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Data on acylglycerophosphate acyltransferase 4 (AGPAT4) during murine embryogenesis and in embryo-derived cultured primary neurons and glia

Whole mouse embryos at three developmental timepoints, embryonic (E) day E10.5, E14.5, and E18.5, were analyzed for Agpat4 mRNA expression. Primary cortical mouse cultures prepared from E18.5 mouse brains were used for immunohistochemistry. Our data show that Agpat4 is differentially expressed at th...

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Autores principales: Bradley, Ryan M., Mardian, Emily B., Marvyn, Phillip M., Vasefi, Maryam S., Beazely, Michael A., Mielke, John G., Duncan, Robin E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4683321/
https://www.ncbi.nlm.nih.gov/pubmed/26759825
http://dx.doi.org/10.1016/j.dib.2015.11.033
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author Bradley, Ryan M.
Mardian, Emily B.
Marvyn, Phillip M.
Vasefi, Maryam S.
Beazely, Michael A.
Mielke, John G.
Duncan, Robin E.
author_facet Bradley, Ryan M.
Mardian, Emily B.
Marvyn, Phillip M.
Vasefi, Maryam S.
Beazely, Michael A.
Mielke, John G.
Duncan, Robin E.
author_sort Bradley, Ryan M.
collection PubMed
description Whole mouse embryos at three developmental timepoints, embryonic (E) day E10.5, E14.5, and E18.5, were analyzed for Agpat4 mRNA expression. Primary cortical mouse cultures prepared from E18.5 mouse brains were used for immunohistochemistry. Our data show that Agpat4 is differentially expressed at three timepoints in murine embryogenesis and is immunodetectable in both neurons and glial cells derived from the developing mouse brain. This paper contains data related to research concurrently published in Bradley et al. (2015) [1].
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spelling pubmed-46833212016-01-12 Data on acylglycerophosphate acyltransferase 4 (AGPAT4) during murine embryogenesis and in embryo-derived cultured primary neurons and glia Bradley, Ryan M. Mardian, Emily B. Marvyn, Phillip M. Vasefi, Maryam S. Beazely, Michael A. Mielke, John G. Duncan, Robin E. Data Brief Data Article Whole mouse embryos at three developmental timepoints, embryonic (E) day E10.5, E14.5, and E18.5, were analyzed for Agpat4 mRNA expression. Primary cortical mouse cultures prepared from E18.5 mouse brains were used for immunohistochemistry. Our data show that Agpat4 is differentially expressed at three timepoints in murine embryogenesis and is immunodetectable in both neurons and glial cells derived from the developing mouse brain. This paper contains data related to research concurrently published in Bradley et al. (2015) [1]. Elsevier 2015-11-24 /pmc/articles/PMC4683321/ /pubmed/26759825 http://dx.doi.org/10.1016/j.dib.2015.11.033 Text en © 2015 Published by Elsevier Inc. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Data Article
Bradley, Ryan M.
Mardian, Emily B.
Marvyn, Phillip M.
Vasefi, Maryam S.
Beazely, Michael A.
Mielke, John G.
Duncan, Robin E.
Data on acylglycerophosphate acyltransferase 4 (AGPAT4) during murine embryogenesis and in embryo-derived cultured primary neurons and glia
title Data on acylglycerophosphate acyltransferase 4 (AGPAT4) during murine embryogenesis and in embryo-derived cultured primary neurons and glia
title_full Data on acylglycerophosphate acyltransferase 4 (AGPAT4) during murine embryogenesis and in embryo-derived cultured primary neurons and glia
title_fullStr Data on acylglycerophosphate acyltransferase 4 (AGPAT4) during murine embryogenesis and in embryo-derived cultured primary neurons and glia
title_full_unstemmed Data on acylglycerophosphate acyltransferase 4 (AGPAT4) during murine embryogenesis and in embryo-derived cultured primary neurons and glia
title_short Data on acylglycerophosphate acyltransferase 4 (AGPAT4) during murine embryogenesis and in embryo-derived cultured primary neurons and glia
title_sort data on acylglycerophosphate acyltransferase 4 (agpat4) during murine embryogenesis and in embryo-derived cultured primary neurons and glia
topic Data Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4683321/
https://www.ncbi.nlm.nih.gov/pubmed/26759825
http://dx.doi.org/10.1016/j.dib.2015.11.033
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