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1 pin, we propose that exchange occurs between homologously aligned duplexes that are extended and unwo
2 ithin a RecA-ssDNA nucleoprotein filament is homologously aligned with the duplex DNA.
3 ex, in which the recombining DNA strands are homologously aligned.
4 ys, that neighboring red and green cones are homologously and heterologously coupled by nonrectifying
5 ple insertions occur both randomly (i.e. non-homologously) and at the targeted locus.
6                                 In fact, non-homologously associated centromeres separate at the begi
7  Kallikrein and BK desensitized the receptor homologously but there was no cross-desensitization.
8 at the internalization of mGluR1a, triggered homologously by glutamate or heterologously by carbachol
9 mately 50% of animals became reinfected when homologously challenged with MoPn, although the secondar
10 murine NIH 3T3-F442A fibroblasts, cells that homologously express GHRs, resulted in tyrosine phosphor
11 this substrate pair was hardly secreted when homologously expressed, it was secreted when co-expresse
12                                Strikingly, a homologously inserted cysteine is also found in Xenopus
13 upled exclusively to other amacrines, either homologously or, more often, through a combination of ho
14                          The enzyme has been homologously overexpressed to provide sufficient quantit
15 tic pathway in Bacillus megaterium and using homologously overproduced enzymes, it has been possible
16 through the formation of joint DNA molecules-homologously paired but metastable DNA intermediates tha
17          In the zip2 mutant, chromosomes are homologously paired but not synapsed.
18       These proteins facilitate formation of homologously paired joint molecules between linear doubl
19 a proteinaceous structure that forms between homologously paired meiotic chromosomes.
20                                     PAFR was homologously phosphorylated and desensitized by PAF, and
21        To improve solubility, the enzyme was homologously produced in the host B. megaterium DSM319.
22 ncluded loxP-flanked selectable markers, and homologously recombined alleles containing the marker an
23 e, effort, and resources required to produce homologously recombined alleles in mice that have been s
24                  Comparing the properties of homologously recombined chimeras with one or two crossov
25 Immortal cell lines and tumor-derived clones homologously recombined extrachromosomal plasmid substra
26 the high rates with which DNA constructs are homologously recombined into its genome.
27                                           We homologously replaced LRb in mice with a receptor with a
28 ooperativity, and stability for all of these homologously structured fragments.
29 ci along the synaptonemal complexes (SCs) of homologously synapsed autosomal bivalents in late zygone
30 zes to discrete foci during leptotene and to homologously synapsed chromosomes.
31 easures like mantle length cannot be applied homologously to all groups.
32 te counterparts, chordin and BMP-4, function homologously to define neural versus non-neural ectoderm
33 s the middle strand s4A in the A beta-sheet, homologously to that of the reactive loop in the latent