Results 121 to 130 of about 5,020 (198)

Rare variant analysis of whole genome sequenced juvenile idiopathic arthritis multiplex pedigrees identifies rare variants in NOD2 and ACVR1. [PDF]

open access: yesG3 (Bethesda)
Avery CN   +9 more
europepmc   +1 more source

The diagnostic journey of fibrodysplasia ossificans progressiva: evidence from a national cohort of 114 patients. [PDF]

open access: yesFront Endocrinol (Lausanne)
Cui L   +14 more
europepmc   +1 more source

BCX9250 is a potent small-molecule inhibitor of Activin A Receptor Type 1 (ACVR1/ALK2) for fibrodysplasia ossificans progressiva. [PDF]

open access: yesJBMR Plus
Wang H   +11 more
europepmc   +1 more source

A pontine-specific niche supports de novo gliomagenesis. [PDF]

open access: yesCell Rep
Pathak A, Wells GB, Bankaitis VA, Xie Z.
europepmc   +1 more source

Hepcidin as a Molecular Hub of Iron Homeostasis: From BMP-SMAD Signaling to Therapeutic Modulation. [PDF]

open access: yesBiomolecules
Duminuco A   +10 more
europepmc   +1 more source

Fibrodysplasia ossificans progressiva in children: diagnostic pitfalls and ACVR1 genotype-phenotype spectrum. [PDF]

open access: yesEur J Pediatr
Acikgoz NB   +10 more
europepmc   +1 more source

USP24-dependent STAT2 stabilization mediates physiologic and pathologic bone formation. [PDF]

open access: yesCell Death Dis
Kim JM   +10 more
europepmc   +1 more source

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