Search Results - "Matsuda, Chie"

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  1. 1

    Obstetrical outcomes of labor with and without analgesia in Robson classification groups 1 and 2a: a single-center retrospective study by Yagi, Taro, Kinose, Yasuto, Bun, Michiko, Horai, Megumi, Matsuda, Chie, Miyake, Tatsuya, Mimura, Kazuya, Otaki, Chiyo, Endo, Masayuki, Kimura, Tadashi

    Published in Journal of anesthesia (01-02-2023)
    “…Purpose This study aimed to elucidate the effects of neuraxial analgesia on labor in women classified based on the Robson classification system. Methods We…”
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    Structural instability of lamin A tail domain modulates its assembly and higher order function in Emery–Dreifuss muscular dystrophy by Mio, Muneyo, Sugiki, Toshihiko, Matsuda, Chie, Mitsuhashi, Hiroaki, Kojima, Chojiro, Chan, Siu Yuen, Hayashi, Yukiko K., Mio, Kazuhiro

    “…The C-terminal Ig-domain of lamin A plays critical roles in cell function via interaction with proteins, DNA, and chromatin. Mutations in this domain are known…”
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    Upregulated expression of FGF13/FHF2 mediates resistance to platinum drugs in cervical cancer cells by Okada, Tomoko, Murata, Kazuhiro, Hirose, Ryoma, Matsuda, Chie, Komatsu, Tsunehiko, Ikekita, Masahiko, Nakawatari, Miyako, Nakayama, Fumiaki, Wakatsuki, Masaru, Ohno, Tatsuya, Kato, Shingo, Imai, Takashi, Imamura, Toru

    Published in Scientific reports (11-10-2013)
    “…Cancer cells often develop drug resistance. In cisplatin-resistant HeLa cisR cells, fibroblast growth factor 13 (FGF13/FHF2) gene and protein expression was…”
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    Augmented autocrine bone morphogenic protein (BMP) 7 signaling increases the metastatic potential of mouse breast cancer cells by Sakai, Hirofumi, Furihata, Mutsuo, Matsuda, Chie, Takahashi, Munehisa, Miyazaki, Hiroshi, Konakahara, Takeo, Imamura, Toru, Okada, Tomoko

    Published in Clinical & experimental metastasis (01-04-2012)
    “…As malignant breast cancers progress, they acquire the ability to spread to other regions of the body, including bone and lung, but the molecular mechanism…”
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    Contribution of dysferlin deficiency to skeletal muscle pathology in asymptomatic and severe dystroglycanopathy models: generation of a new model for Fukuyama congenital muscular dystrophy by Kanagawa, Motoi, Lu, Zhongpeng, Ito, Chiyomi, Matsuda, Chie, Miyake, Katsuya, Toda, Tatsushi

    Published in PloS one (08-09-2014)
    “…Defects in dystroglycan glycosylation are associated with a group of muscular dystrophies, termed dystroglycanopathies, that include Fukuyama congenital…”
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  7. 7

    Successful pulmonary embolectomy for massive pulmonary embolism during pregnancy: a case report by Taenaka, Hiroki, Ootaki, Chiyo, Matsuda, Chie, Fujino, Yuji

    Published in JA clinical reports (25-08-2017)
    “…Background Pulmonary embolism (PE) resulting from venous thromboembolism is a leading cause of maternal mortality in pregnancy. In patients with massive PE and…”
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  8. 8

    Dietary intervention of mice using an improved Multiple Artificial-gravity Research System (MARS) under artificial 1 g by Matsuda, Chie, Kato, Tamotsu, Inoue-Suzuki, Sayo, Kikuchi, Jun, Ohta, Toshiko, Kagawa, Masaharu, Hattori, Masahira, Kobayashi, Hiroe, Shiba, Dai, Shirakawa, Masaki, Mizuno, Hiroyasu, Furukawa, Satoshi, Mukai, Chiaki, Ohno, Hiroshi

