Hisahide Nishio - My portal

Profile Information

Affiliation: Professor, Graduate School of MedicineFaculty of Medical Sciences, Kobe University

Degree: 医学博士(神戸大学)

J-GLOBAL ID: 200901040373289493
researchmap Member ID: 1000032399

Research Interests

Education

- Mar, 1986

Graduate School of Medicine, Kobe University

Committee Memberships

Awards

Nov, 2009

Outstanding Poster Award, in silico estimation for the conjugation capacity of mutant UDP-glucuronosyltransferase 1A1, The 10th International Conference Bioinfo2009

Yutaka Takaoka, Mika Ohta, Kenji Miura, Aki Sugano, Masafumi Matsuo, Hisahide Nishio, Atsuko Takeuchi, Toshiyuki Sakaeda

Papers

220

非侵襲的陽圧換気療法を行った重症型脊髄性筋萎縮症Ｉ型の１例

井上賢治, 木村暢佑, 樋口嘉久, 中本牧子, 今井剛, Nishio Hisahide

脳と発達, 49(2) 141-144, Mar, 2017 Peer-reviewed
Rare renal ciliopathies in non-consanguineous families that were identified by targeted resequencing

Tomohiko Yamamura, Naoya Morisada, Kandai Nozu, Shogo Minamikawa, Shingo Ishimori, Daisaku Toyoshima, Takeshi Ninchoji, Masato Yasui, Mariko Taniguchi-Ikeda, Ichiro Morioka …

CLINICAL AND EXPERIMENTAL NEPHROLOGY, 21(1) 136-142, Feb, 2017 Peer-reviewed
Alternative splicing of a cryptic exon embedded in intron 6 of SMN1 and SMN2

YoshimotoS, HarahapNI, HamamuraY, ArRochmahM, Shima Ai, MorisadaN, ShinoharaM, SaitoT, SaitoK, LaiPS, MatsuoM …

Hum Genome Var, 3 16040-16040, Dec, 2016 Peer-reviewed
「児科雑誌」に発表された仮称所謂脳膜炎(鉛毒性脳症)に関する研究の足跡(11) 1931年から内務省令実施(1935年)まで(第2報)

堀口俊一, 寺本敬子, Nishio Hisahide, 林千代

労働科学, 92(5-6号) 71-82, Oct, 2016 Peer-reviewed
SMN1遺伝子内に微小変異を認めた脊髄性筋萎縮症1型の1例

山田博之, 西田吉伸, 松本貴子, 毎原敏郎, Nishio Hisahide

脳と発達, 48(5号) 343-346, Sep, 2016 Peer-reviewed
HEK293 cells express dystrophin Dp71 with nucleus-specific localization of Dp71ab

Atsushi Nishida, Sato Yasuno, Atsuko Takeuchi, Hiroyuki Awano, Tomoko Lee, Emma Tabe Eko Niba, Takahiro Fujimoto, Kyoko Itoh, Yasuhiro Takeshima, Hisahide Nishio …

HISTOCHEMISTRY AND CELL BIOLOGY, 146(3) 301-309, Sep, 2016 Peer-reviewed
Early detection of tumor relapse/regrowth by consecutive minimal residual disease monitoring in high-risk neuroblastoma patients

Satoshi Hirase, Atsuro Saitoh, Tri Budi Hartomo, Aiko Kozaki, Tomoko Yanai, Daiichiro Hasegawa, Keiichiro Kawasaki, Yoshiyuki Kosaka, Masafumi Matsuo, Nobuyuki Yamamoto …

ONCOLOGY LETTERS, 12(2) 1119-1123, Aug, 2016 Peer-reviewed
Fluorescent protein-based detection of unconjugated bilirubin in newborn serum

Sota Iwatani, Hajime Nakamura, Daisuke Kurokawa, Keiji Yamana, Kosuke Nishida, Sachiyo Fukushima, Tsubasa Koda, Noriyuki Nishimura, Hisahide Nishio, Kazumoto Iijima …

SCIENTIFIC REPORTS, 6 28489, Jun, 2016 Peer-reviewed
Telomeric Region of the Spinal Muscular Atrophy Locus Is Susceptible to Structural Variations

Yoriko Noguchi, Akira Onishi, Yuji Nakamachi, Nobuhide Hayashi, Nur Imma Fatimah Harahap, Mawaddah Ar Rochmah, Ai Shima, Shinichiro Yanagisawa, Naoya Morisada, Talcu Nakagawa …

