S
Stacia E. Rodenbusch
Researcher at University of Texas at Austin
Publications - 13
Citations - 1250
Stacia E. Rodenbusch is an academic researcher from University of Texas at Austin. The author has contributed to research in topics: Dendrimer & Undergraduate research. The author has an hindex of 10, co-authored 13 publications receiving 1044 citations. Previous affiliations of Stacia E. Rodenbusch include UPRRP College of Natural Sciences & University of California, Berkeley.
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Journal ArticleDOI
A Systematic Investigation of p -Nitrophenol Reduction by Bimetallic Dendrimer Encapsulated Nanoparticles.
Zachary D. Pozun,Stacia E. Rodenbusch,Emily L. Keller,Kelly Tran,Wenjie Tang,Keith J. Stevenson,Graeme Henkelman +6 more
TL;DR: This work presents a uniform method for synthesizing pure and bimetallic DENs and demonstrates that their catalytic properties are dependent on the adsorbate’s binding energy.
Journal ArticleDOI
Early Engagement in Course-Based Research Increases Graduation Rates and Completion of Science, Engineering, and Mathematics Degrees
TL;DR: This study shows that participation in course-based undergraduate research experiences improves students’ likelihood of graduating with a STEM degree and graduating within 6 years.
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Size-Dependent Hydrogenation of p-Nitrophenol with Pd Nanoparticles Synthesized with Poly(amido)amine Dendrimer Templates
TL;DR: In this article, the effect of size on the catalytic activity of nanoparticles less than 2 nm in diameter was investigated using poly(amido)amine (PAMAM) dendrimer templates and was evaluated as catalysts using the model reduction of para-nitrophenol.
Journal ArticleDOI
Critical conformational changes in the Arp2/3 complex are induced by nucleotide and nucleation promoting factor.
TL;DR: It is demonstrated that nucleotide binding promotes a substantial conformational change in the Arp2/3 complex, with distinct conformations depending on the bound nucleotide.
Journal ArticleDOI
Identification of DSB-1, a protein required for initiation of meiotic recombination in Caenorhabditis elegans, illuminates a crossover assurance checkpoint.
Ericca L. Stamper,Stacia E. Rodenbusch,Simona Rosu,Julie Ahringer,Anne M. Villeneuve,Abby F. Dernburg,Abby F. Dernburg,Abby F. Dernburg +7 more
TL;DR: This work identifies a novel component of the DSB machinery in C. elegans, sheds light on an important pathway that regulates DSB formation for crossover assurance, and proposes a model for crossover assurances that acts through DSB-1 to maintain a D SB-permissive state until all chromosome pairs acquire crossover precursors.