ログイン
言語:

WEKO3

  • トップ
  • ランキング
To

Field does not validate

To

Field does not validate

To
lat lon distance


インデックスリンク

インデックスツリー

  • RootNode

メールアドレスを入力してください。

WEKO

One fine body…

WEKO

One fine body…

アイテム

  1. 紀要
  2. 札幌医学雑誌
  3. 64巻

生検筋と培養筋におけるDystrophinとDystrophin related proteinの発現について : Duchenne型筋ジストロフィーを中心に

https://doi.org/10.15114/smj.64.227
https://doi.org/10.15114/smj.64.227
3516e5cd-2cc3-449e-9cb8-5434b5959427
名前 / ファイル ライセンス アクション
n0036472X646227.pdf n0036472X646227.pdf (5.3 MB)
Item type 紀要論文 / Departmental Bulletin Paper(1)
公開日 2019-07-31
タイトル
タイトル 生検筋と培養筋におけるDystrophinとDystrophin related proteinの発現について : Duchenne型筋ジストロフィーを中心に
言語 ja
タイトル
タイトル Expression of dystrophin and dystrophin-related protein in biopsied and cultured muscle from patients with Duchenne muscular dystrophy and other muscular diseases
言語 en
言語
言語 jpn
キーワード
言語 en
主題Scheme Other
主題 Duchenne muscular dystrophy
キーワード
言語 en
主題Scheme Other
主題 Dystrophin
キーワード
言語 en
主題Scheme Other
主題 Dystrophin related protein
キーワード
言語 en
主題Scheme Other
主題 Revertant fibers
キーワード
言語 en
主題Scheme Other
主題 a second site in-frame deletion
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
ID登録
ID登録 10.15114/smj.64.227
ID登録タイプ JaLC
著者 渡辺, 幸恵

× 渡辺, 幸恵

渡辺, 幸恵

Search repository
舘, 延忠

× 舘, 延忠

舘, 延忠

Search repository
著者別名
識別子Scheme WEKO
識別子 25631
姓名 Watanabe, Yukie
著者別名
識別子Scheme WEKO
識別子 25632
姓名 Tachi, Nobutada
抄録
内容記述タイプ Abstract
内容記述 The expression of dystrophin and dystrophin-related protein (DRP) in biopsied and cultured muscles from eight Duchenne muscular dystrophy (DMD) patients, four DMD carriers, seven Becker muscular dystrophy (BMD) patients, two dermatomyositis patients and ten normal controls were studied by immunocytochemistry and Western blot analysis. In muscle biopsies, DRP was located on the sarcolemma of dystrophin deficient muscle fibers from patients with DMD, BMD and DMD carriers and regenerating muscle fibers from patients with dermatomyositis. Successive sections of muscles from patients with DMD, DMD carrier, BMD, dermatomyositis, and controls were stained with anti-dystrophin antibodies and anti-DRP antibodies. DRP expression on dystrophin deficient fibers did not completely compensate dystrophin. In muscle cultures, dystrophin was not demonstrable in undifferentiated myoblasts from patients with DMD and controls. After myoblast fusion from control muscles, dystrophin appeared in the cytoplasm of myotubes as discrete round packages in perinuclear resions, and along the surface of more mature myotubes. There was no staining in myotubes from DMD patients. DRP was expressed in the cytoplasm of myoblasts and myotubes from control patients and patients with DMD. Thus far, these results indicate that DRP was expressed by activation of satellite cell irrespective of the cause of muscle damage. Some DMD patients had rare staining dystrophin-positive fibres, termed "revertant fibers". Immunocytochemistry was performed on serial sections from deleted and non-deleted patients by using a panel of anti-dystrophin antibodies. In patients with deletions, revertant fibers did not stain with antibody raised to polypeptide sequences within the deletion. Based on analysis of dystrophin protein in revertant fibers, the most likely mechanism giving rise to revertant fibers appers to be a second site in-frame deletion.
書誌情報 札幌医学雑誌 = The Sapporo medical journal
en : The Sapporo medical journal

巻 64, 号 6, p. 227-237, 発行日 1995-12-01
ISSN
収録物識別子タイプ ISSN
収録物識別子 0036-472X
著者版フラグ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
出版者
出版者 札幌医科大学医学部
戻る
0
views
See details
Views

Versions

Ver.1 2023-05-15 10:07:28.129908
Show All versions

Share

Mendeley Twitter Facebook Print Addthis

Cite as

エクスポート

OAI-PMH
  • OAI-PMH JPCOAR 2.0
  • OAI-PMH JPCOAR 1.0
  • OAI-PMH DublinCore
  • OAI-PMH DDI
Other Formats
  • JSON
  • BIBTEX

Confirm


Powered by WEKO3


Powered by WEKO3