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...
-д хадгалсан:
| Үндсэн зохиолчид: | , , , , , |
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| Формат: | Artigo |
| Хэл сонгох: | Inglês |
| Хэвлэсэн: |
Wiley
2024-12-01
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| Цуврал: | Journal of Cachexia, Sarcopenia and Muscle |
| Нөхцлүүд: | |
| Онлайн хандалт: | https://doi.org/10.1002/jcsm.13579 |
| Шошгууд: |
Шошго байхгүй, Энэхүү баримтыг шошголох эхний хүн болох!
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