Grants

16,469 grants found

24 grants worth up to $22.7M match your search

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HVAC CATALOG SUPPLIES

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Jp Simons & Co

Manufacturing Components and Supplies

2028-01-31

Community DevelopmentHealth

Free to search & build · $99 one-time to unlock the application pack · No subscription

HVAC CATALOG SUPPLIES

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JP SIMONS & COMPANY

Manufacturing Components and Supplies-Pneumatic and hydraulic and electric control systems

2028-12-31

Education

Free to search & build · $99 one-time to unlock the application pack · No subscription

HVAC CATALOG SUPPLIES

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Filterbuy Incorporated

Manufacturing Components and Supplies

2028-01-31

general

Free to search & build · $99 one-time to unlock the application pack · No subscription

HVAC PRODUCTS, INSTALLATION, LABOR RELATED SERVICES

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TRANE US INC

Building and Facility Construction and Maintenance Services

2027-08-31

workforceinfrastructure

Free to search & build · $99 one-time to unlock the application pack · No subscription

HYDE PARK TOWN OF BETTER ROADS

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Transportation Agency

HYDE PARK TOWN OF BETTER ROADS

Up to $7K

2027-10-31

infrastructure

Free to search & build · $99 one-time to unlock the application pack · No subscription

Hydrogen & Fuel Cell Technologies Office (HFTO) Funding

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U.S. Department of Energy

Advances hydrogen production, delivery, storage, and fuel cell technologies to enable clean hydrogen as an energy carrier across sectors.

$500K – $15M

2026-09-01

hydrogenfuel cellsclean energy+1

Free to search & build · $99 one-time to unlock the application pack · No subscription

HYDROGEN AND FUEL CELL TECHNOLOGIES RESEARCH, DEVELOPMENT, AND DEMONSTRATIONS

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Golden Field Office

The Fuel Cell Technologies Office (FCTO) is a key component of the Department of Energy s (DOE) Office of Energy Efficiency and Renewable Energy (EERE) portfolio. FCTO aims to provide clean, safe, secure, affordable, and reliable energy from diverse domestic resources, providing the benefits of increased energy security and reduced criteria pollutants and green-house gas emissions by adopting a technology neutral approach towards applied research, development, and demonstration to address both key technical challenges for fuel cells and hydrogen fuels (i.e. hydrogen production, delivery and storage) and institutional barriers such as hydrogen codes and standards. This Funding Opportunity Announcement (FOA) covers a broad spectrum of the FCTO portfolio with 4 Areas of Interest (AOI): AOI 1: Research and development (R&D) for hydrogen fuel technologies AOI 2: Demonstration and deployment for manufacturing technologies and Climate Action Champions AOI 3: R&D within Consortia for fuel cell performance and durability and hydrogen storage materials AOI 4: Cost and performance analyses for hydrogen production and delivery, hydrogen storage, and fuel cells Submission schedules, cost sharing requirements, eligibility information, applicant requirements (including whether or not a Concept Paper is required), etc. vary by AOI. Please be sure to refer to the appropriate AOI document for specific requirements, schedules, eligibility, etc. The full Funding Opportunity Announcement (FOA) is posted on the EERE eXCHANGE website at https://eere-exchange.energy.gov. To apply to this FOA, Applicants must register with and submit application materials through EERE Exchange at https://eere-Exchange.energy.gov, EERE s online application portal.

$200K – $3M

rolling

energyclean energy

Free to search & build · $99 one-time to unlock the application pack · No subscription

Hydrogen Sulfide for the Prevention of Cisplatin-Induced Atherosclerosis

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NHLBI - National Heart Lung and Blood Institute

