kido jun 城戸淳

… Alternative Names

Kido Jun 城戸淳

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Researcher Number	70721215
Other IDs
Affiliation (Current)	2025: 熊本大学, 大学院生命科学研究部(医), 准教授
Affiliation (based on the past Project Information) *help	2023: 熊本大学, 大学院生命科学研究部(医), 特定研究員 2021 – 2023: 熊本大学, 病院, 講師 2018 – 2020: 熊本大学, 大学院生命科学研究部(医), 助教 2017: 熊本大学, 医学部附属病院小児科学分野, 特任助教 2016 – 2017: 熊本大学, 医学部附属病院, 診療助手 2015: 熊本大学, 医学部附属病院, その他 2014: 熊本大学, 医学部附属病院, 非常勤診療医師
Review Section/Research Field	Principal Investigator Basic Section 52050:Embryonic medicine and pediatrics-related / Pediatrics Except Principal Investigator Basic Section 53050:Dermatology-related / Pediatrics
Keywords	Principal Investigator iPS細胞 / ゴーシェ病 / グロボトリアオシルスフィンゴシン / ろ紙血 / α-Gal A / 新生児スクリーニング / Lyso-Gb3 / LC/MS/MS / ファブリー病 / グルコシルスフィンゴシン … More / ライソソーム / ミトコンドリア機能 / オートファジー / 酸化ストレス / ポストシナプス機能 / プレシナプス機能 / 神経型ゴーシェ病 / 治療薬開発 / Gaucher disease / LAMP1 / GlcSph / 神経型ゴーシェー病 / Neural stem cell / ニューロン / ゴーシェー病 / Neuron / IPS細胞 / 神経幹細胞 / ライソーム病 / 先天代謝異常症 / 遺伝子修復 / 疾患iPS細胞 / 糖原病 / グリコーゲン / 肝臓分化 / 肝臓 / 糖原病Ia型 … More Except Principal Investigator 免疫療法 / メタボローム解析 / 細胞内代謝機能 / 糖尿病 / バイオマーカー / 再生医療 / β細胞 / 1型糖尿病 / エネルギー代謝 / iPS細胞 / 小児糖尿病 Less

血漿Lyso-Gb3と血管内皮細胞解析を駆使した新しいファブリー病診断システムの構築Principal Investigator
- Principal Investigator
  
  城戸淳
- Project Period (FY)
  2023 – 2025
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Kumamoto University
iPS細胞を用いたメラノーマに対する新規がん免疫療法の開発
- Principal Investigator
  
  梶原隆太郎
- Project Period (FY)
  2023 – 2025
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 53050:Dermatology-related
- Research Institution
  Kumamoto University
Development of novel pathological analysis and medicine in neuropathic Gaucher disease.Principal Investigator
- Principal Investigator
  
  城戸淳
- Project Period (FY)
  2020 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Kumamoto University
Development of novel medicine using iPS cells derived from Gaucher disease type II patientsPrincipal Investigator
- Principal Investigator
  
  Kido Jun
- Project Period (FY)
  2017 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Kumamoto University
Prediction of DiabetesMellitus by using with iPS cell technology
- Principal Investigator
  
  MATSUMOTO SHIROU
- Project Period (FY)
  2015 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Kumamoto University
Establish of gene repair methods and analysis of pathological conditions using iPS cells derived from patients with glycogen storage disease type IaPrincipal Investigator
- Principal Investigator
  
  Kido Jun
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Pediatrics
- Research Institution
  Kumamoto University

All 2023 2022 2021 2020 2019 2018 2017 2016 2015

All Journal Article Presentation

[Journal Article] Frequency of iduronate-2-sulfatase gene variants detected in newborn screening for mucopolysaccharidosis type II in Japan2023
- Author(s)
  Hattori Yusuke、Sawada Takaaki、Kido Jun、Sugawara Keishin、Yoshida Shinichiro、Matsumoto Shirou、Inoue Takahito、Hirose Shinichi、Nakamura Kimitoshi
- Journal Title
  
  Molecular Genetics and Metabolism Reports
  
  Volume: 37 Pages: 101003-101003
- DOI
  10.1016/j.ymgmr.2023.101003
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-23K14954, KAKENHI-PROJECT-23K07294, KAKENHI-PROJECT-23K07316
[Journal Article] Gene therapy for spinal muscular atrophy is considerably effective when administered as early as possible after birth.2023
- Author(s)
  Sawada T, Kido J, Yae Y, Yuge K, Nomura K, Okada K, Fujiyama N, Ozasa S, Nakamura K.
- Journal Title
  
  Mol Genet Metab Rep.
  
