Project Grant F30AA033278
- Federal Project Grant Summary The National Institute on Alcohol Abuse and Alcoholism (NIAAA) awarded $249,000 to Indiana University Indianapolis on September 12, 2025, under the Alcohol Research Programs (CFDA 93.273) to support a three-year research project concluding August 31, 2028. The award funds mechanistic research investigating the role of neutrophilic NCF1 (p47phox) in alcohol-associated liver disease (ALD) pathogenesis. The research addresses a critical gap in understanding how...
- Federal Grant Award Summary Loyola University of Chicago's Health Sciences Campus received a $470,066 Project Grant from the National Institute on Alcohol Abuse and Alcoholism (NIAAA) under the Alcohol Research Programs (CFDA 93.273) effective May 1, 2026, with completion targeted for January 31, 2031. The award funds research investigating the molecular mechanisms of ABL (Abelson-like) Kinase 2 in the pathogenesis of alcohol-associated liver disease (ALD). Specifically, the research will...
- Federal Grant Award Summary The National Institute on Alcohol Abuse and Alcoholism (NIAAA) awarded Loyola University of Chicago a Project Grant totaling $248,997.00 under the Alcohol Research Programs (CFDA 93.273) on September 16, 2025, with an ultimate completion date of August 31, 2028. The award supports research investigating RNA splicing regulation, specifically focusing on the poly(C) binding protein 1 (PCBP1) and its role as a molecular mechanism by which chronic alcohol exposure and...
- Federal Grant Award Summary The University of Kansas Medical Center Research Institute, Inc. received a $596,476 Project Grant award from the National Institute on Alcohol Abuse and Alcoholism (NIAAA) under the Alcohol Research Programs (CFDA 93.273), effective May 1, 2026, with completion targeted for February 28, 2031. The project investigates the role of acute phase response (APR) signaling in alcohol-associated liver disease (ALD) resolution following alcohol cessation. The research aims...
- Federal Grant Award Summary The National Institute on Alcohol Abuse and Alcoholism (NIAAA) under the Alcohol Research Programs (CFDA 93.273) awarded a Project Grant of $140,340 to The Regents of the University of Colorado–Denver, with performance from December 1, 2025, through June 30, 2028. The research project investigates the role of the C5 complosome in ethanol-induced immunometabolic dysregulation of Kupffer cells in alcohol-associated liver disease (ALD). Specifically, the research will...
- Federal Grant Award Summary The University of Arizona received a $1,280,415 Project Grant from the National Institute on Alcohol Abuse and Alcoholism (NIAAA) under the Alcohol Research Programs (CFDA 93.273) to investigate the role of hepatocyte Forkhead Box A3 (FOXA3) in the development and progression of alcohol-associated liver disease (ALD). The award, issued September 12, 2025, with a completion date of June 30, 2030, supports research that will employ gain-and-loss-of-function approaches...
- Federal Grant Award Summary The National Institute on Alcohol Abuse and Alcoholism (NIAAA) awarded the University of Texas Health Science Center at Houston a Project Grant of $1,772,733 on September 15, 2025, under the Alcohol Research Programs (CFDA 93.273) to develop a microbial-based platform for assessing organ damage in alcohol use disorders (AUD). The project, scheduled for completion by May 31, 2030, will create a comprehensive, web-based knowledge module integrating microbiota,...
- Federal Project Grant Award Summary Loyola University of Chicago Health Sciences Campus received a $249,000 Project Grant award from the National Institute on Alcohol Abuse and Alcoholism (NIAAA) under the Alcohol Research Programs (CFDA 93.273) on August 21, 2025, with a completion date of July 31, 2028. The award funds research investigating pathological adaptations of glutamatergic AMPA receptor (AMPAR) mechanisms that contribute to alcohol use disorder (AUD) severity, craving, and...
- Federal Grant Award Summary Indiana University Indianapolis received a $138,118 Project Grant from the National Institute on Alcohol Abuse and Alcoholism (NIAAA) under the Alcohol Research Programs (CFDA 93.273) beginning March 9, 2026 and concluding September 8, 2028. The grant funds an integrative multi-omics research project designed to identify cell-type and brain-region specific genetic drivers of Alcohol Use Disorder (AUD). The research employs advanced single-cell sequencing technologies,...
- Federal Grant Award Summary The National Institute on Alcohol Abuse and Alcoholism (NIAAA) awarded The Trustees of Columbia University in the City of New York a Project Grant totaling $2,359,200 under the Alcohol Research Programs (CFDA 93.273) with an award date of July 15, 2026, and completion targeted for June 30, 2030. This research initiative focuses on elucidating the regulation of hepatocyte functions by hepatic stellate cells (HSCs) in the context of steatotic liver diseases (SLD),...
The University of Illinois at Chicago received a $110,228 Project Grant from the National Institute on Alcohol Abuse and Alcoholism (NIAAA) under the Alcohol Research Programs (CFDA 93.273) awarded November 10, 2026, with completion targeted for July 31, 2030. The award funds research to uncover sulfonated high-mobility group box-1 (SO3HMGB1)-mediated mechanisms underlying alcohol-associated liver disease (AALD) progression and recovery through single-nucleus multiomics analysis. The project employs a time-resolved, multi-omic approach to identify transcriptional programs, chromatin states, and cell-cell communication pathways governing AALD across defined disease stages—steatosis, alcoholic hepatitis, and fibrosis—in hepatocytes, hepatic stellate cells, Kupffer cells, and immune populations. The research delivers two primary products: (1) deconvolution of human bulk RNA-sequencing datasets using single-cell RNA-sequencing references to quantify cell-type dynamics across disease stages and establish a human-relevant framework for murine model guidance, and (2) integrated single-nucleus RNA-sequencing and assay for transposase-accessible chromatin sequencing (ATAC-seq) analysis on liver tissues from ethanol-fed mice at control, injury, and recovery stages, with and without SO3HMGB1 treatment. These analyses will elucidate how SO3HMGB1 rewires cell-type-specific gene-regulatory networks and ligand-receptor interactions to suppress inflammation, deactivate fibrogenic cells, and restore hepatocyte function, ultimately advancing therapeutic strategies for AALD treatment.Federal Project Grant Award Summary
Mod # | Description | ReasonForModification | Federal Obligation | Date |
|---|---|---|---|---|
| Not listed | $55.1k | 6/16/26 | ||
| Not listed | $0 | 6/16/26 | ||
| Not listed | $55.1k | 6/16/26 |