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1 t chain variable genes and expression of the surrogate light chain.
2 ostulated to function in the assembly of the surrogate light chain.
3 oth proteins did not inhibit the assembly of surrogate light chain.
5 cell surface mu heavy chain associated with surrogate light chain and the 1E8 immature B cell line e
6 he ability of mu(s)-chains to associate with surrogate light chains and assemble into a pre-B cell re
7 development: one which is activated through surrogate light chains and mIg mu, and an alternative pa
8 pre-BCR), consisting of an Ig mu H chain, Ig surrogate light chain, and associated signal transducing
9 gement and/or efficiency of pairing with the surrogate light chain at the surface Ig-negative, early
10 also to enhance signaling through the micro-surrogate light chain complex of primary pre-B cells.
12 consisting of a rearranged mu heavy chain, a surrogate light chain composed of lambda5/14.1 and VpreB
13 s an immunoglobulin heavy chain (Igmu) and a surrogate light chain composed of the invariant lambda5
14 nd three-parameter flow cytometry for VpreB (surrogate light chain), cytoplasmic mu chain, and surfac
16 .1 completely abrogated the formation of the surrogate light chain, demonstrating that complementatio
17 sion of either one is sufficient to suppress surrogate light chain expression and down-regulate pre-B
18 regulatory factors 4 and 8 (IRF4,8) suppress surrogate light chain expression and down-regulate pre-B
20 s reveal two novel mechanisms for regulating surrogate light chain formation: (i) the presence of an
21 d that loss of the pre-B cell receptors from surrogate light chain gene silencing was linked with exi
22 unction as a genetic switch to down-regulate surrogate light-chain gene expression and induce convent
23 expression of the endogenous immunoglobulin surrogate light chain genes, lambda5 and VpreB, whereas
28 re-B cell receptor, composed of Ig heavy and surrogate light chains, in the negative selection of cel
29 immunoglobulin heavy chain and lambda 5/14.1 surrogate light chain loci disrupt B-cell development to
30 intronic and 3' enhancers, lambda5 and VpreB surrogate light chain promoters, the EBF locus promoter
31 kD intermediate is gradually replaced by the surrogate light chain protein complex, and the Ig(alpha)
33 s, by contrast, a significant portion of the surrogate light chain proteins associate with mu heavy c
36 chain does not associate efficiently with a surrogate light chain, providing a previously unrecogniz
38 se that diminished expression of the lambda5 surrogate light chain results in decreased pre-B cell re
40 receptor (pre-BCR), composed of Ig heavy and surrogate light chain (SLC), signals pre-BII-cell prolif
42 ns, heavy chain association is essential for surrogate light chain survival and transport to the cell
43 an antibody heavy chain (HC) paired with the surrogate light chain, the "unique regions" of VpreB and
44 u heavy chain and subsequent assembly with a surrogate light chain to form the pre-B cell receptor co
45 addition to mu, the pre-BCR consists of the surrogate light chains VpreB and lambda5 and the transme
47 cated, form of mu that cannot associate with surrogate light chains, we have studied the role of surr
51 f two immunoglobulin mu heavy chains and two surrogate light chains, which associate with the signali
52 These experiments lead us to conclude that surrogate light chains, while necessary for the assembly
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