Causal mechanisms of seismo-EM phenomena during the 1965–1967 Matsushiro earthquake swarm

por Enomoto, Yuji, Yamabe, Tsuneaki, Okumura, Nobuo
Publicado 2017

Hereditary Fibrinogen Aα-Chain Amyloidosis in Asia: Clinical and Molecular Characteristics

por Yazaki, Masahide, Yoshinaga, Tsuneaki, Sekijima, Yoshiki, Kametani, Fuyuki, Okumura, Nobuo
Publicado 2018

A Novel Mutation in the Fibrinogen Bβ Chain (c.490G>A; End of Exon 3) Causes a Splicing Abnormality and Ultimately Leads to Congenital Hypofibrinogenemia

por Taira, Chiaki, Matsuda, Kazuyuki, Arai, Shinpei, Sugano, Mitsutoshi, Uehara, Takeshi, Okumura, Nobuo
Publicado 2017

Recombinant γY278H Fibrinogen Showed Normal Secretion from CHO Cells, but a Corresponding Heterozygous Patient Showed Hypofibrinogenemia

por Kamijo, Tomu, Kaido, Takahiro, Yoda, Masahiro, Arai, Shinpei, Yamauchi, Kazuyoshi, Okumura, Nobuo
Publicado 2021

A Novel Amino Acid Substitution, Fibrinogen Bβp.Pro234Leu, Associated with Hypofibrinogenemia Causing Impairment of Fibrinogen Assembly and Secretion

por Kaido, Takahiro, Yoda, Masahiro, Kamijo, Tomu, Arai, Shinpei, Taira, Chiaki, Higuchi, Yumiko, Okumura, Nobuo
Publicado 2020

Congenital Hypofibrinogenemia in a Neonate with a Novel Mutation in the FGB Gene

por Shinozuka, Jun, Okumura, Nobuo, Nagasawa, Mayumi, Nishikado, Motokazu, Kadowaki, Sayaka, Katsuda, Itsuro, Imashuku, Shinsaku
Publicado 2021

Citrullinated fibrinogen-SAAs complex causes vascular metastagenesis

por Han, Yibing, Tomita, Takeshi, Kato, Masayoshi, Ashihara, Norihiro, Higuchi, Yumiko, Matoba, Hisanori, Wang, Weiyi, Hayashi, Hikaru, Itoh, Yuji, Takahashi, Satoshi, Kurita, Hiroshi, Nakayama, Jun, Okumura, Nobuo, Hiratsuka, Sachie
Publicado 2023