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  1. 広島大学の刊行物
  2. Hiroshima Journal of Medical Sciences
  3. 34巻1号

Flow Cytometric Assessment of Neutrophil Oxidative Metabolism in Chronic Granulomatous Disease on Small Quantities of Whole Blood: Heterogeneity in Female Patients

https://hiroshima.repo.nii.ac.jp/records/2013002
https://hiroshima.repo.nii.ac.jp/records/2013002
83eaa830-253b-4885-ab6c-29f80577af5d
名前 / ファイル ライセンス アクション
HiroshimaJMedSci_34_53.pdf HiroshimaJMedSci_34_53.pdf (996.4 KB)
Item type デフォルトアイテムタイプ_(フル)(1)
公開日 2023-03-18
タイトル
タイトル Flow Cytometric Assessment of Neutrophil Oxidative Metabolism in Chronic Granulomatous Disease on Small Quantities of Whole Blood: Heterogeneity in Female Patients
言語 en
作成者 TAGA, Kazuyuki

× TAGA, Kazuyuki

en TAGA, Kazuyuki

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SEKI, Hidetoshi

× SEKI, Hidetoshi

en SEKI, Hidetoshi

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MIYAWAKI, Toshio

× MIYAWAKI, Toshio

en MIYAWAKI, Toshio

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SATO, Tamotsu

× SATO, Tamotsu

en SATO, Tamotsu

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TANIGUCHI, Noboru

× TANIGUCHI, Noboru

en TANIGUCHI, Noboru

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SHOMIYA, Kyoichi

× SHOMIYA, Kyoichi

en SHOMIYA, Kyoichi

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HIRAO, Takao

× HIRAO, Takao

en HIRAO, Takao

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USUI, Tomofusa

× USUI, Tomofusa

en USUI, Tomofusa

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アクセス権
アクセス権 open access
アクセス権URI http://purl.org/coar/access_right/c_abf2
主題
主題Scheme Other
主題 Neutrophil
主題
主題Scheme Other
主題 Oxidative metabolism
主題
主題Scheme Other
主題 Chronic granulomatous disease
主題
主題Scheme Other
主題 Flow Cytometry
主題
主題Scheme NDC
主題 490
内容記述
内容記述 A rapid and sensitive flow cytometric assay is presented for the quantitative estimation of the oxidative metabolic activity of individual polymorphonuclear leukocytes (PMN) on less than 100 td of whole blood. This procedure is a simplified version using whole blood of the method of Bass et al (J. Immunol. 130:1910, 1983) that estimated the metabolic burst activity of phorbol myristate acetate (PMA)-stimulated individual PMN as the intracellular generation of a fluorescence product by a flow cytometric assay. With this method, almost all the PMN from normal subjects responded to PMA as a single cell population generating bright intracellular fluorescence. PMN from a boy with chronic granulomatous disease (CGD), could not respond to PMA with any increase of their fluorescence intensity. His mother had two distinct PMN populations one functionally normal and the other defective, indicating a random lyonization in the carrier mother and the X-linked recessive mode of inheritance. In two female patients with CGD from unrelated families, their PMN responded to PMA, as a whole, with a minimal increase in the fluorescence intensity, but the metabolic defects in their PMN were not so complete as seen in a classical X-linked CGD boy. But, PMN from two female sibling patients from the other family responded to PMA as a single uniform cell population with a weak but definite fluorescence intensity. However, the genetic background of these female patients with CGD remains unclear, since PMN dysfunction could not be identified in their mothers with this method.
言語 en
内容記述
内容記述タイプ Other
内容記述 This work was supported in part by a grant (No. 58440046) from the Ministry of Education of Japan.
出版者
出版者 Hiroshima University School of Medicine
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ departmental bulletin paper
出版タイプ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
関連情報
識別子タイプ PMID
関連識別子 4019240
収録物識別子
収録物識別子タイプ ISSN
収録物識別子 0018-2052
収録物識別子
収録物識別子タイプ NCID
収録物識別子 AA00664312
開始ページ
開始ページ 53
書誌情報 Hiroshima Journal of Medical Sciences
Hiroshima Journal of Medical Sciences

巻 34, 号 1, p. 53-60, 発行日 1985-03
旧ID 49833
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