PEDIATRIC NEUROLOGY, 58 83-89, May, 2016 Peer-reviewed
Next-generation sequencing discloses a nonsense mutation in the dystrophin gene from long preserved dried umbilical cord and low-level somatic mosaicism in the proband mother

Mariko Taniguchi-Ikeda, Yasuhiro Takeshima, Tomoko Lee, Masahiro Nishiyama, Hiroyuki Awano, Mariko Yagi, Ai Unzaki, Kandai Nozu, Hisahide Nishio, Masafumi Matsuo …

JOURNAL OF HUMAN GENETICS, 61(4) 351-355, Apr, 2016 Peer-reviewed
Rituximab treatment for relapsed opsoclonus-myoclonus syndrome

Daisaku Toyoshima, Naoya Morisada, Yuichi Takami, Hiroyuki Kidokoro, Masahiro Nishiyama, Taku Nakagawa, Takeshi Ninchoji, Kandai Nozu, Yasuhiro Takeshima, Satoshi Takada …

BRAIN & DEVELOPMENT, 38(3) 346-349, Mar, 2016 Peer-reviewed
Salbutamol inhibits ubiquitin-mediated survival motor neuron protein degradation in spinal muscular atrophy cells

Nur Imma Fatimah Harahap, Dian Kesumapramudya Nurputra, Mawaddah Ar Rochmah, Ai Shima, Naoya Morisada, Toru Takarada, Atsuko Takeuchi, Yumi Tohyama, Shinichiro Yanagisawa, Hisahide Nishio

Biochemistry and Biophysics Reports, 4 351-356, Dec 1, 2015 Peer-reviewed
High resolution melting analysis of the NR1I3 genetic variants: Is there an association with neonatal hyperbilirubinemia?

Tian Pei Cheung, Hans Van Rostenberghe, Rosliza Ismail, Noor Namirah Nawawi, Nurul Arnierah Abdullah, Noraida Ramli, Nor Rosidah Ibrahim, Noorizan Hj. Abd. Majid, Narazah Mohd Yusoff, Hisahide Nishio …

GENE, 573(2) 198-204, Dec, 2015 Peer-reviewed
Differential expression of minimal residual disease markers in peripheral blood and bone marrow samples from high-risk neuroblastoma patients

Nobuyuki Yamamoto, Aiko Kozaki, Tri Budi Hartomo, Tomoko Yanai, Daiichiro Hasegawa, Keiichiro Kawasaki, Yoshiyuki Kosaka, Masafumi Matsuo, Satoshi Hirase, Takeshi Mori …

ONCOLOGY LETTERS, 10(5) 3228-3232, Nov, 2015 Peer-reviewed
Absolute lymphocyte count at the end of induction therapy is a prognostic factor in childhood acute lymphoblastic leukemia

Satoshi Hirase, Daiichiro Hasegawa, Hironobu Takahashi, Kensuke Moriwaki, Atsuro Saito, Aiko Kozaki, Toshiaki Ishida, Tomoko Yanai, Keiichiro Kawasaki, Nobuyuki Yamamoto …

INTERNATIONAL JOURNAL OF HEMATOLOGY, 102(5) 594-601, Nov, 2015 Peer-reviewed
Trinucleotide insertion in the SMN2 promoter may not be related to the clinical phenotype of SMA

Nur Imma Fatimah Harahap, Atsuko Takeuchi, Surini Yusoff, Koji Tominaga, Takeshi Okinaga, Yukihiro Kitai, Toru Takarada, Yuji Kubo, Kayoko Saito, Nihayatus Sa'adah …

BRAIN & DEVELOPMENT, 37(7) 669-676, Aug, 2015 Peer-reviewed
平成26年度地域における疾病並びに医療等に関する研究調査公衆衛生行政(保健所)医師の育成・確保とその役割に関する研究調査公衆衛生行政の現状と課題をふまえて

伊地智昭浩, 今井雅尚, 河原啓二, 佐藤英之, 中西絵里奈, Nishio Hisahide, Nishimura Noriyuki

神緑会学術誌, 31 7-11, Aug, 2015 Peer-reviewed
Two Japanese Patients With SMA Type 1 Suggest that Axonal-SMN May Not Modify the Disease Severity

