The severe form of type I hyperprolinaemia results from homozygous inactivation of the PRODH gene | Journal of Medical Genetics
PRODH Antibodies
Functional Consequences of PRODH Missense Mutations - ScienceDirect
Diagram of the PRODH gene, representing the variants investigated in... | Download Scientific Diagram
PRODH Gene - GeneCards | PROD Protein | PROD Antibody
Genes for schizophrenia? Recent findings and their pathophysiological implications - The Lancet
Proline oxidase - Wikipedia
Schizophrenia genes, gene expression, and neuropathology: on the matter of their convergence | Molecular Psychiatry
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
PRODH2 Gene - GeneCards | HYPDH Protein | HYPDH Antibody
PRODH Gene - GeneCards | PROD Protein | PROD Antibody
PRODH Gene - GeneCards | PROD Protein | PROD Antibody
Diagram of the PRODH gene, representing the variants investigated in... | Download Scientific Diagram
Northern-blot analysis of the expression of the ProDH gene in... | Download Scientific Diagram
PRODH regulates Cxcl1, Lcn2, and IL17c inflammatory genes a PRODH... | Download Scientific Diagram
![PDF] Relationship between polymorphisms in the proline dehydrogenase gene and schizophrenia risk. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/e15786fea2b6ab6c3225db21489ccbf922eefdf2/5-Figure1-1.png "PDF] Relationship between polymorphisms in the proline dehydrogenase gene and schizophrenia risk. | Semantic Scholar")
PDF] Relationship between polymorphisms in the proline dehydrogenase gene and schizophrenia risk. | Semantic Scholar
Human Proline Dehydrogenase 1, PRODH ELISA Kit - BT LAB
Gene: PRODH (ENSG00000100033) - Summary - Homo_sapiens - Ensembl genome browser 110
PRODH Antibody (NB100-2832): Novus Biologicals
The 22q11 PRODH/DGCR6 deletion is frequent in hyperprolinemic subjects but is not a strong risk factor for ASD.
Human-specific endogenous retroviral insert serves as an enhancer for the schizophrenia-linked gene PRODH | PNAS
Genes | Free Full-Text | Coexisting Conditions Modifying Phenotypes of Patients with 22q11.2 Deletion Syndrome
