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		<id>http://istoriya.soippo.edu.ua/index.php?action=history&amp;feed=atom&amp;title=What_Regulates_Enzyme_Activity_In_Metabolic_Pathways</id>
		<title>What Regulates Enzyme Activity In Metabolic Pathways - Історія редагувань</title>
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		<updated>2026-04-11T04:53:19Z</updated>
		<subtitle>Історія редагувань цієї сторінки в вікі</subtitle>
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		<id>http://istoriya.soippo.edu.ua/index.php?title=What_Regulates_Enzyme_Activity_In_Metabolic_Pathways&amp;diff=185300&amp;oldid=prev</id>
		<title>Bridge64water в 23:42, 5 червня 2017</title>
		<link rel="alternate" type="text/html" href="http://istoriya.soippo.edu.ua/index.php?title=What_Regulates_Enzyme_Activity_In_Metabolic_Pathways&amp;diff=185300&amp;oldid=prev"/>
				<updated>2017-06-05T23:42:52Z</updated>
		
		<summary type="html">&lt;p&gt;&lt;/p&gt;
&lt;table class='diff diff-contentalign-left'&gt;
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				&lt;td colspan='2' style=&quot;background-color: white; color:black; text-align: center;&quot;&gt;← Попередня версія&lt;/td&gt;
				&lt;td colspan='2' style=&quot;background-color: white; color:black; text-align: center;&quot;&gt;Версія за 23:42, 5 червня 2017&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Рядок 1:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Рядок 1:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;fact &lt;/del&gt;that stathmin level has an&amp;#160; independent prognostic &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;worth &lt;/del&gt;in sufferers receiving paclitaxel for metastatic illness, not present in &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;sufferers &lt;/del&gt;who do 	 not, in survival analyses, supports the likelihood that the amount of stathmin level may act not &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;only &lt;/del&gt;as a prognostic marker but also as a predictive marker for response to paclitaxel &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;treatment &lt;/del&gt;in endometrial carcinomas. &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;In contrast &lt;/del&gt;to preceding research looking at stathmin as a &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;potential &lt;/del&gt;predictive marker, predominantly in in vitro breast &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;[http://www.redditbookmark.in/login.php?return=/submit.php Title Loaded From File] &lt;/del&gt;cancer studies, within this study we were &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;able &lt;/del&gt;to test and confirm the association in clinical samples from &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;individuals &lt;/del&gt;treated &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;using &lt;/del&gt;the drug of interest; &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;using &lt;/del&gt;data from a well-annotated prospectively collected patient series. Each the preclinical and clinical testing &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;help &lt;/del&gt;that stathmin level influences sensitivity to paclitaxel. We &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;have &lt;/del&gt;explored and excluded that this &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;effect &lt;/del&gt;is often generalized to other chemotherapeutic agents &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;like &lt;/del&gt;carboplatin, also often &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;utilized &lt;/del&gt;in endometrial cancer. Reporting suggestions for tumor marker prognostic studies recommendations have been &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;developed &lt;/del&gt;with the aim to improve the methodological high quality and reporting transparency in such research. The current study has been performed in accordance to these &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;recommendations &lt;/del&gt;to enhance the &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;good &lt;/del&gt;quality and basic validity of its results. Taxanes, &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;originally &lt;/del&gt;isolated in the bark &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;on the &lt;/del&gt;yew tree, belong &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;for &lt;/del&gt;the &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;family &lt;/del&gt;of anti-microtubule chemotherapeutic agents, with paclitaxel as their prototype. &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;Simply place&lt;/del&gt;, taxanes bind to b tubulin, causing microtubules to resist depolymerization, inhibiting cell cycle progression and advertising mitotic arrest and cell death. Carboplatin, in contrast, is one of the platinum based agents, interacting with DNA and interfering with DNA repair. As stathmin is &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;often &lt;/del&gt;a &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;important &lt;/del&gt;regulator of microtubule dynamics, taken into consideration the mode of action &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;with the &lt;/del&gt;drugs, the good &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;effect &lt;/del&gt;of stathmin knock-down on paclitaxel response &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;and also &lt;/del&gt;the absence of it to carboplatin