Results 211 to 220 of about 169,930 (262)
Aerosol Inhalation of a Recombinant H7N9 Hemagglutinin Antigen Elicits Systemic and Mucosal Immune Responses in Mice. [PDF]
Hou Z +10 more
europepmc +1 more source
Summary Childhood autoimmune neutropenia (AIN) encompasses heterogeneous entities; phenotype‐specific immunological profiles and their relationship to infection outcomes remain incompletely defined. To characterise clinical, immunological and long‐term outcomes across distinct phenotypes of childhood AIN.
Ioanna Saougou +5 more
wiley +1 more source
Recurrence of IgA nephropathy in a kidney transplant patient successfully treated with iptacopan-a case report. [PDF]
Pandav J +9 more
europepmc +1 more source
This study provides the first comprehensive characterization of the functional impact, and mechanistic role of FAT4 in MM. Our findings highlight the tumor‐suppressive role of FAT4 in MM and uncover a novel mechanism by which FAT4 regulates the Hippo/YAP pathway.
Lina Zhang +5 more
wiley +1 more source
Subacute large bowel obstruction as an unusual presentation of selective IgA deficiency. [PDF]
Forouzanfar E +3 more
europepmc +1 more source
Correction: IgA anti-CD74 autoantibodies are associated with treatment escalation in peripheral psoriatic arthritis. [PDF]
Elsaghir A +5 more
europepmc +1 more source
Crosstalk between the microbiome and the mucosal immunoglobulin A system in the lung, in health and disease. [PDF]
Stavart C +5 more
europepmc +1 more source
Serum Eosinophil‐Derived Neurotoxin (EDN) as a Biomarker for Treatment Response in Atopic Dermatitis
Clinical &Experimental Allergy, EarlyView.
J. I. Olydam +3 more
wiley +1 more source
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Serum IgA Class Anti-IgA Antibody in IgA Nephropathy
Nephron, 2008IgA class anti-IgA antibody was sought by an immunoabsorbent technique in sera from patients with IgA nephropathy (IgA-N, n = 62), other forms of primary glomerulonephritis (PGN, n = 41), seropositive rheumatoid arthritis (RF-positive, n = 18) and normal controls (c, n = 50).
Y, Hiki, M, Saitoh, Y, Kobayashi
openaire +2 more sources
Seminars in Immunopathology, 2021
IgA vasculitis (IgAV) is an inflammation of small vessels caused by perivascular deposition of IgA and activation of neutrophils. It may present as systemic vasculitis (IgAV - Henoch-Schönlein purpura) or as a variant restricted to the skin (skin-limited IgAV), while IgA nephropathy presents a variant restricted to the kidneys.
Evangéline Pillebout +1 more
openaire +2 more sources
IgA vasculitis (IgAV) is an inflammation of small vessels caused by perivascular deposition of IgA and activation of neutrophils. It may present as systemic vasculitis (IgAV - Henoch-Schönlein purpura) or as a variant restricted to the skin (skin-limited IgAV), while IgA nephropathy presents a variant restricted to the kidneys.
Evangéline Pillebout +1 more
openaire +2 more sources

