scholarly journals THE LOCATION OF GENETIC FACTORS CONTROLLING A NUMBER OF QUANTITATIVE CHARACTERS IN WHEAT

Genetics ◽  
1967 ◽  
Vol 56 (3) ◽  
pp. 445-461
Author(s):  
C N Law
Genetics ◽  
1988 ◽  
Vol 118 (3) ◽  
pp. 445-459
Author(s):  
A E Shrimpton ◽  
A Robertson

Abstract In the present study an attempt has been made to characterize the genetic ;;factors'' controlling quantitative characters, bristle numbers, in Drosophila melanogaster. A low sternopleural bristle multiple recessive marker third chromosome was used to analyze a high sternopleural third chromosome, in a high sternopleural bristle background. An attempt was made to estimate the minimum number of ;;effective factors'' involved in the difference in bristle score between the tested and marker chromosomes. Apart from sternopleural, scutellar and ocellar bristles, a new character, subprimal bristles, was also scored. The unselected characters were used to help in the factor locations, and an attempt made to detect epistasis. Concentrations of bristle effects were found, as were a few ;factors' of large effect. At least 17 sternopleural bristle factors are required to account for the difference in bristle score between the high tested third chromosome and the low tester third chromosome. There was an ascertainment problem for polygenes with effects of less than about 0.6 phenotypic standard deviation. Only an estimate of the minimum number of factors and approximate locations can be given with any degree of certainty. The results are compatible with the hypothesis (among others) that quantitative characters are under the control of a few major genes supported by numerous genes with smaller effect.


1961 ◽  
Vol 40 (3) ◽  
pp. 371-378 ◽  
Author(s):  
David A. Price Evans

Hepatology ◽  
2004 ◽  
Vol 40 (4) ◽  
pp. 942-950 ◽  
Author(s):  
Nadia Gorman ◽  
Heidi W. Trask ◽  
William J. Bement ◽  
Juliana G. Szakacs ◽  
George H. Elder ◽  
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Keyword(s):  

2010 ◽  
Vol 49 (S 01) ◽  
pp. S64-S68
Author(s):  
E. Dikomey

SummaryIonising irradiation acts primarily via induction of DNA damage, among which doublestrand breaks are the most important lesions. These lesions may lead to lethal chromosome aberrations, which are the main reason for cell inactivation. Double-strand breaks can be repaired by several different mechanisms. The regulation of these mechanisms appears be fairly different for normal and tumour cells. Among different cell lines capacity of doublestrand break repair varies by only few percents and is known to be determined mostly by genetic factors. Knowledge about doublestrand break repair mechanisms and their regulation is important for the optimal application of ionising irradiation in medicine.


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