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Data on the mRNA expression by in situ hybridization of Wnt signaling pathway members in the mouse uterus

Wnt signaling plays an important role in uterine organogenesis and oncogenesis. Our mRNA expression data documents the expression of various Wnt pathway members during the key stages of uterine epithelial gland development. Our data illustrates the expression of Wnt signaling inhibitors (Axin2, Sfrp...

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Autores principales: Goad, Jyoti, Ko, Yi-An, Syed, Shafiq M., Crossingham, Yazmin J., Tanwar, Pradeep S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5393313/
https://www.ncbi.nlm.nih.gov/pubmed/28443299
http://dx.doi.org/10.1016/j.dib.2017.03.047
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author Goad, Jyoti
Ko, Yi-An
Syed, Shafiq M.
Crossingham, Yazmin J.
Tanwar, Pradeep S.
author_facet Goad, Jyoti
Ko, Yi-An
Syed, Shafiq M.
Crossingham, Yazmin J.
Tanwar, Pradeep S.
author_sort Goad, Jyoti
collection PubMed
description Wnt signaling plays an important role in uterine organogenesis and oncogenesis. Our mRNA expression data documents the expression of various Wnt pathway members during the key stages of uterine epithelial gland development. Our data illustrates the expression of Wnt signaling inhibitors (Axin2, Sfrp2, Sfrp4, Dkk1 and Dkk3) in mice uteri at postnatal day 6 (PND 6) and day 15 (PND 15). They also describe the expression pattern of the Wnt ligands (Wnt1, Wnt2, Wnt2b, Wnt3, Wnt3a, Wnt5b, Wnt7b, Wnt8a, Wnt8b, Wnt9a, Wnt9b, Wnt10a and Wnt10b) in mice uteri with or without progesterone treatment. Detailed interpretation and discussion of these data is presented in the research article entitled “Differential Wnt signaling activity limits epithelial gland development to the anti-mesometrial side of the mouse uterus” [1].
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spelling pubmed-53933132017-04-25 Data on the mRNA expression by in situ hybridization of Wnt signaling pathway members in the mouse uterus Goad, Jyoti Ko, Yi-An Syed, Shafiq M. Crossingham, Yazmin J. Tanwar, Pradeep S. Data Brief Data Article Wnt signaling plays an important role in uterine organogenesis and oncogenesis. Our mRNA expression data documents the expression of various Wnt pathway members during the key stages of uterine epithelial gland development. Our data illustrates the expression of Wnt signaling inhibitors (Axin2, Sfrp2, Sfrp4, Dkk1 and Dkk3) in mice uteri at postnatal day 6 (PND 6) and day 15 (PND 15). They also describe the expression pattern of the Wnt ligands (Wnt1, Wnt2, Wnt2b, Wnt3, Wnt3a, Wnt5b, Wnt7b, Wnt8a, Wnt8b, Wnt9a, Wnt9b, Wnt10a and Wnt10b) in mice uteri with or without progesterone treatment. Detailed interpretation and discussion of these data is presented in the research article entitled “Differential Wnt signaling activity limits epithelial gland development to the anti-mesometrial side of the mouse uterus” [1]. Elsevier 2017-04-08 /pmc/articles/PMC5393313/ /pubmed/28443299 http://dx.doi.org/10.1016/j.dib.2017.03.047 Text en © 2017 The Authors 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
Goad, Jyoti
Ko, Yi-An
Syed, Shafiq M.
Crossingham, Yazmin J.
Tanwar, Pradeep S.
Data on the mRNA expression by in situ hybridization of Wnt signaling pathway members in the mouse uterus
title Data on the mRNA expression by in situ hybridization of Wnt signaling pathway members in the mouse uterus
title_full Data on the mRNA expression by in situ hybridization of Wnt signaling pathway members in the mouse uterus
title_fullStr Data on the mRNA expression by in situ hybridization of Wnt signaling pathway members in the mouse uterus
title_full_unstemmed Data on the mRNA expression by in situ hybridization of Wnt signaling pathway members in the mouse uterus
title_short Data on the mRNA expression by in situ hybridization of Wnt signaling pathway members in the mouse uterus
title_sort data on the mrna expression by in situ hybridization of wnt signaling pathway members in the mouse uterus
topic Data Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5393313/
https://www.ncbi.nlm.nih.gov/pubmed/28443299
http://dx.doi.org/10.1016/j.dib.2017.03.047
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