Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Takenori, Nitta"'
Publikováno v:
Clinical and Experimental Neuroimmunology. 14:52-60
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab38168d024c0edf7e9aeecec68a69bb
https://doi.org/10.1111/cen3.12730
https://doi.org/10.1111/cen3.12730
Autor:
AMIEN RAMADHAN ISHAK, RINI PUSPITANINGRUM, RISMA DWI UTARI, MELLA FERANIA, CHRIS ADHIYANTO, TAKENORI NITTA, AB SUSANTO, HATTORI YUKIO, YASUHIRO YAMASHIRO
Publikováno v:
Hayati Journal of Biosciences, Vol 21, Iss 4, Pp 159-165 (2014)
Mitochondrial gene mutation plays a role in the development of type two diabetes mellitus (T2DM). A point mutation in the mitochondrial gene Nicotinamide adenine dinucleotide dehydrogenase 1 (mtDNA ND1) gene mainly reported as the most common mutatio
Externí odkaz:
https://doaj.org/article/0479a323179e4a9ea6e9932868ec907b
Publikováno v:
Electr. Eng. Jpn.. 214:10-17
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b3ff5c4a7926431607eed3e48863590
http://t2r2.star.titech.ac.jp/cgi-bin/publicationinfo.cgi?q_publication_content_number=CTT100846279
http://t2r2.star.titech.ac.jp/cgi-bin/publicationinfo.cgi?q_publication_content_number=CTT100846279
Publikováno v:
IEEJ Transactions on Fundamentals and Materials. 140:292-298
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b6b4f747205b7161dcfe9bd94b94bc2
https://doi.org/10.1541/ieejfms.140.292
https://doi.org/10.1541/ieejfms.140.292
Autor:
Gen-ichiro Nakamura, Tomohiko Otsuka, Tsukasa Furuya, Machiko Nagayoshi, Hiroshi Fujino, Ryo Shoji, Takumi Mukougawa, Takenori Nitta
Publikováno v:
Journal of JSEE. 69:1_45-1_48
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a174bde50848f35f774a7cb68bf96df
https://doi.org/10.4307/jsee.69.1_45
https://doi.org/10.4307/jsee.69.1_45
Autor:
Ferania Mella, Tatehiko Tanaka, Yasuhiro Yamashiro, Masafumi Kimoto, Takenori Nitta, Chris Adhiyanto, Yuki Amao
Publikováno v:
Hemoglobin. 42(1)
We report a new hemoglobin (Hb) variant, Hb Hachioji (HBB: c.187C>T), which was detected in a 32-year-old male with hemolytic anemia. The proband had undergone splenectomy in his childhood after being diagnosed with hereditary spherocytosis (HS) with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49d530300feaa5b355c9865923a78886
https://pubmed.ncbi.nlm.nih.gov/31550961
https://pubmed.ncbi.nlm.nih.gov/31550961
Autor:
Tomoko Ezumi, Mituaki Nishioka, Junji Nakamura, Yasuhiro Yamashiro, Yukio Hattori, Takenori Nitta
Publikováno v:
Annals of Clinical Biochemistry: International Journal of Laboratory Medicine. 52:569-575
Background High performance liquid chromatography and immunological and enzymatic methods are known as the methods for HbA1c measurement. However, the differences in the principles of the methods may cause slight discrepancies, which become problems
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5840bf73b281dd2723e2197af6adea1
https://doi.org/10.1177/0004563214568872
https://doi.org/10.1177/0004563214568872
Autor:
Sajala Salim, Nevin Hareb, Chris Adhiyanto, Takenori Nitta, Minako Hino, Emayla Alba, Mohammed Naveed, Yukio Hattori, Yasuhiro Yamashiro, Maryam Matar
Publikováno v:
Nursing & Health Sciences. 13:105-113
This article reports on efforts to overcome common hurdles that were faced during population-based screening for common hemoglobinopathies in the United Arab Emirates. An Internet-based approach was designed and implemented to increase the acceptance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7ff35e756dbbbf629be760a503bc5b32
https://doi.org/10.1111/j.1442-2018.2011.00599.x
https://doi.org/10.1111/j.1442-2018.2011.00599.x
Autor:
Tomoaki Murata, Tatehiko Tanaka, Fumio Kawano, Takenori Nitta, Chris Adhiyanto, Fumiya Takagi, Yukio Hattori, Yasuhiro Yamashiro, Mella Ferania
Publikováno v:
Hemoglobin. 39(2)
Here we describe a Japanese patient with mild β-thalassemia (β-thal) with an intact β-globin gene but a new missense mutation of c.947G A or p.C316Y in the erythroid Krüppel-Like Factor (KLF1) gene which is strongly associated with the expression
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9de6a9d779341f0a37d8bf715cb82c55
https://pubmed.ncbi.nlm.nih.gov/26794457
https://pubmed.ncbi.nlm.nih.gov/26794457
Autor:
Yukio Hattori, Ferania Mella, Chris Adhiyanto, Takenori Nitta, Yasuhiro Yamashiro, Maryam Matar, Fumiya Takagi, Satsuki Araki, Mizuki Iihoshi
Publikováno v:
Hemoglobin. 38(3)
β-Thalassemia (β-thal), especially β-thalassemia major (β-TM), is reported to be related to reactive oxygen species (ROS) and enhanced oxidation status. It is reflected by increased malondialdehyde (MDA), by membrane lipid peroxidation and decrea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1df901cdd77aedd18dc2ed674daa772c
https://pubmed.ncbi.nlm.nih.gov/24611654
https://pubmed.ncbi.nlm.nih.gov/24611654