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10.1016/j.semcdb.2014.02.005 http://scihub22266oqcxt.onion/10.1016/j.semcdb.2014.02.005 C4043860!4043860 !24560784     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=24560784 &cmd=llinks): Failed to open stream: HTTP request failed! 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Transcriptional control of spermatogonial maintenance and differentiation |pdf=|usr=}}{{24560784 }} gab.com Text Transcriptional control of spermatogonial maintenance and differentiation JO: Semin Cell Dev Biol http://www.kidney.de/pget.php?&tw=1&pmid=24560784 #FOAvip Spermatogenesis is a multistep process that generates millions of spermatozoa per day in mammals. A key to this process is the spermatogonial stem cell (SSC), which has the dual property of continually renewing and undergoing differentiation into a spermatogonial progenitor that expands and further differentiates. In this review, we will focus on how these proliferative and early differentiation steps in mammalian male germ cells are controlled by transcription factors. Most of the transcription factors that have so far been identified as promoting SSC self-renewal (BCL6B, BRACHYURY, ETV5, ID4, LHX1, and POU3F1) are upregulated by glial cell line-derived neurotrophic factor (GDNF). Since GDNF is crucial for promoting SSC self-renewal, this suggests that these transcription factors are responsible for coordinating the action of GDNF in SSCs. Other transcription factors that promote SSC self-renewal are expressed independently of GDNF (FOXO1, PLZF, POU5F1, and TAF4B) and thus may act in non-GDNF pathways to promote SSC cell growth or survival. Several transcription factors have been identified that promote spermatogonial differentiation (DMRT1, NGN3, SOHLH1, SOHLH2, SOX3, and STAT3); some of these may influence the decision of an SSC to commit to differentiate while others may promote later spermatogonial differentiation steps. Many of these transcription factors regulate each other and act on common targets, suggesting they integrate to form complex transcriptional networks in self-renewing and differentiating spermatogonia. Twit Text FOAVip Transcriptional control of spermatogonial maintenance and differentiation ????Semin Cell Dev Biol http://www.kidney.de/pget.php?&tw=1&pmid=24560784 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=24560784 #FOAvip English Wikipedia <ref>{{Cite pmid|24560784 }}</ref> Transcriptional control of spermatogonial maintenance and differentiation #MMPMID24560784 Song HW ; Wilkinson MF Semin Cell Dev Biol 2014[Jun]; 30 (ä): 14-26 PMID24560784 show ga Spermatogenesis is a multistep process that generates millions of spermatozoa per day in mammals. A key to this process is the spermatogonial stem cell (SSC), which has the dual property of continually renewing and undergoing differentiation into a spermatogonial progenitor that expands and further differentiates. In this review, we will focus on how these proliferative and early differentiation steps in mammalian male germ cells are controlled by transcription factors. Most of the transcription factors that have so far been identified as promoting SSC self-renewal (BCL6B, BRACHYURY, ETV5, ID4, LHX1, and POU3F1) are upregulated by glial cell line-derived neurotrophic factor (GDNF). Since GDNF is crucial for promoting SSC self-renewal, this suggests that these transcription factors are responsible for coordinating the action of GDNF in SSCs. Other transcription factors that promote SSC self-renewal are expressed independently of GDNF (FOXO1, PLZF, POU5F1, and TAF4B) and thus may act in non-GDNF pathways to promote SSC cell growth or survival. Several transcription factors have been identified that promote spermatogonial differentiation (DMRT1, NGN3, SOHLH1, SOHLH2, SOX3, and STAT3); some of these may influence the decision of an SSC to commit to differentiate while others may promote later spermatogonial differentiation steps. Many of these transcription factors regulate each other and act on common targets, suggesting they integrate to form complex transcriptional networks in self-renewing and differentiating spermatogonia. |*Cell Differentiation [MESH] |Adult Stem Cells/physiology [MESH] |Animals [MESH] |Cell Proliferation [MESH] |Gene Expression Regulation [MESH] |Gene Regulatory Networks [MESH] |Humans [MESH] |Male [MESH] |Spermatogonia/*physiology [MESH] |Transcription Factors/physiology [MESH]Transcriptional control of spermatogonial maintenance and differentiat(epmc).pdf DeepDyve Pubget Overpricing