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		<id>http://istoriya.soippo.edu.ua/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=Quiet47sailor</id>
		<title>HistoryPedia - Внесок користувача [uk]</title>
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		<updated>2026-04-25T19:51:56Z</updated>
		<subtitle>Внесок користувача</subtitle>
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	<entry>
		<id>http://istoriya.soippo.edu.ua/index.php?title=Pkc_Nf-Kb_Pathway&amp;diff=188204</id>
		<title>Pkc Nf-Kb Pathway</title>
		<link rel="alternate" type="text/html" href="http://istoriya.soippo.edu.ua/index.php?title=Pkc_Nf-Kb_Pathway&amp;diff=188204"/>
				<updated>2017-06-12T14:39:24Z</updated>
		
		<summary type="html">&lt;p&gt;Quiet47sailor: Створена сторінка: Author Contributions Conceived and made the experiments: JD DA JR JF. Performed the experiments: EB VB JR JF. Analyzed the data: EB. Contributed reagents/ mater...&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Author Contributions Conceived and made the experiments: JD DA JR JF. Performed the experiments: EB VB JR JF. Analyzed the data: EB. Contributed reagents/ materials/analysis tools: EB VB JR JF. Wrote the paper: EB. Statistical evaluation: EB. Contributed for the conception and design from the operate: EB VB JD DA DC AW JR JF. Acquisition [http://www.ncbi.nlm.nih.gov/pubmed/18297096  18297096 ] and interpretation of data: VB JD DA DC AW JR JF. Drafted the write-up and revised it critically for critical intellectual content: VB JD DA DC AW JR JF. Approved the final version on the manuscript submitted: EB VB JD DA DC AW JR JF. Acknowledgments We would like to thank all investigators in the MONICA Project for their contribution to the compilation, validation and evaluation of your data. We're grateful to the Institut National de la Statistique et des Etudes Economiques plus the three regional overall health centres for their collaboration. References 1. Inzucchi SE, Bergenstal RM, Buse JB, Diamant M, Ferrannini E, et al. Management of hyperglycaemia in sort 2 diabetes: a patient-centered approach. Position statement in the American Diabetes Association and also the European Association for the Study of Diabetes. Diabetologia 55:1577 1596. two. Action to Handle Cardiovascular Risk in Diabetes Study Group, [http://www.medchemexpress.com/CTEP.html 871362-31-1] Gerstein HC, Miller ME, Byington RP, Goff DC Jr, et al. Effects of intensive glucose lowering in kind 2 diabetes. N Engl J Med 358:25452559. three. Kuulasmaa K, Tunstall-Pedoe H, Dobson A, Fortmann S, Sans S, et al. Estimation of contribution of changes in classic threat aspects to trends in coronaryevent prices across the WHO MONICA Project populations. Lancet 355:675 687. 4. Marques-Vidal P, Ruidavets JB, Amouyel P, Ducimetiere P, Arveiler D, et al. �� Alter in cardiovascular danger components in France, 19851997. Eur J Epidemiol 19:2532. five. Centre de recherche en Epidemiologie et Sante des Populations, INSERM Universite Paris Sud Mise en oeuvre du decret nu 9837 autorisant l'acces aux donnees relatives au deces des personnes inscrites au �� ��Repertoire National d'Identification des Personnes Physiques dans le cadre des recherches dans le domaine de la sante. Accessible: http://cesp.vjf. inserm.fr/svcd. Accessed 2013 Dec 30. 6. The fifth report of the Joint National Committee on Detection, Evaluation, and Treatment of High Blood Stress Arch Intern Med 153:154 183. 7. Friedewald WT, Levy RI, Fredrickson DS Estimation of the concentration of low density lipoprotein cholesterol in plasma without use in the preparative ultracentrifuge. Clin Chem 18:499502. eight. The specialist committee on the diagnosis and classification of diabetes mellitus Report of the expert committee around the diagnosis and classification of diabetes mellitus. Diabetes Care 20:11831197. 9. Saurel-Cubizolles MJ, Chastang JF, Menvielle G, Leclerc A, Luce D, EDISC group Social inequalities in mortality by result in among males and females in France. J Epidemiol Community Overall health 63:197202. 10. Cottel D, Dallongeville J, Wagner A, Ruidavets JB, Arveiler D, et al. The North-East-South gradient of coronary heart disease mortality and case fatality rates in France is consistent having a similar gradient in risk issue clusters. Eur J Epidemiol 16:317322. 11. Boussageon R, Bejan-Angoulvant T, Saadatian-Elahi M, Lafont S, Bergeonneau C, et al. Impact of intensive glucose lowering therapy on all result in mortality, cardiovascular death, and microvascu&lt;/div&gt;</summary>
		<author><name>Quiet47sailor</name></author>	</entry>

