KK0228

1. OKADA Satoshi

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results
2. TSUMURA Miyuki

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results
3. OHARA Osamu

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
4. 湯浅光織

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results

Kagawa Reiko 香川 礼子

Research Projects

Research Products

Co-Researchers

Establishment of a method for functional analysis of CARD9 mutationsPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Study of molecular pathology in which STAT1 gain-of-function mutations cause autoimmune endocrine disordersPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

[Journal Article] Using the C14:1/Medium-Chain Acylcarnitine Ratio Instead of C14:1 to Reduce False-Positive Results for Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency in Newborn Screening in Japan2024

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Blood glucose trends in glycogen storage disease type Ia: A cross‐sectional study2023

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Growth Hormone Injection Log Analysis with Electronic Injection Device for Qualifying Adherence to Low-Irritant Formulation and Exploring Influential Factors on Adherence2023

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Newborn Screening with (C16 + C18:1)/C2 and C14/C3 for Carnitine Palmitoyltransferase II Deficiency throughout Japan Has Revealed C12/C0 as an Index of Higher Sensitivity and Specificity2023

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Enhanced osteoclastogenesis in patients with MSMD due to impaired response to IFN-γ2022

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Inborn errors of immunity with loss- and gain-of-function germline mutations in STAT12022

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Current Perspectives on Neonatal Screening for Propionic Acidemia in Japan: An Unexpectedly High Incidence of Patients with Mild Disease Caused by a Common PCCB Variant2021

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Inherited CARD9 Deficiency in a Child with Invasive Disease Due to Exophiala dermatitidis and Two Older but Asymptomatic Siblings2021

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Pilot Study on Neonatal Screening for Methylmalonic Acidemia Caused by Defects in the Adenosylcobalamin Synthesis Pathway and Homocystinuria Caused by Defects in Homocysteine Remethylation2021

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Autosomal recessive complete STAT1 deficiency caused by compound heterozygous intronic mutations2020

Author(s)

Journal Title

DOI

Data Source

Kagawa Reiko 香川礼子