Underlying data for figures – Part 1: standard diet
Data supporting “The KCNJ11-E23K gene variant reduces glucose tolerance and accelerates diet-induced diabetes progression in mice by impairing glucose-induced insulin secretion”.Underlying data for figures – Part 1: standard diet.Figure 1B – Data on the electrophysiological effect of the Kcnj11-K23...
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creator | Sachse, Gregor Haythorne, Elizabeth Hill, Thomas Proks, Peter Joynson, Russel Terrón-Expósito, Raúl Bentley, Liz Tucker, Stephen Cox, Roger Ashcroft, Frances M. |
description | Data supporting “The KCNJ11-E23K gene variant reduces glucose tolerance and accelerates diet-induced diabetes progression in mice by impairing glucose-induced insulin secretion”.Underlying data for figures – Part 1: standard diet.Figure 1B – Data on the electrophysiological effect of the Kcnj11-K23 allele in isolated beta cells.Figure 2A – Data on the body weight of female and male mice carrying two risk alleles (KK) or none (EE), from 3 to 18 weeks of age.Figure 2B – Data on the fed blood glucose concentration of female and male mice carrying two risk alleles (KK) or none (EE), from 7 to 17 weeks of age.Figures 3A,3C & 3D and supplemental figures 2 & 3 – File 1: Glucose data on the IPGTT of female and male mice carrying two risk alleles (KK) or none (EE), at 12 weeks of age. File 2: Data on the plasma insulin concentrations measured during the IPGTT. Mouse numbering is consistent between file 1 and 2.Figure 3B - Glucose data on the IPITT of female and male mice carrying two risk alleles (KK) or none (EE), at 16 weeks of age.Figure 4A – Data on glucose stimulated insulin secretion from pancreatic islets isolated from female and male mice, carrying two risk alleles (KK) or none (EE), at 18 weeks of age.Figure 4B – Data on islet insulin content from pancreatic islets isolated from female and male mice, carrying two risk alleles (KK) or none (EE), at 18 weeks of age. |
doi_str_mv | 10.6084/m9.figshare.12272873 |
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File 2: Data on the plasma insulin concentrations measured during the IPGTT. Mouse numbering is consistent between file 1 and 2.Figure 3B - Glucose data on the IPITT of female and male mice carrying two risk alleles (KK) or none (EE), at 16 weeks of age.Figure 4A – Data on glucose stimulated insulin secretion from pancreatic islets isolated from female and male mice, carrying two risk alleles (KK) or none (EE), at 18 weeks of age.Figure 4B – Data on islet insulin content from pancreatic islets isolated from female and male mice, carrying two risk alleles (KK) or none (EE), at 18 weeks of age.</description><identifier>DOI: 10.6084/m9.figshare.12272873</identifier><language>eng</language><publisher>figshare</publisher><subject>Endocrinology ; FOS: Biological sciences ; FOS: Clinical medicine ; Molecular Biology ; Physiology</subject><creationdate>2020</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0001-5096-4922</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>780,1894</link.rule.ids><linktorsrc>$$Uhttps://commons.datacite.org/doi.org/10.6084/m9.figshare.12272873$$EView_record_in_DataCite.org$$FView_record_in_$$GDataCite.org$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>Sachse, Gregor</creatorcontrib><creatorcontrib>Haythorne, Elizabeth</creatorcontrib><creatorcontrib>Hill, Thomas</creatorcontrib><creatorcontrib>Proks, Peter</creatorcontrib><creatorcontrib>Joynson, Russel</creatorcontrib><creatorcontrib>Terrón-Expósito, Raúl</creatorcontrib><creatorcontrib>Bentley, Liz</creatorcontrib><creatorcontrib>Tucker, Stephen</creatorcontrib><creatorcontrib>Cox, Roger</creatorcontrib><creatorcontrib>Ashcroft, Frances M.</creatorcontrib><title>Underlying data for figures – Part 1: standard diet</title><description>Data supporting “The KCNJ11-E23K gene variant reduces glucose tolerance and accelerates diet-induced diabetes progression in mice by impairing glucose-induced insulin secretion”.Underlying data for figures – Part 1: standard diet.Figure 1B – Data on the electrophysiological effect of the Kcnj11-K23 allele in isolated beta cells.Figure 2A – Data on the body weight of female and male mice carrying two risk alleles (KK) or none (EE), from 3 to 18 weeks of age.Figure 2B – Data on the fed blood glucose concentration of female and male mice carrying two risk alleles (KK) or none (EE), from 7 to 17 weeks of age.Figures 3A,3C & 3D and supplemental figures 2 & 3 – File 1: Glucose data on the IPGTT of female and male mice carrying two risk alleles (KK) or none (EE), at 12 weeks of age. File 2: Data on the plasma insulin concentrations measured during the IPGTT. Mouse numbering is consistent between file 1 and 2.Figure 3B - Glucose data on the IPITT of female and male mice carrying two risk alleles (KK) or none (EE), at 16 weeks of age.Figure 4A – Data on glucose stimulated insulin secretion from pancreatic islets isolated from female and male mice, carrying two risk alleles (KK) or none (EE), at 18 weeks of age.Figure 4B – Data on islet insulin content from pancreatic islets isolated from female and male mice, carrying two risk alleles (KK) or none (EE), at 18 weeks of age.