  Volume: 35 Pages: 100973-100973
- DOI
  10.1016/j.ymgmr.2023.100973
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K08207, KAKENHI-PROJECT-22K15952, KAKENHI-PROJECT-23K07294
[Journal Article] X-linked intellectual disability related to a novel variant of KLHL152023
- Author(s)
  Kido Jun、Egami Kimiyasu、Misumi Yohei、Sugawara Keishin、Tsuchida Naomi、Matsumoto Naomichi、Ueda Mitsuharu、Nakamura Kimitoshi
- Journal Title
  
  Human Genome Variation
  
  Volume: 10 Issue: 1 Pages: 21-21
- DOI
  10.1038/s41439-023-00248-7
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K08207
[Journal Article] Gene therapy for lysosomal storage diseases: Current clinical trial prospects.2023
- Author(s)
  Kido J, Sugawara K, Nakamura K.
- Journal Title
  
  Front Genet.
  
  Volume: 14 Pages: 1064924-1064924
- DOI
  10.3389/fgene.2023.1064924
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K08207
[Journal Article] Improved sensitivity and specificity for citrin deficiency using selected amino acids and acylcarnitines in the newborn screening2023
- Author(s)
  Kido Jun、Haeberle Johannes、Tanaka Toju、Nagao Masayoshi、Wada Yoichi、Numakura Chikahiko、Bo Ryosuke、Nyuzuki Hiromi、Dateki Sumito、Maruyama Shinsuke、Murayama Kei、Yoshida Shinichiro、Nakamura Kimitoshi
- Journal Title
  
  Journal of Inherited Metabolic Disease
  
  Volume: - Issue: 6 Pages: 1134-1143
- DOI
  10.1002/jimd.12673
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K08207, KAKENHI-PROJECT-23K07294
[Journal Article] Pathogenic variants of ornithine transcarbamylase deficiency: Nation-wide study in Japan and literature review.2022
- Author(s)
  Kido J, Sugawara K, Sawada T, Matsumoto S, Nakamura K.
- Journal Title
  
  Front Genet.
  
  Volume: 13 Pages: 952467-952467
- DOI
  10.3389/fgene.2022.952467
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K08207, KAKENHI-PROJECT-20K08259
[Journal Article] A case report of two siblings with hypertyrosinemia type 1 presenting with hepatic disease with different onset time and severity.2022
- Author(s)
  Kawabata K, Kido J, Yoshida T, Matsumoto S, Nakamura K.
- Journal Title
  
  Mol Genet Metab Rep.
  
  Volume: 32 Pages: 100892-100892
- DOI
  10.1016/j.ymgmr.2022.100892
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K08207
[Journal Article] Newborn screening for spinal muscular atrophy in Japan: One year of experience.2022
- Author(s)
  Sawada T, Kido J, Sugawara K, Yoshida S, Ozasa S, Nomura K, Okada K, Fujiyama N, Nakamura K.
- Journal Title
  
  Newborn screening for spinal muscular atrophy in Japan: One year of experience.
  
  Volume: 32 Pages: 100908-100908
- DOI
  10.1016/j.ymgmr.2022.100908
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K08207, KAKENHI-PROJECT-20K08259
[Journal Article] Clinical manifestation and long-term outcome of citrin deficiency: Report from a nationwide study in Japan2022
- Author(s)
  Kido J, Haberle J, Sugawara K, Tanaka T, Nagao M, Sawada T, Wada Y, Numakura C, Murayama K, Watanabe Y, Kojima-Ishii K, Sasai H, Kosugiyama K, Nakamura K.
- Journal Title
  
  J Inherit Metab Dis .
  