Hiroyuki Yamada, Yoshinobu Nishida, Toshiro Maihara, Nihayatus Sa'adah, Nur Hmna Fatimah Harahap, Dian Kesumapramudya Nurputra, Mawaddah Ar Rochmah, Noriyuki Nishimura, Toshio Saito, Yuji Kubo …

PEDIATRIC NEUROLOGY, 52(6) 638-641, Jun, 2015 Peer-reviewed
A new method for SMN1 and hybrid SMN gene analysis in spinal muscular atrophy using long-range PCR followed by sequencing

Yuji Kubo, Hisahide Nishio, Kayoko Saito

JOURNAL OF HUMAN GENETICS, 60(5) 233-239, May, 2015 Peer-reviewed
A new method for SMN1 and hybrid SMN gene analysis in spinal muscular atrophy using long-range PCR followed by sequencing

Yuji Kubo, Hisahide Nishio, Kayoko Saito

JOURNAL OF HUMAN GENETICS, 60(5) 233-239, May, 2015 Peer-reviewed

Misc.

次世代シークエンサーを用いた先天性腎尿路奇形(CAKUT)の原因遺伝子解析

森貞直哉, 庄野朱美, Nozu Kandai, 叶明娟, 神田祥一郎, 井藤奈央子, 亀井宏一, 伊藤秀一, 山本勝輔, 里村憲一 …

発達腎研究会誌, 24(1) 13-15, Apr, 2016 Peer-reviewed
Contributions of Japanese patients to development of antisense therapy for DMD

Masafumi Matsuo, Yasuhiro Takeshima, Hisahide Nishio

BRAIN & DEVELOPMENT, 38(1) 4-9, Jan, 2016 Peer-reviewed
脊髄性筋萎縮症遺伝子診断から治療戦略まで

Nishio Hisahide

日本小児科学会雑誌, 118(9号) 1315-1323, Sep, 2014 Peer-reviewed
PLS3 expression and SMA phenotype: a commentary on correlation of PLS3 expression with disease severity in children with spinal muscular atrophy

Hisahide Nishio

JOURNAL OF HUMAN GENETICS, 59(2) 64-65, Feb, 2014 Peer-reviewed
Spinal Muscular Atrophy: From Gene Discovery to Clinical Trials

Dian K. Nurputra, Poh San Lai, Nur Imma F. Harahap, Satoru Morikawa, Tomoto Yamamoto, Noriyuki Nishimura, Yuji Kubo, Atsuko Takeuchi, Toshio Saito, Yasuhiro Takeshima …

ANNALS OF HUMAN GENETICS, 77(5) 435-463, Sep, 2013 Peer-reviewed
小児医学最近の進歩脊髄性筋萎縮症とSMN蛋白と低分子量リボ核蛋白合成

Nishio Hisahide, Morikawa Aatoru, Nishimura Noriyuki, Takeshima Yasuhiro

小児科, 52巻, 11号, pp. 1535-1542, Oct, 2011 Peer-reviewed
小児医学最近の進歩脊髄性筋萎縮症up to date 医学的管理

Nishio Hisahide, Nishimura Noriyuki, Morikawa Aatoru, Takeshima Yasuhiro

小児科, 51巻, 13号, pp. 1797-1806, Dec, 2010 Peer-reviewed
小児医学最近の進歩脊髄性筋萎縮症up to date 治療戦略

Nishio Hisahide, Nishimura Noriyuki, Morikawa Aatoru, Takeshima Yasuhiro

小児科, 51巻, 12号, pp. 1687-1695, Nov, 2010 Peer-reviewed
小児医学最近の進歩脊髄性筋萎縮症up to date 遺伝子診断

Nishio Hisahide, Nishimura Noriyuki, Morikawa Aatoru, Matsuo Masafumi

小児科, 51巻, 11号, pp. 1535-1542, Oct, 2010 Peer-reviewed
Genetic disorders associated with neonatal jaundice

Morioka Ichiro, Morikawa Satoru, Nishimura Noriyuki, Nishio Hisahide

Eastern Journal of Medicine, Vol. 15, No. 4, pp. 155-162, 2010 Peer-reviewed
【カルシウムとアンチエイジング】爪カルシウムと加齢、そして骨密度

Nishio Hisahide

Clinical Calcium, 18巻, 7号, pp. 959-966, Jun, 2008
Somatic and germline mosaicism for a mutation of the PHEX gene can lead to genetic transmission of x-linked hypophosphatemic rickets that mimics an autosomal dominant trait

K Goji, K Ozaki, AH Sadewa, H Nishio, M Matsuo

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 91(2) 365-370, Feb, 2006 Peer-reviewed
Frequencies of A(TA)(7)TAA, G71R, and G493R mutations of the UGT1A1 gene in the Malaysian population

S Yusoff, H Van Rostenberghe, NM Yusoff, NA Talib, N Ramli, NZAN Ismail, WPW Ismail, M Matsuo, H Nishio

BIOLOGY OF THE NEONATE, 89(3) 171-176, 2006 Peer-reviewed
Association of multiple risk factors for neonatal jaundice. -eLetters for KADAKOL et al.

