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Cited by 212

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Glycoprotein‐binding site of dystrophin is confined to the cysteine‐rich domain and the first half of the carboxy‐terminal domain

Open access
Suzuki, Atsushi, Yoshida, Mikiharu, Yamamoto, Hideko, Ozawa, Eijiro·1992·FEBS Letters

Abstract

Dystrophin, a protein product of the Duchenne muscular dystrophy gene, is thought to associate with the muscle membrane by way of a glycoprotein complex which was co‐purified with dystrophin. Here, we firstly demonstrate direct biochemical evidence for association of the carboxy‐terminal region of dystrophin with the glycoprotein complex. The binding site is found to lie further inward than previously expected and confined to the cysteine‐rich domain and the first half of the carboxy‐terminal domain. Since this portion corresponds well to the region that, when missing results in severe phenotypes, our findings may provide it molecular basis of the disease.

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Crossref · 10.1016/0014-5793(92)81265-n

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Metadata

Authors
Suzuki, A., Yoshida, M., Yamamoto, H., & Ozawa, E.
Venue
FEBS Letters
Publisher
Wiley
Published
1992-08-17
Volume
308
Issue
2
Pages
154-160
ISSN
  • 0014-5793 (ISSN-L)
  • 1873-3468
OpenAlex
W2016753696
Cited by
212
References
1
FWCI
9.42
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Glycoprotein‐binding site of dystrophin is confined to the cysteine‐rich domain and the first half of the carboxy‐terminal domain. https://app.cochat.ai/papers/10.1016/0014-5793(92)81265-n
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Suzuki, A., Yoshida, M., Yamamoto, H., & Ozawa, E. (1992). Glycoprotein‐binding site of dystrophin is confined to the cysteine‐rich domain and the first half of the carboxy‐terminal domain. FEBS Letters. https://doi.org/10.1016/0014-5793(92)81265-n

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