    Published in NPJ microgravity (08-07-2019)
    “…Japan Aerospace Exploration Agency (JAXA) has developed mouse habitat cage units equipped with an artificial gravity-producing centrifuge, called the Multiple…”
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    Incidence and Cause of Headache after Cesarean Section by MATSUDA, Chie, OOTAKI, Chiyo, KURI, Michioki, YAMAMOTO, Shunske, FUJINO, Yuji

    “…We analyzed a series of 657 parturients that had cesarean sections between January 2016 and April 2019 using data from electronic patient records. Of the 118…”
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  10. 10

    Distal anterior compartment myopathy: A dysferlin mutation causing a new muscular dystrophy phenotype by Illa, Isabel, Serrano-Munuera, Carme, Gallardo, Eduard, Lasa, Adriana, Rojas-García, Ricardo, Palmer, Jaume, Gallano, Pia, Baiget, Montserrat, Matsuda, Chie, Brown, Robert H.

    Published in Annals of neurology (01-01-2001)
    “…We report a family with a new phenotype of autosomal recessive muscle dystrophy caused by a dysferlin mutation. The onset of the illness is distal, in the…”
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  11. 11

    Defective Myotilin Homodimerization Caused by a Novel Mutation in MYOT Exon 9 in the First Japanese Limb Girdle Muscular Dystrophy 1A Patient by Shalaby, Sherine, Mitsuhashi, Hiroaki, Matsuda, Chie, Minami, Narihiro, Noguchi, Satoru, Nonaka, Ikuya, Nishino, Ichizo, Hayashi, Yukiko K

    “…Myotilin is a muscle-specific Z disk protein. Several missense mutations in the myotilin gene (MYOT) have been identified in limb girdle muscular dystrophy…”
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    Ultrasound guided nerve block in infants undergoing pyloromyotomy by Matsuda, Chie, Tachibana, Kazuya, Kinouchi, Keiko

    “…Ultrasound guided nerve block has become popular in pediatric practice. We applied this technique to infants undergoing pyloromyotomy. We retrospectively…”
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    The effect of nitroglycerin 200 microg on uterine relaxation during cesarean delivery by Matsuda, Chie, Hayashi, Shusaku, Kinouchi, Keiko

    “…Rapid and transient uterine relaxation is sometimes required for fetal distress or difficult delivery due to uterine hyperactivity during cesarean section. For…”
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    Ultrasound guided transversus abdominis plane block in early infancy by Matsuda, Chie, Tachibana, Kazuya, Fujii, Masashi, Kinouchi, Keiko

    “…We retrospectively examined the transversus abdominis plane (TAP) block performed in 8 infants (range, 1-115 days) from July 2010 to March 2011. Ultrasound…”
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    Two endoplasmic reticulum-associated degradation (ERAD) systems for the novel variant of the mutant dysferlin: ubiquitin/proteasome ERAD(I) and autophagy/lysosome ERAD(II) by Fujita, Eriko, Kouroku, Yoriko, Isoai, Atsushi, Kumagai, Hiromichi, Misutani, Akifumi, Matsuda, Chie, Hayashi, Yukiko K., Momoi, Takashi

    Published in Human molecular genetics (15-03-2007)
    “…Dysferlin is a type-II transmembrane protein and the causative gene of limb girdle muscular dystrophy type 2B and Miyoshi myopathy (LGMD2B/MM), in which…”
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    Specific phosphorylation of Ser458 of A-type lamins in LMNA-associated myopathy patients by Mitsuhashi, Hiroaki, Hayashi, Yukiko K, Matsuda, Chie, Noguchi, Satoru, Wakatsuki, Shuji, Araki, Toshiyuki, Nishino, Ichizo

    Published in Journal of cell science (15-11-2010)
    “…Mutations in LMNA, which encodes A-type nuclear lamins, cause various human diseases, including myopathy, cardiomyopathy, lipodystrophy and progeria syndrome…”
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