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1 be strong interactions between this tethered J region and the CaM-LD even at basal Ca(2+) concentrati
2 the entire TCR architecture, including V, D, J regions and the complementarity-determining region 3 (
3 ead, that two sequence elements of DnaJ, the J-region and the G/F-rich linker segment, are each requi
4 nal binding protein for immunoglobulin kappa J region) are involved in this process.
5  Vbeta products showed dominant peaks in the J region as well.
6 nal binding protein for immunoglobulin kappa J region) binding and loss of active histone marks on K(
7 or-prone DNA synthesis in immunoglobulin V(D)J regions by error-prone DNA polymerases.
8 g deoxycytidines (dCs) in switch (S) and V(D)J region DNA, respectively, to generate deoxyuracils (dU
9 gment was identified as the highly conserved J-region found in all DnaJ homologues.
10 nal-binding protein for immunoglobulin Kappa J region from DNA binding sites by TNFalpha explaining t
11 uencing of cDNA corresponding to the IgH V-D-J region from the conditional LCL was used to formally s
12 c alpha-chain construct containing the N and J regions from a responsive T hybrid clone and the V alp
13 determining region 3 domain and differential J region gene expression for both TCR alpha- and beta-ch
14 mline promoters (Ko) located upstream of the J region gene segments of the kappa locus also contain a
15 regions in the lgH variable (V) and joining (J) region genes, we analyzed formalin-fixed paraffin-emb
16 00-kb deletion that included D-region genes, J-region genes, and the mu constant-region gene.
17 rders of magnitude, which indicates that the J region has an essential role in stabilizing the struct
18  Ig domains, number and location of joining (J) region-like motifs, presence of transmembrane regions
19  with domain-swap interactions, in which the J region of one protomer interacts extensively with the
20 sesses significant homology to the conserved J region of the DnaJ family of heat shock proteins.
21  sequence (RSS) heptamers present in the V(D)J region of the T lymphocyte receptor gene.
22 DR3alpha and beta loops, indicating that the J regions of both CDR3s are critical for recognition of
23 ion signal sequences (RSSs) flanking V, D or J regions of the antigen-binding genes.
24 formed a deep sequencing analysis of the V(D)J regions of VH and VLK genes, demonstrating the high ab
25 (1-14) portion of PTH and the juxtamembrane (J) region of the receptor, with the latter interaction g
26 mbrane/extracellular loop, or juxtamembrane (J) regions of the receptor.
27 teractions: (i) interaction of DnaK with the J-region of DnaJ and (ii) binding of a peptide or polype
28 nal-binding protein for immunoglobulin Kappa J region partners with the NOTCH2 intracellular domain t
29 nal binding protein for immunoglobulin kappa J region (RBPJ) and caused abnormal fetal megakaryopoies
30 nal-binding protein for immunoglobulin kappa J region (RBPJ) is a transcriptional repressor, but conv
31 nal binding protein for immunoglobulin kappa J region (RBPJ) signaling pathway in controlling the mon
32 nal binding protein for immunoglobulin kappa J region (Rbpj), a crucial mediator of NOTCH signaling,
33 nal binding protein for immunoglobulin kappa J region (Rbpj)-to investigate changes to brain resident
34 nal Binding Protein for Immunoglobulin Kappa J Region (RBPJ).
35 nal binding protein for immunoglobulin kappa J region (RBPjkappa), key modulators of adipogenesis and
36 nal-binding protein for immunoglobulin kappa J region (RBPJkappa).
37  variable (V), (diversity [D]), and joining (J) region recombinases (recombination activating genes [
38 pendent on Rb family binding, mutants in the J region retain the ability to associate with pRb, p107,
39 eta13.6/complementarity-determining region 3/J region sequences.
40 gnal-binding protein of immunoglobulin kappa J region) signaling pathway has been found associated wi
41 n has greater diversity in both the CDR3 and J regions than the C-terminal CLIP reactive subset.
42 ain (CaM-LD)) that is joined via a junction (J) region to the C-terminal end of the kinase catalytic
43 V) region TRAV1-2 rearranged to the joining (J) region TRAJ9 with few nontemplated (N)-region additio
44  peptide-specific TCRs showed a preferential J region usage in both the CDR3alpha and beta loops, ind
45 chains) containing variable (V) and joining (J) region V(alpha)14-J(alpha)18 (V(alpha)14i) rearrangem
46 DnaJ1-75, a polypeptide containing an intact J-region, was found to be incapable of stimulating ATP h
47                             Rearranged IgH D(J) regions were amplified from the spleen and lymph tiss
48  (R27) was generated by introgressing a C57L/J region where Cgnz1 is located to NZM2328.
49    CDPKs contain an autoinhibitory junction (J) region whose calcium-dependent interaction with the t