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1 e requirement for a pre-BCR and pairing with surrogate light chain.
2 t chain variable genes and expression of the surrogate light chain.
3 ostulated to function in the assembly of the surrogate light chain.
4 oth proteins did not inhibit the assembly of surrogate light chain.
6 cell surface mu heavy chain associated with surrogate light chain and the 1E8 immature B cell line e
7 he ability of mu(s)-chains to associate with surrogate light chains and assemble into a pre-B cell re
8 development: one which is activated through surrogate light chains and mIg mu, and an alternative pa
9 pre-BCR), consisting of an Ig mu H chain, Ig surrogate light chain, and associated signal transducing
10 gement and/or efficiency of pairing with the surrogate light chain at the surface Ig-negative, early
11 also to enhance signaling through the micro-surrogate light chain complex of primary pre-B cells.
13 consisting of a rearranged mu heavy chain, a surrogate light chain composed of lambda5/14.1 and VpreB
14 s an immunoglobulin heavy chain (Igmu) and a surrogate light chain composed of the invariant lambda5
15 nd three-parameter flow cytometry for VpreB (surrogate light chain), cytoplasmic mu chain, and surfac
17 .1 completely abrogated the formation of the surrogate light chain, demonstrating that complementatio
18 regulatory factors 4 and 8 (IRF4,8) suppress surrogate light chain expression and down-regulate pre-B
19 sion of either one is sufficient to suppress surrogate light chain expression and down-regulate pre-B
21 s reveal two novel mechanisms for regulating surrogate light chain formation: (i) the presence of an
22 d that loss of the pre-B cell receptors from surrogate light chain gene silencing was linked with exi
23 unction as a genetic switch to down-regulate surrogate light-chain gene expression and induce convent
24 expression of the endogenous immunoglobulin surrogate light chain genes, lambda5 and VpreB, whereas
29 re-B cell receptor, composed of Ig heavy and surrogate light chains, in the negative selection of cel
30 immunoglobulin heavy chain and lambda 5/14.1 surrogate light chain loci disrupt B-cell development to
31 g of the VRC26UCA heavy chain with the mouse surrogate light chain may contribute to this phenotype.
32 intronic and 3' enhancers, lambda5 and VpreB surrogate light chain promoters, the EBF locus promoter
33 kD intermediate is gradually replaced by the surrogate light chain protein complex, and the Ig(alpha)
35 s, by contrast, a significant portion of the surrogate light chain proteins associate with mu heavy c
38 chain does not associate efficiently with a surrogate light chain, providing a previously unrecogniz
40 se that diminished expression of the lambda5 surrogate light chain results in decreased pre-B cell re
42 receptor (pre-BCR), composed of Ig heavy and surrogate light chain (SLC), signals pre-BII-cell prolif
44 ns, heavy chain association is essential for surrogate light chain survival and transport to the cell
45 an antibody heavy chain (HC) paired with the surrogate light chain, the "unique regions" of VpreB and
46 u heavy chain and subsequent assembly with a surrogate light chain to form the pre-B cell receptor co
47 addition to mu, the pre-BCR consists of the surrogate light chains VpreB and lambda5 and the transme
49 cated, form of mu that cannot associate with surrogate light chains, we have studied the role of surr
53 f two immunoglobulin mu heavy chains and two surrogate light chains, which associate with the signali
54 These experiments lead us to conclude that surrogate light chains, while necessary for the assembly