This is a summary of the curriculum vitae (CV) of Dr. Naoyuki Kataoka, Associate Professor, Laboratory of Cellular Biochemistry, Department of Animal Resource Sciences, Graduate School of Agriculture and Life Sciences, University of Tokyo. On May 20, he will give a presentation at Fujita Health University on mRNA splicing, how defects therein can generate “RNA diseases,” and how such diseases may be treated.
Dr. Kataoka is a molecular biologist who specialized in RNA. Professor Akila Mayeda, of Fujita Health University, has highly recommended Dr. Kataoka as one of the leading scientists in the field of pre-mRNA splicing, and states “He has shown quite a flair as a molecular biologist by picking considerable problems in RNA-mediated diseases.” Dr. Kataoka likes to have an overview of—and is well-respected in— his field, as evidenced by him being (associate) editor of several journals and chief editor of the journal RNA & DISEASE. His bird’s eye view perspective should guarantee a great seminar experience, including for those who only have a superficial knowledge of RNA.
Dr. Kataoka studied Biology at Kyoto University, where he specialized in—and got his Ph.D. degree for—RNA research in the Biophysics Department. Here, he showed his promise as a researcher by getting several publications in Nucleic Acids Research. One of his major achievements in this period was the identification of several factors of the nuclear cap binding protein (NCBP) complex that binds to the mRNA cap (the modified 5’ end of mRNA) in the nucleus to help with mRNA processing (e.g., Kataoka et al. 1995).
Then, from 1995 to 2002, he was a postdoc in the group of Dr. Gideon Dreyfuss at Howard Hughes Medical Institute, University of Pennsylvania School of Medicine, in the US. Here, Dr. Kataoka was involved in major findings on how introns are spliced out of pre-mRNA, resulting in papers in Science, Cell, Molecular Cell, Nature Review Molecular Cell Biology, and several papers in EMBO Journal. An especially important finding of Dr. Kataoka during this US period was the identification and characterization of a novel RNA binding protein Y14, which is a critical core component of a complex that mediates a link between mRNA splicing and Nonsense-mediated mRNA Decay (NMD) (e.g., Kataoka et al. 2000).
He then returned to Japan and alternatingly worked in Kyoto and Tokyo. First, from 2002 to 2007, he worked at the Institute for Virus Research at Kyoto University. Then, from 2007 to 2011, he got a position at the Medical Research Institute of Tokyo Dental and Medical University. After this, he returned to Kyoto, to work—from 2011 to 2016—at Kyoto University Graduate School of Medicine. Then again, in 2016, he moved to Tokyo, where he is still working to date at the University of Tokyo in the Graduate School of Agriculture and Life Sciences. During this entire period, he kept studying RNA splicing and got publications in prestigious journals like PNAS and Nucleic Acid Research. He is especially interested in an interplay between mRNA splicing and other gene expression steps. His most important recent contributions to the field concern the molecular mechanisms of how aberrant mRNA splicing can contribute to disease (so-called “RNA diseases”) (e.g., Kataoka et al. 2019).
RNA regulation is a very important contributing factor to the biological/medical phenomenon that most of you study. Therefore, it should be a treat to learn and be updated about this by such an expert as Dr. Kataoka.
Dr. Kataoka has been very kind to give us some personal insights into his science and motivation, and wrote the below sentences and told us his favorite quotes.
MY SCIENCE
(a personal statement about his science by Dr. Kataoka for this blog; bold highlighting and links by me)
Science is my Job, Hobby, and Favorite pastime.
I became interested in RNA when I was a third-year undergraduate student at Kyoto University. In the lectures, I came to know that pre-mRNA undergoes splicing, which is a drastic change. Since then, I am attracted by RNA science.
My favorite quotes are:
RNA: the final frontier. These are the voyages of the RNA scientists. Its continuing mission: to explore strange new worlds. To seek out new functions and new knowledge. To boldly go where no one has gone before!
Original: Space: the final frontier. These are the voyages of the starship Enterprise. Its continuing mission: to explore strange new worlds. To seek out new life and new civilizations. To boldly go where no one has gone before!
(from “STAR TREK: The Next Generation”)
and also
When you have eliminated the impossible, whatever remains, however improbable, must be the truth.
