AWANO HIROYUKI 粟野宏之

… Alternative Names

Hiroyuki Awano 粟野宏之

AWANO Hiroyuki 粟野宏之

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Researcher Number	30437470
Other IDs
Affiliation (Current)	2025: 鳥取大学, 研究推進機構, 教授
Affiliation (based on the past Project Information) *help	2025: 鳥取大学, 研究推進機構, 教授 2022 – 2023: 神戸大学, 医学研究科, 客員教授 2022 – 2023: 鳥取大学, 研究推進機構, 教授 2020 – 2021: 神戸大学, 医学研究科, 特命教授 2019 – 2020: 神戸大学, 医学研究科, 准教授 … More 2018 – 2019: 神戸大学, 医学部附属病院, 講師 2013: 神戸大学, 大学院医学研究科, 特命助教 2012 – 2013: 神戸大学, 医学(系)研究科(研究院), その他 2011: 神戸大学, 医学(系)研究科(研究院), 特命助教 2010 – 2011: 神戸大学, 医学研究科, 特命助教 2010 – 2011: Kobe University, 大学院・医学研究科, 特命助教 2009: Kobe University, 医学部附属病院, 特定助教 Less
Review Section/Research Field	Principal Investigator Basic Section 52050:Embryonic medicine and pediatrics-related / Pediatrics Except Principal Investigator Pediatrics / Basic Section 58060:Clinical nursing-related / Basic Section 52050:Embryonic medicine and pediatrics-related / Basic Section 58070:Lifelong developmental nursing-related
Keywords	Principal Investigator タイチン / Duchenne型筋ジストロフィー / iPS細胞 / αアクチニン3 / 心筋細胞 / 筋ジストロフィー / 筋崩壊 / カルパイン / 国際情報交流 / 非翻訳RNA / レトロトランスポゾン / ジストロフィン遺伝子 … More Except Principal Investigator … More 医療者間連携 / 家族支援 / クライエントの思い / 遺伝カウンセリング / コンパニオン診断 / 遺伝性腫瘍診断 / ゲノム編集 / アンチセンス療法 / SVA型レトロトランスポゾン / 尿中細胞 / レトロトランスポゾン / ロングリードシークエンサー / SVA / 福山型筋ジストロフィー / 相互作用 / 親子 / 多職種 / 家族 / 移行期 / 親子の相互作用 / 意思決定 / セルフケア / 小児 / 慢性疾患 / 家族看護 / 親子関係 / 国際情報交流 / 国際情報研究 / スプライシング / 分子種 / Duchenne型筋ジストロフィー / 精神発達遅滞 / ジストロフィン Less

iPS細胞由来心筋を用いたDMDの心筋障害に対する新規治療標的分子の同定Principal Investigator
- Principal Investigator
  
  粟野宏之
- 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
  Tottori University
αアクチニン3欠損はDMD患者のiPS由来心筋細胞においてタイチン分解を促進するPrincipal Investigator
- Principal Investigator
  
  粟野宏之
- Project Period (FY)
  2022 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Tottori University
がんゲノム医療での遺伝性腫瘍診断目的による患者・家族への医療者間連携に関する研究
- Principal Investigator
  
  笠城典子
- Project Period (FY)
  2022 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 58060:Clinical nursing-related
- Research Institution
  Tottori University
Establishing Diagnostic Methods and Elucidating the Pathogenesis of Fukuyama Congenital Muscular Dystrophy Using Long-Read Sequencers
- Principal Investigator
  
  Nagasaka Miwako
- Project Period (FY)
  2021 – 2023
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Aijinkai Healthcare Corporation Takatsuki General Hospital Clinical Research Center
Development of a multi-professional collaborative program to support the transition of family roles including children with chronic diseases
- Principal Investigator
  
  Honda Junko
- Project Period (FY)
  2019 – 2022
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 58070:Lifelong developmental nursing-related
- Research Institution
  University of Hyogo
Resarch on novel therapeutic molecular target for Duchenne muscular dystrophy that inhibits titin-degrading enzymesPrincipal Investigator
- Principal Investigator
  
  Hiroyuki Awano
- Project Period (FY)
  2018 – 2020
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Kobe University
Correlation between cis-acing elements and effects on inducing exon skipping
- Principal Investigator
  
  YAGI Mariko
- Project Period (FY)
  2011 – 2013
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Kobe University
新規非翻訳RNAのクローニングとグルタミン酸レセプター遺伝子への影響に関する研究Principal Investigator
- Principal Investigator
  
