Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Yasumichi, Toki"'
Autor:
Sohji Nishina, Yasuyuki Tomiyama, Katsuya Ikuta, Yasuaki Tatsumi, Yasumichi Toki, Ayako Kato, Koichi Kato, Naoko Yoshioka, Kyo Sasaki, Yuichi Hara, Keisuke Hino
Publikováno v:
BMC Gastroenterology, Vol 21, Iss 1, Pp 1-7 (2021)
Abstract Background Hereditary hemochromatosis is a heterogenous group of inherited iron-overload conditions that is characterized by increased intestinal absorption and deposition in vital organs. Hepcidin is a soluble regulator that acts to attenua
Externí odkaz:
https://doaj.org/article/67efaf51fab54a8fb71daf0ee916440d
Autor:
Hitoshi Nishio, Yuichi Honma, Keiichiro Kumamoto, Yasumichi Toki, Kahori Morino, Shinji Oe, Koichiro Miyagawa, Michihiko Shibata, Shintaro Abe, Yasuaki Tatsumi, Katsuya Ikuta, Hisao Hayashi, Masaru Harada
Publikováno v:
Kanzo. 63:151-157
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aba7b3608f1d67d8c4d10d914f073570
https://doi.org/10.2957/kanzo.63.151
https://doi.org/10.2957/kanzo.63.151
Autor:
Sho Igarashi, Tsukasa Nozu, Masatomo Ishioh, Takuya Funayama, Chihiro Sumi, Takeshi Saito, Yasumichi Toki, Mayumi Hatayama, Masayo Yamamoto, Motohiro Shindo, Hiroki Tanabe, Toshikatsu Okumura
Publikováno v:
Journal of Physiology and Biochemistry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::62e5a7888fc2c0846aefc14d81b7e006
https://doi.org/10.1007/s13105-023-00962-4
https://doi.org/10.1007/s13105-023-00962-4
Autor:
Akiyoshi Takami, Yasuaki Tatsumi, Katsuhisa Sakai, Yasumichi Toki, Katsuya Ikuta, Yuka Oohigashi, Junko Takagi, Koichi Kato, Kazuhisa Takami
Publikováno v:
Pharmaceuticals, Vol 13, Iss 8, p 195 (2020)
Juvenile hemochromatosis (JH), type 2A hemochromatosis, is a rare autosomal recessive disorder of systemic iron overload due to homozygous mutations of HJV (HFE2), which encodes hemojuvelin, an essential regulator of the hepcidin expression, causing
Externí odkaz:
https://doaj.org/article/59898ac4d9cc4035b03f7a9e26dfefb2
Autor:
Takuya Funayama, Tsukasa Nozu, Masatomo Ishioh, Sho Igarashi, Chihiro Sumi, Takeshi Saito, Yasumichi Toki, Mayumi Hatayama, Masayo Yamamoto, Motohiro Shindo, Hiroki Tanabe, Toshikatsu Okumura
Publikováno v:
Brain Research. 1809:148371
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::559cf13dec93c3fe0b3a206b17cddb33
https://doi.org/10.1016/j.brainres.2023.148371
https://doi.org/10.1016/j.brainres.2023.148371
Autor:
Masaru Harada, Yasuaki Tatsumi, Kazuhiro Sumida, Kahori Morino, Kenji Koikawa, Hisao Hayashi, Koichiro Miyagawa, Shintaro Abe, Shohei Shimajiri, Masahiro Yamasaki, Yuichi Honma, Tsukasa Karasuyama, Katsuya Ikuta, Yasumichi Toki, Keiichiro Kumamoto, Michihiko Shibata, Shinji Oe
Publikováno v:
Medical Molecular Morphology. 54:60-67
Hemochromatosis is a clinical syndrome characterized by iron overload in various organs. We present here a case of type 4 hereditary hemochromatosis due to heterozygous mutation in SLC40A1 gene (p.D157A). SLC40A1 encodes ferroportin, a macromolecule
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::80a61fb55a648d139e83572fa17018dd
https://doi.org/10.1007/s00795-020-00259-1
https://doi.org/10.1007/s00795-020-00259-1
Autor:
Masayo Yamamoto, Motohiro Shindo, Takuya Funayama, Chihiro Sumi, Takeshi Saito, Yasumichi Toki, Mayumi Hatayama, Ken-Ichi Imadome, Yusuke Mizukami, Toshikatsu Okumura
Publikováno v:
Medicine. 101(12)
Posttransplant lymphoproliferative disease (PTLD) is a critical complication of hematopoietic stem cell transplantation (HSCT). PTLD is classified into early and late-onset PTLDs. In post-HSCT patients, late-onset PTLD is rare, particularly PTLD afte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d7516282fb53e808b06fe8b2176bf59
https://pubmed.ncbi.nlm.nih.gov/35357349
https://pubmed.ncbi.nlm.nih.gov/35357349
Autor:
Masayasu Naito, Seiichiro Hoshino, Tatsuyuki Tonan, Takuji Torimura, Takaaki Ohtake, Toshikatsu Okumura, Takumi Kawaguchi, Hisao Hayashi, Koichi Kato, Yasuaki Tatsumi, Yasumichi Toki, Katsuya Ikuta
Publikováno v:
Hepatology Research. 50:144-150
Juvenile hemochromatosis (JH) is known as a progressive iron-storage disease, and causes severe organ impairments, including cardiomyopathy and liver cirrhosis. However, JH is a rare genetic disorder, and information for genetic mutations and phenoty
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a26fd0e8804cf6280538b1610ca88b2
https://doi.org/10.1111/hepr.13423
https://doi.org/10.1111/hepr.13423
Autor:
Daisuke Kato, Riki Tanaka, Toshikatsu Okumura, Naomi Iizuka, Yasumichi Toki, Kotoe Shibusa, Mayumi Hatayama, Kozo Matsui, Takeshi Saito, Katsuya Ikuta
Publikováno v:
Annals of Clinical Biochemistry: International Journal of Laboratory Medicine. 56:654-661
BackgroundAs the saturation of transferrin by iron in the serum is approximately 30%, iron loaded to the blood can bind to transferrin not bearing iron. Nevertheless, prolonged iron influx finally results in full transferrin saturation, and iron not
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17041abaf5f228fd2dbc524292c72351
https://doi.org/10.1177/0004563219861413
https://doi.org/10.1177/0004563219861413
Autor:
Kyo Sasaki, Yuichi Hara, Yasumichi Toki, Keisuke Hino, Yasuaki Tatsumi, Koichi Kato, Sohji Nishina, Naoko Yoshioka, Yasuyuki Tomiyama, Katsuya Ikuta, Ayako Kato
Publikováno v:
BMC Gastroenterology
BMC Gastroenterology, Vol 21, Iss 1, Pp 1-7 (2021)
BMC Gastroenterology, Vol 21, Iss 1, Pp 1-7 (2021)
Background Hereditary hemochromatosis is a heterogenous group of inherited iron-overload conditions that is characterized by increased intestinal absorption and deposition in vital organs. Hepcidin is a soluble regulator that acts to attenuate both i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92bb66080a074ceaeb1340875a266a7a
http://europepmc.org/articles/PMC7934381
http://europepmc.org/articles/PMC7934381