Project Summary Cisplatin (CDDP) is a widely used chemotherapeutic used to treat various cancers, including testicular, lung, head and neck, and ovarian. CDDP use is associated with long-term cardiovascular morbidity and mortality risk, including acute coronary syndrome (ACS). Patients treated with CDDP-based therapies have demonstrated a higher prevalence of cardiovascular risk factors that contribute to the development of ACS. The induction of oxidative stress and pro-inflammatory signaling are known contributing factors in other pathologies of CDDP- induced toxicity. During atherosclerosis progression, pro-inflammatory activation promotes macrophage foam cell death; expansion of the necrotic core, and deterioration of the fibrous cap, resulting in plaque destabilization and coronary artery thrombosis. Hydrogen sulfide (H2S), a gasotransmitter, has gained therapeutic interest due to its known ability to reduce oxidative stress and inflammation. However, H2S has not been studied for its potential to treat CDDP-induced ACS, thus we will assess its protective effects against CDDP-induced plaque instability in a model of atherosclerosis. Based on my preliminary results, I hypothesize that CDDP-induced ROS and inflammation promote macrophage foam cell necroptosis, which may be attenuated by H2S. Our preliminary data support that CDDP induces macrophage foam cell death, which is attenuated by Nec-1, a necroptosis inhibitor, and GYY4137, an H2S donor. We will first assess the activation of necroptosis in CDDP-treated macrophage foam cells by western blot, ELISA, and siRNA knockdown of necroptotic mediators. Furthermore, we will evaluate the ability of H2S to attenuate CDDP-induced cell death. Second, we hypothesize that CDDP administration increases plaque vulnerability in vivo, which may be attenuated with an orally administered H2S donor, SG1002. To test our hypothesis, we will use Ldlr knockout mice placed on a high-fat diet as a model of atherosclerosis. A repeated low-dose model of CDDP toxicity will be used (weekly i.p. injections, for 4 weeks). We will perform aortic dissections to conduct histological and immunocytochemical analysis to assess plaque burden, necrotic core area, fibrous cap thickness, and macrophage-to-smooth muscle ratio. We will then determine the impact of SG1002 administration on the effects of CDDP on plaque vulnerability using the parameters mentioned previously. Identifying the molecular mechanisms contributing to CDDP-induced foam cell death and plaque instability will provide crucial insights into the link between CDDP-based regimens and ACS in cancer survivors. Furthermore, this proposal will present a novel therapeutic approach to circumvent CDDP-induced ACS, which can result in the clinical presentations of myocardial infarction in cancer survivors.

Up to $46K

2027-09-29

health research

Free to search & build · $99 one-time to unlock the application pack · No subscription

Hydrologic Control, Formative Geometry, and Physical Habitat of Sandbars in the Niobrara River, Nebraska

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National Park Service

Study emergent sandbar dynamics along the Niobrara River from Norden Bridge to the confluence with the Missouri River.

$1 – $86K

rolling

Education

Free to search & build · $99 one-time to unlock the application pack · No subscription

Hydrologic Sciences (HS)

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U.S. National Science Foundation

The Hydrologic Sciences Program is a disciplinary program within the Division of Earth Sciences. Hydrologic science has a distinct focus on continental water processes at all scales, and the program supports research with a primary focus on these processes. The program supports fundamental research about water on and beneath the Earth s surface, as well as relationships of water with material and living components of the environment. A major focus is the study of hydrologic processes (e.g., rainfall and runoff; infiltration and subsurface flow; evaporation and transpiration), as well as fluxes of water (e.g. in soils, aquifers, and streams). Many projects involve the study of hydrologic transport (e.g., of dissolved solutes, sediment), coupling of hydrological processes with other systems (e.g., ecosystem processes, geochemical cycles, food and energy systems, socio-ecological systems), or hydrologic responses to change (e.g., changes in land use, climate, or watershed management). Observational, experimental, theoretical, and modeling approaches are supported.

$30K – $1M

rolling

sciencetechnology

Free to search & build · $99 one-time to unlock the application pack · No subscription

HydroNEXT FOA: Innovative Technologies to Advance Non-Powered Dam and Pumped-Storage Hydropower Deve

