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J-GLOBAL ID:202001010142466238   Update date: Oct. 31, 2024

Hijikata Minako

Hijikata Minako
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Research theme for competitive and other funds  (14):
  • 2022 - 2025 Development of an Efficient Screening Method for the Detection of Undiagnosed Primary Ciliary Dyskinesia.
  • 2022 - 2025 肺MAC症に関わる気道上皮細胞におけるエピジェネティック修飾の解析
  • 2020 - 2025 A study on long-term epigenetic immunomodulation caused by latent tuberculosis infection
  • 2020 - 2023 原発性線毛不全症の慢性気道感染病態に見られる微生物叢のメタ16S解析と臨床的意義
  • 2019 - 2022 Comprehensive analysis of changing gene expression of human bronchial epithelial cells by estrogen deficiency
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Papers (113):
  • Minako Hijikata, Kozo Morimoto, Masashi Ito, Keiko Wakabayashi, Akiko Miyabayashi, Hiroyuki Yamada, Naoto Keicho. Genetic Variants Supporting the Diagnosis of Primary Ciliary Dyskinesia in Japan. Clinical Genetics. 2024
  • Hajime Nakamura, Haruka Hikichi, Shintaro Seto, Minako Hijikata, Naoto Keicho. Transcriptional regulators SP110 and SP140 modulate inflammatory response genes in Mycobacterium tuberculosis-infected human macrophages. Microbiology spectrum. 2024. e0010124
  • Masashi Ito, Kozo Morimoto, Masakazu Ohasi, Keiko Wakabayashi, Akiko Miyabayashi, Hiroyuki Yamada, Minako Hijikata, Naoto Keicho. Primary Ciliary Dyskinesia Due to Compound Heterozygous Variants in CFAP221 with Obstructive Azoospermia: Young's Syndrome May Be a Phenotype of Primary Ciliary Dyskinesia. Internal medicine (Tokyo, Japan). 2024
  • 慶長 直人, 土方 美奈子, 伊藤 優志, 森本 耕三. 原発性線毛機能不全症候群. 結核. 2024. 99. 3. 77-77
  • Masashi Ito, Kozo Morimoto, Mikio Saotome, Akiko Miyabayashi, Keiko Wakabayashi, Hiroyuki Yamada, Minako Hijikata, Naoto Keicho, Ken Ohta. Primary Ciliary Dyskinesia Caused by Homozygous DNAAF1 Mutations Resulting from a Consanguineous Marriage: A Case Report from Japan. Internal medicine (Tokyo, Japan). 2024
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MISC (27):
  • 瀬戸 真太郎, 土方 美奈子, 慶長 直人. In vivo研究の視点から見た抗酸菌感染症 プロテオミクスで明らかにする結核肉芽腫のタンパク質ダイナミクス. 結核. 2019. 94. 3. 208-208
  • Genetic analysis of sinobronchial syndrome. 2017. 31. 5. 487-492
  • Primary ciliary dyskinesia. 2017. 31. 1. 84-87
  • 土方 美奈子, 慶長 直人. 難治性気道疾患 : 原発性線毛機能不全・びまん性汎細気管支炎 (特集 ここまで進んだ! びまん性肺疾患の診断と治療) -- (さまざまなびまん性肺疾患の診断・治療). 内科. 2016. 117. 2. 267-270
  • 慶長 直人, 土方 美奈子. 抗酸菌感染症における感受性遺伝子解析 (特集 呼吸器疾患における遺伝子研究の最前線). Respiratory medical research. 2016. 4. 1. 41-45
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