  Volume: none Issue: 3 Pages: 431-444
- DOI
  10.1002/jimd.12483
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K08207, KAKENHI-PROJECT-20K08259, KAKENHI-PROJECT-22K07889
[Journal Article] Newborn screening for Gaucher disease in Japan.2022
- Author(s)
  Sawada T, Kido J, Sugawara K, Yoshida S, Matsumoto S, Shimazu T, Matsushita Y, Inoue T, Hirose S, Endo F, Nakamura K.
- Journal Title
  
  Mol Genet Metab Rep.
  
  Volume: 31 Pages: 100850-100850
- DOI
  10.1016/j.ymgmr.2022.100850
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K08207, KAKENHI-PROJECT-20K08259
[Journal Article] Physical, cognitive, and social status of patients with urea cycle disorders in Japan.2021
- Author(s)
  Kido J, Matsumoto S, Ito T, Hirose S, Fukui K, Kojima-Ishii K, Mushimoto Y, Yoshida S, Ishige M, Sakai N, Nakamura K.
- Journal Title
  
  Mol Genet Metab Rep.
  
  Volume: 27 Pages: 100724-100724
- DOI
  10.1016/j.ymgmr.2021.100724
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K08207
[Journal Article] An iPSC-based neural model of sialidosis uncovers glycolytic impairment-causing presynaptic dysfunction and deregulation of Ca2+ dynamics.2021
- Author(s)
  Odaka H, Numakawa T, Soga M, Kido J, Matsumoto S, Kajihara R, Okumiya T, Tani N, Tanoue Y, Fukuda T, Furuya H, Inoue T, Era T.
- Journal Title
  
  Neurobiol Dis.
  
  Volume: 152 Pages: 105279-105279
- DOI
  10.1016/j.nbd.2021.105279
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K08207, KAKENHI-PROJECT-20K06857, KAKENHI-PROJECT-19K16263
[Journal Article] Current status of surviving patients with arginase 1 deficiency in Japan.2021
- Author(s)
  Kido J*, Matsumoto S, Takeshita E, Hayasaka C, Yamada K, Kagawa J, Nakajima Y, Ito T, Iijima H, Endo F, Nakamura K.
- Journal Title
  
  Mol Genet Metab Rep.
  
  Volume: 29 Pages: 100805-100805
- DOI
  10.1016/j.ymgmr.2021.100805
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K08207
[Journal Article] Current status of newborn screening for Pompe disease in Japan.2021
- Author(s)
  Sawada T, Kido J*, Sugawara K, Momosaki K, Yoshida S, Kojima-Ishii K, Inoue T, Matsumoto S, Endo F, Ohga S, Hirose S, Nakamura K.
- Journal Title
  
  Orphanet J Rare Dis.
  
  Volume: 18 Issue: 1 Pages: 516-516
- DOI
  10.1186/s13023-021-02146-z
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K08207, KAKENHI-PROJECT-20K08259
[Journal Article] Role of liver transplantation in urea cycle disorders: Report from a nationwide study in Japan.2021
- Author(s)
  Kido J*, Matsumoto S, Haberle J, Inomata Y, Kasahara M, Sakamoto S, Horikawa R, Tanemura A, Okajima H, Suzuki T, Nakamura K.
- Journal Title
  
  J Inherit Metab Dis.
  
  Volume: 44 Issue: 6 Pages: 1311-1322
- DOI
  10.1002/jimd.12415
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K08207
[Journal Article] Newborn screening for Fabry disease in the western region of Japan.2020
- Author(s)
  Sawada T, Kido J, Yoshida S, Sugawara K, Momosaki K, Inoue T, Tajima G, Sawada H, Mastumoto S, Endo F, Hirose S, Nakamura K.
- Journal Title
  
  Mol Genet Metab Rep.
  
  Volume: 22 Pages: 100562-100562
- DOI
  10.1016/j.ymgmr.2019.100562
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K10054, KAKENHI-PROJECT-17K10055, KAKENHI-PROJECT-20K08259
[Journal Article] Fabry disease screening in high-risk populations in Japan: a nationwide study.2020
- Author(s)
  Yoshida S, Kido J, Sawada T, Momosaki K, Sugawara K, Matsumoto S, Endo F, Nakamura K.
- Journal Title
  
  Orphanet J Rare Dis.
  
