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

Genetic pathways disrupted by ENPP1 deficiency provide insight into mechanisms of osteoporosis, osteomalacia, and paradoxical mineralization

ENPP1 缺乏症破坏的遗传途径为骨质疏松症、骨软化症和反常矿化机制提供了见解

Nathan D Maulding, Dillon Kavanagh, Kristin Zimmerman, Gianfilippo Coppola, Thomas O Carpenter, Nathaniel K Jue, Demetrios T Braddock

Human Heterozygous ENPP1 Deficiency Is Associated With Early Onset Osteoporosis, a Phenotype Recapitulated in a Mouse Model of Enpp1 Deficiency

人类杂合 ENPP1 缺乏症与早发性骨质疏松症有关,这种表型在 Enpp1 缺乏症小鼠模型中重现

Ralf Oheim, Kristin Zimmerman, Nathan D Maulding, Julian Stürznickel, Simon von Kroge, Dillon Kavanagh, Paul R Stabach, Uwe Kornak, Steven M Tommasini, Mark C Horowitz, Michael Amling, David Thompson, Thorsten Schinke, Björn Busse, Thomas O Carpenter, Demetrios T Braddock