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Homeobox protein MOX-2 is a protein that in humans is encoded by the MEOX2gene.
Function
This gene encodes a member of a subfamily of non-clustered, diverged, antennapedia-like homeobox-containing genes. The encoded protein may play a role in the regulation of vertebrate limb myogenesis. Mutations in the related mouse protein may be associated with craniofacial and/or skeletal abnormalities, in addition to neurovascular dysfunction observed in Alzheimer's disease. MEOX2 has been implicated in the initiation of tumors in glioma. Additionally, MEOX2 influences several critical processes in lung cancer, including cellular proliferation, invasion, metastasis, angiogenesis, and the development of drug resistance.
"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
LePage DF, Altomare DA, Testa JR, Walsh K (December 1994). "Molecular cloning and localization of the human GAX gene to 7p21". Genomics. 24 (3): 535–540. doi:10.1006/geno.1994.1663. PMID7713505.
Peralta-Arrieta I, Trejo-Villegas OA, Armas-López L, Ceja-Rangel HA, Ordóñez-Luna MD, Pineda-Villegas P, et al. (January 2022). "Failure to EGFR-TKI-based therapy and tumoural progression are promoted by MEOX2/GLI1-mediated epigenetic regulation of EGFR in the human lung cancer". European Journal of Cancer. 160: 189–205. doi:10.1016/j.ejca.2021.10.032. PMID34844838.
Grigoriou M, Kastrinaki MC, Modi WS, Theodorakis K, Mankoo B, Pachnis V, et al. (April 1995). "Isolation of the human MOX2 homeobox gene and localization to chromosome 7p22.1-p21.3". Genomics. 26 (3): 550–555. doi:10.1016/0888-7543(95)80174-K. PMID7607679.
Reardon W, McManus SP, Summers D, Winter RM (October 1993). "Cytogenetic evidence that the Saethre-Chotzen gene maps to 7p21.2". American Journal of Medical Genetics. 47 (5): 633–636. doi:10.1002/ajmg.1320470510. PMID8266988.
Quinn LM, Latham SE, Kalionis B (2000). "The homeobox genes MSX2 and MOX2 are candidates for regulating epithelial-mesenchymal cell interactions in the human placenta". Placenta. 21 Suppl A: S50 – S54. doi:10.1053/plac.1999.0514. PMID10831122.
Gorski DH, Leal AJ (May 2003). "Inhibition of endothelial cell activation by the homeobox gene Gax". The Journal of Surgical Research. 111 (1): 91–99. doi:10.1016/S0022-4804(03)00042-8. PMID12842453.
Wu Z, Guo H, Chow N, Sallstrom J, Bell RD, Deane R, et al. (September 2005). "Role of the MEOX2 homeobox gene in neurovascular dysfunction in Alzheimer disease". Nature Medicine. 11 (9): 959–965. doi:10.1038/nm1287. PMID16116430. S2CID12998034.