scholarly journals Inverted insertion (9)(q34.3q22.3q21.2) and its recombination product: Duplication 9q21.2q22.3

1987 ◽  
Vol 32 (1) ◽  
pp. 45-48 ◽  
Author(s):  
Tadashi Kajii ◽  
Shinya Matsuura ◽  
Ichiro Murano ◽  
Akira Kuwano
1978 ◽  
Vol 33 (3) ◽  
pp. 293-299 ◽  
Author(s):  
Joachim Stauff ◽  
Wolfgang Jaeschke

Abstract The reactions of diluted aqueous solutions of SO2 resp. HSO3-ions with MnO4-or Ce4+ ions in the pH range 1-4 produce chemiluminescence in the spectral region of 450-600 nm. Measurements of the time course of the light emission and their simulation on an analog computer led to a reaction scheme in which a recombination product of primarily formed HSO3 radicals -of a lifetime of about 1 second -appears as precursor of electronically excited SO2 molecules. The participation of singlet oxygen can be excluded because at least the reaction with Ce4+ ions proceeds also in the absence of oxygen.


2008 ◽  
Vol 42 (4) ◽  
pp. 178-185 ◽  
Author(s):  
S. Stengel-Rutkowski ◽  
K. Lohse ◽  
C. Herzog ◽  
C. Apacik ◽  
J. Couturier ◽  
...  

2020 ◽  
Vol 132 (34) ◽  
pp. 14402-14408 ◽  
Author(s):  
Yuxing Zhang ◽  
Chaoqun Wang ◽  
Stefan Mecking ◽  
Zhongbao Jian

1979 ◽  
Vol 32 (2) ◽  
pp. 261 ◽  
Author(s):  
DEA Catcheside

In crosses between his-3(K874) and ad-3A(K118), the presence of rec-2+ reduces the frequency of formation of both prototrophic recombinants (his-3+ ad-3A +) and double mutant recombinants (his-3 ad-3A) to a similar degree. This is consistent with the hypothesis that the product of the rec-2+ gene acts to block the initiation of recombination events and indicates that rec-2+ does not determine the frequency of formation of prototrophic recombinants by influencing the type of recombination product which predominates.


1986 ◽  
Vol 6 (11) ◽  
pp. 3948-3953 ◽  
Author(s):  
P Bullock ◽  
J Miller ◽  
M Botchan

Sequencing studies have shown that in somatic cells alternating runs of purines and pyrimidines are frequently associated with recombination crossover points. To test whether such sequences actually promote recombination, we have examined the effects of poly[d(pGpT).d(pApC)] and poly[d(pCpG).d(pCpG)] repeats on a homologous recombination event. The parental molecule used in this study, pSVLD, is capable of generating wild-type simian virus 40 DNA via recombination across two 751-base-pair regions of homology and has been described previously (Miller et al., Proc. Natl. Acad. Sci. USA 81:7534-7538, 1984). Single inserts of either a poly[d(pGpT).d(pApC)] repeat or a poly[d(pCpG).d(pCpG)] repeat were positioned adjacent to one region of homology in such a way that the recombination product, wild-type simian virus 40 DNA, could be formed only by recombination within the homologies and not by recombination across the alternating purine-pyrimidine repeats. We have found that upon transfection of test DNAs into simian cells, a poly[d(pCpG).d(pCpG)] repeat enhanced homologous recombination 10- to 15-fold, whereas a poly[d(pGpT).d(pApC)] repeat had less effect. These results are discussed in terms of the features of these repeats that might be responsible for promoting homologous recombination.


2006 ◽  
Vol 25 (5) ◽  
pp. 798-828 ◽  
Author(s):  
Nigel G. Adams ◽  
Viktoriya Poterya ◽  
Lucia M. Babcock

Sign in / Sign up

Export Citation Format

Share Document