Van Rostenberghe H, Yusoff S, Yusoff NM, NISHIO, Hisahide

Biology Of The Neonate, Vol. 89, No. 3, pp. 171-176, Oct, 2005
ACE gene polymorphism in children with nephrotic syndrome in the Indonesian population

Teguh Haryo Sasongko, Ahmad Hamim Sadewa, Pungky Ardani Kusuma, Martua Parlindungan, Damanik, LEE, Meijin, AYAKI, Hitoshi, NOZU, kandai, Akinobu Goto …

The Kobe Journal Of Medical Sciences, Vol. 51, No. 3-4, pp. 41-47(3) 41-47, 2005 Peer-reviewed
男女共同参画社会の形成が少子化に歯止めをかける

NISHIO, Hisahide

さんぎょうほけんひょうご, 29巻, , pp. 1-2, Oct, 2004
少子化対策－新「子育て」教育の提案

NISHIO, Hisahide

公衆衛生, 67巻, 8, pp. 568-569, Aug, 2003
産業衛生学の動向

NISHIO HISAHIDE

公衆衛生, 67巻, 3号, pp. 217-220, Mar, 2003

Books and Other Publications

最新臨床検査学講座免疫検査学第1版第1刷 / 第4章II．輸血用血液製剤の種類と特性

坊池義浩, Nishio Hisahide

医師薬出版株式会社, Feb, 2017
脊髄性筋萎縮症診療マニュアル / ５章遺伝子疾患としてのSMA 5-1小児期発症SMAの原因と病態は何ですか。

Nishio Hisahide

金芳堂, May, 2012
脊髄性筋萎縮症診療マニュアル / １２章SMAの新しい治療法の開発研究

Nishio Hisahide

金芳堂, May, 2012
子育て支援のための子ども保健学 / わが国における母子保健福祉事業

Nishio Hisahide

日本小児医事出版社, Mar, 2012
臨床検査学講座免疫検査学第２版 / II．輸血用血液製剤の種類と特性

Nishio Hisahide (Role: Joint author)

医歯薬出版株式会社, Mar, 2010
臨床検査学講座免疫検査学 / II. 輸血用血液製剤の種類と特性

Nishio Hisahide (Role: Joint author)

医歯薬出版株式会社, Jun, 2008
Women and Aging: New Research / Aging and Calcium Paradox. Increase of Red Cell Calcium Content with Age and its Reversal by Calcium Supplementation

Nishio Hisahide (Role: Joint author)

Nova Science Publishers, Inc., 2008
産業医学実践講座 / 第9章労働者保護

NISHIO HISAHIDE (Role: Joint author)

南江堂, Jan, 2007
産業医活動をする人のために / 少子化対策：子育てしやすい企業風土

NISHIO HISAHIDE (Role: Joint author)

財団法人産業医学振興財団, Oct, 2005
子育て支援のための小児保健学第２版 / 少子化社会の到来

NISHIO HISAHIDE (Role: Joint author)

日本小児医事出版社, Mar, 2005
子育て支援のための小児保健学初版 / 第1章小児の健康と小児保健の意義と目的

NISHIO HISAHIDE (Role: Joint author)

日本小児医事出版社, Mar, 2003
Child Health and Child Care

NAKAMURA, Hajiem, MATSUO, Masafumi, INAGAKI, Yuko, NISHIO, Hisahide, OKADA, Yuka (Role: Joint author)

日本小児医事出版社, Mar, 2003

Presentations

183

保健所実習は公衆衛生に興味を持たせる絶好の機会

白井千香, 松林恵介, 藤山理世, 千原三枝子, 片上祐子, 横山真一, 渡辺雅子, 谷畑健生, 三品浩基, 伊地智昭浩, Nishio Hisahide

The 75th Annual Meeting of Japanese Society of Public Health, Oct, 2016, JAPANESE SOCIETY OF PUBLIC HEALTH Invited
脊髄性筋萎縮症(SMA)原因遺伝子、SMN のヒト神経細胞モデルにおける機能の解析

佐々木彪曜, Shima Ai, 森田寛之, 田畑裕幸, Nishio Hisahide, 通山由美

第66回日本薬学会近畿支部総会, Oct, 2016, The Pharmaceutical Society of Japan Kinki Branch Invited
Spinal Muscular Atrophy (SMA): Advances in Therapeutic Development.

