Emily L Germain-Lee
8PUBLICATIONS
7CO-AUTHORS
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Publications (8)
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|Apr 21, 2025
Alpha-smooth muscle actin-expressing dermal sheath cells are a major cellular contributor to heterotopic subcutaneous ossifications in a mouse model of Albright hereditary osteodystrophy.Patrick McMullan, Peter Maye, Sierra H Root
|Jul 01, 2024
Hair follicle-resident progenitor cells are a major cellular contributor to heterotopic subcutaneous ossifications in a mouse model of Albright hereditary osteodystrophy.Patrick McMullan, Peter Maye, Sierra H Root
|Jan 20, 2023
Prevalence of Chiari malformation type 1 is increased in pseudohypoparathyroidism type 1A and associated with aberrant bone development.Neetu Krishnan, Patrick McMullan, Qingfen Yang
|Feb 28, 2022
Aberrant Bone Regulation in Albright Hereditary Osteodystrophy dueto Gnas Inactivation: Mechanisms and Translational Implications.Patrick McMullan, Emily L Germain-Lee
|Jan 26, 2022
Parental Origin of Gsα Inactivation Differentially Affects Bone Remodeling in a Mouse Model of Albright Hereditary Osteodystrophy.Patrick McMullan, Peter Maye, Qingfen Yang
|Aug 13, 2021
Local versus systemic control of bone and skeletal muscle mass by components of the transforming growth factor-β signaling pathway.Yewei Liu, Adam Lehar, Renata Rydzik
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