  Volume: 15 Issue: 1 Pages: 220-220
- DOI
  10.1186/s13023-020-01494-6
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K08207, KAKENHI-PROJECT-20K08259
[Journal Article] Role of induced pluripotent stem cells in lysosomal storage diseases.2020
- Author(s)
  Kido J, Nakamura K, Era T.
- Journal Title
  
  Mol Cell Neurosci.
  
  Volume: 108 Pages: 103540-103540
- DOI
  10.1016/j.mcn.2020.103540
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K08207, KAKENHI-PROJECT-20K08259
[Journal Article] Detection of novel Fabry disease-associated pathogenic variants in Japanese patients by newborn and high-risk screening.2020
- Author(s)
  Sawada T, Kido J, Sugawara K, Matsumoto S, Takada F, Tsuboi K, Ohtake A, Endo F, Nakamura K.
- Journal Title
  
  Mol Genet Genomic Med.
  
  Volume: 11 Issue: 11
- DOI
  10.1002/mgg3.1502
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K08207, KAKENHI-PROJECT-20K08259
[Journal Article] Associations among amino acid, lipid, and glucose metabolic profiles in childhood obesity.2019
- Author(s)
  Suzuki Y, Kido J, Matsumoto S, Shimizu K, Nakamura K.
- Journal Title
  
  BMC Pediatr.
  
  Volume: 19 Issue: 1 Pages: 273-273
- DOI
  10.1186/s12887-019-1647-8
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K10054
[Journal Article] Newborn screening for Pompe disease in Japan: report and literature review of mutations in the GAA gene in Japanese and Asian patients.2019
- Author(s)
  Momosaki K, Kido J, Yoshida S, Sugawara K, Miyamoto T, Inoue T, Okumiya T, Matsumoto S, Endo F, Hirose S, Nakamura K.
- Journal Title
  
  J Hum Genet.
  
  Volume: 64 Issue: 8 Pages: 741-755
- DOI
  10.1038/s10038-019-0603-7
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K10054, KAKENHI-PROJECT-17K10055, KAKENHI-PROJECT-16H06276
[Journal Article] Rhabdomyolysis in organic acidemia patients manifesting with metabolic decompensation.2019
- Author(s)
  Kido J, Matsumoto S, Sawada T, Endo F, Nakamura K.
- Journal Title
  
  Hemodial Int.
  
  Volume: 23 Issue: 4
- DOI
  10.1111/hdi.12778
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K10054
[Journal Article] High-risk screening for Gaucher disease in patients with neurological symptoms.2018
- Author(s)
  Momosaki K, Kido J, Matsumoto S, Yoshida S, Takei A, Miyabayashi T, Sugawara K, Endo F, Nakamura K.
- Journal Title
  
  J Hum Genet.
  
  Volume: 63 Issue: 6 Pages: 717-721
- DOI
  10.1038/s10038-018-0438-7
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K10054, KAKENHI-PROJECT-17K10055
[Journal Article] A significant difference in the blood carnitine values obtained by the enzymatic cycling and andem mass spectrometry methods2018
- Author(s)
  Kido J, Inoue H, Suzuki Y, Tanaka M, Mitsubuchi H, Nakamura K, Endo F, Matsumoto S.
- Journal Title
  
  Clinical Lab.
  
  Volume: 64(1) Issue: 01+02/2018 Pages: 211-215
- DOI
  10.7754/clin.lab.2017.170805
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15K09625, KAKENHI-PROJECT-17K10055
[Journal Article] Pulmonary artery hypertension in methylmalonic acidemia.2017
- Author(s)
  Kido J, Mitsubuchi H, Sakanashi M, Matsubara J, Matsumoto S, Sakamoto R, Endo F, Nakamura K.
- Journal Title
  
  Hemodial Int.
  
