Figure 3.
Figure 3. DH gene segment use in transplanted sources of hematopoietic precursors. DH gene segment use for sIgM+ (A) and sIgM- (B) cells from adult bone marrow (▪), cord blood (▦), and fetal (□) sources are shown for DH gene use. For adult bone marrow (sIgM+, n = 135 + 28; sIgM-, n = 50 + 49) and cord blood (sIgM+, n = 172 + 87 + 112; sIgM-, n = 87 + 19 + 48) LP sources and one experiment for the fetal LP source (sIgM+, n = 173; sIgM-, n = 51, 2 experiments). DH6 (P = .03 and P = .003) and DH7 (P = .008 and P = .02) in sIgM- and sIgM+ cells were significant for an age-related trend. In addition DH4 (P = .02) in sIgM+ and DH3 (P = .01) in sIgM- cells showed a significant age-related trend. Error bars indicate standard error.

DH gene segment use in transplanted sources of hematopoietic precursors. DH gene segment use for sIgM+ (A) and sIgM- (B) cells from adult bone marrow (▪), cord blood (▦), and fetal (□) sources are shown for DH gene use. For adult bone marrow (sIgM+, n = 135 + 28; sIgM-, n = 50 + 49) and cord blood (sIgM+, n = 172 + 87 + 112; sIgM-, n = 87 + 19 + 48) LP sources and one experiment for the fetal LP source (sIgM+, n = 173; sIgM-, n = 51, 2 experiments). DH6 (P = .03 and P = .003) and DH7 (P = .008 and P = .02) in sIgM- and sIgM+ cells were significant for an age-related trend. In addition DH4 (P = .02) in sIgM+ and DH3 (P = .01) in sIgM- cells showed a significant age-related trend. Error bars indicate standard error.

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