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ProteomicsCD177 deficiency defines a stable subtype of human neutrophil granulocytes
CD177 is a surface protein on human neutrophil granulocytes whose function is related, but not limited to, tissue infiltration. While a fraction of the population is completely CD177-deficient (CD177d), most individuals express CD177. Expression levels on cells are not uniform and in every individua...
ORGANISM(S): Homo sapiens (Human) 
2026-09-07 | PXD068607 | Pride
Human neutrophils Proteomics Circulation Inflammation Lfq Cd177 
GenomicsCD177+ neutrophils restrict neuroinflammation following CNS injury
CD177+ neutrophils restrict neuroinflammation following CNS injury
PRJNA1242790 | ENA
GenomicsGeneration of pancreatic β cells from CD177+ anterior definitive endoderm
Generation of pancreatic β cells from CD177+ anterior definitive endoderm
PRJNA453996 | ENA
UnknownCD177 is a novel IgG Fc receptor and CD177 genetic variants affect IgG-mediated function.
Not available
S-EPMC11316256 | biostudies-literature
UnknownThe CD177 c.1291A Allele Leads to a Loss of Membrane Expression and Mimics a CD177-Null Phenotype.
Not available
S-EPMC10931634 | biostudies-literature
UnknownIncrease expression of CD177 in Kawasaki disease.
Not available
S-EPMC6446352 | biostudies-literature
TranscriptomicsCD177+ neutrophils restrict neuroinflammation following CNS injury
Neutrophils are the most abundant circulating leukocyte population that play critical roles in neuroinflammation after ischemic stroke. CD177, a glycoprotein on neutrophils, is emerging as an important immune regulator which fundamentally affects multiple inflammatory diseases. However, the role and...
ORGANISM(S): Mus musculus 
2025-03-27 | GSE293098 | GEO
UnknownHeterogeneity of Human Neutrophil CD177 Expression Results from CD177P1 Pseudogene Conversion.
Not available
S-EPMC4882059 | biostudies-literature
UnknownCharacterization of a novel mouse model with genetic deletion of CD177.
Not available
S-EPMC4312768 | biostudies-literature
TranscriptomicsGeneration of pancreatic β cells from CD177+ anterior definitive endoderm
Methods for differentiating human pluripotent stem cells to pancreatic and liver lineages in vitro have been limited by the inability to identify and isolate distinct endodermal subpopulations specific to these two organs. Here we report that pancreatic and hepatic progenitors can be isolated using ...
ORGANISM(S): Homo sapiens 
2020-04-27 | GSE113791 | GEO
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