  Volume: Apr;21(2) Issue: 2
- DOI
  10.1111/hdi.12506
- Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26870544, KAKENHI-PROJECT-17K10055
[Journal Article] Plasma exchange and chelator therapy rescues acute liver failure in Wilson disease without liver transplantation.2017
- Author(s)
  Kido J, Matsumoto S, Momosaki K, Sakamoto R, Mitsubuchi H, Inomata Y, Endo F, Nakamura K
- Journal Title
  
  Hepatol Res.
  
  Volume: Mar;47(4) Issue: 4 Pages: 359-363
- DOI
  10.1111/hepr.12711
- Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26870544, KAKENHI-PROJECT-15K09625
[Journal Article] Hyperammonemia crisis following parturition in a female patient with ornithine transcarbamylasedeficiency.2017
- Author(s)
  Kido J, Kawasaki T, Mitsubuchi H, Kamohara H, Ohba T, Matsumoto F, Endo F, Nakamura K.
- Journal Title
  
  World J Hepatol.
  
  Volume: 9(6) Issue: 6 Pages: 343-348
- DOI
  10.4254/wjh.v9.i6.343
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26461919, KAKENHI-PROJECT-26870544, KAKENHI-PROJECT-26462757, KAKENHI-PROJECT-17K10055
[Journal Article] Amelioration by glycine of brain damage in neonatal rat brain following hypoxia-ischemia2017
- Author(s)
  Mori Hiroko、Momosaki Ken、Kido Jun、Naramura Tetsuo、Tanaka Kenichi、Matsumoto Shirou、Nakamura Kimitoshi、Mitsubuchi Hiroshi、Endo Fumio、Iwai Masanori
- Journal Title
  
  Pediatrics International
  
  Volume: 59 Issue: 3 Pages: 321-327
- DOI
  10.1111/ped.13164
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K10055, KAKENHI-PROJECT-15K09625
[Journal Article] Advanced Endometrial Cancer in Phenylketonuria2016
- Author(s)
  Jun Kido, Hiroshi Mitsubuchi, Fumiko Itoh, Takanobu Yoshida, Shirou Matsumoto, Rieko Sakamoto, Fumio Endo, Kimitoshi Nakamura
- Journal Title
  
  Med Sci Case Rep
  
  Volume: 3 Pages: 108-111
- DOI
  10.12659/mscr.901499
- Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26870544
[Journal Article] Evaluation of the skin-prick test for predicting the outgrowth of cow's milk allergy.2016
- Author(s)
  Kido J, Hirata M, Ueno H, Nishi N, Mochinaga M, Ueno Y, Yanai M, Johno M, Matsumoto T.
- Journal Title
  
  Allergy Rhinol (Providence)
  
