Poster Lightning Round ⚡
| IMPACT Lightning Round
|
POSTER SIZE
POSTER REQUIREMENTS
PRINT & PICKUP ONSITE
For your convenience, there is a FedEx Print center located within a 1-2 minute walk of the EPNEC building if you prefer to order online and pickup your poster onsite.
POSTER LIGHTNING ROUNDThe poster lightning round session will take place on October 28 from 4:15 to 4:45 pm. Five trainees will be selected to present during the Poster Lightning Round. The top presenter will win a $500 award to be presented during the Day 2 award session.
POSTER SESSION & JUDGING
The interactive poster session and reception will take place on October 28 from 5:15 – 7:15 pm. Graduate students who would like to compete for the Promega Poster Award must be present for judging during their assigned time and are expected to have a 3 – 4 minute oral summary of their poster prepared for the judges. The top scored poster and two runners up will be provided $500, $250, and $250 during the Day 2 award session.
Judging A - 5:15 - 6:15 pm | Judging B - 6:15 - 7:15 pm |
Odd numbered posters (P-01, etc.) | Even numbered posters (P-02, etc.) |
![]() ADDC is proud to announce that we will have an ADDC Lightning Round Poster Award at the ADDC 2025 Colloquium. The
top oral presenter will receive a $500 award to be presented during the Day 2 award
session. | ![]() ADDC is equally pleased to announce that Promega has sponsored a Best Poster Award at the ADDC 2025 Colloquium. The top poster presenter will receive a $500 award to be presented during the Day 2 award session. | Judging CriteriaScoring criteria for both awards will be based on:
|
Poster# |
Presenting Author |
Abstract Title |
Category |
P-01 |
Olanrewaju Akande |
Validation of a novel microfluidic device as an early-stage research training tool |
Academic |
P-02 |
Nadia Alamri |
Fusion of extracellular matrix binder motifs to GMCSF for localized cancerimmunotherapy |
Academic |
P-03 |
Soumendranath Bhakat |
Generalizable Protein Dynamics in Kinases: Physics is the key |
Trainee |
P-04 |
Julie Conkright-Fincham |
Adapting Lumit p-ERK assay to high-throughput screening using Novartis Chemogenetic LMW library |
Commercial |
P-05 |
Joseph DeCorte |
GrowTAC: protein-context aware optimization of PROTAC linkers |
Trainee |
P-06 |
Umesh Desai |
A Synthetic, Allosteric Inhibitor of Human Factor XIa for Lung Cancer Associated Thrombosis |
Academic |
P-07 |
Sharanya Duvvuri |
Pharmacological Evaluation of novel HBV RNase H Inhibitors |
Trainee |
P-08 |
Heather Fears |
MegaUni: A Scalable Platform for AI-Powered Compound Screening |
Commercial |
P-09 |
Anthony Ferranti |
Investigating the mGlu7/8 Heterodimer as a Novel Drug Target for Neurodevelopmental Disorders Associated with Hippocampal Dysfunction |
Trainee |
P-10 |
Tomas Friman |
Employing CETSA in Primary Screening for p53 Binders |
Commercial |
P-11 |
Khalid Garman |
Intersectional high-throughput screening uncovers a synergistic drug combination for a rare and lethal skin cancer |
Trainee |
P-12 |
Niki Harris |
Modulation of metabotropic glutamate receptor 7 (mGlu7) as a novel mechanism to correct NMDAR antagonist-induced cognitive impairments: implications for schizophrenia |
Trainee |
P-13 |
Md. Zahid Hossain |
Neuro-Informed Algorithms: Accelerating CNS Drug Discovery with Predictive AI |
Academic |
P-14 |
Meixiang Huang |
Dendrimer-Conjugated Propofol Enables Non-Sedating Neuroinflammation Therapy With >30-Fold Therapeutic Index Gain |
Trainee |
P-15 |
Meixiang Huang |
Next-Generation nSMase2 Inhibitor Blocks Tau Propagation in an Alzheimer’s Model |
Trainee |
P-16 |
Genevieve Hunn |
Investigating dysregulated microRNAs in Rett syndrome that regulate the GRM7 3’UTR |
Trainee |
P-17 |
Wei Li |
Discovery of a potent and highly brain-penetrable anti-mitotic agent as a potential new treatment for breast cancer brain metastasis |
Academic |
P-18 |
Wei Li |
Advancing Drug Discovery Through DNA-Encoded Library Technologies: Innovations, Applications, and Future Directions |
Commercial |
P-19 |
Mengchu Li |
Identification of a Drug-like Negative Allosteric Modulator of the Mu-Opioid Receptor (Mu-NAM) |
Trainee |
P-20 |
Natalia Martinez |
Integrating Machine Learning and High Throughput Screening to identify chemical probe candidates for Aldehyde Dehydrogenases |
Academic |
P-21 |
Marvin Meyers |
