Gene · 94
Papers4,014
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
121 to 140 of 4,014
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| A novel SMAD9 nonsense variant in an 11-year-old Japanese patient with diffuse pulmonary arteriovenous malformation: A case report. | J Cardiol Cases | 2025 | 40270704 | PubTator, text mining | PubMed |
| Arteriovenous cerebral high-flow shunts: genetic analysis of patients from a pediatric tertiary care center. | Front Genet | 2025 | 40259928 | PubTator, text mining | PubMed |
| ACVRL1 and MTHFR double variants in an adolescent with paradoxical cerebral embolism. | Pediatr Int | 2025 | 40243618 | PubTator, text mining | PubMed |
| Rapid improvement in postpartum pulmonary hypertension associated with hereditary hemorrhagic telangiectasia: A case report and review of literature. | World J Clin Cases | 2025 | 40242231 | PubTator, text mining | PubMed |
| A generalized higher-order correlation analysis framework for multi-omics network inference. | PLoS Comput Biol | 2025 | 40228208 | PubTator, text mining | PubMed |
| ACVRL1 variation-induced hereditary hemorrhagic telangiectasia presenting with pulmonary arterial hypertension: clinical and genetic analyses of three case studies. | BMC Cardiovasc Disord | 2025 | 40205542 | PubTator, text mining | PubMed |
| Imaging manifestations of hereditary hemorrhagic telangiectasia with pulmonary arterial hypertension: a case report. | Front Cardiovasc Med | 2025 | 40190465 | PubTator, text mining | PubMed |
| Case report: Novel homozygous ACVRL1 missense variant in a family with hereditary hemorrhagic telangiectasia and pulmonary arterial hypertension: findings suggest a hypomorphic allele. | Front Genet | 2025 | 40160294 | PubTator, text mining | PubMed |
| Study on the changes of extracellular matrix morphology and components in COPD animal model by using lung decellularized scaffold. | FASEB J | 2025 | 40150895 | PubTator, text mining | PubMed |
| Screening of Phytocompounds Against the NF-kB Pathway Genes and Lung Elevated Proteins Associated with Acute Respiratory Distress Syndrome. | Recent Adv Inflamm Allergy Drug Discov | 2025 | 40129159 | PubTator, text mining | PubMed |
| Prognostic Value of Ferroptosis-Immunity-Related Signature Genes in Cervical Cancer Radiotherapy Resistance and Risk Modeling. | Cancer Manag Res | 2025 | 40093571 | PubTator, text mining | PubMed |
Consistent Safety and Efficacy of Sotatercept for Pulmonary Arterial Hypertension in BMPR2 Mutation Carriers and Noncarriers: A Planned Analysis of a Phase II, Double-Blind, Placebo-controlled Clinical Trial (PULSAR). | Am J Respir Crit Care Med | 2025 | 40035659 | PubTator, text mining | PubMed |
| Basic Knowledge and Overview of Brain AVMs. | J Neuroendovasc Ther | 2025 | 40018280 | PubTator, text mining | PubMed |
| Transcytosis of LDL Across Arterial Endothelium: Mechanisms and Therapeutic Targets. | Arterioscler Thromb Vasc Biol | 2025 | 40013359 | PubTator, text mining | PubMed |
| STANCE: a unified statistical model to detect cell-type-specific spatially variable genes in spatial transcriptomics. | Nat Commun | 2025 | 39979358 | PubTator, text mining | PubMed |
| Arteriovenous malformation from a patient with JP-HHT harbours two second-hit somatic DNA alterations in SMAD4. | J Med Genet | 2025 | 39939156 | PubTator, text mining | PubMed |
| Updates on the Pathogenesis and Therapeutic Approaches for Hereditary Hemorrhagic Telangiectasia. | Curr Vasc Pharmacol | 2025 | 39901690 | PubTator, text mining | PubMed |
| AntiCD30-Conjugated Antibody Plus Standard BEAM as Conditioning Regimen for Autologous Hematopoietic Stem Cell Transplantation in Systemic Anaplastic Large Cell Lymphoma. | Hematol Rep | 2025 | 39846607 | PubTator, text mining | PubMed |
| Potential Therapeutic Drug Targets for Hypertension Identified Using Proteomics and Mendelian Randomization. | Am J Hypertens | 2025 | 39844355 | PubTator, text mining | PubMed |
| An activin receptor-like kinase 1-governed monocytic lineage shapes an immunosuppressive landscape in breast cancer metastases. | J Clin Invest | 2025 | 39808498 | PubTator, text mining | PubMed |
gene-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.
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