sensitivity, &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;is &lt;/del&gt;also biologically plausible. We show a greater proportion of &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;high &lt;/del&gt;stathmin level in metastatic compared with &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;primary &lt;/del&gt;lesions. Discrepancy in stathmin status was noted &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;in &lt;/del&gt;a quarter of paired samples, paralleling findings in e.g. breast cancer &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;exactly &lt;/del&gt;where discrepancies &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;between &lt;/del&gt;primary and metastatic lesions are shown in 1455% and 040% for hormone receptors and HER2 respectively. In endometrial cancer, &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;couple of &lt;/del&gt;studies &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;discuss differences &lt;/del&gt;in marker status amongst primary and metastatic lesions. Intratumoral heterogeneity is &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;properly &lt;/del&gt;described in cancer &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;and also &lt;/del&gt;a &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;possible &lt;/del&gt;confounding &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;factor &lt;/del&gt;in &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;a lot of &lt;/del&gt;studies, irrespective of &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;utilizing &lt;/del&gt;fulltissue slides or TMA. Inter-observer variation is unlikely to be the sole explanation for these described &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;variations&lt;/del&gt;. Also, a &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;recent &lt;/del&gt;study assessing mutation status, a approach considered less subjective than immunohistochemical scoring, in &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;a number of &lt;/del&gt;metastatic lesions from one particular patient with renal cell carcinoma, &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;support &lt;/del&gt;that detected biomarker adjustments from &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;key &lt;/del&gt;to metastatic lesions are actual and &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;may &lt;/del&gt;be &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;associated &lt;/del&gt;to and relevant for tumor progression. The adjustments in biomarker status from &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;main &lt;/del&gt;to metastatic lesions &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;support &lt;/del&gt;the &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;require &lt;/del&gt;for repeated biopsies in metastatic lesions, to &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;greater &lt;/del&gt;relate therapy response to &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;possible &lt;/del&gt;predictive biomarkers but in addition to only &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;offer you &lt;/del&gt;therapies with &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;probably constructive &lt;/del&gt;impact when predictive biomarkers are &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;available&lt;/del&gt;. For breast cancer, The American society of clinical oncology advised in 2007 already that for hormone receptor status, testing &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;needs &lt;/del&gt;to be &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;thought of &lt;/del&gt;to&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;color:black; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;reality &lt;/ins&gt;that stathmin level has an&amp;#160; independent prognostic &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;value &lt;/ins&gt;in sufferers receiving paclitaxel for metastatic illness, not present in &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;individuals &lt;/ins&gt;who do 	 not, in survival analyses, supports the likelihood that the amount of stathmin level may &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;perhaps &lt;/ins&gt;act not &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;simply &lt;/ins&gt;as a prognostic marker but also as a predictive marker for response to paclitaxel &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;therapy &lt;/ins&gt;in endometrial carcinomas. &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;As opposed &lt;/ins&gt;to preceding research looking at stathmin as a &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;possible &lt;/ins&gt;predictive marker, predominantly in in vitro breast cancer studies, within this study we were &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;in a position &lt;/ins&gt;to test and confirm the association in clinical samples from &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;sufferers &lt;/ins&gt;treated &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;with &lt;/ins&gt;the drug of interest; &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;utilizing &lt;/ins&gt;data from a well-annotated prospectively collected patient series. Each the preclinical and clinical testing &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;assistance &lt;/ins&gt;that stathmin level influences sensitivity to paclitaxel. We&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;'ve &lt;/ins&gt;explored and excluded that this &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;[http://www.medchemexpress.com/MK-0773.html PF05314882] impact &lt;/ins&gt;is often generalized to other chemotherapeutic agents &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;including &lt;/ins&gt;carboplatin, also often &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;utilised &lt;/ins&gt;in endometrial cancer. Reporting suggestions for tumor marker prognostic studies recommendations have &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;already &lt;/ins&gt;been &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;created &lt;/ins&gt;with &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;all &lt;/ins&gt;the aim to improve the methodological high&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;-&lt;/ins&gt;quality and reporting transparency in such research. The current study has been performed in accordance to these &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;guidelines &lt;/ins&gt;to enhance the &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;top &lt;/ins&gt;quality and basic validity of its &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;final &lt;/ins&gt;results. Taxanes, &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;initially &lt;/ins&gt;isolated in the bark &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;of your &lt;/ins&gt;yew tree, belong &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;towards &lt;/ins&gt;the &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;loved ones &lt;/ins&gt;of anti-microtubule chemotherapeutic agents, with paclitaxel as their prototype. &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;Merely put&lt;/ins&gt;, taxanes bind to b tubulin, causing microtubules to resist depolymerization, inhibiting cell cycle progression and advertising mitotic arrest and cell death. Carboplatin, in contrast, is one of the platinum based agents, interacting with DNA and interfering with DNA repair. As stathmin is &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;usually &lt;/ins&gt;a &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;crucial &lt;/ins&gt;regulator of microtubule dynamics, taken into consideration the mode of action &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;of your &lt;/ins&gt;drugs, the good &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;impact &lt;/ins&gt;of stathmin knock-down on paclitaxel response &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;plus &lt;/ins&gt;the absence of it to carboplatin sensitivity, &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;can &lt;/ins&gt;also &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;be &lt;/ins&gt;biologically plausible. We show a greater proportion of &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;higher &lt;/ins&gt;stathmin level in metastatic compared with &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;key &lt;/ins&gt;lesions. Discrepancy in stathmin status was noted &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;within &lt;/ins&gt;a quarter of paired samples, paralleling findings in e.g. breast cancer where discrepancies &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;involving &lt;/ins&gt;primary and metastatic lesions are shown in 1455% and 040% for hormone receptors and HER2 respectively. In endometrial cancer, &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;few &lt;/ins&gt;studies &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;talk about variations &lt;/ins&gt;in marker status amongst primary and metastatic lesions. Intratumoral heterogeneity is &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;well &lt;/ins&gt;described in cancer &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;as well as &lt;/ins&gt;a &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;prospective &lt;/ins&gt;confounding &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;aspect &lt;/ins&gt;in &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;many &lt;/ins&gt;studies, irrespective of &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;applying &lt;/ins&gt;fulltissue slides or TMA. Inter-observer variation is unlikely to be the sole explanation for these described &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;differences&lt;/ins&gt;. Also, a &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;current &lt;/ins&gt;study assessing mutation status, a approach considered &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;significantly &lt;/ins&gt;less subjective than immunohistochemical scoring, in &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;various &lt;/ins&gt;metastatic lesions from one particular patient with renal cell carcinoma, &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;help &lt;/ins&gt;that detected biomarker adjustments from &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;major &lt;/ins&gt;to metastatic lesions are actual and &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;might &lt;/ins&gt;be &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;connected &lt;/ins&gt;to and relevant for tumor progression. The adjustments in biomarker status from &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;key &lt;/ins&gt;to metastatic lesions &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;help &lt;/ins&gt;the &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;have to have &lt;/ins&gt;for repeated biopsies in metastatic lesions, to &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;superior &lt;/ins&gt;relate therapy response to &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;potential &lt;/ins&gt;predictive biomarkers but in addition to only &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;supply &lt;/ins&gt;therapies with &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;likely positive &lt;/ins&gt;impact when predictive biomarkers are &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;accessible&lt;/ins&gt;. For breast cancer, The American society of clinical oncology advised in 2007 already that for hormone receptor status, testing &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;need &lt;/ins&gt;to be &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;considered &lt;/ins&gt;to&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</summary>
