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Cited by 320

The DOI matches its Crossref record; 218 of the 218 references it cites were found in a registry or an index.

Role of RANKL in physiological and pathological bone resorption and therapeutics targeting the RANKL–RANK signaling system

Tanaka, Sakae, Nakamura, Kozo, Takahasi, Naoyuki, Suda, Tatsuo·2005·Immunological Reviews

Abstract

Summary: Osteoclasts are primary cells for physiological and pathological bone resorption, and receptor activator of nuclear factor‐κB ligand (RANKL) is critically involved in the differentiation, activation, and survival of these cells. Recently, therapeutics for pathological bone destruction targeting RANKL pathways has attracted a great deal of attention. Herein, we review the recent advances in the research on osteoclast biology and discuss the advantages and disadvantages of anti‐RANKL therapies.

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Crossref · 10.1111/j.0105-2896.2005.00327.x

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Metadata

Authors
Tanaka, S., Nakamura, K., Takahasi, N., & Suda, T.
Venue
Immunological Reviews
Publisher
Wiley
Published
2005-11-22
Volume
208
Issue
1
Pages
30-49
ISSN
  • 0105-2896 (ISSN-L)
  • 1600-065X
OpenAlex
W2052712126
Cited by
320
References
218
FWCI
0.99
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Role of RANKL in physiological and pathological bone resorption and therapeutics targeting the RANKL–RANK signaling system. https://app.cochat.ai/papers/10.1111/j.0105-2896.2005.00327.x
The paper
Tanaka, S., Nakamura, K., Takahasi, N., & Suda, T. (2005). Role of RANKL in physiological and pathological bone resorption and therapeutics targeting the RANKL–RANK signaling system. Immunological Reviews. https://doi.org/10.1111/j.0105-2896.2005.00327.x

Data sources

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.