@article{PalmaVeraReyerLanghammeretal.2022,
  author    = {Palma-Vera, Sergio E. and Reyer, Henry and Langhammer, Martina and Reinsch, Norbert and Derezanin, Lorena and Fickel, J{\"o}rns and Qanbari, Saber and Weitzel, Joachim M. and Franzenburg, Soeren and Hemmrich-Stanisak, Georg and Sch{\"o}n, Jennifer},
  title     = {Genomic characterization of the world's longest selection experiment in mouse reveals the complexity of polygenic traits},
  series = {BMC Biology},
  volume    = {20},
  journal   = {BMC Biology},
  number    = {1},
  publisher = {BMC},
  address   = {London},
  issn      = {1741-7007},
  doi       = {10.1186/s12915-022-01248-9},
  pages     = {20},
  year      = {2022},
  abstract  = {Background Long-term selection experiments are a powerful tool to understand the genetic background of complex traits. The longest of such experiments has been conducted in the Research Institute for Farm Animal Biology (FBN), generating extreme mouse lines with increased fertility, body mass, protein mass and endurance. For >140 generations, these lines have been maintained alongside an unselected control line, representing a valuable resource for understanding the genetic basis of polygenic traits. However, their history and genomes have not been reported in a comprehensive manner yet. Therefore, the aim of this study is to provide a summary of the breeding history and phenotypic traits of these lines along with their genomic characteristics. We further attempt to decipher the effects of the observed line-specific patterns of genetic variation on each of the selected traits. Results Over the course of >140 generations, selection on the control line has given rise to two extremely fertile lines (>20 pups per litter each), two giant growth lines (one lean, one obese) and one long-distance running line. Whole genome sequencing analysis on 25 animals per line revealed line-specific patterns of genetic variation among lines, as well as high levels of homozygosity within lines. This high degree of distinctiveness results from the combined effects of long-term continuous selection, genetic drift, population bottleneck and isolation. Detection of line-specific patterns of genetic differentiation and structural variation revealed multiple candidate genes behind the improvement of the selected traits. Conclusions The genomes of the Dummerstorf trait-selected mouse lines display distinct patterns of genomic variation harbouring multiple trait-relevant genes. Low levels of within-line genetic diversity indicate that many of the beneficial alleles have arrived to fixation alongside with neutral alleles. This study represents the first step in deciphering the influence of selection and neutral evolutionary forces on the genomes of these extreme mouse lines and depicts the genetic complexity underlying polygenic traits.},
  language  = {en}
}
@article{KaruwanarintPhonratTungtrongchitretal.2018,
  author    = {Karuwanarint, Piyaporn and Phonrat, Benjaluck and Tungtrongchitr, Anchalee and Suriyaprom, Kanjana and Chuengsamarn, Somlak and Schweigert, Florian J. and Tungtrongchitr, Rungsunn},
  title     = {Vitamin D-binding protein and its polymorphisms as a predictor for metabolic syndrome},
  series = {Biomarkers in medicine},
  volume    = {12},
  journal   = {Biomarkers in medicine},
  number    = {5},
  publisher = {Future Medicine},
  address   = {London},
  issn      = {1752-0363},
  doi       = {10.2217/bmm-2018-0029},
  pages     = {465 -- 473},
  year      = {2018},
  abstract  = {Aim: To investigate the relationship of vitamin D-binding protein (GC) and genetic variation of GC (rs4588, rs7041 and rs2282679) with metabolic syndrome (MetS) in the Thai population. Materials \& methods: GCglobulin concentrations were measured by quantitative western blot analysis in 401 adults. All participants were genotyped using TaqMan allelic discrimination assays. Results: GC-globulin levels were significatly lower in MetS subjects than in control subjects, in which significant negative correlations of GC-globulin levels with systolic blood pressure, glucose and age were found. Male participants who carried the GT genotype for rs4588 showed an increased risk of MetS compared with the GG wild-type (odds ratio: 3.25; p = 0.004). Conclusion: GC-globulin concentrations and variation in GC rs4588 were supported as a risk factor for MetS in Thais.},
  language  = {en}
}
@article{SchertlO'Brien2013,
  author    = {Schertl, Hans-Peter and O'Brien, Patrick},
  title     = {Continental crust at mantle depths - key minerals and microstructures},
  series = {Elements : an international magazine of mineralogy, geochemistry, and petrology},
  volume    = {9},
  journal   = {Elements : an international magazine of mineralogy, geochemistry, and petrology},
  number    = {4},
  publisher = {Mineralogical Society of America},
  address   = {Chantilly},
  issn      = {1811-5209},
  doi       = {10.2113/gselements.9.4.261},
  pages     = {261 -- 266},
  year      = {2013},
  abstract  = {Finding evidence for ultrahigh-pressure (UHP) metamorphism in crustal rocks is far from straightforward. The index minerals coesite and diamond are incredibly inconspicuous and are therefore difficult to use as UHP prospecting tools. Consequently, petrographers rely on recognizing subtle breakdown microstructures that result from pressure release during the return to the surface of the once deeply buried rock. Similarly, many other UHP minerals are first suspected on the basis of typical reaction or exsolution microstructures. Thus, the painstaking use of microscopic techniques has been fundamental to the tremendous advances in characterizing, quantifying, and understanding macroscopic-scale, deep continental subduction, rapid exhumation, and mountain-building processes.},
  language  = {en}
}