131 ApoE allele frequencies and ApoE mutations in endogenous hypertriglyceridemia

1997 ◽  
Vol 130 ◽  
pp. S34 ◽  
Author(s):  
Frits HAF de Man ◽  
Peter de Knijff ◽  
Femke de Beer ◽  
Louis M Havekes ◽  
Augustinus HM Smelt ◽  
...  
1997 ◽  
Vol 20 (4) ◽  
pp. 741-743 ◽  
Author(s):  
Guilherme B. Marin ◽  
Marli H. Tavella ◽  
João F. Guerreiro ◽  
Sidney E.B. Santos ◽  
Marco A. Zago

Determination of the ApoE allele distribution in five South American Amerindian tribes revealed absence of the ApoE2 allele, accompanied by high ApoE3 and low ApoE4 allele frequencies for most tribes, a distribution only previously reported for the Inuit Eskimo from Greenland.


1994 ◽  
Vol 177 (1-2) ◽  
pp. 100-102 ◽  
Author(s):  
Sandro Sorbi ◽  
Benedetta Nacmias ◽  
Paolo Forleo ◽  
Stefania Latorraca ◽  
Ida Gobbini ◽  
...  

1998 ◽  
Vol 43 (4) ◽  
pp. 545-545 ◽  
Author(s):  
Owen S. Morgan ◽  
Denise A. Eldemire ◽  
Charles H. Thesiger ◽  
J. Luseko ◽  
Amrik Sahota ◽  
...  

PLoS ONE ◽  
2017 ◽  
Vol 12 (11) ◽  
pp. e0188501 ◽  
Author(s):  
Timothy J. Hohman ◽  
Logan Dumitrescu ◽  
Amy Oksol ◽  
Madison Wagener ◽  
Katherine A. Gifford ◽  
...  

Author(s):  
Sarah F. Barclay ◽  
Kendra Potocki ◽  
Ford Burles ◽  
N. Torben Bech-Hansen ◽  
Giuseppe Iaria

The three common alleles of the APOE gene, ɛ2/ɛ3/ɛ4, have been linked to human spatial orientation. We investigated the genetic role of APOE in developmental topographical disorientation (DTD), a lifelong condition that results in topographical disorientation. We genotyped the APOE ɛ2/ɛ3/ɛ4 alleles in a cohort of 20 unrelated DTD probands, and found allele frequencies not statistically different from the those seen in the population as a whole. Therefore, we found no evidence that DTD occurs preferentially on a genetic background containing any particular APOE allele, making it unlikely that these APOE alleles are contributing to the development of DTD.


Genetics ◽  
1999 ◽  
Vol 151 (3) ◽  
pp. 1053-1063 ◽  
Author(s):  
Ilik J Saccheri ◽  
Ian J Wilson ◽  
Richard A Nichols ◽  
Michael W Bruford ◽  
Paul M Brakefield

Abstract Polymorphic enzyme and minisatellite loci were used to estimate the degree of inbreeding in experimentally bottlenecked populations of the butterfly, Bicyclus anynana (Satyridae), three generations after founding events of 2, 6, 20, or 300 individuals, each bottleneck size being replicated at least four times. Heterozygosity fell more than expected, though not significantly so, but this traditional measure of the degree of inbreeding did not make full use of the information from genetic markers. It proved more informative to estimate directly the probability distribution of a measure of inbreeding, σ2, the variance in the number of descendants left per gene. In all bottlenecked lines, σ2 was significantly larger than in control lines (300 founders). We demonstrate that this excess inbreeding was brought about both by an increase in the variance of reproductive success of individuals, but also by another process. We argue that in bottlenecked lines linkage disequilibrium generated by the small number of haplotypes passing through the bottleneck resulted in hitchhiking of particular marker alleles with those haplotypes favored by selection. In control lines, linkage disequilibrium was minimal. Our result, indicating more inbreeding than expected from demographic parameters, contrasts with the findings of previous (Drosophila) experiments in which the decline in observed heterozygosity was slower than expected and attributed to associative overdominance. The different outcomes may both be explained as a consequence of linkage disequilibrium under different regimes of inbreeding. The likelihood-based method to estimate inbreeding should be of wide applicability. It was, for example, able to resolve small differences in σ2 among replicate lines within bottleneck-size treatments, which could be related to the observed variation in reproductive viability.


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