AWANO HIROYUKI 粟野宏之

… Alternative Names

Researcher Number	30437470
Other IDs
Affiliation (Current)	2020: 神戸大学, 医学研究科, 准教授
Affiliation (based on the past Project Information) *help	2020: 神戸大学, 医学研究科, 准教授 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 … More
Review Section/Research Field	Principal Investigator Pediatrics / Basic Section 52050:Embryonic medicine and pediatrics-related Except Principal Investigator Pediatrics / Basic Section 58070:Lifelong developmental nursing-related
Keywords	Principal Investigator ジストロフィン遺伝子 / レトロトランスポゾン / 非翻訳RNA / 国際情報交流 / 筋ジストロフィー / カルパイン / Duchenne型筋ジストロフィー / タイチン Except Principal Investigator ジストロフィン / 精神発達遅滞 … More

Development of a multi-professional collaborative program to support the transition of family roles including children with chronic diseasesOngoing
- Principal Investigator
  
  本田順子
- 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
タイチン分解酵素を阻害するDuchenne型筋ジストロフィーの新しい治療標的Principal InvestigatorOngoing
- Principal Investigator
  
  粟野宏之
- 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 2018 2014 2013 2012 2011 2010 Other

All Journal Article Presentation

[Journal Article] Differences in carrier frequency between mothers of Duchenne and Becker muscular dystrophy patients2014
- Author(s)
  Lee T, Takeshima Y, Kusunoki N, Awano H, Yagi M, Matsuo M, Iijima K.
- Journal Title
  
  J Hum Genet
  
  Volume: 59 Pages: 46-50
- 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 8years 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 Xq282013
- Author(s)
  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 Pages: 33-39
- DOI
  10.1038/jhg.2012.131
- NAID
  10031145898
- Peer Reviewed
- Data Source
  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 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 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)
  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] 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] 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 plicing regulatory factors as decision markers.2012
- 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 Genet
  
  Volume: 13(23) 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 mutations2012
- Author(s)
  Ota M, Takeshima Y, Nishida A, Awano H, Lee T, Yagi M, Matsuo M.
- Journal Title
  
  Genet Test Mol Biomarkers
  
  Volume: 16 Pages: 3-8
- DOI
  10.1089/gtmb.2010.0276
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591495, 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) Pages: 347-53
- DOI
  10.1089/nat.2011.0310
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591496
[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] 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] 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] Chemical treatment enhances skipping of amutated 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
  
  Nature Communications
  
  Volume: 2 Pages: 308-308
- DOI
  10.1038/ncomms1306
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22500288, KAKENHI-PROJECT-22603002, KAKENHI-PUBLICLY-23112706, KAKENHI-PROJECT-23591496
[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 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] 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] 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] 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] 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] 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] 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] (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] 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)
  HIROYUKI AWANO
- Organizer
  Pediatric Academic Sociieties
- Place of Presentation
  Boston
- Data Source
  KAKENHI-PROJECT-23791174
[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
  日本人類遺伝学会第57回大会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-23591496
[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] 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
  日本人類遺伝学会第56回大会
- Place of Presentation
  千葉
- 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] 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] 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] 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] 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] 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] 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: 23 results
2. TAKESHIMA Yasuhiro (40281141)

# of Collaborated Projects: 2 results

# of Collaborated Products: 24 results
3. MATSUO Masafumi (10157266)

# of Collaborated Projects: 1 results

# of Collaborated Products: 6 results
4. 本田順子 (50585057)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
5. 勝田仁美 (00254475)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
6. 山口未久 (20771132)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
7. 宮脇郁子 (80209957)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
8. 山口智子 (80843052)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
9. 福井美苗 (70882207)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
10. HAGIWARA Masatoshi

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results
11. 高岡裕

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
12. 片岡直行

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
13. 中川卓

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

AWANO HIROYUKI 粟野 宏之

粟野 宏之 アワノ ヒロユキ

AWANO Hiroyuki 粟野 宏之

Research Projects

Research Products

Co-Researchers

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

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

タイチン分解酵素を阻害するDuchenne型筋ジストロフィーの新しい治療標的Principal InvestigatorOngoing

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

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

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

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

Project Period (FY)

Research Category

Research Field

Research Institution

Genes responsible for mental retardation complicating to Duchenne muscular dystrophy

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

A study of mobile element inserted into dystrophin genePrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] Differences in carrier frequency between mothers of Duchenne and Becker muscular dystrophy patients2014

Author(s)

Journal Title

DOI

NAID

Data Source

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

Author(s)

Journal Title

DOI

Data Source

[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 Xq282013

Author(s)

Journal Title

DOI

NAID

Data Source

[Journal Article] A Japanese child with geleophysic dysplasia caused by a novel mutation of FBN1.2012

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Pathogenic orphan transduction created by a non-reference LINE-1retrotransposon2012

Author(s)

Journal Title

Data Source

[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)

Journal Title

Data Source

[Journal Article] Pathogenic orphan transduction created by a nonreference LINE-1 retrotransposon2012

Author(s)

Journal Title

Data Source

[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)

Journal Title

Data Source

AWANO HIROYUKI 粟野宏之

粟野宏之アワノヒロユキ

AWANO Hiroyuki 粟野宏之