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 輸血・細胞プロセシング科
Summary Research grants & projects Published papers
Academic conference presentation


Professor:
   菅野 仁
   下平 滋隆
Assistant Professor:
   UTSUGISAWA Taiju
Assistant Professor:
   Shimojima Keiko
■ Summary
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■ Research grants & projects
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■ Research works
Journal Book Presentation Other presentations
JapaneseEnglish JapaneseEnglish Domesticinternational
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■ Published papers
Original article
1. Yamamoto-Shimojima Keiko, Osawa K, Saito M, Yamamoto T*:  iPSCs established from a female patient with Xq22 deletion confirm that BEX2 escapes from X-chromosome inactivation.  Congenital Anomalies  61 :63-67 , 2021.3   DOI:https://doi.org/10.1111/cga.12403 Link
2. Ogura H, Ohga S, Aoki T, Utsugisawa T, Takahashi H, Iwai A, Watanabe K, Okuno Y, Yoshida K, Ogawa S, Miyano S, Kojima S, Yamamoto T, Yamamoto-Shimojima K*, Kanno H.:  Novel COL4A1 mutations identified in infants with congenital hemolytic anemia in association with brain malformations.  Human Genome Variation  7 :42 , 2020.11   DOI:https://doi.org/10.1038/s41439-020-00130-w Link
3. 牧野茂義, 菅野仁, 岡本好雄, 北澤 淳一, 山本晃士, 安村敏, 米村雄士, 横濱章彦, 松下正:  改善されてきたわが国の輸血医療、その現状と課題 ~血液製剤使用実態調査から見えてくるもの~.  日本輸血細胞治療学会誌  66 (4) :619-628 , 2020.8
4. Kamio T, Kamio H, Aoki T, Ondo Y, Uchiyama T, Yamamoto-Shimojima K, Watanabe M, Okamoto T, Kanno H, Yamamoto T*.:  Molecular Profiles of Breast Cancer in a Single Institution.  Anticancer Research  40 (8) :4567-4570 , 2020.8   DOI:doi: 10.21873/anticanres.14462 Link
5. Tanaka Junji*, Tanaka Norina, Wang Yan-Hua, Mitsuhashi Kenjiro, Ryuzaki Michiko, Iizuka Yuki, Watanabe Aya, Ishiyama Midori, Shinohara Akihito, Kazama Hiroshi, Hagiwara Shotaro, Yoshinaga Kentaro, Kougen Yumi, Kobayashi Hirohito, Kanno Hitoshi, Shiseki Masayuki:  Phase I study of cellular therapy using ex vivo expanded NK cell from autologous peripheral blood mononuclear cells combined with rituximab-containing chemotherapy for relapsed CD20-positive malignant lymphoma patients.  Haematologica  105 (4) :e190-e193 , 2020.4   DOI:10.3324/haematol.2019.226696
Review article
1. 大賀正一, 石村匡崇, 江口克秀, 長谷川一太, 小倉浩美, 槍澤大樹, 菅野仁:  新生児の遺伝性溶結性貧血 ― 遺伝子診断の臨床的意義 ―.  臨床血液  61 (5) :484-490 , 2020.5
Case report
1. KOYAMAISHI Shun, KAMIO Takuya, KOBAYASHI Akie, SATO Tomohiko, KUDO Ko, SASAKI Shinya, KANEZAKI Rika, HASEGAWA Daiichiro, MURAMATSU Hideki, TAKAHASHI Yoshiyuki, SASAHARA Yoji, HIRAMATSU Hidefumi, KAKUDA Harumi, TANAKA Miyuki, ISHIMURA Masataka, NISHI Masanori, ISHIGURO Akira, YABE Hiromasa, SARASHINA Takeo, YAMAMOTO Masaki, YUZA Yuki, HYAKUMA Nobuyuki, YOSHIDA Kenichi, KANNO Hitoshi, OHGA Shouichi, OHARA Akira, KOJIMA Seiji, MIYANO Satoru, OGAWA Seishi, TOKI Tsutomu, TERUI Kiminori, ITO Etsuro:  Reduced-intensity conditioning is effective for hematopoietic stem cell transplantation in young pediatric patients with Diamond-Blackfan anemia.  Bone Marrow Transplant  :online , 2020.9   DOI:10.1038/s41409-020-01056-1
2. SUZUKI Tomoko, TOGAWA Takao, KANNO Hitoshi, OGURA Hiromi, YAMAMOTO Toshiyuki, SUGIURA Takahiro, KOUWAKI Masanori, SAITOH Shinji:  A Novel α-Spectrin Pathogenic Variant in Trans to α-Spectrin LELY Causing Neonatal Jaundice With Hemolytic Anemia From Hereditary Pyropoikilocytosis Coexisting With Gilbert Syndrome.  J Pediatr Hematol Oncol.  :1796 , 2020.4   DOI:10.1097/MPH.0000000000001796
3. Yamamoto-Shimojima K, Kimoto Y, WatanabeY, Yamamoto T*:  Two different MLC1 variants compounded with a common variant S93L in Japanese patients of megalencephalic leukoencephalopathy with subcortical cysts.  Tokyo Women's Medical University Journal  4 :94-97 , 2020   DOI:https://doi.org/10.24488/twmuj.2020007 Link
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■ Academic conference presentation
1. ◎Grace Rachael F, Boscoe Audra N, Bowden Chris, Glader Bertil, 菅野 仁, Layton D Mark, Beers Eduard van, Corrons Joan-Lluis Vives, Yan Yan, Bianchi Paola: Baseline Characteristics of Patients in Peak: A Global, Longitudinal Registry of Patients with Pyruvate Kinase Deficiency.  62nd American Society of Hematology (ASH),  San Diego U.S.A.,  2020/12
2. ◎山本圭子, 澤石由記夫, 山本俊至: Inverted-duplication-deletionの領域にさらに不均衡転座が付加された過去に報告のない染色体構造異常の1例.  第43回日本小児遺伝学会学術集会,  松本(WEB),  2021/01
3. ◎山本俊至, 山本圭子, 岡本伸彦: SMARCA2のhot spot変異は従来のSWI/SNF複合体症候群とは異なる表現型を示す.  第43回日本小児遺伝学会学術集会,  松本(WEB),  2021/01
4. ◎難波貴弘, 樋口洋介, 越智元春, 西村佑真 , 浦田奈生子, 江渕有紀, 森茂弘, 井上拓志, 清水順也, 古城真秀子, 菅野仁, 久保俊英: 重症な溶血性貧血のため輸血を要した乳児濃縮赤血球症の1例.  第72回中国四国小児科学会,  広島市,  2020/11
5. ◎山本圭子, 小野浩明, 今泉太一, 山本俊至: 白質異常を端緒に特定された新規LAMA2バリアント.  日本人類遺伝学会第65回大会,  名古屋(Web),  2020/11
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