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1 phocytes with biallelic expression of IgH or TCRbeta genes.
2 ression of a fully rearranged and functional TCRbeta gene, and most cells that fail to produce a func
3 s method involves sequencing of TCRalpha and TCRbeta genes, and amplifying functional genes character
5 is study, we demonstrate that a preassembled TCRbeta gene, but not a preassembled DbetaJbeta complex
6 rangement and expression of TCRgammadelta or TCRbeta genes, but whether it is an instructive or a sto
7 go RAG-dependent rearrangement of endogenous TCRbeta genes, driving surface expression of novel TCRs.
8 use bone marrow that have not rearranged the TCRbeta gene; express a variety of genes associated with
10 Rbeta rearrangements needed for a productive TCRbeta gene further increased frequencies of ATM-defici
12 e that suppress rearrangements of endogenous TCRbeta genes in normal DN cells are engaged by activate
13 xpression of both prerearranged TCRalpha and TCRbeta genes, indicating a critical role for TCR signal
15 n, Dbeta1 and Dbeta2 DJ rearrangement of the TCRbeta gene may be differentially regulated and thus se
17 impaired pre-TCR checkpoint with failure of TCRbeta gene rearrangement and increased apoptosis, resu
18 play obligatory roles both before and after TCRbeta gene rearrangement during the alpha/beta lineage
20 " scid thymocyte that undergoes a productive TCRbeta gene rearrangement is susceptible to the oncogen
22 among T cell progenitors that have completed TCRbeta gene rearrangement without producing a functiona
23 typical B-cell marker, T-cell receptor beta (TCRbeta) gene rearrangement indicated a T-cell origin.
25 SCL and LMO1 and additionally suggests that TCRbeta gene rearrangements may be required for the onco
29 d gender-specific V(D)J recombinase-mediated TCRbeta gene usage and coding joint processing at immune
32 pression of either a preassembled functional TCRbeta gene (Vbeta1(NT)) or the prosurvival BCL2 protei
33 Here, we show that the T cell receptor-beta (TCRbeta) gene, which acquires in-frame nonsense codons a
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