Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Hidehiko Iwabuki"'
Autor:
Chihiro Yagi, Takeshi Inukai, Hidehiko Iwabuki, Mariko Eguchi, Wenming Gao, Zhouying Wu, Eiichi Ishii, Hisamichi Tauchi, Kanji Sugita, Minenori Eguchi-Ishimae
Publikováno v:
British Journal of Haematology. 171:818-829
Acute lymphoblastic leukaemia (ALL) in infants is an intractable cancer in childhood. Although recent intensive chemotherapy progress has considerably improved ALL treatment outcome, disease cure is often accompanied by undesirable long-term side eff
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fe132e3fb2b1395a1957fc2e596ed5f
https://doi.org/10.1111/bjh.13763
https://doi.org/10.1111/bjh.13763
Autor:
Eiichi Yamamoto, Hidehiko Iwabuki, Minenori Eguchi-Ishimae, Mariko Eguchi, Toshiyuki Chisaka, Koji Takemoto, Kikuko Murao, Takashi Higaki, Keiichi Isoyama, Eiichi Ishii, Masaaki Ohta, Mayumi Ohshima
Publikováno v:
Journal of Molecular Medicine. 89:43-50
HDR syndrome is an autosomal dominant disorder characterized by hypoparathyroidism, sensorineural deafness, and renal anomaly caused by mutation of the GATA3 gene located at chromosome 10p15. We report the case of a neonate with HDR syndrome and a no
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12a09263e6931c989a3254179cf48452
https://doi.org/10.1007/s00109-010-0702-6
https://doi.org/10.1007/s00109-010-0702-6
Autor:
Hirofumi Inoue, Miki Hieda, Chie Morimoto, Hidehiko Iwabuki, Shigeki Higashiyama, Natsuki Matsushita
Publikováno v:
Cancer Science. 99:214-220
The epidermal growth factor (EGF) family and the EGF receptor (EGFR, ErbB) tyrosine kinase family have been spearheading the studies of signal transduction events that determine cell fate and behavior in vitro and in vivo. The EGFR family and their s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f7c0097ed4649d08966b62f5aba64c7
https://doi.org/10.1111/j.1349-7006.2007.00676.x
https://doi.org/10.1111/j.1349-7006.2007.00676.x
Autor:
Hiroshi Iwasaki, Tatsuo Yoshinobu, Masamitsu Futai, Toshihide Okajima, Katsuyuki Tanizawa, Daisuke Kitaguchi, Hidehiko Iwabuki, Seigo Kodera, Shun'ichi Kuroda
Publikováno v:
Analytical Biochemistry. 321:65-70
We have applied spectroscopic ellipsometry to sensitive detection of specific protein-protein interactions on SiO2/Si substrates. First, the change of ellipticity of the reflected polarized light (600-1100 nm) was correlated with the thickness of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c68fac41865515e56941605533b4b3e2
https://doi.org/10.1016/s0003-2697(03)00422-6
https://doi.org/10.1016/s0003-2697(03)00422-6
Autor:
Tadanori Yamada, Hideki Fukuda, Marinee Chuah, Shun'ichi Kuroda, Akihiko Kondo, Thierry VandenDriessche, Hiroko Tada, Katsuyuki Tanizawa, Hidehiko Iwabuki, Masaharu Seno, Masakazu Ueda, Yasushi Iwasaki
Publikováno v:
Nature Biotechnology. 21:885-890
Hepatitis B virus envelope L particles form hollow nanoparticles displaying a peptide that is indispensable for liver-specific infection by hepatitis B virus in humans. Here we demonstrate the use of L particles for the efficient and specific transfe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9e74b97144faa38ccbf45c8e9269bc8
https://doi.org/10.1038/nbt843
https://doi.org/10.1038/nbt843
Autor:
Hisamichi Tauchi, Mariko Eguchi, Hidehiko Iwabuki, Eiichi Ishii, Sanae Kawakami, Minenori Eguchi-Ishimae, Kiriko Tokuda
Publikováno v:
European journal of haematology. 94(2)
Juvenile myelomonocytic leukemia (JMML) is a clonal disease arising from abnormal hematopoietic stem cells, although the involvement of lymphoid lineage differs among reported cases. Here, we present a case of JMML with a KRAS G13D mutation. The muta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8341b8c9285e96586119014d78295360
https://pubmed.ncbi.nlm.nih.gov/24766281
https://pubmed.ncbi.nlm.nih.gov/24766281
Autor:
Jong Keun Kim, Bart Devreese, Ayse Hacisalihoglu, Isabel Vandenberghe, Johannis A. Duine, Katsuyuki Tanizawa, Toshihide Okajima, Osao Adachi, Shun'ichi Kuroda, Hidehiko Iwabuki, Jozef Van Beeumen, Jaap A. Jongejan
Publikováno v:
Journal of Biological Chemistry. 276:42923-42931
Pseudomonas putida contains an amine dehydrogenase that is called a quinohemoprotein as it contains a quinone and two hemes c as redox active groups. Amino acid sequence analysis of the smallest (8.5 kDa), quinone-cofactor-bearing subunit of this het
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a74df1ca645ec6d3db75b0e87ad7ceaa
https://doi.org/10.1074/jbc.m107164200
https://doi.org/10.1074/jbc.m107164200
Autor:
Takeshi Inukai, Zhouying Wu, Minenori Eguchi-Ishimae, Wenming Gao, Masanori Nishi, Mariko Eguchi, Yuhei Hamasaki, Kanji Sugita, Sanae Kawakami, Hisamichi Tauchi, Eiichi Ishii, Hidehiko Iwabuki
Publikováno v:
Leukemia. 27(2)
MicroRNAs (miRNAs) regulate cell proliferation and differentiation by controlling the expression of proteins involved in many signaling pathways. Recent studies have shown that dysregulation of miRNA expression is associated with increased tumorigeni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f14096f4ae40db15cb3664b783cbb869
https://pubmed.ncbi.nlm.nih.gov/22918121
https://pubmed.ncbi.nlm.nih.gov/22918121
Autor:
Eiichi Yamamoto, Hidehiko Iwabuki, Zhouying Wu, Takashi Higaki, Mariko Eguchi, Minenori Eguchi-Ishimae, Wenming Gao, Issei Imoto, Masaaki Ohta, Hidemi Takata, Eiichi Ishii
Publikováno v:
Human Genome Variation
Cardiac anomaly is one of the hallmarks of DiGeorge syndrome (DGS), observed in approximately 80% of patients. It often shows a characteristic morphology, termed as conotruncal heart defects. In many cases showing only the conotruncal heart defect, d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6565560f5c7ceb45540d2c0beb02c5e7
http://europepmc.org/articles/PMC4785558
http://europepmc.org/articles/PMC4785558
Autor:
Wen Ming, Takeshi Inukai, Hidehiko Iwabuki, Kanji Sugita, Mariko Eguchi, Eiichi Ishii, Zhouying Wu, Minenori Eguchi-Ishimae
Publikováno v:
Blood. 124:2244-2244
Leukemic cells of acute lymphoblastic leukemia (ALL) in infants are frequently characterised by chromosome translocations involving 11q23, resulting in the rearrangement of the mixed-lineage leukemia (MLL) gene and subsequent generation of MLL fusion
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::709869633bc2b660cdd5dcb84fa48814
https://doi.org/10.1182/blood.v124.21.2244.2244
https://doi.org/10.1182/blood.v124.21.2244.2244