  粟野宏之
- Project Period (FY)
  2011 – 2012
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Pediatrics
- Research Institution
  Kobe University
Genes responsible for mental retardation complicating to Duchenne muscular dystrophy
- Principal Investigator
  
  MATSUO Masafumi
- Project Period (FY)
  2009 – 2011
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  Kobe Gakuin University
  Kobe University
A study of mobile element inserted into dystrophin genePrincipal Investigator
- Principal Investigator
  
  AWANO Hiroyuki
- Project Period (FY)
  2009 – 2010
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Pediatrics
- Research Institution
  Kobe University

All 2020 2018 2013 2012 2011 2010 Other

All Journal Article Presentation

[Journal Article] The ACTN3 577XX Null Genotype Is Associated with Low Left Ventricular Dilation-Free Survival Rate in Patients with Duchenne Muscular Dystrophy2020
- Author(s)
  Masashi Nagai, Hiroyuki Awano, Tetsushi Yamamoto, Ryosuke Bo, Masafumi Matsuo, Kazumoto Iijima
- Journal Title
  
  Journal of Cardiac Failure Home
  
  Volume: 26(10) Issue: 10 Pages: 841-848
- DOI
  10.1016/j.cardfail.2020.08.002
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K17564, KAKENHI-PROJECT-18K07845
[Journal Article] Differences in carrier frequency between mothers of Duchenne and Becker muscular dystrophy patients.2013
- Author(s)
  Lee T, Takeshima Y, Kusunoki N, Awano H, Yagi M, Matsuo M, Iijima K.
- Journal Title
  
  J Hum Genet.
  
  Volume: 59 Issue: 1 Pages: 46-51
- DOI
  10.1038/jhg.2013.119
- NAID
  40019946811
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591496
[Journal Article] A prostaglandin D2 metabolite is elevated in the urine of Duchenne muscular dystrophy patients and increases further from 8 years old.2013
- Author(s)
  Nakagawa T, Takeuchi A, Kakiuchi R, Lee T, Yagi M, Awano H, Iijima K, Takeshima Y, Urade Y, Matsuo M.
- Journal Title
  
  Clin Chim Acta.
  
  Volume: 423 Pages: 10-14
- DOI
  10.1016/j.cca.2013.03.031
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591496, KAKENHI-PROJECT-24791060
[Journal Article] Molecular characterization of an X(p21.2;q28) chromosomal inversion in a Duchenne muscular　dystrophy patient with mental retardation reveals a novel long non-coding gene on Xq28.2013
- Author(s)
  Thu Tran TH, Zhang Z, Yagi M, Lee T, Awano H, Nishida A, Okinaga T, Takeshima Y, Matsuo M.
- Journal Title
  
  J Hum Genet
  
  Volume: 58 Issue: 1 Pages: 33-39
- DOI
  10.1038/jhg.2012.131
- NAID
  10031145898
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591496
[Journal Article] Pathogenic orphan transduction created by a non-reference LINE-1retrotransposon2012
- Author(s)
  Solyom S, Ewing AD, Hancks DC, Takeshima Y, Awano H, Matsuo M, Kazazian H Jr
- Journal Title
  
  Hum. Mutat
  
  Volume: 33 Pages: 369-371
- Data Source
  KAKENHI-PROJECT-21390311
[Journal Article] Categorization of 77 dystrophin exons into 5 groups by a decision tree using indexes of splicing regulatory factors as decision markers2012
- Author(s)
  Rusdy Ghazali Malueka, Yutaka Takaoka, Mariko Yagi, Hiroyuki Awano, Tomoko Lee, Ery Kus Dwianingsih, Atsushi Nishida, Yasuhiro Takeshima, Masafumi Matsuo
- Journal Title
  
  BMC Genetics
  
  Volume: 13(23) Issue: 1 Pages: 23-23
- DOI
  10.1186/1471-2156-13-23
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22590653, KAKENHI-PROJECT-23591495, KAKENHI-PROJECT-23591496
[Journal Article] athogenic orphan transduction created by a non-reference LINE-1 retrot ransposon2012
- Author(s)
  Solyom S, Ewing AD, Hancks DC, Takeshima Y, Awano H, Matsuo M, Kazazian HH Jr
- Journal Title
  
