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2 cted, suggesting that most if not all of the cross-hybridizing bands in genomic Southern blots repres
3 urveys with a sigF-specific probe identified cross-hybridizing bands in other slow-growing mycobacter
7 he immunoglobulin superfamily (OB-BP1) and a cross-hybridizing clone (OB-BP2) that is identical to a
8 (Gossypium barbadense L.; AD genome), 83 non-cross-hybridizing DNA clones contain dispersed repeats t
10 igonucleotide probe that was used to clone a cross-hybridizing DNA fragment from V. fischeri genomic
11 and genetic organization, and their genomes cross-hybridize extensively, but they differ in biologic
12 thern analyses indicated the presence of two cross-hybridizing genes in the human genome and expressi
18 synthase cDNA clones on chromosome 6 do not cross-hybridize on genomic DNA gel blots with putative s
19 m the mouse wt1 5'-flanking region contained cross-hybridizing sequence with significant homology to
20 Genomic Southern analysis with HRG4 showed cross-hybridizing sequences in six different species, an
21 s unreliable to use MM probe signal to track cross-hybridizing signal on a corresponding PM probe.
24 lysis revealed that approximately 75% of the cross-hybridizing subclones contained sequences ortholog
26 and 86% of cosmids derived from chromosome 3 cross-hybridize to a subset of these locations, many to
28 20,696 (10.5%) nonspecific probes that could cross-hybridize to multiple genes and a total of 18,363
29 amplified 3'-untranslated region from pLE16 (cross-hybridizing to a third gene in L. pennellii, namel
30 se positives and to efficient knockdown of a cross-hybridizing transcript, raising a cautionary note
33 data, a second isoform exists which does not cross-hybridize with the leaf form in RNA blots at high
34 Using probes from the maize p1 gene that cross-hybridize with the sorghum Y gene, we isolated the
35 Five genes, spanning 1.9 cM of the region, cross-hybridized with maize genomic DNA and were genetic
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