(from “Adventures of Sherlock Holmes”)
CURRICULUM VITAE
EDUCATION
1989 B.Sc., Biology, Kyoto University
1991 M.Sc., Department of Biophysics, Kyoto University (Prof. Yoshiro Shimura)
Thesis : The role of the cap structure in pre-mRNA splicing
1995 Ph.D., Biophysics, Kyoto University (Prof. Yoshiro Shimura)
Thesis : Study of the cap structure and nuclear cap binding protein
PROFESSIONAL EXPERIENCE
1995-2001 Post-doctoral Fellow (Dr. Gideon Dreyfuss)
Howard Hughes Medical Institute
Department of Biochemistry and Biophysics
University of Pennsylvania School of Medicine
Philadelphia, PA, U.S.A.
2001-2002 Research Associate (Dr. Gideon Dreyfuss)
Howard Hughes Medical Institute
Department of Biochemistry and Biophysics
University of Pennsylvania School of Medicine
Philadelphia, PA, U.S.A.
2002-2007 Assistant Professor (Prof. Mutsuhito Ohno)
Institute for Virus Research, Kyoto University
2007-2011 Lecturer
Medical Top Track Program, Medical Research Institute,
Tokyo Dental and Medical University
2011.4-2011.10 Associate Professor (Prof. Masatoshi Hagiwara)
Department of Anatomy and Developmental Biology
Kyoto University Graduate School of Medicine
2011-2016 Associate Professor, Principal Investigator
Medical Innovation Center
Laboratory for Malignancy Control Research / DSK Project
Kyoto University Graduate School of Medicine
2016-2019 Associate Professor (Prof. Shin-Ichiro Takahashi)
Graduate School of Agriculture and Life Sciences
Departments of Applied Animal Sciences and Applied
Biological Chemistry
Laboratory of Cell Regulation
University of Tokyo
2019-present Associate Professor (Prof. Satoshi Tanaka)
Graduate School of Agriculture and Life Sciences
Department of Animal Resource Sciences
Laboratory of Cellular Biochemistry
University of Tokyo
AWARDS
2008 Best presentation award for young scientists
Medical Research Institute
Tokyo Dental and Medical University
2010 Best presentation award for young scientists
Medical Research Institute
Tokyo Dental and Medical University
EDITORSHIPS
● Frontiers in Genetics, Associate Editor
● Frontiers in Molecular Biosciences, Associate Editor
● Frontiers in Endocrinology, Associate Editor
● International Journal of Molecular Sciences, Editor
● RNA & DISEASE, Editor in Chief
MEMBERSHIPS
● The RNA Society of Japan
(Secretariat 2010~2013, Committee member 2014~2017)
● The Molecular Biology Society of Japan.
● Japanese Cancer Society
● The RNA Society (USA)
PUBLICATIONS
Research Articles
1. Ohno, M. Kataoka, N. and Shimura, Y. (1990)
A nuclear cap binding protein from HeLa cells.
Nucleic Acids Research, 18: 6989-6995.
2. Kataoka, N., Hashimoto, S. and Shimura, Y. (1993)
Heat treatment of nuclear extract alters selection of the 3′ splice site in pre-mRNA splicing.
Biochemical and Biophysical Research Communications, 190: 223-228.
3. Kataoka, N., Ohno, M., Kangawa, K., Tokoro, Y. and Shimura, Y. (1994)
Cloning of a complementary DNA encoding an 80 kilodalton nuclear cap binding protein.
Nucleic Acids Research, 22: 3861-3865.
4. Kataoka, N., Ohno, M., Moda, I. and Shimura, Y. (1995)
Identification of the factors that interact with NCBP, an 80 kDa nuclear cap binding protein.
Nucleic Acids Research, 23: 3638-3641.
5. Siomi, M.C., Eder, P.S., Kataoka, N., Wan, L., Liu, Q. and Dreyfuss, G. (1997)
Transportin-mediated nuclear import of heterogeneous Nuclear RNP Proteins.
Journal of Cell Biology, 138: 1181-1192.
6. Pellizoni, L., Kataoka, N., Charroux, B. and Dreyfuss, G. (1998)
A novel function of SMN, the spinal muscular atrophy disease gene product, in
pre-mRNA splicing.
7. Kataoka, N., Bachorik, J.L. and Dreyfuss G. (1999)
Transportin-SR, a nuclear import receptor for SR proteins.
Journal of Cell Biology, 145: 1145-1152.