  Hum.Mutat
  
  Volume: 33 Pages: 369-371
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390311
[Journal Article] A G-to-T transversion at the splice acceptor site of dystrophin exon 14 shows multiple splicing outcomes that are not exemplified by transition mutations.2012
- Author(s)
  Ota M, Takeshima Y, Nishida A, Awano H, et al.
- Journal Title
  
  Genet Test Mol Biomarkers
  
  Volume: 16 Pages: 3-8
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23791174
[Journal Article] Categorization of 77 dystrophin exons into 5 groups by a decision tree using indexes of splicing regulatory factors as decision markers2012
- Author(s)
  Malueka RG, Takaoka Y, Yagi M, Awano H, et al.
- Journal Title
  
  BMC Genet
  
  Volume: 31 Pages: 13-23
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23791174
[Journal Article] A G-to-T transversion at the splice acceptor site of dystrophin exon 14 shows multiple splicing outcomes that are not exemplified by transition mutations.2012
- Author(s)
  Ota M, Takeshima Y, Nishida A, Awano H, Lee T, Yagi M, Matsuo M.
- Journal Title
  
  Genet Test Mol Biomarkers.
  
  Volume: 16 Issue: 1 Pages: 3-8
- DOI
  10.1089/gtmb.2010.0276
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591495, KAKENHI-PROJECT-23591496
[Journal Article] A Japanese child with geleophysic dysplasia caused by a novel mutation of FBN1.2012
- Author(s)
  Lee T, Takeshima Y, Okizuka Y, Hamahira K, Kusunoki N, Awano H, Yagi M, Sakai N, Matsuo M, Iijima K
- Journal Title
  
  Gene
  
  Volume: 512 Issue: 2 Pages: 456-459
- DOI
  10.1016/j.gene.2012.10.060
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591496
[Journal Article] Pathogenic orphan transduction created by a nonreference LINE-1 retrotransposon2012
- Author(s)
  Solyom S, Ewing AD, Hancks DC, Takeshima Y, Awano H, et al.
- Journal Title
  
  Hum Muta.
  
  Volume: 33 Pages: 369-71
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23791174
[Journal Article] Chemical treatment enhances skipping of a mutated exon in the dystrophin gene2011
- Author(s)
  Nishida A, Kataoka N, Takeshima Y,Yagi M, Awano, H, Ota, M, Itoh K, Hagiwara M, and Matsuo M
- Journal Title
  
  Nat Commun
  
  Volume: 2 Issue: 1 Pages: 308-308
- DOI
  10.1038/ncomms1306
- NAID
  120003001398
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22500288, KAKENHI-PROJECT-22603002, KAKENHI-PUBLICLY-23112706, KAKENHI-PROJECT-23591496
[Journal Article] Antisense oligonucleotide induced dystrophin exon 45 skipping at a low half-maximal effective concentration in a cell-free splicing system2011
- Author(s)
  Malueka RG, Yagi M, Awano H, Lee T, Dwianingsih EK, Nishida A, Takeshima Y, Matsuo M
- Journal Title
  
  Nucleic Acid Ther
  
  Volume: 21(5) Issue: 5 Pages: 347-53
- DOI
  10.1089/nat.2011.0310
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591496
[Journal Article] A patient with mitochondrial trifunctional protein deficiency due to the mutations in the HADHB gene showed recurrent myalgia since early childhood and was diagnosed in adolescence.2011
- Author(s)
  Yagi M, Lee T., Awano H, Tsuji M, et al.
- Journal Title
  
  Mol Genet Metab.
  
  Volume: 104 Pages: 556-9
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23791174
[Journal Article] Antisense oligonucleotide induced dystrophin exon 45 skipping at a low half-maximal effective concentration in a cell-free splicing system.2011
- Author(s)
  Malueka RG, Yagi M, Awano H, Lee T, et al.
- Journal Title
  
  Nucleic Acid Ther.
  
  Volume: 21 Pages: 347-53
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23791174
[Journal Article] 非侵襲的陽圧換気療法と器械による咳介助を活用し気管内挿管から離脱した脊髄性筋委縮症1型2011
- Author(s)
  粟野宏之
- Journal Title
  
  日本小児科学会雑誌
  
  Volume: 115 Pages: 1451-1455
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23791174
[Journal Article] Contemporary retrotransposition of a novel non-coding gene induces exon-skipping in dystrophin mRNA2010
- Author(s)
  Hiroyuki Awano
- Journal Title
  
