![MCM7 serves as a prognostic marker in diffuse-type gastric adenocarcinoma and siRNA-mediated knockdown suppresses its oncogenic function MCM7 serves as a prognostic marker in diffuse-type gastric adenocarcinoma and siRNA-mediated knockdown suppresses its oncogenic function](https://www.spandidos-publications.com/article_images/or/31/5/OR-31-05-2071-g00.jpg)
MCM7 serves as a prognostic marker in diffuse-type gastric adenocarcinoma and siRNA-mediated knockdown suppresses its oncogenic function
![Homozygous mutation in MCM7 causes autosomal recessive primary microcephaly and intellectual disability | Journal of Medical Genetics Homozygous mutation in MCM7 causes autosomal recessive primary microcephaly and intellectual disability | Journal of Medical Genetics](https://jmg.bmj.com/content/jmedgenet/59/5/453/F2.large.jpg)
Homozygous mutation in MCM7 causes autosomal recessive primary microcephaly and intellectual disability | Journal of Medical Genetics
![Schematic diagram of interplay of PKC, RACK1, and MCM7. PKC binding... | Download Scientific Diagram Schematic diagram of interplay of PKC, RACK1, and MCM7. PKC binding... | Download Scientific Diagram](https://www.researchgate.net/publication/234122908/figure/fig2/AS:267605931982890@1440813634530/Schematic-diagram-of-interplay-of-PKC-RACK1-and-MCM7-PKC-binding-with-TPA-leads-to.png)
Schematic diagram of interplay of PKC, RACK1, and MCM7. PKC binding... | Download Scientific Diagram
![MCM complex members MCM3 and MCM7 are associated with a phenotypic spectrum from Meier-Gorlin syndrome to lipodystrophy and adrenal insufficiency | European Journal of Human Genetics MCM complex members MCM3 and MCM7 are associated with a phenotypic spectrum from Meier-Gorlin syndrome to lipodystrophy and adrenal insufficiency | European Journal of Human Genetics](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41431-021-00839-4/MediaObjects/41431_2021_839_Fig1_HTML.png)
MCM complex members MCM3 and MCM7 are associated with a phenotypic spectrum from Meier-Gorlin syndrome to lipodystrophy and adrenal insufficiency | European Journal of Human Genetics
![Phosphorylation of Minichromosome Maintenance Protein 7 (MCM7) by Cyclin/Cyclin-dependent Kinase Affects Its Function in Cell Cycle Regulation - ScienceDirect Phosphorylation of Minichromosome Maintenance Protein 7 (MCM7) by Cyclin/Cyclin-dependent Kinase Affects Its Function in Cell Cycle Regulation - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S002192582045687X-gr2.jpg)
Phosphorylation of Minichromosome Maintenance Protein 7 (MCM7) by Cyclin/Cyclin-dependent Kinase Affects Its Function in Cell Cycle Regulation - ScienceDirect
![Homozygous mutation in MCM7 causes autosomal recessive primary microcephaly and intellectual disability | Journal of Medical Genetics Homozygous mutation in MCM7 causes autosomal recessive primary microcephaly and intellectual disability | Journal of Medical Genetics](https://jmg.bmj.com/content/jmedgenet/59/5/453/F1.large.jpg)