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Marieke Verleih

Researcher at Leibniz Association

Publications -  31
Citations -  523

Marieke Verleih is an academic researcher from Leibniz Association. The author has contributed to research in topics: Rainbow trout & Trout. The author has an hindex of 12, co-authored 29 publications receiving 387 citations. Previous affiliations of Marieke Verleih include Leibniz Institute for Neurobiology.

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Transcriptome Profiling of Gill Tissue in Regionally Bred and Globally Farmed Rainbow Trout Strains Reveals Different Strategies for Coping with Thermal Stress

TL;DR: An overview of the genes of the multifunctional gills in rainbow trout that are mandated after temperature change is provided, suggesting links between the different temperature-dependent pathways and gene networks.
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Transcriptome Profiling Reveals Insight into Distinct Immune Responses to Aeromonas salmonicida in Gill of Two Rainbow Trout Strains

TL;DR: Dynamic but moderate changes in the expression of a broad range of immune-relevant features implying the gill’s involvement in pathogen defense strategies are uncovered.
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Impact of Thermal Stress on Kidney-Specific Gene Expression in Farmed Regional and Imported Rainbow Trout.

TL;DR: A general overview of stress-induced transcriptional patterns in rainbow trout trunk kidney is provided in addition to identifying genes and networks that contribute to the robustness of the BORN strain, and analyses suggest SERPINH1 and CIRBP as general marker genes for heat stress and cold stress in trout.
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Novel insights into the peritoneal inflammation of rainbow trout (Oncorhynchus mykiss)

TL;DR: Results represent the first complete description of the immune reaction protecting the peritoneal cavity of the fish and shed some light on the conservation of these processes during the evolution.
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Creatine metabolism differs between mammals and rainbow trout (Oncorhynchus mykiss).

TL;DR: The expression data showed clear differences between the creatine system in rainbow trout and mammals, as the spatial distribution of the enzyme-encoding gene expression was clearly different from the patterns described for mammals.