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Golden Field Office

The complete Notice of Intent can be viewed on the EERE Exchange website - https://eere-exchange.energy.gov The purpose of this notice is to inform potential applicants that EERE intends to issue DE-FOA-0001455 HydroNEXT FOA: Innovative Technologies to Advance Non-Powered Dam and Pumped-Storage Hydropower Development." The overall objective of this FOA is to further the development of non-powered dams (NPD) and pumped storage hydropower (PSH) resources by reducing capital costs and deployment timelines. These objectives will be achieved by funding projects in two topic areas. Projects awarded under Topic Area 1 will develop low-head, modular, and standard turbine/generation technologies for NPD applications that can reduce civil works activities and can operate efficiently over a range of flows. Civil works include the infrastructure of a hydropower project, such as dams, conduits, powerhouses, tunnels, and penstocks. Under Topic Area 2, projects awarded will demonstrate the concept feasibility of innovative closed-loop PSH systems that can reduce development costs and timelines by applying concepts of modularity and creatively producing head differentials (e.g. pressurizing water using compressed air or weights). This is a Notice of Intent (NOI) only. EERE may issue a FOA as described, may issue a FOA that is significantly different than the FOA described, or EERE may not issue a FOA at all. EERE will not respond to questions concerning this Notice. Once the FOA has been released, EERE will provide an avenue for potential Applicants to submit questions.

$300K – $1.5M

rolling

energyclean energy

Free to search & build · $99 one-time to unlock the application pack · No subscription

Hypersensitivity Pneumonitis - Early Identification and Mechanisms of Disease (R01)

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National Institutes of Health

-Purpose. To address the importance of continued research about forms of Hypersensitivity Pneumonitis Lung Diseases, especially the early recognition of disease and a better understanding of immune mechanisms involved in the cause and pathogenesis. -Mechanism of Support. This FOA will utilize the R01 mechanism. This R01 mechanism will support different types of projects including pilot and feasibility studies; small, self-contained research projects; and development of new research technology. -Eligible Institutions/Organizations. Public/State Controlled Institution of Higher Education; Private Institution of Higher Education; Nonprofit with 501(c)(3) IRS Status (Other than Institution of Higher Education); Nonprofit without 501(c)(3) IRS Status (Other than Institution of Higher Education); Small Business; For-Profit Organization (Other than Small Business); State Government; U.S. Territory or Possession; Indian/Native American Tribal Government (Federally Recognized); Indian/Native American Tribal Government (Other than Federally Recognized); Indian/Native American Tribally Designated Organization; Non-domestic (non-U.S.) Entity (Foreign Organization); Hispanic-serving Institution; Historically Black Colleges and Universities (HBCUs); Tribally Controlled Colleges and Universities (TCCUs); Alaska Native and Native Hawaiian Serving Institutions; Regional Organization; Other(s): Eligible agencies of the Federal government; Faith-based or community based organizations.

rolling

Healthhealthcare

Free to search & build · $99 one-time to unlock the application pack · No subscription

HYPERSPECTRAL IMAGERY DATA COLLECTION

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SpecTIR LLC

Information Technology Broadcasting and Telecommunications

2028-11-30

infrastructuretechnology

Free to search & build · $99 one-time to unlock the application pack · No subscription

Hypoxia-associated L-2-hydroxyglutarate in regulation of germinal center responses

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NIAID - National Institute of Allergy and Infectious Diseases

