Results 91 to 100 of about 33,919 (161)

Heterozygous mutations in the C-terminal domain of COPA underlie a complex autoinflammatory syndrome

open access: yesThe Journal of Clinical Investigation
Mutations in the N-terminal WD40 domain of coatomer protein complex subunit α (COPA) cause a type I interferonopathy, typically characterized by alveolar hemorrhage, arthritis, and nephritis. We described 3 heterozygous mutations in the C-terminal domain
Selket Delafontaine   +33 more
doaj   +1 more source

A Rare Case of COPA Syndrome: Multisystem Relapse and Fatal Septic Complication. [PDF]

open access: yesRespirol Case Rep
Castro Velasco Fernandes F   +7 more
europepmc   +1 more source

Recurrent COPA mutation drives R-spondin-independent Wnt activation in intestinal tumors. [PDF]

open access: yesNat Genet
Fujii M   +15 more
europepmc   +1 more source

COPI Coatomer Regulates Several Steps of HDL Metabolism. [PDF]

open access: yesArterioscler Thromb Vasc Biol
Panteloglou G   +32 more
europepmc   +1 more source

Bacterial extracellular vesicles and direct microbial contact drive species-specific corneal epithelial reprogramming. [PDF]

open access: yesFront Cell Infect Microbiol
Blanco-Agudín N   +5 more
europepmc   +1 more source

Golgi-derived COPI vesicles fuel the biogenesis of coronavirus replication organelles. [PDF]

open access: yesHlife
Wang Z   +12 more
europepmc   +1 more source

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