ライフサイエンスコーパス: Ig gene rearrangement

1 nship between CD127 expression/signaling and Ig gene rearrangement.

2 the induction of the machinery that mediates Ig gene rearrangement.

3 e marker expression, gene transcription, and Ig gene rearrangement.

4 the confines of the bone marrow by secondary Ig gene rearrangements.

5 homas and suggesting that each had different Ig gene rearrangements.

6 n of a B cell subset coexpressing endogenous Ig gene rearrangements.

7 al or oligoclonal pattern of immunoglobulin (Ig) gene rearrangement.

8 e (MRD) by real-time PCR directed to TCR and Ig gene rearrangements allows a refined evaluation of re

9 as determined by 1) the restoration of V(H) Ig gene rearrangement and 2) the appearance of immature

10 Given that abnormalities in Ig gene rearrangement and DNA damage repair are hallmark

11 ot its catalytic activities, is required for Ig gene rearrangement and production of B cell receptors

12 mice succumbed to lymphoid tumors containing Ig gene rearrangements and immunophenotypes characterist

13 an algorithm designed to fully characterize Ig gene rearrangements and oncogenic translocations from

14 review the data currently available on both Ig gene rearrangements and protein patterns seen in myel

15 e that occurred concomitantly with decreased Ig gene rearrangements and rag-1 transcripts.

16 Immunoglobulin (Ig) gene rearrangements and oncogenic translocations are

17 o programmed cell death due to nonproductive Ig gene rearrangements are cleared from the bone marrow

18 Immunoglobulin (Ig) gene rearrangements are used to define clonality of

19 that E-protein activity regulates secondary Ig gene rearrangement at the immature B cell stage and c

20 lts suggest that IL-7-mediated inhibition of Ig gene rearrangement blocks maturation of B cell precur

21 Interestingly, they possess Ig gene rearrangements, but lack Ig molecule expression

22 naling, we show that PI3K signaling inhibits Ig gene rearrangement by suppressing the expression of t

23 Ig gene rearrangements could generate V(H)-D-J(H) joinin

24 omparative analysis of platelet-reactive Fab Ig gene rearrangements from each patient suggested that

25 The amplification of nonproductive Ig gene rearrangements from HED-ID B cells reflects the

26 B in human V(D)J recombination, we amplified Ig gene rearrangements from individual peripheral B cell

27 ive analysis of productive and nonproductive Ig gene rearrangements from transgenic mice engineered t

28 V(H) genes; however, Pax5 did not induce any Ig gene rearrangement in the absence of Ikaros.

29 In addition to this, the analysis of Ig gene rearrangements in B-cell neoplasms provides info

30 We found intact Ig gene rearrangements in immunoglobulin heavy (IgH) and

31 pment and Ab selection in humans we analyzed Ig gene rearrangements in pro-B cells from two patients

32 Analysis of Ig gene rearrangements indicates monoclonality or oligoc

33 cell differentiation when the machinery for Ig gene rearrangement is in place but rearrangement has

34 Together, our results suggest that ordered Ig gene rearrangement is regulated by distinct activitie

35 tance of EBF1 in regulating target genes and Ig gene rearrangements necessary for B cell lineage spec

36 phocyte-associated genes and immunoglobulin (Ig) gene rearrangement occurred before CD45R acquisition

37 Receptor editing or secondary Ig gene rearrangement occurs in immature, autoreactive B

38 exhibit the skewed Ig V gene repertoire and Ig gene rearrangement patterns associated with these spe

39 Moreover, sequencing of Ig gene rearrangement products showed that a diverse rep

40 lerance mechanism that operates by secondary Ig gene rearrangements to change the specificity of auto

41 breaks (DSBs) are essential intermediates in Ig gene rearrangements: V(D)J and class switch recombina

42 tumors arose at high incidence and displayed Ig gene rearrangement with downregulated expression of B