PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 31229844-2 2019 The core fucosylation is dramatically up-regulated at the transition from CD4-CD8- (DN) to CD4+CD8+ (DP) in the thymic development. dp 101-103 CD4 antigen Mus musculus 74-77 33428991-5 2021 This phenomenon might be explained by an inhibition of the DN-to-DP-cell transition and stimulation of DP cell conversion into CD4+ /CD8+ SP thymocytes. dp 103-105 CD4 antigen Mus musculus 127-130 31229844-2 2019 The core fucosylation is dramatically up-regulated at the transition from CD4-CD8- (DN) to CD4+CD8+ (DP) in the thymic development. dp 101-103 CD4 antigen Mus musculus 91-94 29310022-6 2018 Genetic studies suggested that the altered balance between transcription factors T-bet, Runx3, and Th-POK underlies the induction of the DP-IEL-like phenotype in Eed-deficient CD4+ cells. dp 137-139 CD4 antigen Mus musculus 176-179 22927977-4 2012 CONCLUSION/SIGNIFICANCE: This study shows that the developmental dynamics of DN iNKT cells in DP(dim) are very rapid and that it takes less than 1 day to down-regulate CD4 and CD8 and become DN. dp 94-96 CD4 antigen Mus musculus 168-171 24592261-10 2014 In the post-DP compartment, 91.7% undergo death by negative selection, 4.7% become CD4 SP, and 3.6% become CD8 SP. dp 12-14 CD4 antigen Mus musculus 83-86 23093039-16 2012 Our lab has developed the HY(cd4) model, in which the transgenic HY TCRalpha is conditionally expressed at the DP stage, allowing negative selection to occur during the DP to SP transition as occurs in wildtype mice(10). dp 111-113 CD4 antigen Mus musculus 29-32 15792999-2 2005 Intrathymic precursor transfer experiments and the identification of CD4(+)8+ double-positive (DP), V alpha 14J alpha 18 natural T (iNKT) cells suggest that commitment to this lineage might occur at the DP stage. dp 95-97 CD4 antigen Mus musculus 69-72 20599940-4 2010 This occurs at the transition from a double positive (DP) to a single positive (SP) phenotype, resulting in higher numbers of CD4 and CD8 SP cells, and to a lesser extent at the transition from double negative (DN) to DP cells. dp 54-56 CD4 antigen Mus musculus 126-129 17911179-8 2008 Finally, in competitive reaggregation thymic organ cultures, CCR9(-/-) preselection DP thymocytes were disadvantaged significantly in their ability to generate CD4 single-positive (SP) thymocytes, a finding that correlated with a reduced ability to form TCR-MHC-dependent conjugates with thymic epithelial cells. dp 84-86 CD4 antigen Mus musculus 160-163 9881968-5 1998 Activation of the Notch signaling pathway also upregulated a number of other markers that, like steroid resistance, correlate with DP maturation into both the CD4 and CD8 lineages. dp 131-133 CD4 antigen Mus musculus 159-162 10975810-5 2000 Production of CD4+ T cells required TCR signaling in the reaggregates, indicating that transient recognition of self-ligands by DP is inadequate for full differentiation. dp 128-130 CD4 antigen Mus musculus 14-17 11097211-5 2000 Examination of the CD4/CD8 populations in dy/dy thymi showed large relative increases in the DN (CD4- CD8-) and SP (CD4+ CD8-, CD4- CD8+) populations and a significant decrease in the DP (CD4+ CD8+) population. dp 184-186 CD4 antigen Mus musculus 19-22 10477603-6 1999 Specifically, a dramatic increase in the CD4low/-CD8+CD5lowHSA+TCRlow/- immature single positive population and a concomitant decrease in the subsequent DP population are observed. dp 153-155 CD4 antigen Mus musculus 41-44 14768939-6 2003 These thymic SP and DP populations with reduced levels of CD4 and/or CD8 markers had a lower rate of apoptosis in the tg than in the non-tg mice. dp 20-22 CD4 antigen Mus musculus 58-61 9144482-10 1997 Even in a viable DP population, high incidences of DNA strand breaks were detected in the CD4(low)CD8(low) compartment. dp 17-19 CD4 antigen Mus musculus 90-93 8671594-7 1996 The size of the F3Ag- DP subset is positively correlated with the efficacy of positive selection into the CD4(+) SP compartment. dp 22-24 CD4 antigen Mus musculus 106-109