  Journal of Human Genetics
  
  Volume: 55 Pages: 785-790
- NAID
  10030737817
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21790988
[Journal Article] Molecular characterization of the 5'-UTR of retinal dystrophin reveals a cryptic intron that regulates translational activity2010
- Author(s)
  Kubokawa, I., Takeshima, Y., Ota, M., Enomoto, M., Okizuka, Y., Mori, T., Nishimura, N., Awano, H., Yagi, M., Matsuo, M.
- Journal Title
  
  Molecular vision
  
  Volume: 16 Pages: 2590-2597
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390311
[Journal Article] Moleculaar chaaracterizatioon of the 5'-UUTR of retinnal dysstrophin reveals a cryptiic intron thaat reggulates transslational acttivity2010
- Author(s)
  Kubokawa, I., Takeshima, Y., Ota, M., Enomoto, M., Okizuka, Y., Mori, T., Nishimura, N., Awano, H., Yagi, M., Matsuo, M
- Journal Title
  
  Mol Vis
  
  Volume: 16 Pages: 2590-2597
- Data Source
  KAKENHI-PROJECT-21390311
[Journal Article] Contemporary retrotransposition of a novel non-coding gene induces exon-skipping in dystrophin mRNA.
- Author(s)
  Awano H, Malueka RG, Yagi M, Okizuka Y, Takeshima Y, Matsuo M.
- Journal Title
  
