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Jürg Bähler

Researcher at University College London

Publications -  237
Citations -  24955

Jürg Bähler is an academic researcher from University College London. The author has contributed to research in topics: Schizosaccharomyces pombe & Gene. The author has an hindex of 67, co-authored 227 publications receiving 21327 citations. Previous affiliations of Jürg Bähler include University of Debrecen & European Bioinformatics Institute.

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Transient structural variations have strong effects on quantitative traits and reproductive isolation in fission yeast

TL;DR: It is shown that copy number variants (CNVs) frequently segregate within closely related clonal populations, are weakly linked to single nucleotide polymorphisms (SNPs), and show other genetic signals consistent with rapid turnover that have broad implications for evolution and for the understanding of quantitative traits including complex human diseases.
Posted ContentDOI

A natural variant of the sole pyruvate kinase of fission yeast lowers glycolytic flux triggering increased respiration and oxidative-stress resistance but decreased growth

TL;DR: Low Pyk1 activity provided no growth advantage but stress tolerance, despite increased respiration, and the genetic tuning of glycolytic flux by a single-nucleotide change might reflect an adaptive trade-off in a species lacking pyruvate-kinase isoforms.
Journal ArticleDOI

Co-Expression Network Models Suggest that Stress Increases Tolerance to Mutations.

TL;DR: It is found that exposure to stress decreases the average damage from node removal, suggesting stress induces greater tolerance to loss of function mutations, and the shape of the damage distribution is changed upon stress.
Posted ContentDOI

Temporal Transcriptome and Promoter Architecture of the African Swine Fever Virus

TL;DR: The results reveal that the ASFV-RNAP undergoes transcript slippage at the 5’ end of transcription units that in a promoter sequence-specific manner results in the addition of 5‘-AT and 5�’-ATAT tails to mRNAs.
Posted ContentDOI

Uncovering Natural Longevity Alleles from Intercrossed Pools of Aging Fission Yeast Cells

TL;DR: It is proposed that Ppk31 and SPBC409.08 may function together to modulate lifespan, thus linking Rim15/Ppk 31 with spermidine metabolism, and single and double allele replacement suggests that both variants, alone or combined, have subtle effects on cellular longevity.