  Volume: Jan 1;7(3) Issue: 3 Pages: 139-143
- DOI
  10.2500/ar.2016.7.0175
- Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26870544
[Presentation] Development of drug screening system using neural stem cells derived from a patient with Type II Gaucher Disease.2019
- Author(s)
  Jun Kido, Tadahiro Numakawa, Shirou Matsumoto, Haruki Odaka, Minami Soga, Ryutarou Kajihara, Fumio Endo, Kimitoshi Nakamura, Takumi Era.
- Organizer
  SSIEM annual symposium 2019
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K10054
[Presentation] Perinatal diagnosis and amino acid profiles of a large family with ornithine transcarbamylase deficiency.2018
- Author(s)
  Shirou Matsumoto, Jun Kido, Hiroshi Mitsubuchi, Fumio Endo and Kimitoshi Nakamura
- Organizer
  the International Conference on Ureagenesis Defects
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09625
[Presentation] 小児生活習慣病患者における血中アミノ酸プロファイル2017
- Author(s)
  鈴木陽輔、城戸淳、黒澤茶々、水洗添泉、坂本理恵子、中村公俊、松本志郎、遠藤文夫
- Organizer
  日本アミノ酸学会第 11 回学術大会(JSAAS2017)
- Data Source
  KAKENHI-PROJECT-15K09625
[Presentation] MATI/III deficiency with demyelination of central tegmental tract during neonatal period.2017
- Author(s)
  Shirou Matsumoto, Jun Kido, Endo Fumio, Kimitoshi nakamrua.
- Organizer
  The 12th Asia-Pacific Conference of Human Genetics.
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09625
[Presentation] Development of drug screening system using iPS cells derived from a patient with Gaucher Disease Type II2017
- Author(s)
  Jun Kido, Tadahiro Numakawa, Shirou Matsumoto, Hiroki Odaka,　Minami Soga,　Ryutarou Kajihara, Fumio Endo, Kimitoshi Nakamura,Takumi Era.
- Organizer
  The 59th Annual Meeting of the Japanese Society for Inherited Metabolic Diseases
- Data Source
  KAKENHI-PROJECT-17K10054
[Presentation] Plasma exchange and chelator therapy rescues acute liver failure in Wilson disease without liver transplantation2016
- Author(s)
  Jun Kido, Shirou Matsumoto, Ken Momosaki, Rieko Sakamoto, Hiroshi Mitsubuchi,
- Organizer
  第58回日本先天代謝異常学会
- Place of Presentation
  東京
- Year and Date
  2016-10-27
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26870544
[Presentation] Improved neurodevelopmental outcomes in patients with urea cycle disorders after liver transplantation.2016
- Author(s)
  Kido Jun
- Organizer
  Society for the study of inborn errors of metabolism
- Place of Presentation
  ローマ
- Year and Date
  2016-09-06
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26870544
[Presentation] Induced pluripotent stem cell research: Basic Research for Development of New Drugs for Organic Acidemia.2015
- Author(s)
  Shirou Matsumoto, Jun Kido, Rieko Sakamoto, Takumi Era, Fumio Endo
- Organizer
  The 3rd Annual Symposium of the Asian Society of Inherited Metabolic Disorders
- Place of Presentation
  大阪国際会議場
- Year and Date
  2015-11-12
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09625

1. MATSUMOTO SHIROU (70467992)

# of Collaborated Projects: 3 results

# of Collaborated Products: 23 results
2. 沼川忠広 (40425690)

# of Collaborated Projects: 3 results

# of Collaborated Products: 3 results
3. 梶原隆太郎 (00738221)

# of Collaborated Projects: 3 results

# of Collaborated Products: 1 results
4. NAKAMURA KIMITOSHI (30336234)

# of Collaborated Projects: 2 results

# of Collaborated Products: 11 results
5. 曽我美南 (80768002)

# of Collaborated Projects: 2 results

# of Collaborated Products: 3 results
6. 小高陽樹 (40831243)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
7. 澤田貴彰 (40839065)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
8. KAMOHARA Hidenobu

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

kido jun 城戸 淳

Kido Jun 城戸 淳

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血漿Lyso-Gb3と血管内皮細胞解析を駆使した新しいファブリー病診断システムの構築Principal Investigator

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iPS細胞を用いたメラノーマに対する新規がん免疫療法の開発

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Development of novel pathological analysis and medicine in neuropathic Gaucher disease.Principal Investigator

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Development of novel medicine using iPS cells derived from Gaucher disease type II patientsPrincipal Investigator

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Prediction of DiabetesMellitus by using with iPS cell technology

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Establish of gene repair methods and analysis of pathological conditions using iPS cells derived from patients with glycogen storage disease type IaPrincipal Investigator

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[Journal Article] Frequency of iduronate-2-sulfatase gene variants detected in newborn screening for mucopolysaccharidosis type II in Japan2023

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[Journal Article] Gene therapy for spinal muscular atrophy is considerably effective when administered as early as possible after birth.2023

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[Journal Article] X-linked intellectual disability related to a novel variant of KLHL152023

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[Journal Article] Gene therapy for lysosomal storage diseases: Current clinical trial prospects.2023

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[Journal Article] Improved sensitivity and specificity for citrin deficiency using selected amino acids and acylcarnitines in the newborn screening2023

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[Journal Article] Pathogenic variants of ornithine transcarbamylase deficiency: Nation-wide study in Japan and literature review.2022

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[Journal Article] A case report of two siblings with hypertyrosinemia type 1 presenting with hepatic disease with different onset time and severity.2022

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[Journal Article] Newborn screening for spinal muscular atrophy in Japan: One year of experience.2022

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kido jun 城戸淳

Kido Jun 城戸淳