	<entry>
		<id>http://istoriya.soippo.edu.ua/index.php?title=Metabolic_Enzyme_Reactions&amp;diff=187123</id>
		<title>Metabolic Enzyme Reactions</title>
		<link rel="alternate" type="text/html" href="http://istoriya.soippo.edu.ua/index.php?title=Metabolic_Enzyme_Reactions&amp;diff=187123"/>
				<updated>2017-06-09T08:26:35Z</updated>
		
		<summary type="html">&lt;p&gt;Quiet47sailor: Створена сторінка: minantly cytoplasmic, as reported  in literature. Representative images from immunohistochemistry with weak and robust stathmin staining are shown in Stathmin P...&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;minantly cytoplasmic, as reported  in literature. Representative images from immunohistochemistry with weak and robust stathmin staining are shown in Stathmin Predicts Response in Endometrial Cancer Variable FIGO I/II III/IV Histology Endometrioid Non-endometrioid Histological differentiation1 I/II III Age Below/equal to Above Menopausal status Pre/perimenopausal Postmenopausal Stathmin expression2 Normal Higher expression info missing for 1 patient. information and facts missing for four individuals. doi:ten.1371/journal.pone.0090141.t001 two 1 Paclitaxel n Other therapy n P-value 0.712 five 17 15 41 0.765 13 9 31 25 0.365 6 16 21 34 0.031 15 7 23 33 0.255 three 19 three 53 0.891 15 6 37 16 ical characteristics nevertheless remained similar, except that this subgroup was considerably older. Sufferers with regular stathmin level clearly responded substantially far better to therapy than sufferers with higher stathmin level. Stathmin level didn't predict response to other chemotherapy regimens or therapy modalities. Approaching from a distinctive angle, normally, patients with higher stathmin level showed a reduced disease particular survival, in line with stathmins function as a prognostic biomarker. Even so, inside the subgroup of patients with metastatic disease treated with paclitaxel containing chemotherapy, disease distinct survival was substantially poorer in those individuals with higher compared to typical stathmin. In individuals who received other treatments for metastatic illness, prognosis was unrelated to stathmin level, adjusted for FIGO stage and histological subtype, but not inside the subgroup getting other therapies. Inside the paired primary-metastasis samples, 35% of metastatic lesions showed high stathmin level. A discordance of 26% amongst metastatic lesions and their primaries was observed. In 16% there was a adjust to higher level in metastases and in 10% to regular level. Discussion Discordant biomarker status in principal and metastatic lesions The percentage of individuals with higher stathmin level was drastically higher in metastases when compared with main lesions with pathologic levels noted in 18% on the latter in comparison to 37% in metastatic samples . Stathmin Predicts Response in Endometrial Cancer guishing it from other mechanisms of cell death, like necrosis. The enhanced apoptotic physique formation noted by microscopy in the stathmin knock-down cell lines fits with enhanced [http://www.medchemexpress.com/av-412.html MedChemExpress AV412] apoptosis. In our prospectively collected, retrospectively analyzed patient series, we also demonstrated a striking distinction in response to paclitaxel containing chemotherapy comparing patients with regular to these with high stathmin level, also when correcting for one of the most critical clinicopathological prognostic variables. Even when exploring such a large clinical series with endometrial cancer individuals as ours, collected over more than ten years, with sufficient follow-up and RECIST compliant documentation of response, eventually only a smaller sized number of sufferers  had been treated with the remedy of interest, underlining the difficulty of collecting series with adequate patient numbers for specific marker research; but at the identical time the significance to exploit these big prospectively collected population primarily based series for predictive biomarkers recommended in preclinical studies, and discover potential clinical validity prior to clinical trial stage. The statistically important correlation involving high stathmin level and poor paclitaxel response in accordance with RECIST criteria in clinical samples and the&lt;/div&gt;</summary>
		<author><name>Quiet47sailor</name></author>	</entry>

	<entry>
		<id>http://istoriya.soippo.edu.ua/index.php?title=Metabolic_Yeast_Enzyme_Dietary_Beauty_Supplements&amp;diff=187114</id>
		<title>Metabolic Yeast Enzyme Dietary Beauty Supplements</title>
		<link rel="alternate" type="text/html" href="http://istoriya.soippo.edu.ua/index.php?title=Metabolic_Yeast_Enzyme_Dietary_Beauty_Supplements&amp;diff=187114"/>
				<updated>2017-06-09T08:10:31Z</updated>
		
		<summary type="html">&lt;p&gt;Quiet47sailor: Створена сторінка: minantly cytoplasmic, as reported  in literature. Representative photographs from immunohistochemistry with weak and powerful stathmin staining are shown in Sta...&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;minantly cytoplasmic, as reported  in literature. Representative photographs from immunohistochemistry with weak and powerful stathmin staining are shown in Stathmin Predicts Response in Endometrial Cancer Variable FIGO I/II III/IV Histology Endometrioid Non-endometrioid Histological differentiation1 I/II III Age Below/equal to Above Menopausal status Pre/perimenopausal Postmenopausal Stathmin expression2 Typical Higher expression details missing for 1 patient. facts missing for 4 sufferers. doi:10.1371/journal.pone.0090141.t001 2 1 Paclitaxel n Other treatment n P-value 0.712 5 17 15 41 0.765 13 9 31 25 0.365 six 16 21 34 0.031 15 7 23 33 0.255 3 19 3 53 0.891 15 six 37 16 ical traits nonetheless remained equivalent, except that this subgroup was substantially older. Sufferers with normal stathmin level clearly responded a lot greater to therapy than sufferers with high stathmin level. Stathmin level didn't predict response to other chemotherapy regimens or therapy modalities. Approaching from a unique angle, generally, individuals with higher stathmin level showed a reduced illness [http://www.medchemexpress.com/TEPP-46.html get ML-265] certain survival, in line with stathmins function as a prognostic biomarker. Nonetheless, within the subgroup of individuals with metastatic disease treated with paclitaxel containing chemotherapy, disease specific survival was drastically poorer in those sufferers with high in comparison to regular stathmin. In patients who received other treatment options for metastatic disease, prognosis was unrelated to stathmin level, adjusted for FIGO stage and histological subtype, but not inside the subgroup getting other therapies. Within the paired primary-metastasis samples, 35% of metastatic lesions showed high stathmin level. A discordance of 26% amongst metastatic lesions and their primaries was observed. In 16% there was a modify to high level in metastases and in 10% to typical level. Discussion Discordant biomarker status in principal and metastatic lesions The percentage of individuals with high stathmin level was significantly larger in metastases in comparison to key lesions with pathologic levels noted in 18% of the latter in comparison to 37% in metastatic samples . Stathmin Predicts Response in Endometrial Cancer guishing it from other mechanisms of cell death, such as necrosis. The elevated apoptotic body formation noted by microscopy in the stathmin knock-down cell lines fits with improved apoptosis. In our prospectively collected, retrospectively analyzed patient series, we also demonstrated a striking difference in response to paclitaxel containing chemotherapy comparing individuals with regular to these with higher stathmin level, also when correcting for the most crucial clinicopathological prognostic variables. Even when exploring such a big clinical series with endometrial cancer patients as ours, collected more than much more than 10 years, with sufficient follow-up and RECIST compliant documentation of response, eventually only a smaller sized number of individuals  had been treated with the remedy of interest, underlining the difficulty of collecting series with adequate patient numbers for certain marker research; but at the same time the value to exploit these massive prospectively collected population primarily based series for predictive biomarkers recommended in preclinical research, and discover possible clinical validity prior to clinical trial stage. The statistically substantial correlation between high stathmin level and poor paclitaxel response based on RECIST criteria in clinical samples along with the&lt;/div&gt;</summary>
		<author><name>Quiet47sailor</name></author>	</entry>

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