Results 211 to 220 of about 169,930 (262)

Phenotype‐specific immune profiles and outcomes in childhood autoimmune neutropenia: A 20‐year cohort study

open access: yesBritish Journal of Haematology, EarlyView.
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]

open access: yesFront Immunol
Pandav J   +9 more
europepmc   +1 more source

Decreased Expression of FAT4 Promotes Multiple Myeloma Proliferation and Migration by Targeting the Hippo/YAP Pathway

open access: yesCancer Science, EarlyView.
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]

open access: yesJ Allergy Clin Immunol Glob
Forouzanfar E   +3 more
europepmc   +1 more source

Crosstalk between the microbiome and the mucosal immunoglobulin A system in the lung, in health and disease. [PDF]

open access: yesFront Cell Infect Microbiol
Stavart C   +5 more
europepmc   +1 more source

Serum Eosinophil‐Derived Neurotoxin (EDN) as a Biomarker for Treatment Response in Atopic Dermatitis

open access: yes
Clinical &Experimental Allergy, EarlyView.
J. I. Olydam   +3 more
wiley   +1 more source
Some of the next articles are maybe not open access.

Related searches:

Serum IgA Class Anti-IgA Antibody in IgA Nephropathy

Nephron, 2008
IgA 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

IgA vasculitis

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

Home - About - Disclaimer - Privacy