PROJECT SUMMARY/ABSTRACT Germinal centers (GCs) are sites where B cells engage in T cell-dependent selection and ultimately differentiate to antibody-secreting plasma cells or long-lived memory B cells, a process that generates high- quality antibodies and helps to provide protection against pathogens and maintain immunological memory. Previous studies have shown that GCs are hypoxic compared to surrounding tissues and further suggest that this hypoxic environment is crucial for GC B cell responses. However, the mechanisms by which germinal center hypoxia governs GC B cell selection and differentiation are not fully understood. Hypoxia induces generation of the metabolite L-2-hydroxyglutarate (L-2HG), an inhibitor of α-ketoglutarate (αKG) dependent dioxygenases, including ten-eleven translocation (TET) and Jumonji-C domain containing lysine (K) demethylase (KDM) enzymes. TET and KDM enzymes mediate DNA and histone demethylation, respectively, and are known to be critical regulators of B cell fate. In mice with B cell specific deletion of L-2HG dehydrogenase (L2HGDH), the enzyme that metabolizes L-2HG to αKG, I observed an expansion of GC B cells and skewing towards memory fates. However, it is unknown how L-2HG-directed epigenetic changes affect DNA and histone methylation at key B cell regulatory genes, and how these changes may contribute to GC B cell fate decisions. Based on these preliminary results, I hypothesize that L-2HG produced under germinal center hypoxia influences B cell fate decisions through epigenetic reprogramming. In Aim 1, I will determine the role of L-2HG in regulation of GC B cell differentiation and memory commitment. I will use genetic models of B cell specific L2hgdh deficiency and overexpression to study the effects of altered L-2HG levels on GC B cell differentiation and memory. I will also use an immunization-infection model of influenza A to examine the functional effects of enhanced L-2HG levels on immunological memory. In Aim 2, I will elucidate the mechanisms of L-2HG-mediated epigenetic reprogramming in B cells. Using CUT&Tag and whole genome bisulfide sequencing (WGBS), I will assess the effects of increased L-2HG levels on histone and DNA methylation and assess transcriptional changes with single-cell RNA sequencing. I will further test the effects of DNA methylation inhibition to rescue the transcriptional, epigenetic, and differentiation changes induced by L-2HG treatment in B cells. Together, these studies will provide clear genetic evidence for an important role of L-2HG in memory B cell lineage commitment and define the precise mechanisms by which L-2HG influences transcriptional and epigenetic states in B cells.

Up to $45K

2030-05-31

health research

Free to search & build · $99 one-time to unlock the application pack · No subscription

Hyundai Foundation Expanded Programs

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Hyundai Foundation

Supports community mobility, environmental programs, and arts/culture in Hyundai markets worldwide.

$25K – $1M

Rolling

community mobilityEnvironmentalarts

Free to search & build · $99 one-time to unlock the application pack · No subscription

Hyundai Foundation Grants

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Hyundai Foundation

Funds education, culture, and social welfare programs in Korea and internationally.

$20K – $200K

Rolling

Educationculturesocial welfare

Free to search & build · $99 one-time to unlock the application pack · No subscription

I-SLEPT: Integrated Sleep and Life Engagement Program for Transitions

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NIH

Significance to VA: This project will create I-SLEPT (Integrated Sleep and Life Engagement Program for Transitions), a novel intervention to enhance sleep health and life engagement during the transition period following discharge from VA subacute rehabilitation. The development of I-SLEPT will be informed by both Veterans and experts. Including the Veteran perspective is essential [to reflect Veterans’ choice, ensure access to timely care, and prioritize effective care solutions to improve Veterans’ health and well-being.] Veterans are more likely to report poor sleep and medical complexities than non-Veterans [which may further complicate their readjustment to their home environment after discharge.] Innovation and Impact: VA is a leader in creating programs and interventions to support Veterans in their transitions from inpatient settings to home and the community. I-SLEPT will further add to VA efforts by being the first intervention to simultaneously target sleep health and life engagement during a vulnerable period of recovery. Experts guiding intervention development are from psychology, medicine, occupational therapy and [nursing], thus laying the groundwork for future trials where I-SLEPT is implemented by clinicians from an array of disciplines, allowing for greater accessibility and positive impact on [Veteran] health and well-being. Specific Aims: Aim 1. Define I-SLEPT and Develop Intervention [Protocol] (Years 1-2) 1.1 Identify core components of I-SLEPT integrating knowledge based on CDA-1 data, [the literature, and Veteran survey data (N=20)]. 1.2 Review and refine I-SLEPT based on Veteran feedback [(N=10)] in structured interviews. 1.3 Review and refine I-SLEPT based on expert panel feedback [(N=6)]. Aim 2. Refine I-SLEPT Intervention Protocol (Years 2-3) 2.1 Pilot I-SLEPT protocol in Veterans (N=5) discharged from VA Boston subacute rehabilitation. 2.2 Assess preliminary acceptability, [appropriateness, and feasibility] of intervention through structured interviews in Veterans. 2.3 Review and refine I-SLEPT for strength and efficiency based on preliminary results and expert panel feedback. Aim 3. Determine Proof-of-Concept for I-SLEPT Intervention (Years 3-5) 3.1 Conduct a preliminary evaluation of the I-SLEPT protocol in Veterans [(N=40)] discharged from VA Boston subacute rehabilitation. 3.2 Assess for clinically significant results of I-SLEPT intervention by examining within person changes. 3.3 Review progress of treatment with expert panelists. Methodology: The proposed study is a single arm clinical trial. Veterans aged 50+ discharged home from the subacute rehabilitation units at VA Boston’s Community Living Center will be recruited to complete [surveys and] interviews informing I-SLEPT creation (Aim 1), complete a preliminary trial (Aim 2) or complete a Proof-of- Concept trial (Aim 3). Veterans participating in Aims 2 or 3 will complete assessments of sleep health (e.g., [sleep satisfaction]) and life engagement (e.g., [participation in pleasant activities]), as well as acceptability measures. Path to Translation/Implementation: Results from this CDA-2 will provide preliminary data for future large- scale randomized controlled trials (RDT IIR Merit). Results may also inform future work adapting this intervention to other transitional phases (e.g., discharge from acute hospitalization), support Veterans across the lifespan, and support intervention implementation by staff from multiple disciplines [and specialties], including nursing, social work, physical therapy, occupational therapy, [and Veteran peer specialists].