8. Nakielny, S., Kataoka, N., Siomi, H., Wan, L., Siomi, M. and Dreyfuss, G. (1999)
Ran-regulated interactions of nuclear import and export receptors with nucleoporins.
Biochemistry and Cell Biology, 77:403.
9. Kataoka, N., Yong, J., Kim, V.N., Valazquez, F., Perkinson, R.A., Wang, F. and Dreyfuss G. (2000)
Pre-mRNA splicing imprints mRNA in the nucleus with a novel RNA-binding protein that persists in the cytoplasm.
10. Kim, V.N., Yong, J., Kataoka, N., Abel, L., Diem, M. and Dreyfuss, G. (2001)
Y14 communicates the position of exon-exon junctions to the cytoplasm.
11. Kim, V.N., Kataoka, N. and Dreyfuss, G. (2001)
Role of the nonsense-mediated decay factor hUpf3 in the splicing-dependent
exon-exon junction complex.
12. Mourelatos, Z., Abel, L, Yong, J., Kataoka, N. and Dreyfuss, G. (2001)
SMN interacts with a novel family of hnRNP and spliceosomal proteins.
13. Kataoka, N., Diem, M. D., Kim, V.N., Yong, J. and Dreyfuss, G. (2001)
Magoh, a human homolog of Drosophila mago nashi protein, is a component of splicing-dependent exon-exon junction complex.
14. Kawano, T., Kataoka, N., Dreyfuss, G. and Sakamoto, H. (2004)
Ce-Y14 and MAG-1, components of the exon-exon junction complex, are required for embryogenesis and germline sexual switching in C. elegans.
Mechanism of Development, 121: 27-35.
15. Kataoka, N. and Dreyfuss, G. (2004)
A simple whole-cell lysate system for in vitro splicing reveals a stepwise-assembly of the exon-exon junction complex.
Journal of Biological Chemistry, 279: 7009-7013.
16. Masuyama, K., Taniguchi, I., Kataoka N. and Ohno, M. (2004)
RNA length defines RNA export pathway.
Genes & Development, 18: 2074-2085.
17. Masuyama, K., Taniguchi, I., Kataoka, N. and Ohno, M. (2004)
SR proteins preferentially associate with mRNAs in the nucleus and facilitate their export to the cytoplasm.
18. Okuda, J., Toyotome,T., Kataoka, N., Ohno, M., Abe, H., Shimura, Y., Seyedarabi, A., Pickersgill, R. and Sasakawa, C. (2005)
Shigella effector IpaH9.8 binds to a splicing factor U2AF35 to modulate host immune responses.
Biochemical and Biophysical Research Communications, 333: 531-539.
19. Kashima, I., Yamashita, A., Izumi, N., Kataoka, N., Morishita, R., Hoshino, S., Ohno, M., Dreyfuss, G. and Ohno, S. (2006)
Binding of a novel SMG-1-Upf1-eRF1-eRF3 complex (SURF) to the exon junction complex triggers Upf1 phosphorylation and nonsense-mediated mRNA decay.
Genes & Development, 20: 355-367.
20. Fukumura, K., Kato, A., Jin, Y., Ideue, T., Hirose, T., Kataoka, N., Fujiwara, T., Sakamoto, H. and Inoue, K. (2007)
Tissue-specific splicing regulator Fox-1 induces exon skipping by interfering E complex formation on the downstream intron of human F1gamma gene.
Nucleic Acids Research, 35: 5303-5311.
21. Yomoda, J., Muraki, M., Kataoka, N., Hosoya, T., Suzuki, M., Hagiwara, M. and Kimura, H. (2008)
Combination of Clk family kinase and SRp75 modulates alternative splicing of Adenovirus E1A.
22. Yoshimoto, R., Kataoka, N.*, Okawa, K. and Ohno, M.*(2009) (*Corresponding authors)
Isolation and characterization of post-splicing lariat-intron complexes.
Nucleic Acids Research, 37: 891-902.
23. Kataoka, N.#,*, Fujita, M.# and Ohno, M* (2009). (#Equally contributed first authors, *Corresponding authors)
Functional association of the Microprocessor complex with spliceosome.
Molecular and Cellular Biology, 29: 3243-3254.
24. Nojima, T., Oshiro-Ideue, T., Nakanoya, H., Kawamura, H., Morimoto, T., Kawaguchi, Y., Kataoka, N. and Hagiwara, M. (2009)
Herpesvirus protein ICP27 switches PML isoform by altering mRNA splicing.