Discovery of Potent Therapeutics for Treatment of Cryptosporidiosis |
Academic |
P-22 |
Sorrayut Mongkoltipparat |
Proteomics-Based LC–MRM–MS/MS Platform for Kinetic and Selectivity Profiling of Covalent Inhibitors |
Academic |
P-23 |
Omar Moukha-Chafiq |
Novel Pyrrolopyrimidine Nucleoside Analogs as Anti-Hepatitis B Virus Agents |
Academic |
P-24 |
Harrison Parent |
Investigating Metabotropic Glutamate Receptor 7 as a Drug Target for Cognitive Phenotypes in Neurofibromatosis Type 1 |
Trainee |
P-25 |
Barnali Paul |
Structure guided efficacy modulation to design opioid sparing agents |
Academic |
P-26 |
ARGHYA POLLEY |
Allosteric modulation of mu opioid receptor |
Academic |
P-27 |
Thomas Prisinzano |
Searching for Synthetic Opioid Rescue Agents: Identification of a Potent Opioid Agonist with Reduced Respiratory Depression |
Academic |
P-28 |
Nokomis Ramos-Gonzalez |
Modulating efficacy and functional selectivity of the kappa opioid receptor |
Trainee |
P-29 |
Mark Rutherford |
Development of the first subtype selective AMPA-type glutamate receptor pore blocker to halt glutamate excitotoxicity: Calcium-permeable AMPA receptors in noise-induced hearing loss and ischemic stroke. |
Academic |
P-30 |
Matthew Shaffer |
Early Preclinical CMC Development of SAgA-T1D: A Protein-Polysaccharide Conjugate to Treat Type 1 Diabetes |
Academic |
P-31 |
Yu Su |
Orally Bioavailable GCPII Inhibitor Promotes Remyelination After Peripheral Nerve Injury |
Trainee |
P-32 |
Razia Tajwar |
Truncated variant of Hepatitis B virus polymerase catalyzes cryptic and e RNA-dependent protein priming reactions |
Academic |
P-33 |
Steve Valentino |
Miniaturized Biophysical Screening of Cereblon with Dianthus uHTS and Echo Acoustic Liquid Handling |
Commercial |
P-34 |
Balazs R. Varga |
Structure-guided partial 5-HT2A agonism achieves antinociception with reduced central liabilities |
Trainee |
P-35 |
Sestina Ventresca Wilburn |
Enhancement of cAMP levels by α-MSH, ACTH, and the API from Purified Cortrophin® Gel at Five Melanocortin Receptors |
Trainee |
P-36 |
Holly Walden |
Biological and pharmacological characteristics of a novel HBV ribonuclease H inhibitor class |
Trainee |
P-37 |
Kristen Wang |
Designing antigen-based therapeutics to modulate Type 1 Diabetes-associated autoimmune cell signaling |
Academic |
P-38 |
Emma Webb |
Protease-activated Receptor 4 (PAR4) is an Essential Mediator of Inflammation |
Trainee |
P-39 |
Noah Yocum |
Structure-Guided Optimization of Imidazopyridine Amine Inhibitors of the Epigenetically Dysregulated Nutrient Carrier SLC1A1/EAAT3 for Renal Cell Carcinoma |
Academic |
P-40 |
Puhan Zhao |
Exploiting Molecular Dynamics-Derived 5HT3A Receptor Conformational Ensembles for Structure-Based Virtual Screening |
Trainee |
P-41 |
Bin Zhao |
Fragment-Based NMR Screening to Disrupt the YAP–TEAD Interaction |
Academic |
P-42 |
Haoran Zhu |
Structural Based Discovery on Kappa Opioid Receptor Agonists |
Trainee |
P-43 |
Silviya Zustiak |
Glioblastoma spheroid growth and chemotherapeutic responses in single and dual-stiffness hydrogels |
Academic |
P-44 |
Maaike Everts |
Making Translation Work: TRxA - A Real-World Solution for Academic Research |
Academic |
P-45 |
Christopher Goins |
The Center for Therapeutics Discovery at Cleveland Clinic Research |
Academic |
P-46 |
Charles Hart |
Applications of AI in Early-Stage Drug Discovery and Chemical Biology at UCSF’s Small Molecule Discovery Center |
Academic |
P-47 |
Ma. Xenia Ilagan |
Translating Discovery into Therapeutics: The WashU Center for Drug Discovery |
Academic |
P-48 |
Chafiq Hamdouchi |
Advancing Oncology Innovation through the Indiana University Simon Comprehensive Cancer Center's Cancer Drug Discovery & Development Accelerator (CD3A) |
Academic |
P-49 |
Christopher Moth |
Meiler Lab: Transatlantic computational methods development for Drug Discovery |
Academic |
P-50 |
John Tavis |
Saint Louis University Institute for Drug and Biotherapeutic Innovation |
Academic |
P-51 |
Peter Toogood |
Identification of Selective Pyruvate Dehydrogenase Kinase 1 (PDHK1) Inhibitors by Virtual Screening |
Academic |
P-52 |
Peter Toogood |
Introduction to Michigan Drug Discovery |
Academic |
P-53 |
Henry Valle |
Unlocking New Insights Into Targeting LRRK2 for Parkinson's Disease: Advancing Drug Discovery with the CAS Biofinder Discovery Platform |
Commercial |