Population genetics of red cell phosphoglucomutase (E C 2.7.5.1): Gene frequencies in Southwestern Germany

1968 ◽  
Vol 5 (3) ◽  
Author(s):  
B. Wille ◽  
Elke Schmidt ◽  
H. Ritter
Genetics ◽  
1993 ◽  
Vol 133 (3) ◽  
pp. 711-727
Author(s):  
B K Epperson

Abstract The geographic distribution of genetic variation is an important theoretical and experimental component of population genetics. Previous characterizations of genetic structure of populations have used measures of spatial variance and spatial correlations. Yet a full understanding of the causes and consequences of spatial structure requires complete characterization of the underlying space-time system. This paper examines important interactions between processes and spatial structure in systems of subpopulations with migration and drift, by analyzing correlations of gene frequencies over space and time. We develop methods for studying important features of the complete set of space-time correlations of gene frequencies for the first time in population genetics. These methods also provide a new alternative for studying the purely spatial correlations and the variance, for models with general spatial dimensionalities and migration patterns. These results are obtained by employing theorems, previously unused in population genetics, for space-time autoregressive (STAR) stochastic spatial time series. We include results on systems with subpopulation interactions that have time delay lags (temporal orders) greater than one. We use the space-time correlation structure to develop novel estimators for migration rates that are based on space-time data (samples collected over space and time) rather than on purely spatial data, for real systems. We examine the space-time and spatial correlations for some specific stepping stone migration models. One focus is on the effects of anisotropic migration rates. Partial space-time correlation coefficients can be used for identifying migration patterns. Using STAR models, the spatial, space-time, and partial space-time correlations together provide a framework with an unprecedented level of detail for characterizing, predicting and contrasting space-time theoretical distributions of gene frequencies, and for identifying features such as the pattern of migration and estimating migration rates in experimental studies of genetic variation over space and time.


1972 ◽  
Vol 17 (1) ◽  
pp. 79-80 ◽  
Author(s):  
S. Bissbort ◽  
J. Kömpf
Keyword(s):  

1975 ◽  
Vol 24 (3-4) ◽  
pp. 337-338
Author(s):  
A. Kalos ◽  
K. Melissinos ◽  
A. Archimandritis ◽  
G. Kourounis ◽  
B. Angelopoulos

Red cell acid phosphatase polymorphism was studied by starch gel electrophoresis in 70 b-thalassemia patients and in 310 healthy Greeks. Our results gave the following gene frequencies: b-thalassemia patients: pa 0.321, pb 0.643, pc 0.036; healthy Greeks: pa 0.302, pb 0.653, pc 0.045. No statistically significant differences were found between the two groups.


1992 ◽  
Vol 7 (3) ◽  
pp. 1-10 ◽  
Author(s):  
P. Amirshahi ◽  
E. Sunderland ◽  
D. D. Farhud ◽  
S. H. Tavakoli ◽  
P. Daneshmand ◽  
...  

2009 ◽  
pp. 75-111
Author(s):  
T. L. White ◽  
W. T. Adams ◽  
D. B. Neale

Hematology ◽  
2002 ◽  
Vol 2002 (1) ◽  
pp. 35-57 ◽  
Author(s):  
David J. Weatherall ◽  
Louis H. Miller ◽  
Dror I. Baruch ◽  
Kevin Marsh ◽  
Ogobara K. Doumbo ◽  
...  

Abstract Because of the breakdown of malaria control programs, the constant emergence of drug resistant parasites, and, possibly, climatic changes malaria poses a major problem for the developing countries. In addition, because of the speed of international travel it is being seen with increasing frequency as an imported disease in non-tropical countries. This update explores recent information about the pathophysiology of the disease, its protean hematological manifestations, and how carrier frequencies for the common hemoglobin disorders have been maintained by relative resistance to the malarial parasite. In Section I, Dr. Louis Miller and colleagues consider recent information about the pathophysiology of malarial infection, including new information about interactions between the malarial parasite and vascular endothelium. In Section II, Dr. David Roberts discusses what is known about the complex interactions between red cell production and destruction that characterize the anemia of malaria, one of the commonest causes of anemia in tropical countries. In Section III, Dr. David Weatherall reviews recent studies on how the high gene frequencies of the thalassemias and hemoglobin variants have been maintained by heterozygote advantage against malaria and how malaria has shaped the genetic structure of human populations.


1975 ◽  
Vol 25 (5) ◽  
pp. 414-417 ◽  
Author(s):  
S.G. Welch ◽  
J. Lee ◽  
I.A. McGregor ◽  
K. Williams

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