MCM7 (minichromosome maintenance complex component 7)
Transcriptional expression and prognostic roles of MCM7 in human bladder, breast, and lung cancers: a multi-omics analysis | SpringerLink
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
MCM7 antibody (67446-1-Ig) | Proteintech
Gene: MCM7 (ENSG00000166508) - Summary - Homo_sapiens - Ensembl genome browser 110
MCM7 Antibody (141.2) | SCBT - Santa Cruz Biotechnology
Anti-MCM7 Antibody (A35457) | Antibodies.com
MCM7 (MSVA-507R) - MS Validated Antibodies
Micro Hi-Fi System MCM7/22 | Philips
Mcm7, a Subunit of the Presumptive MCM Helicase, Modulates Its Own Expression in Conjunction with Mcm1*
Operational amplifiers - Elettronica Veneta S.p.A.
MCM7 Antibody | Cell Signaling Technology
MCM proteins and checkpoint kinases get together at the fork | PNAS
-Western-Blot-NBP2-59613-img0004.jpg "MCM7 Antibody (MCM7/1469) (NBP2-59613): Novus Biologicals")
MCM7 Antibody (MCM7/1469) (NBP2-59613): Novus Biologicals
Anti-MCM7 Antibody PA1792
Molecules | Free Full-Text | Computational Screening of Natural Compounds for Identification of Potential Anti-Cancer Agents Targeting MCM7 Protein
MCM7 (Proliferation Marker) - Clone MCM7/2832R | 4176
MCM7 antibody | Biorbyt
MCM7 supports the stemness of bladder cancer stem-like cells by enhancing autophagic flux - ScienceDirect
MCM7 (minichromosome maintenance complex component 7)
Discordance of MCM7 mRNA and its Intronic MicroRNA Levels Under Hypoxia | Anticancer Research
Role of MCM2–7 protein phosphorylation in human cancer cells | Cell & Bioscience | Full Text
Micro Hi-Fi System MCM7/37 | Philips
MCM7 (MSVA-507R) - MS Validated Antibodies
MCM7 serves as a prognostic marker in diffuse-type gastric adenocarcinoma and siRNA-mediated knockdown suppresses its oncogenic function
MCM7 amplification and overexpression promote cell proliferation, colony formation and migration in esophageal squamous cell carcinoma by activating the AKT1/mTOR signaling pathway
MCM7 Gene - GeneCards | MCM7 Protein | MCM7 Antibody
Homozygous mutation in MCM7 causes autosomal recessive primary microcephaly and intellectual disability | Journal of Medical Genetics
