Leptin signalling altered in infantile nephropathic cystinosis‐related bone disorder
Abstract Background The CTNS gene mutation causes infantile nephropathic cystinosis (INC). Patients with INC develop Fanconi syndrome and chronic kidney disease (CKD) with significant bone deformations. C57BL/6 Ctns−/− mice are an animal model for studying INC. Hyperleptinaemia results from the kidn...
保存先:
| 主要な著者: | , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Wiley
2024-12-01
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| シリーズ: | Journal of Cachexia, Sarcopenia and Muscle |
| 主題: | |
| オンライン･アクセス: | https://doi.org/10.1002/jcsm.13579 |
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