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1 CDR1 accumulates in intercellular fluid in response to p
2 CDR1 disruption had a partial effect, reducing fluconazo
3 CDR1 elements of both subunits of NITR dimers form ligan
4 CDR1, which directly interacted with adaptor protein 1 (
6 ncoded complementarity determining region 1 (CDR1) and CDR2 of the V alpha element can be responsible
7 nts in complementarity-determining region 1 (CDR1) and CDR2, and less than two replacements in the fr
8 ted in complementarity-determining region 1 (CDR1) and CDR2, which exhibited higher replacement-to-si
10 30 in complementarity-determining region 1 (CDR1) of the TCR alpha-chain interacts with the I-A alph
12 er the complementarity-determining region 1 (CDR1) or CDR2 were sufficient to change selection from t
13 which complementarity-determining region 1 (CDR1), CDR2, and framework region 3 (FR3) are predicted
16 ormation of disulfide bonds between CDR3 and CDR1, FW2, or CDR2 was also observed, as described in ca
17 significantly inhibited LUSC metastases and CDR1 was sufficient to promote migration and metastases.
18 of CDR1 generates a small mobile signal, and CDR1 action is blocked by the protease inhibitor pepstat
22 termining region of the TcR beta chain (beta:CDR1) points outward and interacts with highly conserved
23 id-dependent cooperative interaction between CDR1 and CDR3 residues that are separated by more than 9
24 th studies revealed that the antigen-binding CDR1 loop is the least protected part in the variable do
26 Movements of the CD8alpha CDR2 and CD8beta CDR1 and CDR2 loops as well as the flexibility of the H-
28 an residues including one in the heavy chain CDR1 and a tryptophan in close proximity to heavy chain
29 g to the anti-Id were located in heavy chain CDR1 and CDR2 and were peripheral to the residues within
30 geting non-germline hot spots in heavy chain CDR1 and CDR3 were generated but did not produce Fv with
32 human mAb; a large insert in the light chain CDR1 of mAb SN66E3 distinguished it from both CRll-351 a
34 interactions between the DRVIA7 light-chain CDR1 and the N terminus with N276 and V5 glycans of gp12
36 16 microg ml(-1)) similarly show coordinate CDR1-PDH1 upregulation, and in one of these (F15) a puta
37 two parts of the CDR region here designated CDR1 and CDR2 (closest to the carboxyl end) each consist
39 hese anti-DKK1 antibody leads targeting DKK1 CDR1 are potent in inhibition of tumor growth and may ha
41 ity during Ag recognition while gene-encoded CDR1 and CDR2 contribute to the fine specificity of the
42 Within this hotspot, key germline-encoded CDR1 and CDR2 loop residues and a crucial but commonly c
44 and antibodies, whereas the germline-encoded CDR1 and CDR2 sequences are much more cross-reactive.
46 tified key positions in the VH gene encoding CDR1, CDR2, and the immunoglobulin framework that are cr
48 2) of the beta-chain and, to lesser extents, CDR1 and hypervariable region 4 (HV4), bind in a cleft b
50 extends the database of canonical forms for CDR1 and CDR2, and has implications for antigen recognit
51 have explored the sequence requirements for CDR1 and CDR2 of the TCR alpha-chain in a human T cell r
59 ficity change despite the proximity of the H:CDR1 hapten contact residue Asn-35 to the cardenolide 16
60 resistance of a cka2 mutant, as expected if CDR1 and CDR2 overexpression is responsible for fluconaz
62 n requirements for particular side chains in CDR1 and CDR2 and in their relative binding contribution
66 so, when another carbohydrate was present in CDR1, CDR2, or CDR3 of the L chain, the V(H) CDR2 glycan
69 TCRs show that germline-encoded residues in CDR1 and CDR3 regions of TRBV4-1-encoded sequences inter
71 ant bias toward replacement substitutions in CDR1; in Tm clones there was no significant bias toward
72 ctedly, every TCR mutant, including those in CDR1 and CDR2, retained remarkable peptide specificity.
