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1 nstream acceptor S region, with a DSB in Smu being joined to a DSB in the acceptor S region at suffic
2 turn-helix DNA-binding and dimerizing domain is joined to a C-terminal effector and multimerizing dom
3  termed hybrid joints, in which a signal end is joined to a hairpin coding end.
4 r step wherein the processed donor substrate is joined to a nonspecific target DNA.
5 Cys)] is a modified vinylogous cysteine that is joined to a novel ketide [3,7-dihydroxy-2,5,8,8-tetra
6 truct in which a folded quadruplex structure is joined to a standard double helix.
7                     Further, the T59 peptide was joined to a cell adhesive sequence and used to promo
8                             Hybrid promoters were joined to a lacZ reporter gene and assayed by trans
9 To determine this chirality, the cleaved DNA is joined to an oligonucleotide by DNA ligase.
10               An extracellular region of DAF was joined to an antibody combining site with specificit
11                  Lumen and vessel boundaries are joined to create the coronary wall.
12 the rearranged hybrid switch region sequence was joined to DNA from chromosome 4p16, suggesting that
13 ree base porphyrins in the tetrad and pentad are joined to each other via p-phenylene linkers whereas
14 n variable region of a murine anti-dansyl Ab was joined to either human kappa or lambda constant regi
15 ative data sets and active surveillance data were joined to estimate influenza-associated hospitaliza
16 s were processed separately and subsequently were joined to evaluate the effect of synergy on the inf
17 o macrocycles with chemically distinct faces are joined to form a catenane, the structure is chiral,
18 his analysis reveals that two cysteines that are joined to form a structural disulfide can play diffe
19 functional units and whether these units can be joined to form a larger composition with dual functio
20 yeast cells, generating signal ends that can be joined to form signal joints.
21 us- and minus-strand primers; these ends can be joined to form two-long-terminal repeat circles.
22 he linear DNA molecules with homologous ends are joined to generate the plasmid with the desired muta
23 fferent receptor gene loci could potentially be joined to generate interlocus joints.
24                                      Helix 1 is joined to helix 2 by a flexible linker.
25 ian sarcoma virus retroviral vector DNA that is joined to host DNA in the population of infected cell
26 ce hypothesis would require these results to be joined to independent and reliable estimates of reass
27 ncode information for archival data storage, are joined to linker sequences at either end.
28  bundle fold (ca 45 residues in length) that is joined to N- and C-terminal flanking immunoglobulin d
29 sions in which PAX3 or PAX7 is postulated to be joined to novel genomic loci.
30               In addition, S-region DSBs can be joined to other chromosomes to generate translocation
31 creased GCR rates, but their telomeres could be joined to other DNAs resulting in chromosome fusions.
32    N-terminal or C-terminal fragments of RAP were joined to PE to produce two novel fusion proteins w
33 tions in which individual 3' transposon ends are joined to separate strands of the target DNA.
34                       The lux reporter genes were joined to seven uncharacterized open reading frames
35                                 The two have been joined to support growing environmental markets wit
36 ch the 3'-OH groups produced by Rag cleavage are joined to target DNA.
37 he 3' ends of linear transposon or donor DNA are joined to the 5' phosphates of a double-stranded cut
38                        The added nucleotides are joined to the growing RNA chain by 3',5'-phosphodies
39  resulting recessed 3' ends of the viral DNA are joined to the host DNA.
40                    The aberrant end can then be joined to the host DNA by unusual processes that do n
41                               The RNA strand is joined to the 5' end of the DNA chain via a 2'-5' lin
42 ly active aziridine-containing fragment that is joined to the aromatic moiety in a highly convergent
43 and each contains a 5' leader sequence which is joined to the body of the mRNA through a conserved ju
44 ing the splicing reaction, the 5' intron end is joined to the branchpoint nucleotide, selecting the n
45 n, containing an additional alpha-helix that is joined to the C terminus of the homeodomain by a turn
46  of the brain mRNA that in non-brain tissues is joined to the coding region by alternative splicing,
47 Mistranslation occurs when glycine or serine is joined to the G3.U70-containing tRNAs, and is prevent
48 a is a large, broad puboischiadic plate that is joined to the iliac process of a hypertrophied sacral
49  approximately 251 nucleotides (nt) long and is joined to the main body of the transcript upon remova
50                       This C-terminal domain is joined to the rest of FliM by a segment (residues 237
51          In both adducts C5 of the inhibitor is joined to the sulfur of C67.
52 which the variable domain of the heavy chain is joined to the variable domain of the light chain thro
53 h a truncated form of Pseudomonas exotoxin A is joined to the variable region of a broadly neutralizi
54 in which the carboxyl terminus of one domain was joined to the amino terminus of the second domain vi
55          Three kb of the peroxidase promoter was joined to the coding region of the Escherichia coli
56 mphotropic env of the helper packaging virus was joined to the long terminal repeat (LTR) of the Molo
57 artery thrombosis, and double donor arteries were joined to the bifurcation of the recipient hepatic
58 ce sites within an intron can, in principle, be joined to those within any other intron during pre-mR
59 aminoacylation reactions whereby amino acids are joined to tRNAs bearing the anticodons of the geneti
60                                 Each subunit is joined to two of its neighbors by ligation of the sid