  Journal of Human Genetics 55巻
  
  Pages: 785-90
- NAID
  10030737817
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21790988
[Presentation] ACTN3ヌル遺伝子型はＤＭＤの拡張型心筋症の早期発症と関連する2020
- Author(s)
  永井正志、粟野宏之、山本哲志、坊亮輔、西尾久英、松尾雅文、飯島一誠
- Organizer
  第62回日本小児神経学会
- Data Source
  KAKENHI-PROJECT-18K07845
[Presentation] DMD患者の心電図異常と関係するジストロフィンの新規アイソフォーム2020
- Author(s)
  松尾雅文、ラニアブヂュル、山本哲志、川口達也、前田和宏、粟野宏之
- Organizer
  第62回日本小児神経学会
- Data Source
  KAKENHI-PROJECT-18K07845
[Presentation] 尿中タイチンはDuchenne型筋ジストロフィー診断のバイオマーカーである2018
- Author(s)
  粟野宏之
- Organizer
  第60回日本小児神経学会
- Data Source
  KAKENHI-PROJECT-18K07845
[Presentation] URINARY TITIN IS A NON-INVASIVE BIOMARKER TO DIAGNOSE DUCHENNE MUSCULAR DYSTROPHY EVEN IN ADVANCED STAGE2018
- Author(s)
  Hiroyuki　Awano
- Organizer
  15th International Congress on Neuromuscular Diseases
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07845
[Presentation] Dystrophin gene mutations in three dystrophinopathy patients with severe cardiomyopathy2012
- Author(s)
  HIROYUKI AWANO
- Organizer
  Pediatric Academic Sociieties
- Place of Presentation
  Boston
- Data Source
  KAKENHI-PROJECT-23791174
[Presentation] Duchenne/Becker型筋ジストロフィーにおけるジストロフィン遺伝子の微小変異の割合は増加傾向にある2012
- Author(s)
  李知子、楠典子、粟野宏之、八木麻理子、竹島泰弘、松尾雅文、飯島一誠
- Organizer
  日本人類遺伝学会第57回大会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-23591496
[Presentation] (1) Dystrophin gene mutations in three dystrophynopathy patients with severe cardiomyopathy.2012
- Author(s)
  Hiroyuki Awano
- Organizer
  Pediatric Academic Societies annual meeting
- Place of Presentation
  Boston
- Year and Date
  2012-04-29
- Data Source
  KAKENHI-PROJECT-23791174
[Presentation] Duchenne/Becker型筋ジストロフィー兄弟例における心機能障害の検討2012
- Author(s)
  李知子、粟野宏之、八木麻理子、竹島泰弘、松尾雅文、飯島一誠
- Organizer
  第115回日本小児科学会学術集会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-23591496
[Presentation] Duchenne型筋ジストロフィーにおける尿プロスタグランディンD2代謝産物の排泄の増加2012
- Author(s)
  中川卓、李知子、粟野宏之、八木麻理子、松尾雅文、竹島泰弘
- Organizer
  第54回日本小児神経学会総会
- Place of Presentation
  札幌
- Data Source
  KAKENHI-PROJECT-23591496
[Presentation] Duchenne/Becker型筋ジストロフィーにおけるジストロフィン遺伝子の微小変異の割合は増加傾向にある2012
- Author(s)
  李知子、楠典子、粟野宏之、八木麻理子、竹島泰弘、松尾雅文、飯島一誠
- Organizer
  日本人類遺伝学会57回大会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-23591496
[Presentation] A small chemical, TG003, enhances skipping of mutated dystrophin exons: the third example revealing a decrease of exonic splicing enhancer density in common.2012
- Author(s)
  Nishida A, Takeshima Y, Kataoka N, Yagi M, Awano H, Lee T, Iijima K, Hagiwara M, Matsuo M.
- Organizer
  The American Society of Human Genetics, the 62th Annual Meeting
- Place of Presentation
  San Francisco
- Data Source
  KAKENHI-PROJECT-23591496
[Presentation] A small chemical, TG003, enhances skipping of mutated dystrophin exons : the third example revealing a decrease of exonic splicing enhancer density in common2012
- Author(s)
  Nishida A, Takeshima Y, Kataoka N, Yagi M, Awano H, Lee T, Iijima K, Hagiwara M, Matsuo M
- Organizer
  The American Society of Human Genetics, the 62th Annual Meeting
- Place of Presentation
  San Francisco
- Data Source
  KAKENHI-PROJECT-23591496
[Presentation] ベサフィブラートにより骨格筋症状が改善した極長鎖アシルCoA脱水素酵素欠損症の1例2012
- Author(s)
  八木麻理子、楠典子、李知子、粟野宏之、但馬剛、小林弘典、長谷川有紀、山口清次、竹島泰弘、飯島一誠
- Organizer
  第54回日本先天代謝異常学会
- Place of Presentation
  岐阜
- Data Source
  KAKENHI-PROJECT-23591496
[Presentation] Dystrophin gene mutations in three dystrophinopathy patients with severe cardiomyopathy2012
- Author(s)
  Awano H, Lee T, Yagi M, Takeshima Y, Matsuo M, Iijima K
- Organizer
  Pediatric Academic Societies Annual Meeting
- Place of Presentation
  Boston
- Data Source
  KAKENHI-PROJECT-23591496
[Presentation] ジストロフィン遺伝子エクソンスキッピングを誘導する低分子化合物の同定と治療への応用2011
- Author(s)
  八木麻理子、李知子、粟野宏之、伊東恭子、竹島泰弘、松尾雅文
- Organizer
  第53回日本小児神経学会総会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-23591496
[Presentation] 左室内径短縮率をもちいたDuchenne型筋ジストロフィーの小児期における心機能の検討2011
- Author(s)
  粟野宏之
- Organizer
  日本小児神経学会
- Place of Presentation
  パシフィコ横浜
- Data Source
  KAKENHI-PROJECT-23791174
[Presentation] MLPA法を用いたジストロフィン遺伝子解析のピットフォール2011
- Author(s)
  粟野宏之
- Organizer
  日本人類遺伝学会
- Place of Presentation
  幕張メッセ
- Data Source
  KAKENHI-PROJECT-23791174
[Presentation] MLPA法を用いたジストロフィン遺伝子解析のピットフォール2011
- Author(s)
  粟野宏之
- Organizer
  日本人類遺伝学会第56回大会
- Place of Presentation
  千葉
- Data Source
  KAKENHI-PROJECT-23591496
[Presentation] Antisense RNA/Ethylene-bridged nucleic acid chimera induces exon 45 skipping in cultured myocytes from DMD patients with 6 different deletion mutaions2011
- Author(s)
  Yagi M, Lee T, Awano H, Takeshima Y, Matsuo M
- Organizer
  The American Society of Human Genetics 61th Annual Meeting
- Place of Presentation
  Montreal
- Data Source
  KAKENHI-PROJECT-23591496
[Presentation] Genotype-phenotype correlation of the dystrophinopathy cases with small mutations in the dystrophin gene.2010
- Author(s)
  粟野宏之
- Organizer
  アメリカ小児科学会
- Place of Presentation
  バンクーバーコンベンションセンター
- Year and Date
  2010-05-02
- Data Source
  KAKENHI-PROJECT-21790988
[Presentation] Genotype-phenotype correlation of the dystrophinopathy cases with small mutations in the dystrophin gene2010
- Author(s)
  Awano H, Takeeshima Y, YaYagi M, Yamaauchi Y, MMalueka RGG, Dwianingssih EK, Maatsuo M
- Organizer
  Pediatric Academic Societies. 2010 Annual Meeting
- Place of Presentation
  Vancouver
- Data Source
  KAKENHI-PROJECT-21390311
[Presentation] Chemical treatment of muscular dystrophy that enhances skiping of the mutated exon in the dystrophin gene2010
- Author(s)
  Nishida A, Kataoka N, Takeshima Y, Yagi M, Awano H, Ota M, Itoh K, Hagiwara M, Matsuo M
- Organizer
  The American Society of Human Genetics60th Anual Meeting
- Place of Presentation
  Washigton, DC
- Data Source
  KAKENHI-PROJECT-21390311
[Presentation] Genotype-phenotype correlation of the dystrophinopathy cases with small mutations in the dystrophin gene2010
- Author(s)
  粟野宏之
- Organizer
  アメリカ小児科学会
- Place of Presentation
  Vancouver Convention Centre(Canada)
- Year and Date
  2010-05-02
- Data Source
  KAKENHI-PROJECT-21790988
[Presentation] Evolutionary acquired alternative splicing in the 5'-UTR of retinal dystrophin transcript is a default pathway with weaker translational activity than nonspliced retina specific form
- Author(s)
  Kubokawa I, Yagi M, Awano H, Ota M, Nishida A, Dwianingsih EK, Malueka RG, Takeshima Y, Matsuo M
- Data Source
  KAKENHI-PROJECT-21390311

