Biology is designed for multi-semester biology courses for science majors. It is …
Biology is designed for multi-semester biology courses for science majors. It is grounded on an evolutionary basis and includes exciting features that highlight careers in the biological sciences and everyday applications of the concepts at hand. To meet the needs of today’s instructors and students, some content has been strategically condensed while maintaining the overall scope and coverage of traditional texts for this course. Instructors can customize the book, adapting it to the approach that works best in their classroom. Biology also includes an innovative art program that incorporates critical thinking and clicker questions to help students understand—and apply—key concepts.
By the end of this section, you will be able to:Describe the …
By the end of this section, you will be able to:Describe the overall result in terms of molecules produced in the breakdown of glucose by glycolysisCompare the output of glycolysis in terms of ATP molecules and NADH molecules produced
By the end of this section, you will be able to:Describe the …
By the end of this section, you will be able to:Describe the overall result in terms of molecules produced in the breakdown of glucose by glycolysisCompare the output of glycolysis in terms of ATP molecules and NADH molecules produced
This resource is a video abstract of a research paper created by …
This resource is a video abstract of a research paper created by Research Square on behalf of its authors. It provides a synopsis that's easy to understand, and can be used to introduce the topics it covers to students, researchers, and the general public. The video's transcript is also provided in full, with a portion provided below for preview:
"Neurotrophins activate multiple signalling pathways in neuronal cells by binding to their receptors, regulating processes such as cell survival and differentiation. γ-Enolase exerts neurotrophic effects dependent on its γ1-syntrophin-mediated translocation to the plasma membrane, but the molecule(s) that γ-enolase binds to at the membrane remain unclear. To learn more, researchers recently investigated the plasma membrane binding partners of γ-enolase in differentiated SH-SY5Y cells. In cells with reduced γ1-syntrophin levels (RNAi SNTG1), γ-enolase-Trk receptor binding was decreased due to impairment of either γ-enolase translocation or Trk activity. Treatment with the γ-enolase-mimicking peptide γ-Eno enhanced Trk receptor internalization and endosomal trafficking, as indicated by reduced Trk levels in clathrin-coated vesicles and increased Trk levels in late endosomes. These effects triggered Rap1 activation, which was necessary for γ-Eno’s neurotrophic activity..."
The rest of the transcript, along with a link to the research itself, is available on the resource itself.
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