Foundation directory

Emerald Foundation Inc Co Solomon Blum Heymann Grants

Private foundation · EIN 13-3912580 · IRS 990-PF filings through tax year 2024

Total grants paid
$1.5M
Grants reported
31
Median grant
$50K
Future commitments
None reported

Giving by tax year

Tax yearGrants paidAmount
202431$1.5M

Where Emerald Foundation Inc Co Solomon Blum Heymann gives

States of grant recipients reported on the foundation's 990-PF filings, by dollars received.

Largest reported grants

The biggest individual grants on file, as reported by the foundation to the IRS.

RecipientLocationPurposeTax yearAmount
MASSACHUSETTS INSTITUTE OF TECHNOLOCambridge, MATo study how ferroptosis-based strategies can enhance the efficacy of immunotherapies in breast cancer.2024$87.5K
UNIVERSITY OF MARYLAND SCH OF MEDICBALTIMORE, MDTO INVESTIGATE THE REGULATION OF TREG LYMPHATIC TUMOR MIGRATION AND THE INTERACTION AMONG TREGS, LYMPHATIC ENDOTHELIAL CELLS, AND TUMORS TO DEVELOP STRATEGIES OF DELIVERING TARGETED THERAPIES LOCALLY INSTEAD OF SYSTEMICALLY.2024$75K
MASSACHUSETTS INSTITUTE OF TECHNOLOCAMBRIDGE, MATo enhance nanoparticle accumulation in desired cell types to develop more effective and safer targeted nanotherapies.2024$75K
UNIVERSITY OF MARYLAND SCH OF MEDICBALTIMORE, MDTo investigate the regulation of Treg lymphatic tumor migration and the interaction among Tregs, lymphatic endothelial cells, and tumors to develop strategies of delivering targeted therapies locally instead of systemically.2024$75K
NYU SCHOOL OF MEDICINENew York, NYTo examine the cellular mechanisms through which dendrite-centric Alzheimer's disease pathologies result in cognitive dysfunction and hyper-excitability.2024$75K
WEILL CORNELL MEDICINENew York, NYTo identify regulators of lineage reversion that impact resistance to WNT-targeted therapies in colorectal cancer.2024$75K
JOHN HOPKINS UNIVERSITYBALTIMORE, MDTo investigate how the colon microbiota and host genetics intersect to alter responsiveness to immunotherapy in colorectal cancer.2024$50K
SALK INSTITUTE FOR BIOLOGICAL STUDILA JOLLA, CATO USE INNOVATIVE CELL BIOLOGY TECHNIQUES COUPLED WITH GENOMICS TO INVESTIGATE THE ROLE OF MITOCHONDRIAL-DERIVED VESICLES IN CANCER CELL METABOLISM.2024$50K
UNIVERSITY OF KENTUCKYLEXINGTON, KYTO UNDERSTAND HOW MALADAPTIVE CHANGES TO THE INTEGRATED STRESS RESPONSE PATHWAY ALTER THE FORCE GENERATING ABILITY OF HUMAN HEART CELLS AND DETERMINE IF PHARMACOLOGICAL MANIPULATION CAN RESCUE CARDIOMYOCYTE FUNCTION.2024$50K
SALK INSTITUTE FOR BIO STUDIESLA JOLLA, CATo use innovative cell biology techniques coupled with genomics to investigate the role of mitochondrial-derived vesicles in cancer cell metabolism.2024$50K
WHITEHEAD INST FOR BIOMEDICAL RESEACAMBRIDGE, MATo identify molecular mechanisms that help anaerobes cope with oxygen exposure and/or oxidative stress.2024$50K
WHITEHEAD INST FOR BIOMEDICAL RESEACAMBRIDGE, MATo identify molecular mechanisms that help anaerobes cope with oxygen exposure and/or oxidative stress.2024$50K
INSERM DR GRAND OUESTNANTES, Cedex 1To determine the mechanism through which breast cancer cell clusters dissociate into single cells and proliferate at distant sites and to determine the impact of the new environment on metastasis formation.2024$50K
UNIVERSITY OF PENNSYLVANIAPhiladelphia, PATo understand the molecular mechanism underlying immunosuppression and immunoactivation and develop new treatment strategies for hepatic malignancies.2024$50K
DANA-FARBER CANCER INSTITUTEBOSTON, MATo map the transcriptional and protein changes induced by lactate and identify the mechanisms that cause NK suppression, on both NK and tumor cells, using high-throughput and unbiased approaches.2024$50K
UNIVERSITY OF MICHIGANAnn Arbor, MITo use tumor organoid and mouse models to determine how loss of Claudin proteins impacts tumor invasion and metastasis.2024$50K
DANA-FARBER CANCER INSTITUTEBoston, MATo map the transcriptional and protein changes induced by lactate and identify the mechanisms that cause NK suppression, on both NK and tumor cells, using high-throughput and unbiased approaches.2024$50K
WHITEHEAD INST FOR BIOMEDICAL RESEACAMBRIDGE, MATo uncover the set of cell-surface proteins that mediate essential interactions between PDAC cells and their microenvironment.2024$50K
UNIVERSITY OF PENNSYLVANIAPhiladelphia, PATo understand the molecular mechanism underlying immunosuppression and immunoactivation and develop new treatment strategies for hepatic malignancies.2024$50K
UNIVERSITY OF KENTUCKYLexington, KYTo understand how maladaptive changes to the integrated stress response pathway alter the force generating ability of human heart cells and determine if pharmacological manipulation can rescue cardiomyocyte function.2024$50K
WEILL CORNELL MEDICINENew York, NYTo characterize exosomes from nave and tumor-educated platelets and determine their contribution to metastatic dormancy and recurrence.2024$37.5K
JOHN HOPKINS UNIVERSITYBALTIMORE, MDTo use tumor organoid and mouse models to determine how loss of claudin proteins impacts tumor invasion and metastasis.2024$37.5K
WEILL CORNELL MEDICINENEW YORK, NYTo characterize exosomes from nave and tumor-educated platelets and determine their contribution to metastatic dormancy and recurrence.2024$37.5K
FOX CHASE CANCER CENTERPHILADELPHIA, PATo investigate the role of Brg1-dependent epigenetic regulation on PDAC fibroblast pro-tumorigenic functions.2024$37.5K
CALIFORNIA INSITUTE OF TECHNOLOGYPASADENA, CATo develop interpretable machine learning methods that link spatial phenotypes in imaging data of solid tumors with patient outcomes.2024$37.5K

How to apply

This foundation reports on its 990-PF that it only makes contributions to preselected organizations and does not accept unsolicited applications.

About this data

Figures are aggregated from Emerald Foundation Inc Co Solomon Blum Heymann's IRS Form 990-PF electronic filings (1 filing on file, most recent tax year 2024). Totals reflect grants the foundation reported as paid, and can lag the current year because foundations file annually and often on extension. Source: IRS 990-PF e-file archive.

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