Gene · 8913
NIH grants1,078
NIH grants whose papers are about the gene, through NIH's grant-paper links.
601 to 620 of 1,078
Download this page as JSON| Grant | Title | CACNA1G papers | Newest fiscal year |
|---|---|---|---|
| R01CA185357 | (PQD3)Molecular Profiles associated with Long-Term Survival in pancreas Cancer | 1 | 2017 |
| R01DA034856 | Homeostatic Regulation and Dysregulation in Cocaine Craving | 1 | 2017 |
| R01DA036216 | Adult consequences of youth substance use: Twin study enriched for SUD risk | 1 | 2017 |
| R01GM048430 | Greatwall Kinase and the Mitotic Control of Phosphatase Activity | 1 | 2017 |
| R01GM098320 | Mechanisms of neuropeptide signaling in the modulation of a serotonergic synapse | 1 | 2017 |
| R01GM113182 | Toll-like receptor signaling in sensory neuron differentiation and function. | 1 | 2017 |
| R01HL088243 | Protein Kinase A Inhibitor Peptide (PKI) and Cardiac Protection in Heart Failure | 1 | 2017 |
| R01HL092217 | Positional Cloning and Candidate Gene Approach to Familial Atrial Fibrilation | 1 | 2017 |
| R01HL096453 | Effects of HIV antiretroviral therapy on pulmonary function in a randomized trial | 1 | 2017 |
| R01HL121706 | Regulations of Myoendothelial Function By Signaling Microdomains in Hypertension | 1 | 2017 |
| R01HL123364 | Leukotriene C4 and STIM/Orai channels in airway smooth muscle remodeling | 1 | 2017 |
| R01MH097993 | 2/2 - Identification of rare variants of OCD | 1 | 2017 |
| R01MH099216 | Identifying de novo mutations causing OCD in trios by whole exome sequencing | 1 | 2017 |
| R01MH104680 | Integration of brain imaging with genomic and epigenomic data | 1 | 2017 |
| R01NS058529 | COMPLEX GENOMIC REARRANGEMENTS IN NEUROLOGICAL DISEASE | 1 | 2017 |
| R03AR066875 | The Mechanical Phenotype of Fetal Fibroblasts as a Model for Regenerative Repair | 1 | 2017 |
| R15GM124013 | Voltage-Gated Calcium Channel Modulation by RGK proteins | 1 | 2017 |
| R21AI125997 | Identifying Novel Ion Channels Regulating T cell Function | 1 | 2017 |
| R21CA201865 | Using DNA methylation markers to improve the predictive accuracy and utility of needle biopsiesfor determining prostate cancer aggressiveness | 1 | 2017 |
| R21CA205475 | Splicing factors and RNA processing alternations: exploring new players in glioblastoma development | 1 | 2017 |
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/v1/8913/grants?page=31