Nishio Hisahide

The 1st International Conference on Health Sciences, Oct, 2016, Gadjah Mada University Invited
Advancement in diagnosis and therapy of congenital diseases.

Nishio Hisahide

The 1st International Conference on Health Sciences, Oct, 2016, Gadjah Mada University Invited
脊髄性筋萎縮症における遺伝子解析

野口依子, 中町祐司, 林伸英, Saegusa Jun, Kawano Seiji, 中川卓, Shima Ai, Nishio Hisahide

65th JAMT CONGRESS, Sep, 2016, The Japanese Association of Medical Technologists Invited
Telomeric regions of the spinal muscular atrophy locus are susceptible to structural variations.

Yoriko Noguchi, Yuji Nakamachi, Nobuhide Hayashi, Saegusa Jun, Kawano Seiji, Taku Nakagawa, Shima Ai, Nishio Hisahide

The 32nd World Congress of Biomedical Laboratory Science, Sep, 2016 Invited
脊髄性筋萎縮症（SMA）モデル神経細胞では神経突起様構造の伸長が抑制される

Shima Ai, 森田寛之, 通山由美, Nishio Hisahide

The 2nd Annual Meeting of Japan Muscle Society, Aug, 2016, Japan Muscle Society Invited
臍帯由来間葉系幹細胞を用いた脊髄性筋萎縮症の病態解析の試み

Iwatani Souta, 福嶋祥代, 德田央士, Nishida Kosuke, Fujita Kaori, Yamana Keiji, Kurokawa Daisuke, 長坂美和子, 香田翼, Morioka Ichiro, Nishio Hisahide, Iijima Kazumoto, Nishimura Noriyuki

第52回日本周産期・新生児医学会学術集会, Jul, 2016 Invited
Lecture of acupuncture for medical students in Kobe University.

Takaoka Yutaka, Ohta Mika, Sugano Aki, Nishio Hisahide

The 48th Annual Meeting of the Japan Society for Medical Education, Jul, 2016, Japan Society for Medical Education Invited
CAKUT及び原因不明の小児期発症慢性腎機能障害患者への包括的原因遺伝子解析

森貞直哉, Nozu Kandai, Shono Akemi, Ninchoji Takeshi, 叶明娟, 井藤奈央子, 神田祥一郎, 亀井宏一, 石倉健司, 伊藤秀一, 山本勝輔, 里村憲一, 服部元史, 田中亮二郎, Nishio Hisahide, Iijima Kazumoto

The 51st Annual Meeting of the Japanese Society for Pediatric Nephrology, Jul, 2016, The Japanese Society for Pediatric Nephrology Invited
Rab6B mediates the progression of neuroblastoma through the interaction with MTMR5

Nishimura Noriyuki, Pham TVH, Thwin KK, Yamamoto Nobuyuki, Mori Takeshi, Hayakawa A, Nishio Hisahide, Matsuo M, Hasegawa D, Kawasaki K, Kosaka Y, Iijima Kazumoto

Advances in Neuroblastoma Research Conference 2016, Jun, 2016 Invited
DENN domain protein DENND2A regulates the progression of neuroblastoma.

Yamamoto Nobuyuki, Thwin KK, Fujimura J, Nakanishi K, Mori Takeshi, Hayakawa A, Nishio Hisahide, Matsuo M, Hasegawa D, Kawasaki K, Kosaka Y, Iijima Kazumoto, Nishimura Noriyuki

Advances in Neuroblastoma Research Conference 2016, Jun, 2016 Invited
脊髄性筋萎縮症（SMA）のヒト神経細胞モデル作製と表現型の解析

Shima Ai, 森田寛之, Nishio Hisahide, 通山由美

The 63th Annual Meeting of the Japanese Biochemical Society, Kinki Branch, May, 2016, The Japanese Biochemical Society, Kinki Branch Invited
Minimal residual disease monitoring in neuroblastoma patients.