Nucleic Acids Research, 37: 6515-6527.
25. Nishida, A.#, Kataoka, N.#, Takeshima. Y., Yagi, M. Awano, H., Ota, M., Itoh, K., Hagiwara, M. and Matsuo, M. (2011) (#Equally contributed first authors)
Chemical treatment enhances skipping of a mutated exon in the dystrophin gene.
26. Kataoka, N.*, #, Diem, M.D., Yoshida, M., Hatai, C., Dobashi, I., Dreyfuss, G, Hagiwara, M. and Ohno, M#. (2011) (*Corresponding author, #Equally contributed authors)
Specific Y14 domains mediate its nucleo-cytoplasmic shuttling and association with spliced mRNA.
27. Ninomiya, K., Kataoka, N. and Hagiwara, M. (2011)
Stress-responsive maturation of Clk1/4 pre-mRNAs promotes phosphorylation of SR splicing factor.
Journal of Cell Biology, 195: 27-40.
28. Kataoka, N.*, #, Dobashi, I., Hagiwara, M. and Ohno, M#. (2013) (*Corresponding author, #Equally contributed authors)
hDbr1 is a nucleocytoplasmic shuttling protein with a protein phosphatase-like motif essential for debranching activity.
29. Ozoe, A., Sone, M., Fukushima, T., Kataoka, N., Arai, T., Chida, K., Asano, T., Hakuno, F. and Takahashi, S-I. (2013)
Insulin Receptor Substrate-1 (IRS-1) Forms a Ribonucleoprotein Complex Associated with Polysomes.
30. Yoshimoto, R., Okawa, K., Yoshida, M., Ohno, M.* and Kataoka, N.*(2014) (*Corresponding authors)
Identification of a novel component C2ORF3 in the lariat-intron complex: Lack of C2ORF3 interferes with pre-mRNA splicing via intron turnover pathway.
31. Ozoe, A., Sone, M., Fukushima, T., Kataoka, N., Chida, K., Asano, T., Hakuno, F. and Takahashi, S-I. (2014)
Insulin receptor substrate-1 (IRS-1) associates with small nucleolar RNA which contributes to ribosome biogenesis.
Frontiers in Cancer Endocrinology 5: 24.
32. Melero, R., Uchiyama, A., Castaño, R., Kataoka, N., Kurosawa, H., Ohno, S., Yamashita, A. and Llorca, O. (2014)
Structures of SMG1-UPFs complexes: SMG1 contributes to regulate UPF2-dependent activation of UPF1 in NMD.
33. Masaki, S., Yoshimoto, R., Kaida, D., Hata, A., Satoh, T., Ohno, M. and Kataoka, N.* (2015) (*Corresponding author)
Identification of the specific interactors of the human lariat RNA debranching enzyme 1 protein.
International Journal of Molecular Sciences, 16: 3705-3721.
34. Yoshida, M., Kataoka, N.*, Miyauchi, K., Iida, K., Usui, T., Ohe, K., Yoshida, S., Nojima, T., Okuno, Y., Onogi, H., Takeuchi, A., Hosoya, T., Suzuki, T. and Hagiwara, M.* (2015) (*Corresponding authors)
Rectifier of aberrant mRNA splicing recovers tRNA modification in familial dysautonomia.
Proceedings of the National Academy of Science, U.S.A., 112: 2764-2769.
35. Masaki, S., Kii, I., Sumida, Y, Kato-Sumida, T, Ogawa, Y., Ito, N., Nakamura, M., Sonamoto, R., Kataoka, N., Hosoya, T., and Hagiwara, M. (2015)
Design and synthesis of a potent inhibitor of class 1 DYRK kinases as a suppressor of adipogenesis.
Bioorganic & Medicinal Chemistry, 23: 4434-4441.
36. López-Perrote, A., Castaño, R., Melero, R., Zamarro, T., Kurosawa, H., Ohnishi, T., Uchiyama, A., Aoyagi, K., Buchwald, G., Kataoka, N., Yamashita, A. and Llorca, O. (2016)
Human nonsense-mediated mRNA decay factor UPF2 interacts directly with eRF3 and the SURF complex.
Nucleic Acids Research, 44: 1909-1923.
