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1 CD4(+) CD8(+) T-cell progenitors as well as T-cell receptor excision circles.
2 onset of infections by means of screening of T-cell-receptor excision circles, a biomarker for thymic
3 , whereas thymic function was assessed using T-cell receptor excision circle analyses as well as flow
4 assess thymic output, T-cell proliferation (T-cell receptor excision circle analysis), and T-cell re
6 shorter telomeres but increased single-joint T-cell receptor excision circle content and CD31(+) naiv
7 RO(-)CD27(+)CD95(low)) are all equivalent in T-cell receptor excision circle content, a marker for th
8 s in increased IL-2 responsiveness and lower T-cell receptor excision circle content, implying a hist
9 aller increases in naive T cells but greater T cell receptor-excision circle DNA content after 48 wee
11 eceptor diversity positively correlated with T-cell receptor excision circle levels, a reflection of
12 y quantification of recent thymic emigrants, T-cell receptor excision circle levels, and T-cell recep
13 had significantly fewer naive T cells, lower T-cell receptor excision circle levels, fewer CD4 centra
16 ines in the frequency and absolute number of T-cell receptor excision circle-positive (TREC(+)) cells
18 rn screening test on Guthrie cards using the T-cell receptor excision circle quantification method.
20 NA levels, lymphocyte immunophenotyping, and T cell receptor excision circle (TREC) levels were measu
21 khead box protein P3 (FoxP3) expression, and T cell receptor excision circle (TREC) measurements in T
22 ignificant correlation between the counts of T cell receptor excision circle (TREC)-containing CD4 T
29 opulation-based screening for SCID using the T-cell receptor excision circle (TREC) assay began in Wi
31 une assessment, including the development of T-cell receptor excision circle (TREC) assays of thymopo
32 e sought to study thymic function, including T-cell receptor excision circle (TREC) quantification, i
33 unophenotyping, intracellular Ki67 staining, T-cell receptor excision circle (TREC) quantitation in s
35 -dependent progeny with increased numbers of T-cell receptor excision circle (TREC)-positive T cells,
37 Cultured T cells expressed a high level of T-cell receptor excision circles (TREC), demonstrating d
39 ring telomere shortening and the dilution of T cell receptor excision circles (TRECs) or the dye CFSE
40 obust triplex PCR method for quantitation of T-cell receptor excision circles (TRECs) and kappa-delet
41 ed doses of KGF showed the highest levels of T-cell receptor excision circles (TRECs) and the lowest
42 munodeficiency (SCID) using assays to detect T-cell receptor excision circles (TRECs) began in Wiscon
46 the factors that influence thymic function, T-cell receptor excision circles (TRECs) were examined i
47 s considered for SCID screening, testing for T-cell receptor excision circles (TRECs), a DNA biomarke
49 ghout the third trimester, concentrations of T-cell-receptor excision circles (TRECs) were 10 per 100
50 hymus function in adults (the measurement of T cell receptor excision circles, TRECs), and studies of
51 numbers of total thymocytes and signal joint T-cell receptor excision circles were observed in the hi
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