Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Kohei Ogata"'
Autor:
Tatsuya Kubota, Erika Kurihara, Kazuya Watanabe, Kohei Ogata, Ryosuke Kaneko, Masaru Goto, Toshihisa Ohshima, Kazuaki Yoshimune
Publikováno v:
Communications Biology, Vol 5, Iss 1, Pp 1-7 (2022)
Heat-induced maturation of homoserine dehydrogenase from a hyperthermophilic archaeon requires conformational changes within the catalytic region.
Externí odkaz:
https://doaj.org/article/13843f348b5b4fd6bf590f12efb216a5
Publikováno v:
Remote Sensing, Vol 10, Iss 7, p 1126 (2018)
The tsunami generated by the 2011 Tohoku-Oki earthquake was the first time that the velocity fields of a tsunami were measured by using high-frequency oceanographic radar (HF radar) and since then, the development of HF radar systems for tsunami dete
Externí odkaz:
https://doaj.org/article/9f016c6b7c0d4c8f8877451bb686cde5
Autor:
Mayumi Takano, Kotaro Hine, Sumito Nagasaki, Junya Sakuma, Makiko Shimabukuro, Hikari Kotaki, Keiko Saito, Kohei Ogata, Hitoshi Yoda, Masahiko Nakata
Publikováno v:
Prenatal Diagnosis. 42:1448-1457
To investigate the differences in amniotic fluid cardiac biomarkers and clinical features among types of right ventricular outflow tract (RVOT) abnormality in monochorionic (MC) twins.This prospective study included MC twins that underwent laser surg
Publikováno v:
Congenital Heart Disease. 16:369-371
Autor:
Kohei Ogata, Sanenori Nakamura, Toshihisa Ohshima, Yui Yajima, Masaru Goto, Ryosuke Kaneko, Kazuaki Yoshimune
Publikováno v:
Scientific Reports, Vol 8, Iss 1, Pp 1-8 (2018)
Scientific Reports
Scientific Reports
Homoserine dehydrogenase (EC 1.1.1.3, HSD) is an important regulatory enzyme in the aspartate pathway, which mediates synthesis of methionine, threonine and isoleucine from aspartate. Here, HSD from the hyperthermophilic archaeon Sulfolobus tokodaii
Publikováno v:
Journal of Japan Society of Civil Engineers, Ser. B2 (Coastal Engineering). 75:I_1309-I_1314
Publikováno v:
Journal of Japan Society of Civil Engineers, Ser. B2 (Coastal Engineering). 73:I_1615-I_1620
Publikováno v:
Clinical genetics. 11(3)
The case of a 4-month-old male infant with retarded psychomotor development and multiple anomalies is presented. Cytogenetic studies on peripheral blood and skin cultures revealed a normal male complement with a supernumerary small metacentric chromo