37. Fukumura, K., Wakabayashi, S. Kataoka, N., Sakamoto, H., Suzuki, Y., Nakai, K., Mayeda, A. and Inoue, K. (2016)
The Exon Junction Complex Controls the Efficient and Faithful Splicing of a Subset of Transcripts Involved in Mitotic Cell-Cycle Progression.
International Journal of Molecular Sciences, 17: 1153-1165.
38. Ninomiya, K., Ohno, M. and Kataoka, N.* (2016) (*Corresponding author)
Dendritic Transport Element of human arc mRNA confers RNA degradation activity in a translation-dependent manner.
Genes to Cells, 21: 1263-1269.
39. Ohe, K., Yoshida, M., Nakano-Kobayashi, A., Hosokawa, M., Sako, Y., Sakuma, M., Okuno, Y., Usui, T., Ninomiya, K., Nojima, T., Kataoka, N.* and Hagiwara, M.* (2017) (*Corresponding authors)
RBM24 promotes U1 snRNP recognition of the mutated 5′ splice site in the IKBKAP gene of familial dysautonomia.
40. Wang, D.O., Ninomiya, K., Mori, C., Koyama, A., Haan, M., Kitabatake, M., Hagiwara, M., Chida, K., Takahashi, S-I., Ohno, M.* and Kataoka, N.* (2017) (*Corresponding authors)
Transport Granules Bound with Nuclear Cap Binding Protein and Exon Junction Complex are associated with microtubules and spatially separated from eIF4E granules and P bodies in Human Neuronal Processes.
Frontiers in Molecular Biosciences, 4:93.
41. Nishi, H., Yamanaka, D., Kamei, H., Goda, Y., Kumano, M., Toyoshima, Y., Takenaka, A., Masuda, M., Nakabayashi, Y., Shioya, R., Kataoka, N., Hakuno, F. and Takahashi, S-I. (2018)
Importance of Serum Amino Acid Profile for Induction of Hepatic Steatosis under Protein Malnutrition.
42. Cho, H., Gleghorn, M.L., Rambout, X. Nguyen, P., Phipps, C.R., Miyoshi, K., Fasan, R., Myers, J.R., Kataoka, N. and Maquat, L.E. (2018)
Transcriptional coactivator PGC-1α contains a novel CBP80-binding motif that orchestrates efficient target-gene expression.
Genes & Development, 32: 555-567.
43. Furuta, H., Yoshihara, H., Fukushima, T., Yosuke Yoneyama, Y., Ito, A., Worrall, C., Girnita, A., Girnita, L., Minoru Yoshida, M., Asano, T., Komada, M., Kataoka, N., Chida, K., Hakuno, F., and Takahashi1, S-I. (2018)
IRS-2 deubiquitination by USP9X maintains anchorage-independent cell growth via Erk1/2 activation in prostate carcinoma cell line.
44. Masaki, S.*, Ikeda, S., Hata, A., Shiozawa, Y., Kon, A., Ogawa, S., Suzuki, K., Hakuno, F., Takahashi, S-IT. and Kataoka, N.* (2019) (*Corresponding authors)
Myelodysplastic syndrome-associated SRSF2 mutations cause splicing changes by altering binding motif sequences.
Frontiers in Genetics, 10:338.
45. Hase, K, Contu, VR., Kabuta, C., Sakai, R., Takahashi, M., Kataoka, N., Hakuno, F., Takahashi, SI., Fujiwara, Y., Wada, K. and Kabuta, T. (2020)
Cytosolic domain of SIDT2 carries an arginine-1 rich motif that binds to RNA/DNA and is important for the direct transport of nucleic acids into lysosomes.
46. Chen, R., Sugiyama, A, Takaishi, S, Kataoka, N., Sugimoto, M., Seno, H., Fukuda, A. and Yokoyama, S. (2020)
Promoter-level transcriptome identifies stemness associated with relatively high proliferation in pancreatic cancer cells
Frontiers in Oncology, 10:316.
47. Masaki, S., Kabuto, T., Suzuki, K. and Kataoka, N.* (2020) (*Corresponding author)
Multiple nuclear localization sequences in SRSF4 protein.
48. Masaki, S., Hashimoto, K., Kihara, D., Tsuzuki, C., Kataoka, N. and Suzuki, K. (2020)
The cysteine residue at 424th of pyruvate kinase M2 is crucial for tetramerization and responsiveness to oxidative stress
Biochemical and Biophysical Research Communications, 526: 973-977.
