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Cristina C. Rohena

Researcher at University of California, San Diego

Publications -  23
Citations -  491

Cristina C. Rohena is an academic researcher from University of California, San Diego. The author has contributed to research in topics: Microtubule & Tubulin. The author has an hindex of 10, co-authored 23 publications receiving 408 citations. Previous affiliations of Cristina C. Rohena include University of Texas at San Antonio & University of Texas Health Science Center at San Antonio.

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Drosophila Ringmaker regulates microtubule stabilization and axonal extension during embryonic development

TL;DR: The characterization of Drosophila Ringmaker (Ringer) is reported, and it is demonstrated that Ringer regulates axonal growth by affecting microtubular organization during CNS development.
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GIV•Kindlin Interaction Is Required for Kindlin-Mediated Integrin Recognition and Activation.

TL;DR: How the GIV•Kindlin-2 complex has a 2-fold impact is elucidate: it allosterically synergizes integrin activation and enables β1-integrins to indirectly access and modulate trimeric GTPases via the complex.
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Biochemical, Biophysical and Cellular Techniques to Study the Guanine Nucleotide Exchange Factor, GIV/Girdin.

TL;DR: This work provides the most up‐to‐date overview of protocols that have generated most of what the authors know today about noncanonical G protein activation by GIV and its relevance in health and disease.
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Biological Characterization of an Improved Pyrrole-Based Colchicine Site Agent Identified through Structure-Based Design.

TL;DR: A refined model of the colchicine site on tubulin was used to design an improved analog of the pyrrole parent compound, JG-03-14, and the optimized compound, NT-7-16, was evaluated in biological assays that confirm that it has potent activities as a new colchichine site microtubule depolymerizer.
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Janus Compounds, 5-Chloro-N4-methyl-N4-aryl-9H-pyrimido[4,5-b]indole-2,4-diamines, Cause Both Microtubule Depolymerizing and Stabilizing Effects

TL;DR: The identification of synthetically tractable, small molecules that elicit microtubule stabilizing effects is a significant finding with the potential to identify new mechanisms of microtubules stabilization.