</description><subject>Endocrinology</subject><subject>FOS: Biological sciences</subject><subject>FOS: Clinical medicine</subject><subject>Molecular Biology</subject><subject>Physiology</subject><fulltext>true</fulltext><rsrctype>dataset</rsrctype><creationdate>2020</creationdate><recordtype>dataset</recordtype><sourceid>PQ8</sourceid><recordid>eNo1zz1OAzEQBWA3FChwAwpfYBeP7fXO0KGIPykSKUJtTfwTVsouyGuKdNyBG3ISiCDVa56e3ifEFajWKbTXI7V52M2vXFILWvcae3MuupcpprI_DNNORq4s81uRv72Pkmb5_fkl11yqhBs5V54ilyjjkOqFOMu8n9Plfy7E5v5us3xsVs8PT8vbVRMJTBMtMSjFyaFF2yExKoDUh5g12BAMBdwSse4CO2tQk8HoMGXoto50Mgth_2aPz8JQk38vw8jl4EH5I8qP5E8of0KZH2QsR8Y</recordid><startdate>20200508</startdate><enddate>20200508</enddate><creator>Sachse, Gregor</creator><creator>Haythorne, Elizabeth</creator><creator>Hill, Thomas</creator><creator>Proks, Peter</creator><creator>Joynson, Russel</creator><creator>Terrón-Expósito, Raúl</creator><creator>Bentley, Liz</creator><creator>Tucker, Stephen</creator><creator>Cox, Roger</creator><creator>Ashcroft, Frances M.</creator><general>figshare</general><scope>DYCCY</scope><scope>PQ8</scope><orcidid>https://orcid.org/0000-0001-5096-4922</orcidid></search><sort><creationdate>20200508</creationdate><title>Underlying data for figures – Part 1: standard diet</title><author>Sachse, Gregor ; Haythorne, Elizabeth ; Hill, Thomas ; Proks, Peter ; Joynson, Russel ; Terrón-Expósito, Raúl ; Bentley, Liz ; Tucker, Stephen ; Cox, Roger ; Ashcroft, Frances M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-d913-d49a100ae68484589a8011e7cdf214cc39c8b99a25ca64382938d68ef15b692e3</frbrgroupid><rsrctype>datasets</rsrctype><prefilter>datasets</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Endocrinology</topic><topic>FOS: Biological sciences</topic><topic>FOS: Clinical medicine</topic><topic>Molecular Biology</topic><topic>Physiology</topic><toplevel>online_resources</toplevel><creatorcontrib>Sachse, Gregor</creatorcontrib><creatorcontrib>Haythorne, Elizabeth</creatorcontrib><creatorcontrib>Hill, Thomas</creatorcontrib><creatorcontrib>Proks, Peter</creatorcontrib><creatorcontrib>Joynson, Russel</creatorcontrib><creatorcontrib>Terrón-Expósito, Raúl</creatorcontrib><creatorcontrib>Bentley, Liz</creatorcontrib><creatorcontrib>Tucker, Stephen</creatorcontrib><creatorcontrib>Cox, Roger</creatorcontrib><creatorcontrib>Ashcroft, Frances M.</creatorcontrib><collection>DataCite (Open Access)</collection><collection>DataCite</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Sachse, Gregor</au><au>Haythorne, Elizabeth</au><au>Hill, Thomas</au><au>Proks, Peter</au><au>Joynson, Russel</au><au>Terrón-Expósito, Raúl</au><au>Bentley, Liz</au><au>Tucker, Stephen</au><au>Cox, Roger</au><au>Ashcroft, Frances M.</au><format>book</format><genre>unknown</genre><ristype>DATA</ristype><title>Underlying data for figures – Part 1: standard diet</title><date>2020-05-08</date><risdate>2020</risdate><abstract>Data supporting “The KCNJ11-E23K gene variant reduces glucose tolerance and accelerates diet-induced diabetes progression in mice by impairing glucose-induced insulin secretion”.Underlying data for figures – Part 1: standard diet.Figure 1B – Data on the electrophysiological effect of the Kcnj11-K23 allele in isolated beta cells.Figure 2A – Data on the body weight of female and male mice carrying two risk alleles (KK) or none (EE), from 3 to 18 weeks of age.Figure 2B – Data on the fed blood glucose concentration of female and male mice carrying two risk alleles (KK) or none (EE), from 7 to 17 weeks of age.Figures 3A,3C & 3D and supplemental figures 2 & 3 – File 1: Glucose data on the IPGTT of female and male mice carrying two risk alleles (KK) or none (EE), at 12 weeks of age. File 2: Data on the plasma insulin concentrations measured during the IPGTT. Mouse numbering is consistent between file 1 and 2.Figure 3B - Glucose data on the IPITT of female and male mice carrying two risk alleles (KK) or none (EE), at 16 weeks of age.Figure 4A – Data on glucose stimulated insulin secretion from pancreatic islets isolated from female and male mice, carrying two risk alleles (KK) or none (EE), at 18 weeks of age.Figure 4B – Data on islet insulin content from pancreatic islets isolated from female and male mice, carrying two risk alleles (KK) or none (EE), at 18 weeks of age.</abstract><pub>figshare</pub><doi>10.6084/m9.figshare.12272873</doi><orcidid>https://orcid.org/0000-0001-5096-4922</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Endocrinology FOS: Biological sciences FOS: Clinical medicine Molecular Biology Physiology |
title | Underlying data for figures – Part 1: standard diet |
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