Nishimura Noriyuki, トゥインキンキモン, Yamamoto Nobuyuki, Mori Takeshi, 早川晶, 長谷川大一郎, 川崎圭一郎, 小阪嘉之, Nishio Hisahide, Iijima Kazumoto

The 119th Annual Meeting of the Japan Pedeatric Society, May, 2016, Japan Pediatric Society Invited
次世代シークエンサーによる重症心身障害者施設での原因遺伝子解析

森貞直哉, 加藤威, 加藤神奈, Shima Ai, Fujita Kaori, Nishimura Noriyuki, Nishio Hisahide, 和田博子, Iijima Kazumoto

第119回日本小児科学会学術集会, May, 2016 Invited
Studies on the history of lead poisoning (15) the literature on lead poisoning refered by Igaku-chuo-zasshi (1913-1926)3

堀口俊一, 寺本敬子, Nishio Hisahide, 林千代

The 89th Annual Meeting of the Japan Society for Occupational Health, May, 2016, Japan Society for Occupational Health Invited
当院における稀少遺伝性難病の出生前診断の現状

Ikeda Mariko, 李知子, 竹島泰弘, Nishio Hisahide, Tairaku Shinya, 田中敬子, 運﨑愛, Hiroyuki Awano, Morioka Ichiro, Yamada Hideto, Iijima Kazumoto, Toda Tatsushi

第40回日本遺伝カウンセリング学会, Apr, 2016 Invited
The comprehensive genetic analysis of congenital anomalies of the kidney and urinary tract (CAKUT) in Japan.

Naoya Morisada, Shono Akemi, Ikeda Mariko, Nozu Kandai, Koichi Kamei, Kenji Ishikura, Shuichi Ito, Ryojiro Tanaka, Nishio Hisahide, Iijima Kazumoto

The 13th International Congress of Human Genetics, Apr, 2016 Invited
Sulbutamol inhibits ubiquitin-mediated survival motor neuron protein degradation in spinal muscular atrophy cells.

Nur Imma Fatimah Harahap, Dian Kesumapramudya Nurputra, Mawaddah Ar Rochmah, Shima Ai, Naoya Morisada, Toru Takarada, Atsuko Takeuchi, Yumi Tohyama, Shinichiro Yanagisawa, Nishio Hisahide

The 13th International Congress of Human Genetics, Apr, 2016 Invited
Gender effects on the severity of spinal muscular atrophy (SMA) in 286 Japanese patients diagnosed in 1996-2015.

Shima Ai, Mawaddah Ar Rochmah, Naoya Morisada, Shinichiro Yanagisawa, Nur Imma Fatimah Harahap, Toshio Saito, Aiko Umeno, Kaori Kaneko, Kayoko Saito, Iijima Kazumoto, Nishio Hisahide

The 13th International Congress of Human Genetics, Apr, 2016 Invited

Teaching Experience

Professional Memberships

Research Projects

Rabファミリー低分子量G蛋白質を標的とした神経芽腫の新しい治療法に関する研究

学術研究助成基金助成金／基盤研究(C), Apr, 2014 - Mar, 2017

西村範行
細胞内シグナル伝達経路を標的とする脊髄性筋萎縮症治療法の開発

学術研究助成基金助成金／基盤研究(C), Apr, 2013 - Mar, 2016

西尾久英
Ｒａｂファミリー低分子量Ｇ蛋白質の神経芽腫がん幹細胞の発生・分化における機能解明

学術研究助成基金助成金／基盤研究(C), 2011

西村範行
ＳＭＮ２遺伝子転写制御を中核技術とする脊髄性筋萎縮症治療法の開発

科学研究費補助金／基盤研究(C), 2010

西尾久英
神経芽腫の予後決定因子としてのＲａｂファミリー低分子量Ｇ蛋白質の役割に関する研究

科学研究費補助金／基盤研究(C), 2009

李明鎮
ＳＭＮ遺伝子スプライシング制御を中核技術とする脊髄性筋萎縮症治療法の開発

科学研究費補助金／基盤研究(C), 2006

西尾久英
スプライシングの抑制／回復に関わる金属を利用したスプライシング関連蛋白の検出

科学研究費補助金／基盤研究(C), 2006

李明鎭
発がん性化学物質が選択的スプライシングに及ぼす影響の評価

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