Regulation of the TCRα repertoire by the survival window of CD4+CD8+ thymocytes
By Jian Guo, A. Hawwari, Hong Li, Zuoming Sun, S. Mahanta, Dan R. Littman, M. Krangel, You-Wen He. Nature Immunology, 2002
192 citations recorded by the source corpus.
Subfields: Immunology
View Paper: https://www.semanticscholar.org/paper/d3b199d1c2b6fd7c65e7820e72117103bb961368
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Immunology
Citations in the corpus
- Raising the NKT cell family (2010, background): “The DNA excision circles are limited in size, and the expression of distal (3′) segments that require multiple excisions is dependent on an extended lifespan of DP thymocyte”
- Origin and evolution of the adaptive immune system: genetic events and selective pressures (2010, background): “The many J segments in the α locus allow extensive receptor editing in developing T cells, resulting in greater opportunities for modification of the antigen receptor, followed by potential selection of self-MHC-restricted TCRs in the thymu”
- An essential function for the nuclear receptor RORγt in the generation of fetal lymphoid tissue inducer cells (2004, result): “5 fetuses, in contrast to earlier findings based on the detection of Rorc (γt) mRN”
- Enforcing order within a complex locus: current perspectives on the control of V(D)J recombination at the murine T‐cell receptor α/δ locus (2004, background): “Analysis of TCRa rearrangements in fetal thymocytes and in early DP thymocytes of adult mice demonstrates a strong 50 bias to Ja usage (7, 25, 40) (Fig.”