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Institution

Bielefeld University

EducationBielefeld, Nordrhein-Westfalen, Germany
About: Bielefeld University is a education organization based out in Bielefeld, Nordrhein-Westfalen, Germany. It is known for research contribution in the topics: Population & Quantum chromodynamics. The organization has 10123 authors who have published 26576 publications receiving 728250 citations. The organization is also known as: University of Bielefeld & UNIVERSITAET BIELEFELD.


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17 Dec 2015
TL;DR: In this paper, the existence of solutions to Fokker-planck-kolmogorov equations is investigated and the uniqueness problem of the infinite-dimensional case is investigated.
Abstract: * Stationary Fokker-Planck-Kolmogorov equations* Existence of solutions* Global properties of densities* Uniqueness problems* Associated semigroups* Parabolic Fokker-Planck-Kolmogorov equations* Global parabolic regularity and upper bounds* Parabolic Harnack inequalities and lower bounds* Uniquess of solutions to Fokker-Planck-Kolmogorov equations* The infinite-dimensional case* Bibliography* Subject index

218 citations

Journal ArticleDOI
TL;DR: In this article, the authors considered the hard scattering processes gg→3S1 g and gq→3P0,1,2q with subsequent decay 3PJ→ 3S1γ as the main mechanisms at large transverse momenta.

218 citations

Journal ArticleDOI
TL;DR: High-throughput DNA sequencing was used to estimate genome-wide heterozygosity based on over 10,000 loci and found it to accurately reflect inbreeding, providing the strongest evidence to date of an HFC being due to inbreeding depression in a natural population lacking a pedigree.
Abstract: Proxy measures of genome-wide heterozygosity based on approximately 10 microsatellites have been used to uncover heterozygosity fitness correlations (HFCs) for a wealth of important fitness traits in natural populations. However, effect sizes are typically very small and the underlying mechanisms remain contentious, as a handful of markers usually provides little power to detect inbreeding. We therefore used restriction site associated DNA (RAD) sequencing to accurately estimate genome-wide heterozygosity, an approach transferrable to any organism. As a proof of concept, we first RAD sequenced oldfield mice (Peromyscus polionotus) from a known pedigree, finding strong concordance between the inbreeding coefficient and heterozygosity measured at 13,198 single-nucleotide polymorphisms (SNPs). When applied to a natural population of harbor seals (Phoca vitulina), a weak HFC for parasite infection based on 27 microsatellites strengthened considerably with 14,585 SNPs, the deviance explained by heterozygosity increasing almost fivefold to a remarkable 49%. These findings arguably provide the strongest evidence to date of an HFC being due to inbreeding depression in a natural population lacking a pedigree. They also suggest that under some circumstances heterozygosity may explain far more variation in fitness than previously envisaged.

218 citations

Journal ArticleDOI
TL;DR: The suitability of the p SG5 vector family for mutating chromosomal genes by gene disruption was demonstrated: pBN10, a pSG5 derivative containing an internal fragment of the phosphinothricyl-alanyl-alanine (PTT) resistance gene pat, was integrated into the chromosomal pat gene of the PTT-producer Streptomyces viridochromogenes thus inactivating PTT resistance.
Abstract: Replication of the Streptomyces ghanaensis plasmid pSG5 was shown to be temperature sensitive. The pSG5 replicon is stably inherited at temperatures below 34° C, but is lost at incubation temperatures above this. A family of cloning vectors was constructed using the pSG5 minimal replicon and different marker genes. The vectors obtained are small in size, have an intermediate copy number, possess a broad host range and are compatible with some other streptomycete vector systems. By increasing the incubation temperature, these vectors can be eliminated from their host cells very efficiently. The suitability of the pSG5 vector family for mutating chromosomal genes by gene disruption was demonstrated: pBN10, a pSG5 derivative containing an internal fragment of the phosphinothricyl-alanyl-alanine (PTT) resistance gene pat, was integrated into the chromosomal pat gene of the PTT-producer Streptomyces viridochromogenes thus inactivating PTT resistance. The integrated pBN10 plasmid was rescued from the chromosome, together with an adjacent fragment carrying DNA of the PTT biosynthetic cluster.

217 citations

Journal ArticleDOI
TL;DR: The missense mutation L967Q in Vps54 in the wobbler mouse, an animal model of amyotrophic lateral sclerosis, is identified and a lethal allele, Vps 54β-geo is characterized, indicating that VPS54 has an essential role in these processes.
Abstract: Vacuolar-vesicular protein sorting (Vps) factors are involved in vesicular trafficking in eukaryotic cells. We identified the missense mutation L967Q in Vps54 in the wobbler mouse, an animal model of amyotrophic lateral sclerosis, and also characterized a lethal allele, Vps54(beta-geo). Motoneuron survival and spermiogenesis are severely compromised in the wobbler mouse, indicating that Vps54 has an essential role in these processes.

217 citations


Authors

Showing all 10375 results

NameH-indexPapersCitations
Stefan Grimme113680105087
Alfred Pühler10265845871
James Barber10264242397
Swagata Mukherjee101104846234
Hans-Joachim Werner9831748508
Krzysztof Redlich9860932693
Graham C. Walker9338136875
Christian Meyer93108138149
Muhammad Farooq92134137533
Jean Willy Andre Cleymans9054227685
Bernhard T. Baune9060850706
Martin Wikelski8942025821
Niklas Luhmann8542142743
Achim Müller8592635874
Oliver T. Wolf8333724211
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023150
2022511
20211,696
20201,655
20191,410
20181,299