日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

FLNA-filaminopathy skeletal phenotypes are not due to an osteoblast autonomous loss-of-function

FLNA丝状蛋白病引起的骨骼表型并非由成骨细胞自主功能丧失所致。

Wade, Emma M; Goodin, Elizabeth A; Wang, Yongqiang; Morgan, Tim; Callon, Karen E; Watson, Maureen; Daniel, Philip B; Cornish, Jillian; McCulloch, Christopher A; Robertson, Stephen P

Craniosynostosis and multiple skeletal anomalies in humans and zebrafish result from a defect in the localized degradation of retinoic acid.

人类和斑马鱼的颅缝早闭和多发性骨骼畸形是由视黄酸局部降解缺陷引起的

Laue Kathrin, Pogoda Hans-Martin, Daniel Philip B, van Haeringen Arie, Alanay Yasemin, von Ameln Simon, Rachwalski Martin, Morgan Tim, Gray Mary J, Breuning Martijn H, Sawyer Gregory M, Sutherland-Smith Andrew J, Nikkels Peter G, Kubisch Christian, Bloch Wilhelm, Wollnik Bernd, Hammerschmidt Matthias, Robertson Stephen P