Sort   by:  
 Page size 
TranscriptomicsIncreased CD226 Expression on CD8+ T cells in Patients with Systemic Sclerosis
Systemic sclerosis (SSc) is an autoimmune disease characterized by vascular damage, and fibrosis of the skin and internal organs. Because activated and oligoclonally expanded CD8+ T cells can be detected in peripheral blood and lung of SSc patients, effector memory CD8+ T cells may play a critical r...
ORGANISM(S): Homo sapiens 
2014-12-06 | E-GEOD-63903 | biostudies-arrayexpress
UnknownHIV Impacts CD34+ Progenitors Involved in T-Cell Differentiation During Coculture With Mouse Stromal OP9-DL1 Cells.
Not available
S-EPMC6361802 | biostudies-literature
UnknownAge-associated increase in lifespan of naive CD4 T cells contributes to T-cell homeostasis but facilitates development of functional defects.
Not available
S-EPMC2759371 | biostudies-literature
UnknownA new species of the genus Arrup from a limestone cave in Akiyoshi-dai, Western Japan (Chilopoda, Geophilomorpha, Mecistocephalidae).
Not available
S-EPMC6428782 | biostudies-literature
UnknownICOS+CD4+ T cells define a high susceptibility to anti-PD-1 therapy-induced lung pathogenesis.
Not available
S-EPMC12128994 | biostudies-literature
UnknownSIKs Regulate HDAC7 Stabilization and Cytokine Recall in Late-Stage T Cell Effector Differentiation.
Not available
S-EPMC10842463 | biostudies-literature
UnknownComplete Sequences of the Human T-Cell Leukemia Virus Type 1 Proviral Genomes from Newly Established Adult T-Cell Leukemia Cell Lines in Oita Prefecture, Japan.
Not available
S-EPMC6013615 | biostudies-literature
UnknownAging-associated and CD4 T-cell-dependent ectopic CXCL13 activation predisposes to anti-PD-1 therapy-induced adverse events.
Not available
S-EPMC9303859 | biostudies-literature
UnknownA Human ABC Transporter ABCC4 Gene SNP (rs11568658, 559 G > T, G187W) Reduces ABCC4-Dependent Drug Resistance.
Not available
S-EPMC6356542 | biostudies-literature
UnknownPEX12, the pathogenic gene of group III Zellweger syndrome: cDNA cloning by functional complementation on a CHO cell mutant, patient analysis, and characterization of PEX12p.
Not available
S-EPMC109016 | biostudies-literature
Sort   by:  
 Page size