2031-03-31

health research

Free to search & build · $99 one-time to unlock the application pack · No subscription

I3-2026-INV1 - Interregional Innovation Investments Strand 1

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European Commission - I3

I3-2026-INV1 - Interregional Innovation Investments Strand 1. Call: Interregional Innovation Investments Strand 1. Programme: I3. Keywords: Business coaching and mentoring, Business development, Business environment (legal and administrative), Business management, Business models, Business plan, Business strategies, Business support services, Evaluation of programmes/projects, Innovation methodologies, Regional development, SME support, Smart Specialisation strategies, Supply chain management. Open call from the EU Funding & Tenders Portal.

$50K

2026-11-12

environmenttechnologyBusiness Development

Free to search & build · $99 one-time to unlock the application pack · No subscription

I3-2026-INV2a - Interregional Innovation Investments Strand 2a

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European Commission - I3

I3-2026-INV2a - Interregional Innovation Investments Strand 2a. Call: Interregional Innovation Investments Strand 2a. Programme: I3. Keywords: Business coaching and mentoring, Business development, Business environment (legal and administrative), Business management, Business models, Business plan, Business strategies, Business support services, Evaluation of programmes/projects, Innovation methodologies, Regional development, SME support, Smart Specialisation strategies, Supply chain management. Open call from the EU Funding & Tenders Portal.

$50K

2026-11-12

environmenttechnologyBusiness Development

Free to search & build · $99 one-time to unlock the application pack · No subscription

IA State Arts Council — General Operating Grant

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IA Arts Council

General operating and project support for arts organizations and individual artists in IA. Funds visual arts, performing arts, literary arts, and arts education.

$2K – $50K

2026-12-31

artsculture

Free to search & build · $99 one-time to unlock the application pack · No subscription

IBM Call for Code

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IBM

Global challenge calling developers to build solutions for natural disaster preparedness and climate change using cloud, AI, blockchain, and IoT.

$25K – $200K

2026-07-31

climatedisaster preparednesstechnology+1

Free to search & build · $99 one-time to unlock the application pack · No subscription

IBM Foundation Education & Health Grants

open

IBM Foundation

Funds education innovation, public health programs, and workforce readiness initiatives through technology-driven solutions.

$25K – $500K

Rolling

EducationHealthworkforce development

Free to search & build · $99 one-time to unlock the application pack · No subscription

ICE Clear Credit LLC; Order Granting an Application for Registration as a Clearing Agency Under Section 17A of the Securities Exchange Act of 1934

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Securities and Exchange Commission

ICE Clear Credit LLC; Order Granting an Application for Registration as a Clearing Agency Under Section 17A of the Securities Exchange Act of 1934

See notice

Community Development

Free to search & build · $99 one-time to unlock the application pack · No subscription

ICFJ Journalism Fellowship

open

International Center for Journalists

Fellowships and grants for journalists worldwide covering critical beats with innovative approaches.

$10K – $75K

2026-09-30

international journalismfellowship

Free to search & build · $99 one-time to unlock the application pack · No subscription

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