Zobrazeno 1 - 10
of 118
pro vyhledávání: '"Yoshiyuki Takahashi"'
Autor:
Valentina Sas, Sergiu Pasca, Ancuta Jurj, Laura Pop, Hideki Muramatsu, Hiroko Ono, Delia Dima, Patric Teodorescu, Sabina Iluta, Cristina Turcas, Anca Onaciu, Raluca Munteanu, Alina-Andreea Zimta, Cristina Blag, Gheorghe Popa, Elias Daniel Alexander von Gamm, Smaranda Arghirescu, Margit Serban, Sorin Man, Mirela Marian, Bobe Petrushev, Cristian Berce, Anca Colita, Mihnea Zdrenghea, Seiji Kojima, Diana Gulei, Yoshiyuki Takahashi, Ciprian Tomuleasa
Publikováno v:
Cellular Physiology and Biochemistry, Vol 54, Iss 5, Pp 994-1012 (2020)
Externí odkaz:
https://doaj.org/article/386eda9b6f0745e2ab7430ba6e883f14
Autor:
Takuya Takeichi, Yusuke Okuno, Akane Kawamoto, Takeshi Inoue, Eiko Nagamoto, Chiaki Murase, Eri Shimizu, Kenichi Tanaka, Yuichi Kageshita, Satoshi Fukushima, Michihiro Kono, Junko Ishikawa, Hironobu Ihn, Yoshiyuki Takahashi, Masashi Akiyama
Publikováno v:
Journal of Lipid Research, Vol 59, Iss 12, Pp 2413-2420 (2018)
Neu-Laxova syndrome (NLS) is a very rare autosomal recessive congenital disorder characterized by disturbed development of the central nervous system and the skin and caused by mutations in any of the three genes involved in de novo l-serine biosynth
Externí odkaz:
https://doaj.org/article/831482703d28463483b0693e3974d333
Autor:
Franco Locatelli, Hyoung Jin Kang, Bénédicte Bruno, Virginie Gandemer, Fanny Rialland, Maura Faraci, Yoshiyuki Takahashi, Katsuyoshi Koh, Henrique Bittencourt, Grace Cleary, Christine Rosko, Pantelia Roussou, Annie St. Pierre, Anirudh Prahallad, Cristina Díaz-de-Heredia
Publikováno v:
Blood. 140:1376-1378
Autor:
Yoshiyuki Takahashi, Nobuhiro Nishio, Hideki Muramatsu, Rieko Taniguchi, Yuichi Ishikawa, Makoto Murata, Nozomu Kawashima, Eri Nishikawa, Ryo Hanajiri, Motoharu Hamada, Atsushi Narita
Publikováno v:
Blood. 138:3831-3831
Introduction: Chimeric antigen receptor-modified T cells targeting CD19 (CD19.CAR-T cells) have shown clinical success in patients with hematological malignancies. Despite the encouraging results obtained with this novel therapy, a major concern to i
Publikováno v:
Organic letters. 22(3)
The nickel-catalyzed hydroarylation of 1,3-dienes with arylboronic acids using a secondary homoallyl carbonate as a surrogate for the 1,3-diene and hydride source has been developed. The synthetic strategy allowed an efficient access to a wide array
Autor:
Ayako Hattori, Yoshiyuki Takahashi, Kazuhito Satou, Seiji Kojima, Yusuke Okuno, Ikumi Hori, Yuji Nakamura, Daisuke Ieda, Shinji Saitoh, Yutaka Negishi, Hideki Muramatsu, Kei Ohashi, Tomoko Kawai
Publikováno v:
Human Genome Variation
Human Genome Variation, Vol 6, Iss 1, Pp 1-4 (2019)
Human Genome Variation, Vol 6, Iss 1, Pp 1-4 (2019)
Patients with variants in CUL4B exhibit syndromic intellectual disability (MIM #300354). A seven-year-old boy presented with intellectual disability, a history of seizure, characteristic facial features, and short stature. Whole-exome sequencing dete
Publikováno v:
Tetrahedron Letters. 68:152916
The use of a malonate nucleophile in the transition metal-catalyzed hydroalkylation of 1,3-dienes remains immature. Herein, we report the nickel-catalyzed hydroalkylation of 1,3-dienes with malonates using a homoallyl carbonate as the 1,3-diene and h
Autor:
Masayuki Imaya, Tomoo Ogi, Yoshiyuki Takahashi, Manabu Wakamatsu, Eri Nishikawa, Masafumi Ito, Hideki Muramatsu, Kotaro Narita, Daisuke Ichikawa, Seiji Kojima, Atsushi Narita, Rieko Taniguchi, Nobuhiro Nishio, Yusuke Okuno, Shunsuke Miwata, Taro Yoshida, Motoharu Hamada, Asahito Hama, Nozomu Kawashima, Ayako Yamamori
Publikováno v:
Blood. 136:9-9
BACKGROUND: Inherited bone marrow failure syndromes (IBMFSs) are a heterogeneous group of genetic disorders characterized by bone marrow failure, physical anomalies, and various kinds of organ complications. In addition to classical IBMFSs, such as F
Autor:
Haichan Xu, Biljana Horn, Rui Zhang, Sanfang Tu, Le-Ping Zhang, Cheng Jiao, Yu-Chen Liu, Yuan Sun, Yuhua Li, Yoshiyuki Takahashi, Zhouyang Liu, Bin Wang, Jia Feng, Yuchen Li, Lung-Ji Chang, Xue Song, Yi-Fei Cheng, Yongping Zhang, Huyong Zheng, Juan Xiao, Kai Wang, Nobuhiro Nishio
Publikováno v:
Blood. 136:7-7
BACKGROUND: Allogeneic haematopoietic stem cell transplantation (allo-HCT) is a standard treatment for relapsed/refractory B-cell acute lymphoblastic leukemia (r/r B-ALL). However ~30-40% of patients (pts) still relapse after HCT. We report a cohort
Autor:
Yoshiyuki Takahashi, Seiji Kojima, Manabu Wakamatsu, Norihiro Murakami, Hironobu Kitazawa, Yusuke Okuno, Hideki Muramatsu
Publikováno v:
Blood. 134:4213-4213
Background Juvenile myelomonocytic leukemia (JMML) is a rare pediatric myelodysplastic/myeloproliferative disease. Approximately 85% of patients with JMML harbor germline and/or somatic mutations in RAS pathway genes, such as PTPN11, NF1, CBL, NRAS,