Fibrodysplasia Ossificans Progressiva: Clinical and Genetic Aspects [PDF]
Robert J Pignolo +2 more
core +1 more source
The HIF-1α and mTOR Pathways Amplify Heterotopic Ossification
Fibrodysplasia ossificans progressiva (FOP; MIM# 135100) is an ultra-rare congenital disorder caused by gain-of-function point mutations in the Activin receptor A type I (ACVR1, also known as ALK2) gene.
Haitao Wang +2 more
doaj +1 more source
Histone Variant H3.3: A versatile H3 variant in health and in disease [PDF]
core +1 more source
The Mütter Museum of the College of Physicians of Philadelphia: An introduction to its history and resources for the teaching of human developmental biology [PDF]
Grunwald, Gerald B.
core +4 more sources
Orosomucoid 2 promotes colorectal cancer liver metastasis by suppressing natural killer cell-mediated antitumor immunity by remodeling the serine and one-carbon metabolism pathway. [PDF]
Zhou J +9 more
europepmc +1 more source
Comparison of the enzymatic and cellular profiles of clinical JAK inhibitors for the treatment of myelofibrosis. [PDF]
Celik H +11 more
europepmc +1 more source
The role of muscle fascia in heterotopic ossification and maintenance of skeletal muscle integrity in fibrodysplasia ossificans progressiva. [PDF]
Hanson LR +4 more
europepmc +1 more source
ACVR mutation [NM_001105.4:c.774G>T (p.Arg258Ser)] in pediatric fibrodysplasia ossificans progressiva complicated by scoliosis: a case report. [PDF]
Yang F, Liu M, Pei S, Huang J, Wang H.
europepmc +1 more source
Compound KTI-2338 Inhibits ACVR1 Receptor Signaling in Fibrodysplasia Ossificans Progressiva. [PDF]
Rosenberg NM +6 more
europepmc +1 more source