76 ng GD2 affinity, the double mutation D32H (L-CDR1) and E1K (L-FR1) did not further improve anti-tumor
77 t in affinity of hu3F8 with a single D32H (L-CDR1) mutation translated into a approximately 12-fold i
82 indicates that transient gene duplication of CDR1 and ERG11 causes the observed age-dependent enhance
83 is flipped into a cavity formed by Gly35 of CDR1, thereby increasing the hydrophilicity of the V(H):
85 studies revealed transient overexpression of CDR1 and ERG11 mRNA in the presence of fluconazole that
86 2T increased the amyloidogenic propensity of CDR1 loop, decreased its protection in the native struct
87 he PPR and B2542 strains, the replacement of CDR1 of fCD134 (amino acids 1 to 64) with human CD134 (h
89 tides containing the amino acid sequences of CDR1 and CDR2 (designated bCDR1 and bCDR2) were synthesi
94 uted at the peptidic termini at the putative CDR1 contact regions show improved recognition in B6 mic
95 est that some amino acids in variable region CDR1 and CDR2s almost always react in a consistent way w
96 uence, the complementary determining regions CDR1 and CDR3 of the TCR Valpha and Vbeta domains make t
97 ermline complementarity determining regions (CDR1 and 2) in MHC restriction is not well understood.
98 second complementarity determining regions (CDR1 and CDR2) of this Valpha are shorter than the CDRs
99 s three complementarity-determining regions (CDR1-CDR3), which contribute to antigen specificity.
100 identified constitutive disease resistance (CDR1) encoding an apoplastic aspartic protease, the over
101 diverse peptides, and moderately diverse TCR CDR1 and CDR2 regions contact moderately diverse MHC alp
103 to the high amino acid diversity of the TCR CDR1 and CDR2 loops, and that such conservation is unlik
106 he TCRs in complex with QL9-L(d) showed that CDR1, CDR2, and CDR3beta conformations and docking orien
110 ntify a fibrillogenic hotspot located at the CDR1 and beta-strand C of the protein, which was confirm
112 unit(s) in the heterodimer or homodimer, the CDR1 loop of CD8beta tilts away from its corresponding C
115 identified and implies that residues in the CDR1 and CDR2-equivalent loops of CD8beta are occluded u
117 hat alanine substitutions of residues in the CDR1 loop of CD8beta have no effect on CD8alphabeta core
120 ally, 8 of 9 of these events occurred in the CDR1 or CDR2, following a pattern consistent with select
121 beta mutants and identified mutations in the CDR1, CDR2, and CDR3 loops that decreased binding to MHC
122 e conservative F substitution of Y 26 in the CDR1-like region also reduced binding to CD80 and CD86.
124 nment of the V region, and especially of the CDR1 and CDR2, is highly evolved to recruit mutations to
125 gs are inconsistent with the notion that the CDR1 and CDR2 loops of the TCR are responsible for MHC r
127 all conformational changes, localized to the CDR1 contact regions, may play a significant role in TCR
128 at a fibrillogenic hotspot associated to the CDR1 is also encoded by several kappa and lambda germlin
129 of homologous peptides corresponding to the CDR1 segments of human Vbeta gene products, a major epit
131 erminal of the MYPPPY region, and within the CDR1-like region of CTLA-4, eliminated both CD80 and CD8
133 and neonate in the first 6 weeks have unique CDR1 and CDR2 sequences, permitting each to be identifie
134 owever, so-called "hybrid" VH genes that use CDR1 of one VH gene and the CDR2 of another are frequent
137 volutionarily selected germline Valpha/Vbeta CDR1/CDR2 loops to create highly MHC/peptide cross-react
139 , RSB1, RPN4, YLR346c and YMR102c along with CDR1, PDH1 and PDR1 itself) or downregulated (PDR12); ro
140 lementarity-determining regions (CDRs), with CDR1 and CDR2 encoded by the V segment and CDR3 encoded
141 exclusively bearing VDJ rearrangements with CDR1, CDR2, and nearly intact DH segments in germline co