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Federation of European Neuroscience Societies high-throughput microarray
High Throughput Microarray, supplied by Federation of European Neuroscience Societies, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/high+throughput+microarray+platform/high+throughput+microarray/pm27117587-57-31-13
Average 90 stars, based on 1 article reviews
high-throughput microarray - by Bioz Stars, 2026-10
90/100 stars

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Related Articles

Infection:

Article Title: Plasmodium meets AAV-the (un)likely marriage of parasitology and virology, and how to make the match.
Article Snippet: Edited by Wilhelm Just The increasing use of screening technologies in malaria research has substantially expanded our knowledge on cellular factors hijacked by the Plasmodium parasite in the infected host, including those that participate in the clinically silent liver stage.. This rapid gain in our understanding of the hepatic interaction partners now requires a means to validate and further disentangle parasite–host networks in physiologically relevant liver model systems.. Here, we outline seminal work that contributed to our present knowledge on the intrahepatic Plasmodium host factors, followed by a discussion of surrogate models of mammalian livers or hepatocytes.

Microarray:

Article Title: Plasmodium meets AAV-the (un)likely marriage of parasitology and virology, and how to make the match.
Article Snippet: Edited by Wilhelm Just The increasing use of screening technologies in malaria research has substantially expanded our knowledge on cellular factors hijacked by the Plasmodium parasite in the infected host, including those that participate in the clinically silent liver stage.. This rapid gain in our understanding of the hepatic interaction partners now requires a means to validate and further disentangle parasite–host networks in physiologically relevant liver model systems.. Here, we outline seminal work that contributed to our present knowledge on the intrahepatic Plasmodium host factors, followed by a discussion of surrogate models of mammalian livers or hepatocytes.

Genome Wide:

Article Title: Plasmodium meets AAV-the (un)likely marriage of parasitology and virology, and how to make the match.
Article Snippet: Edited by Wilhelm Just The increasing use of screening technologies in malaria research has substantially expanded our knowledge on cellular factors hijacked by the Plasmodium parasite in the infected host, including those that participate in the clinically silent liver stage.. This rapid gain in our understanding of the hepatic interaction partners now requires a means to validate and further disentangle parasite–host networks in physiologically relevant liver model systems.. Here, we outline seminal work that contributed to our present knowledge on the intrahepatic Plasmodium host factors, followed by a discussion of surrogate models of mammalian livers or hepatocytes.



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Number of present miRNAs at different stages (day 0, day 12, day 19 and day 26) during cardiomyocyte specific differentiation and <t> maturation. </t>
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Image Search Results


Number of present miRNAs at different stages (day 0, day 12, day 19 and day 26) during cardiomyocyte specific differentiation and  maturation.

Journal: PLoS ONE

Article Title: MicroRNA Profiling during Cardiomyocyte-Specific Differentiation of Murine Embryonic Stem Cells Based on Two Different miRNA Array Platforms

doi: 10.1371/journal.pone.0025809

Figure Lengend Snippet: Number of present miRNAs at different stages (day 0, day 12, day 19 and day 26) during cardiomyocyte specific differentiation and maturation.

Article Snippet: In the present manuscript paper, a transgenic mouse ES cell clone was used to generate uniform Cor.At® cardiomyocytes. miRNAs were profiled for undifferentiated transgenic ES cells (day 0) and at time points day 12, day 19 and day 26 during cardiomyocyte-specific differentiation and maturation using 2 high throughput microarray platforms provided from Affymetrix and Febit.

Techniques:

The number of up/down regulated miRNAs at different maturation stages (day 12, day 19 and day 26) compared to undifferentiated ES cells were denoted with arrows up/down.

Journal: PLoS ONE

Article Title: MicroRNA Profiling during Cardiomyocyte-Specific Differentiation of Murine Embryonic Stem Cells Based on Two Different miRNA Array Platforms

doi: 10.1371/journal.pone.0025809

Figure Lengend Snippet: The number of up/down regulated miRNAs at different maturation stages (day 12, day 19 and day 26) compared to undifferentiated ES cells were denoted with arrows up/down.

Article Snippet: In the present manuscript paper, a transgenic mouse ES cell clone was used to generate uniform Cor.At® cardiomyocytes. miRNAs were profiled for undifferentiated transgenic ES cells (day 0) and at time points day 12, day 19 and day 26 during cardiomyocyte-specific differentiation and maturation using 2 high throughput microarray platforms provided from Affymetrix and Febit.

Techniques: