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The EMBO Journal<p>EMBO Journal Issue 4/23:<br>- Commentary on <a href="https://sciencemastodon.com/tags/creativity" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>creativity</span></a> needs in research<br>- <a href="https://sciencemastodon.com/tags/Degron" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>Degron</span></a> recognition in orphan complex subunits by CLR4-DCAF12 E3 <a href="https://sciencemastodon.com/tags/ubiquitin" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>ubiquitin</span></a> <a href="https://sciencemastodon.com/tags/ligase" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>ligase</span></a><br>- <a href="https://sciencemastodon.com/tags/Plasmamembrane" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>Plasmamembrane</span></a> topography of <a href="https://sciencemastodon.com/tags/IgM" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>IgM</span></a> <a href="https://sciencemastodon.com/tags/Bcell" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>Bcell</span></a> receptors<br>- <a href="https://sciencemastodon.com/tags/YAP" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>YAP</span></a> roles and regulation in <a href="https://sciencemastodon.com/tags/tumorigenesis" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>tumorigenesis</span></a><br>- <a href="https://sciencemastodon.com/tags/Brassinosteroid" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>Brassinosteroid</span></a> interplay with <a href="https://sciencemastodon.com/tags/katanin" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>katanin</span></a> <a href="https://sciencemastodon.com/tags/microtubule" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>microtubule</span></a> severing</p><p>Cover by Satarupa Bhaduri, Analine Aguayo, Sonya Neal et al<br><a href="https://www.embopress.org/toc/14602075/2023/42/4" rel="nofollow noopener" target="_blank"><span class="invisible">https://www.</span><span class="ellipsis">embopress.org/toc/14602075/202</span><span class="invisible">3/42/4</span></a></p>
Thiago Carvalho<p><a href="https://qoto.org/tags/Telomeres" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>Telomeres</span></a> <a href="https://qoto.org/tags/Telomerase" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>Telomerase</span></a> <a href="https://qoto.org/tags/tumorigenesis" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>tumorigenesis</span></a> <a href="https://qoto.org/tags/Preprint" class="mention hashtag" rel="nofollow noopener" target="_blank">#<span>Preprint</span></a> from Charles Kinzig, Titia de Lange et al</p><p>"Here, we aimed to determine whether telomerase can add telomeric DNA to DSBs in human cells and how this process is regulated. The data indicate that telomerase can create a functional neotelomere at a Cas9-induced DSB that bears the TS sequence at one 3′ end. The frequency of neotelomere formation is increased upon overexpression of telomerase, suggesting that the low level of telomerase in most human cells minimizes these deleterious events. In addition, neotelomere formation is inhibited by ATR signaling at resected DSBs. We discuss these findings in the context of genome instability during tumorigenesis, where neotelomere formation by telomerase might end BFB cycles as originally proposed by McClintock."</p><p><a href="https://www.biorxiv.org/content/10.1101/2022.10.31.514589v1" rel="nofollow noopener" target="_blank"><span class="invisible">https://www.</span><span class="ellipsis">biorxiv.org/content/10.1101/20</span><span class="invisible">22.10.31.514589v1</span></a></p>