49. Kawamura, H., Nojima, T., Oshiro-Ideue, T., Kataoka, N.* and Hagiwara, M.* (2020) (*Corresponding authors)
RNA binding activity of HSV-2 ICP27 protein
50. Muraoka, S., Fukumura, K., Hayashi, M., Kataoka, N., Mayeda, A. and Kaida, D. (2020)
Rbm38 suppresses transcription elongation defect of SMEK2 gene caused by splicing deficiency
International Journal of Molecular Sciences, 21: E8799.
51. Nakura, T., Ozoe, A., Narita, Y., Matsuo, M., Hakuno, F., Kataoka, N.* and Takahashi, SI.* (2021) (*Corresponding authors)
Rbfox2 mediates exon 11 inclusion in insulin receptor pre-mRNA splicing in hepatoma cells
52. Fukushima, S., Nishi, H., Kumano, M., Yamanaka, D., Kataoka, N., Hakuno, F. and Takahashi, SI. (2021)
A Novel Amino Acid Signaling Process Governs Glucose-6-phosphatase Transcription
53. Goda, Y., Yamanaka, D., Nishi, H., Masuda, M., Kamei, H., Kumano, M., Ito, K., Katsumata, M., Yamanouchi, K., Kataoka, N., Hakuno, F., Takahashi, SI. (2021)
Dietary lysine restriction induces lipid accumulation in skeletal muscle through an increase in serum threonine levels in rats
Journal of Biological Chemistry, 297(4):101179.
Review articles
1. Dreyfuss, G., Kim, V.N. and Kataoka, N. (2002)
Messenger-RNA-binding proteins and the messages they carry
Nature Review Molecular Cell Biology 3: 195 -205.
2. Kataoka, N.* (2015) (*Corresponding author)
Human RNA lariat Debranching Enzyme Protein 1 –A surveillant for branch RNAs for degradation.
3. Kataoka, N.* (2017) (*Corresponding author)
Modulation of aberrant splicing in human RNA diseases by chemical compounds.
Human Genetics, 136: 1237-1245.
4. Kataoka, N.*, Mayeda, A. and Ohno, K. (2019) (*Corresponding author)
Editorial: RNA Diseases in Humans – From Fundamental Research to Therapeutic Applications.
Frontiers in Molecular Biosciences, 6:53.
5. Nakayama, K.* and Kataoka, N.* (2019) (*Corresponding authors)
Regulation of gene expression under hypoxic conditions.
International Journal of Molecular Sciences, 20:3278.
6. Tan, X., Kataoka, N. and Guan, X. (2019)
Editorial: Non-coding RNA: From Bench to Bedside
7. Zhang, W., Tan, X., Kataoka, N. and Guan, X. (2020)
Editorial: Non-coding RNA in breast cancer.
8. Kataoka, N.*, Matsumoto, E. and Masaki, S. (2021) (*Corresponding author)
Mechanistic Insights of Aberrant Splicing with Splicing Factor Mutations Found in Myelodysplastic Syndromes.
International Journal of Molecular Sciences, 22:7789.
9. Zhang, W., Kataoka, N. and Guan, X. (2021)
Editorial: Non-Coding RNAs in Breast Cancer.
Frontiers in Oncology, 11:789798.
10. Kataoka, N.* and Cho, W.C. (2021) (*Corresponding author)
Editorial: Interplay Between RNA Processing Machinery and Epigenetic Regulation in Gene Expression.
Frontiers in Genetics, 12:799874.
Book chapters
1. Kataoka, N. and Dreyfuss, G. (2008)
Preparation of efficient splicing extracts from whole cells, nuclei, and cytoplasmic fractions.
RNA-Protein Interaction Protocols, 2nd edition. (Editor: Ren-Jang Lin)
Methods in Molecular Biology, 488: 357-365.
2. Kataoka N.* (2016) (*Corresponding author)
Purification of RNA-Protein Splicing Complexes Using a Tagged Protein from In Vitro Splicing Reaction Mixture.
RNA-Protein Complexes and Interactions (Editor: Ren-Jang Lin)
Methods in Molecular Biology, 1421: 45-52.
3. Kataoka N.* (2018) (*Corresponding author)
Modulation of Abnormal Splicing of RNA Diseases by Small Chemical Compounds
Applied RNA Bioscience (Editors: Seiji Masuda, Shingo Izawa), 115-130.