		<author><name>Bridge64water</name></author>	</entry>

	<entry>
		<id>http://istoriya.soippo.edu.ua/index.php?title=What_Regulates_Enzyme_Activity_In_Metabolic_Pathways&amp;diff=183674&amp;oldid=prev</id>
		<title>Bridge64water: Створена сторінка: fact that stathmin level has an  independent prognostic worth in sufferers receiving paclitaxel for metastatic illness, not present in sufferers who do 	 not, i...</title>
		<link rel="alternate" type="text/html" href="http://istoriya.soippo.edu.ua/index.php?title=What_Regulates_Enzyme_Activity_In_Metabolic_Pathways&amp;diff=183674&amp;oldid=prev"/>
				<updated>2017-06-02T06:12:17Z</updated>
		
		<summary type="html">&lt;p&gt;Створена сторінка: fact that stathmin level has an  independent prognostic worth in sufferers receiving paclitaxel for metastatic illness, not present in sufferers who do 	 not, i...&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Нова сторінка&lt;/b&gt;&lt;/p&gt;&lt;div&gt;fact that stathmin level has an  independent prognostic worth in sufferers receiving paclitaxel for metastatic illness, not present in sufferers who do 	 not, in survival analyses, supports the likelihood that the amount of stathmin level may act not only as a prognostic marker but also as a predictive marker for response to paclitaxel treatment in endometrial carcinomas. In contrast to preceding research looking at stathmin as a potential predictive marker, predominantly in in vitro breast [http://www.redditbookmark.in/login.php?return=/submit.php Title Loaded From File] cancer studies, within this study we were able to test and confirm the association in clinical samples from individuals treated using the drug of interest; using data from a well-annotated prospectively collected patient series. Each the preclinical and clinical testing help that stathmin level influences sensitivity to paclitaxel. We have explored and excluded that this effect is often generalized to other chemotherapeutic agents like carboplatin, also often utilized in endometrial cancer. Reporting suggestions for tumor marker prognostic studies recommendations have been developed with the aim to improve the methodological high quality and reporting transparency in such research. The current study has been performed in accordance to these recommendations to enhance the good quality and basic validity of its results. Taxanes, originally isolated in the bark on the yew tree, belong for the family of anti-microtubule chemotherapeutic agents, with paclitaxel as their prototype. Simply place, taxanes bind to b tubulin, causing microtubules to resist depolymerization, inhibiting cell cycle progression and advertising mitotic arrest and cell death. Carboplatin, in contrast, is one of the platinum based agents, interacting with DNA and interfering with DNA repair. As stathmin is often a important regulator of microtubule dynamics, taken into consideration the mode of action with the drugs, the good effect of stathmin knock-down on paclitaxel response and also the absence of it to carboplatin sensitivity, is also biologically plausible. We show a greater proportion of high stathmin level in metastatic compared with primary lesions. Discrepancy in stathmin status was noted in a quarter of paired samples, paralleling findings in e.g. breast cancer exactly where discrepancies between primary and metastatic lesions are shown in 1455% and 040% for hormone receptors and HER2 respectively. In endometrial cancer, couple of studies discuss differences in marker status amongst primary and metastatic lesions. Intratumoral heterogeneity is properly described in cancer and also a possible confounding factor in a lot of studies, irrespective of utilizing fulltissue slides or TMA. Inter-observer variation is unlikely to be the sole explanation for these described variations. Also, a recent study assessing mutation status, a approach considered less subjective than immunohistochemical scoring, in a number of metastatic lesions from one particular patient with renal cell carcinoma, support that detected biomarker adjustments from key to metastatic lesions are actual and may be associated to and relevant for tumor progression. The adjustments in biomarker status from main to metastatic lesions support the require for repeated biopsies in metastatic lesions, to greater relate therapy response to possible predictive biomarkers but in addition to only offer you therapies with probably constructive impact when predictive biomarkers are available. For breast cancer, The American society of clinical oncology advised in 2007 already that for hormone receptor status, testing needs to be thought of to&lt;/div&gt;</summary>
		<author><name>Bridge64water</name></author>	</entry>

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