Gene · 6007
NIH grants1,059
NIH grants whose papers are about the gene, through NIH's grant-paper links.
121 to 140 of 1,059
Download this page as JSON| Grant | Title | RHD papers | Newest fiscal year |
|---|---|---|---|
| R01CA251436 | Mediators Of Arrested Differentiation In Pediatric Rhabdomyosarcoma | 1 | 2025 |
| R01CA251858 | Predicting Relapse at the Time of Diagnosis in Acute Lymphoblastic Leukemia | 1 | 2025 |
| R01CA255446 | Role of PRC1 in RUNX1-ETO-mediated transcriptional control | 1 | 2025 |
| R01CA255960 | Targeting STAT3 for the Treatment of CDK4/6 Inhibitor Resistant Advanced Estrogen Receptor Positive Breast Cancer Patients | 1 | 2025 |
| R01CA262790 | The Role of Immature Tumor Subpopulations In Pediatric Rhabdomyosarcoma | 1 | 2025 |
| R01CA266600 | EXPLORE AND TARGET THE EPIGENETIC VULNERABILITY OF PAX3-FOXO1-DRIVEN RHABDOMYOSARCOMA | 1 | 2025 |
| R01CA272872 | Understanding Infantile Rhabdomyosarcoma Biology and Therapeutic Targets | 1 | 2025 |
| R01CA276480 | Advanced Oncolytic Adenovirus Enabling Systemic Therapy of PDAC | 1 | 2025 |
| R01DC007864 | Molecular genetics of gustatory detection | 1 | 2025 |
| R01DC016278 | Opsins as a new class of evolutionarily conserved taste receptors | 1 | 2025 |
| R01DK075787 | Biological Insights from Genetic Investigation of ANthropometric Traits (GIANT) Across the Allelic Spectrum | 1 | 2025 |
| R01DK127037 | Mechanisms of telomere-induced disease: Role of intestinal malabsorption, barrier dysfunction and dsybiosis. | 1 | 2025 |
| R01EY012146 | Patterning Genes in Retinal Development | 1 | 2025 |
| R01GM071940 | High-Resolution CryoEM Reconstruction of Large Complexes | 1 | 2025 |
| R01HD085901 | Mapping the ciliary interactome, an extensive protein interaction network underlying human ciliopathies | 1 | 2025 |
| R01HD105868 | Genomics and functional dissection of fetal brain abnormalities using a prenatal cohort | 1 | 2025 |
| R01HG006677 | Computational Methods for Gene Discovery, Genome Annotation, and Genome Assembly | 1 | 2025 |
| R01HG010149 | Refining Mendelian disease analysis via detection of clinically relevant repeat variants | 1 | 2025 |
| R01HG011649 | Detection and genotyping complex human genetic variation using single-molecule sequencing | 1 | 2025 |
| R01HL057181 | Cardiogenesis: Molecular Mechanisms | 1 | 2025 |
Source NIH's project filesgene-search-2026-11-11-0.2.0
Sources 12
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ChEMBL, through Open TargetsCC BY-SA 3.0
- ClinicalTrials.govNo license stated
- EMBL-EBI's patent proteinsNo added restrictions. Attribution expected
- GenBank's patent filesNo restrictions from NCBI. Submitters may hold rights
- HGNCCC0
- NCBI GenePublic domain (US government)
- NIH's project files and grant-paper linksPublic domain
- Open TargetsCC0 1.0
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- ClinicalTrials.govnone stated
- EMBL-EBI's patent proteinsEMBL-EBI's patent protein files from the EPO, JPO, KIPO and USPTO. EMBL-EBI: "EMBL-EBI itself places no additional restrictions on the use or redistribution of the data available via its Data Resources and Tools other than those provided by the original data owners" and "EMBL-EBI expects attribution (e.g. in publications, services or products) for the use of any of its Data Resources and Tools." Read on 11 Nov 2026 at https://www.ebi.ac.uk/about/terms-of-use
- GenBank's patent filesGenBank's patent files. NCBI: "NCBI places no restrictions on the use or distribution of the GenBank data. However, some submitters may claim patent, copyright, or other intellectual property rights in all or a portion of the data they have submitted." Read on 11 Nov 2026 at https://www.ncbi.nlm.nih.gov/genbank/about/
- HGNCCC0: https://www.genenames.org/about/license/
- NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
- NIH's project files and grant-paper linksPublic domain (NIH RePORTER)
- Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this list from software.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/genes/v1/6007/grants?page=7