1. YAGI Mariko (60362787)

# of Collaborated Projects: 2 results

# of Collaborated Products: 21 results
2. TAKESHIMA Yasuhiro (40281141)

# of Collaborated Projects: 2 results

# of Collaborated Products: 22 results
3. MATSUO Masafumi (10157266)

# of Collaborated Projects: 1 results

# of Collaborated Products: 6 results
4. Honda Junko (50585057)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
5. Nagasaka Miwako (70723998)

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6. 山口未久 (20771132)

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7. 福井美苗 (70882207)

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8. 宮脇郁子 (80209957)

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9. 山口智子 (80843052)

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10. 勝田仁美 (00254475)

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11. 池田真理子 (00410738)

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12. 加藤武馬 (20387690)

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13. 青井貴之 (00546997)

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14. 笠城典子 (60185741)

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15. 鈴木康江 (10346348)

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16. 前垣義弘 (80252849)

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17. 岡崎哲也 (30465299)

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18. HAGIWARA Masatoshi

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19. 高岡裕

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20. 永井正志

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AWANO HIROYUKI 粟野 宏之

Hiroyuki Awano 粟野 宏之

AWANO Hiroyuki 粟野 宏之

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iPS細胞由来心筋を用いたDMDの心筋障害に対する新規治療標的分子の同定Principal Investigator

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αアクチニン3欠損はDMD患者のiPS由来心筋細胞においてタイチン分解を促進するPrincipal Investigator

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がんゲノム医療での遺伝性腫瘍診断目的による患者・家族への医療者間連携に関する研究

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Establishing Diagnostic Methods and Elucidating the Pathogenesis of Fukuyama Congenital Muscular Dystrophy Using Long-Read Sequencers

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Development of a multi-professional collaborative program to support the transition of family roles including children with chronic diseases

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Resarch on novel therapeutic molecular target for Duchenne muscular dystrophy that inhibits titin-degrading enzymesPrincipal Investigator

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Correlation between cis-acing elements and effects on inducing exon skipping

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新規非翻訳RNAのクローニングとグルタミン酸レセプター遺伝子への影響に関する研究Principal Investigator

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Genes responsible for mental retardation complicating to Duchenne muscular dystrophy

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A study of mobile element inserted into dystrophin genePrincipal Investigator

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[Journal Article] The ACTN3 577XX Null Genotype Is Associated with Low Left Ventricular Dilation-Free Survival Rate in Patients with Duchenne Muscular Dystrophy2020

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[Journal Article] Differences in carrier frequency between mothers of Duchenne and Becker muscular dystrophy patients.2013

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[Journal Article] A prostaglandin D2 metabolite is elevated in the urine of Duchenne muscular dystrophy patients and increases further from 8 years old.2013

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AWANO HIROYUKI 粟野宏之

Hiroyuki Awano 粟野宏之

AWANO Hiroyuki 粟野宏之

[Journal Article] Molecular characterization of an X(p21.2;q28) chromosomal inversion in a Duchenne muscular　dystrophy patient with mental retardation reveals a novel long non-coding gene on Xq28.2013