ライフサイエンスコーパス: variable heavy chain

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1 dues, whereas S1-15 utilizes exclusively the variable heavy chain.

2 The germline immunoglobulin (Ig) variable heavy chain 4-34 (VH4-34) gene segment encodes

3 ology (a mouse that expresses human antibody-variable heavy chains and kappa light chains) alongside

4 ragment (scFv) that consists of the antibody variable heavy chain connected to the variable light cha

5 eliminated by point mutation (Y100bP) in the variable heavy-chain domain to create an scFv (B6-2) tha

6 ovement between the variable light chain and variable heavy chain domains within the antibody, but no

7 B cells of the largest Ig variable heavy chain gene (VH) family, VH3, are reported

8 malignant cells and unmutated immunoglobulin variable heavy chain gene have similarly been validated

9 Variable heavy chain gene usage was restricted, but simi

10 s (N- to C-terminal) a pelB leader sequence, variable heavy chain, glycine-serine polylinker, variabl

11 alphaGal-containing N-linked glycan on a mAb variable heavy chain has potential clinical interest, as

12 displays somatically mutated immunoglobulin variable heavy chain (IgV(H)) genes, which suggests an o

13 adjacent to significant glycosylation of the variable heavy chain on asparagine 85 in Framework Regio

14 hain locus and 5'-flanking sequences of some variable heavy chain promoters.

15 ied ASCs punctuated by clones expressing the variable heavy-chain region VH4-34 that produced dominan

16 istal rearrangement of the gene encoding the variable heavy-chain region.

17 or post-GC phenotype and carrying mutated Ig variable heavy chain sequences.

18 the BCL-6 5'-noncoding region and in the Ig variable heavy chain sequences.

19 s, extensive somatic hypermutation and long, variable heavy-chain third complementarity-determining r

20 e presence or absence of immunoglobulin (Ig) variable heavy chain (V(H)) gene mutations.

21 ructed by diversifying a scaffold: the human variable heavy chain (V(H)) germ line gene 3-23, which w

22 that these anti-bodies display a restricted variable heavy chain (V(H)) repertoire and lack somatic

23 Immunoglobulin rearrangement from variable heavy chain (V(H)) to diversity (D)-joining hea

24 st position (Kabat numbering) in CDR3 of the variable heavy chain (V(H)), having aspartic acid (Asp)

25 tolerance using gene-targeted immunoglobulin variable heavy-chain (V(H)) alleles 3H9 or 56R, which en

26 at positions S31R and W33T of the associated variable heavy chain (VH) allele were identified and con

27 y fragments, consisting of an interconnected variable heavy chain (VH) and variable light chain (VL),

28 y to interact with many members of an entire variable heavy chain (VH) or variable light chain gene f

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