Search Results - "Takezawa, Yuka"

Avoidance behavior and experience-dependent tolerance in response to bitter compounds in Caenorhabditis elegans by Ishikawa, Seiryu, Iida, Chiharu, Takezawa, Yuka, Chiba, Kyoko, Kage-Nakadai, Eriko

“…ABSTRACT This study investigates the mechanisms governing experience-dependent tolerance of bitter compounds in Caenorhabditis elegans. The nematodes showed an…”
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Experience-Dependent Behavioral Plasticity in Avoiding Epigallocatechin Gallate (EGCG) Requires DAF-16/FOXO in the AIY Interneurons of Caenorhabditis elegans by ISHIKAWA, Seiryu, TAKEZAWA, Yuka, IIDA, Chiharu, YAMADA, Yuko, CHIBA, Kyoko, ALI, Mohammad Shaokat, SUN, Simo, KAGE-NAKADAI, Eriko

“…Bitterness and astringency are the aversive tastes in mammals. In humans, aversion to bitterness and astringency may be reduced depending on the eating…”
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Acquired dysfibrinogenemia: monoclonal λ-type IgA binding to fibrinogen caused lower functional plasma fibrinogen level and abnormal clot formation by Arai, Shinpei, Kamijo, Tomu, Takezawa, Yuka, Sugano, Mitsutoshi, Nakazawa, Hideyuki, Yanagisawa, Ryu, Uehara, Takeshi, Honda, Takayuki, Okumura, Nobuo

“…We report a case of acquired dysfibrinogenemia with monoclonal gammopathy of undetermined significance presenting λ -type IgA M protein. The patient showed…”
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Nonsense-mediated mRNA decay was demonstrated in two hypofibrinogenemias caused by heterozygous nonsense mutations of FGG , Shizuoka III and Kanazawa II by Soya, Keisuke, Takezawa, Yuka, Okumura, Nobuo, Terasawa, Fumiko

“…Abstract We report two novel hypofibrinogenemias, Shizuoka III and Kanazawa II, which are caused by heterozygous mutations in FGG . Shizuoka III showed…”
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The fibrous form of intracellular inclusion bodies in recombinant variant fibrinogen-producing cells is specific to the hepatic fibrinogen storage disease-inducible variant fibrinogen by Arai, Shinpei, Ogiwara, Naoko, Mukai, Saki, Takezawa, Yuka, Sugano, Mitsutoshi, Honda, Takayuki, Okumura, Nobuo

“…Fibrinogen storage disease (FSD) is a rare disorder that is characterized by the accumulation of fibrinogen in hepatocytes and induces liver injury. Six…”
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Clinical utility of urinary mulberry bodies/cells testing in the diagnosis of Fabry disease by Nakamura, Katsuya, Mukai, Saki, Takezawa, Yuka, Natori, Yuika, Miyazaki, Akari, Ide, Yuichiro, Takebuchi, Mayu, Nanato, Kana, Katoh, Mizuki, Suzuki, Harue, Sakyu, Akiko, Kojima, Tomomi, Kise, Emiko, Hanafusa, Hiroaki, Kosho, Tomoki, Kuwahara, Koichiro, Sekijima, Yoshiki

“…Variants in the galactosidase alpha (GLA) gene cause Fabry disease (FD), an X-linked lysosomal storage disorder caused by α-galactosidase A (α-GAL) deficiency…”
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γ375W fibrinogen-synthesizing CHO cells indicate the accumulation of variant fibrinogen within endoplasmic reticulum by Kobayashi, Tamaki, Arai, Shinpei, Ogiwara, Naoko, Takezawa, Yuka, Nanya, Mai, Terasawa, Fumiko, Okumura, Nobuo

“…Abstract Background Hepatic endoplasmic reticulum (ER) storage disease (HERSD) associated with hypofibrinogenemia has been reported in patients with four types…”
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Richter Transformation in the Brain from Chronic Lymphocytic Leukemia by Ishida, Fumihiro, Nakazawa, Hideyuki, Takezawa, Yuka, Matsuda, Kazuyuki, Asano, Naoko, Sano, Kenji, Sakai, Hitoshi, Ito, Toshiro

“…Richter syndrome (RS) involves the development of an aggressive lymphoma in patients with chronic lymphocytic leukemia (CLL). Diffuse large B-cell lymphoma…”
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Factor H gene variants in Japanese: Its relation to atypical hemolytic uremic syndrome by Mukai, Saki, Hidaka, Yoshihiko, Hirota-Kawadobora, Masako, Matsuda, Kazuyuki, Fujihara, Noriko, Takezawa, Yuka, Kubota, Seiko, Koike, Kenichi, Honda, Takayuki, Yamauchi, Kazuyoshi

“…► We analyze FH1 in Japanese aHUS. ► Japanese aHUS have FH1 mutations in its exon 23. ► Interestingly, healthy Japanese have the well-known disease risk…”
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Molecular analysis of afibrinogenemic mutations caused by a homozygous FGA1238 bp deletion, and a compound heterozygous FGA1238 bp deletion and novel FGA c.54+3A>C substitution by Takezawa, Yuka, Terasawa, Fumiko, Matsuda, Kazuyuki, Sugano, Mitsutoshi, Tanaka, Aiko, Fujiwara, Mitsuhiro, Kainuma, Keigo, Okumura, Nobuo

