Epigenome-wide gene–age interaction analysis reveals reversed effects of PRODH DNA methylation on survival between young and elderly early-stage NSCLC patients - Figure f3 | Aging
![Frontiers | Appropriate Activity Assays Are Crucial for the Specific Determination of Proline Dehydrogenase and Pyrroline-5-Carboxylate Reductase Activities Frontiers | Appropriate Activity Assays Are Crucial for the Specific Determination of Proline Dehydrogenase and Pyrroline-5-Carboxylate Reductase Activities](https://www.frontiersin.org/files/Articles/602939/fpls-11-602939-HTML/image_m/fpls-11-602939-g001.jpg)
Frontiers | Appropriate Activity Assays Are Crucial for the Specific Determination of Proline Dehydrogenase and Pyrroline-5-Carboxylate Reductase Activities
![Effect of the PRODH CpG island on hsERV PRODH-enhancer activity. (A)... | Download Scientific Diagram Effect of the PRODH CpG island on hsERV PRODH-enhancer activity. (A)... | Download Scientific Diagram](https://www.researchgate.net/publication/258446197/figure/fig4/AS:668294260461588@1536345176846/Effect-of-the-PRODH-CpG-island-on-hsERV-PRODH-enhancer-activity-A-The-PRODH-gene.jpg)
Effect of the PRODH CpG island on hsERV PRODH-enhancer activity. (A)... | Download Scientific Diagram
![Genes | Free Full-Text | Coexisting Conditions Modifying Phenotypes of Patients with 22q11.2 Deletion Syndrome Genes | Free Full-Text | Coexisting Conditions Modifying Phenotypes of Patients with 22q11.2 Deletion Syndrome](https://pub.mdpi-res.com/genes/genes-14-00680/article_deploy/html/images/genes-14-00680-g001.png?1678353548)
Genes | Free Full-Text | Coexisting Conditions Modifying Phenotypes of Patients with 22q11.2 Deletion Syndrome
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PDF] Relationship between polymorphisms in the proline dehydrogenase gene and schizophrenia risk. | Semantic Scholar
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The severe form of type I hyperprolinaemia results from homozygous inactivation of the PRODH gene | Journal of Medical Genetics
![The severe form of type I hyperprolinaemia results from homozygous inactivation of the PRODH gene | Journal of Medical Genetics The severe form of type I hyperprolinaemia results from homozygous inactivation of the PRODH gene | Journal of Medical Genetics](https://jmg.bmj.com/content/jmedgenet/40/1/e7/F2.large.jpg)
The severe form of type I hyperprolinaemia results from homozygous inactivation of the PRODH gene | Journal of Medical Genetics
![Human-specific endogenous retroviral insert serves as an enhancer for the schizophrenia-linked gene PRODH | PNAS Human-specific endogenous retroviral insert serves as an enhancer for the schizophrenia-linked gene PRODH | PNAS](https://www.pnas.org/cms/10.1073/pnas.1318172110/asset/95083703-24f4-4bf5-b55d-260771bef08a/assets/graphic/pnas.1318172110fig01.jpeg)
Human-specific endogenous retroviral insert serves as an enhancer for the schizophrenia-linked gene PRODH | PNAS
![Diagram of the PRODH gene, representing the variants investigated in... | Download Scientific Diagram Diagram of the PRODH gene, representing the variants investigated in... | Download Scientific Diagram](https://www.researchgate.net/profile/Sintia-Belangero/publication/260157536/figure/fig1/AS:297214447505422@1447872854848/Diagram-of-the-PRODH-gene-representing-the-variants-investigated-in-this-study-and-their_Q320.jpg)