about
B cells and CD22 are dispensable for the immediate antiinflammatory activity of intravenous immunoglobulins in vivo.DC subset-specific induction of T cell responses upon antigen uptake via Fcγ receptors in vivo.Inflammatory monocytes and Fcγ receptor IV on osteoclasts are critical for bone destruction during inflammatory arthritis in mice.Fc-gamma receptors are not involved in cartilage damage during experimental osteoarthritis.Catchup: a mouse model for imaging-based tracking and modulation of neutrophil granulocytes.Unlocking the bone: Fcγ-receptors and antibody glycosylation are keys to connecting bone homeostasis to humoral immunity.Differential antibody glycosylation in autoimmunity: sweet biomarker or modulator of disease activity?Releasing the Brakes: Targeting FcγRIIB on B Cells to Enhance Antibody-Dependent Lymphoma ImmunotherapyBroad requirement for terminal sialic acid residues and FcγRIIB for the preventive and therapeutic activity of intravenous immunoglobulins in vivoA Humanized Mouse Identifies the Bone Marrow as a Niche with Low Therapeutic IgG ActivityInfluence of activating Fcgamma receptors on osteoclast differentiation and bone metabolismOral administration of the selective GPR120/FFA4 agonist compound A is not effective in alleviating tissue inflammation in mouse models of prototypical autoimmune diseasesCorrigendum to “Fc-gamma receptors are not involved in cartilage damage during experimental osteoarthritis” [Osteoarthritis Cartilage 23 (2015) 1221–1225]
P50
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P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
ricercatrice
@it
հետազոտող
@hy
name
Michaela Seeling
@ast
Michaela Seeling
@en
Michaela Seeling
@es
Michaela Seeling
@sl
type
label
Michaela Seeling
@ast
Michaela Seeling
@en
Michaela Seeling
@es
Michaela Seeling
@sl
prefLabel
Michaela Seeling
@ast
Michaela Seeling
@en
Michaela Seeling
@es
Michaela Seeling
@sl
P106
P21
P214
122144647644651342662
P31
P496
0000-0002-4788-4021
P735
P7859
viaf-122144647644651342662