“…We identified two afibrinogenemic girls in two Japanese families and performed molecular analysis to clarify the mechanisms of fibrinogen defects. Genetic…”
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Comparison of fibrinogen synthesis and secretion between novel variant fibrinogen, nagakute (gamma305Thr --> Ala), and other variants located in gamma305-308 residues by Kobayashi, Tamaki, Takezawa, Yuka, Terasawa, Fumiko, Okumura, Nobuo

“…We found and identified a novel heterozygous dysfibrinogenemia with gammaT305A (ACA --> GCA) mutation in a 6-month old boy. Since his plasma antigenic…”
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Functional analysis for dysfibrinogenemias, Toyama and Adachi, which have a mutation of Aalpha16Arg-->His (CGT-->CAT) with aberrant fibrinopeptide A release by Soya, Keisuke, Takezawa, Yuka, Terasawa, Fumiko, Okumura, Nobuo

“…We found and identified four heterozygous dysfibrinogenemias with AalphaR16H(CGT-->CAT) mutation in two families by coagulation tests and direct sequence…”
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Role of fibrinogen Bbeta-chain D-region 454-458 residues for assembly and secretion of intact fibrinogen by Terasawa, Fumiko, Takezawa, Yuka, Hirota-Kawadobora, Masako, Okumura, Nobuo

“…To examine the role of fibrinogen Bbeta-chain D region in the assembly and/or secretion of multichain protein, we synthesized eight variant fibrinogens with…”
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Paediatric acute lymphoblastic leukaemia‐associated haemophagocytic lymphohistiocytosis develops during prednisolone prephase by Tanabe, Sota, Furui, Yu, Saito, Shoji, Okura, Eri, Ide, Yuichiro, Takezawa, Yuka, Maruyama, Yuta, Sakamoto, Kenichi, Hirabayashi, Koichi, Tanaka, Miyuki, Yanagisawa, Ryu, Nakazawa, Yozo

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Development of multiplex short tandem repeat (STR)-PCR for chimerism analysis in patients with hematological malignancies and comparison of chimerism in different sample sources by Taira, Chiaki, Matsuda, Kazuyuki, Takezawa, Yuka, Ito, Toshiro, Ishida, Fumihiro, Hidaka, Eiko, Kumagai, Toshiko, Honda, Takayuki

“…Polymerase chain reaction analysis of short-tandem repeat (STR) markers (STR-PCR) has been used for chimerism testing to assess engraftment following…”
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Immature Platelet Fraction and Its Kinetics in Neonates by Kobayashi, Jun, Takezawa, Yuka, Saito, Shoji, Kubota, Noriko, Sakashita, Kazuo, Nakazawa, Yozo, Higuchi, Yumiko, Tozuka, Minoru, Ishida, Fumihiro

“…Thrombocytopenia is a common abnormality encountered in the neonatal period, and immature platelet fraction (IPF) may be an informative indicator of…”
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Immature Platelet Fraction and its Kinetics in Neonates by Kobayashi, Jun, Takezawa, Yuka, Saito, Shoji, Kubota, Noriko, Sakashita, Kazuo, Nakazawa, Yozo, Higuchi, Yumiko, Tozuka, Minoru, Ishida, Fumihiro

“…Thrombocytopenia is a common abnormality encountered in the neonatal period, and immature platelet fraction (IPF) may be an informative indicator of…”
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Case with intrauterine fetus death: interphase fluorescence in situ hybridization using buccal cells is useful for examining chromosomal abnormalities when placental villus not available by Takezawa, Yuka, Kosho, Tomoki, Matsuda, Kazuyuki, Taira, Chiaki, Ito, Yurika, Hidaka, Eiko, Sugano, Mitsutoshi, Narumi, Yoko, Mizuuchi, Asako, Kobara, Hisanori, Wakui, Keiko, Okumura, Nobuo, Fukushima, Yoshimitsu, Honda, Takayuki

“…The proband was a male fetus who died at 18 weeks of gestation. The fetus had growth retardation, hydrocephalus, exophthalmos, and micrognathia. The placental…”
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Real-time nanodiamond thermometry probing in vivo thermogenic responses by Fujiwara, Masazumi, Sun, Simo, Dohms, Alexander, Nishimura, Yushi, Suto, Ken, Takezawa, Yuka, Oshimi, Keisuke, Zhao, Li, Sadzak, Nikola, Umehara, Yumi, Teki, Yoshio, Komatsu, Naoki, Benson, Oliver, Shikano, Yutaka, Kage-Nakadai, Eriko

“…Real-time temperature monitoring inside living organisms provides a direct measure of their biological activities. However, it is challenging to reduce the…”
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Recombinant γT305A fibrinogen indicates severely impaired fibrin polymerization due to the aberrant function of hole ‘a’ and calcium binding sites by Ikeda, Minami, Kobayashi, Tamaki, Arai, Shinpei, Mukai, Saki, Takezawa, Yuka, Terasawa, Fumiko, Okumura, Nobuo

“…Abstract Introduction We examined a 6-month-old girl with inherited fibrinogen abnormality and no history of bleeding or thrombosis. Routine coagulation…”
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