MEOX1

Mesenchyme homeobox 1, also known as MEOX1, is a human gene.cite web | title = Entrez Gene: MEOX1 mesenchyme homeobox 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=4222| accessdate = ]

PBB_Summary
section_title =
summary_text = 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 molecular signaling network regulating somite development. Alternatively spliced transcript variants encoding different isoforms have been described.cite web | title = Entrez Gene: MEOX1 mesenchyme homeobox 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=4222| accessdate = ]

References

Further reading

PBB_Further_reading
citations =
*cite journal | author=Jones KA, Black DM, Brown MA, "et al." |title=The detailed characterisation of a 400 kb cosmid walk in the BRCA1 region: identification and localisation of 10 genes including a dual-specificity phosphatase. |journal=Hum. Mol. Genet. |volume=3 |issue= 11 |pages= 1927–34 |year= 1995 |pmid= 7874108 |doi=
*cite journal | author=Futreal PA, Cochran C, Rosenthal J, "et al." |title=Isolation of a diverged homeobox gene, MOX1, from the BRCA1 region on 17q21 by solution hybrid capture. |journal=Hum. Mol. Genet. |volume=3 |issue= 8 |pages= 1359–64 |year= 1995 |pmid= 7987315 |doi=
*cite journal | author=Stelnicki EJ, Kömüves LG, Holmes D, "et al." |title=The human homeobox genes MSX-1, MSX-2, and MOX-1 are differentially expressed in the dermis and epidermis in fetal and adult skin. |journal=Differentiation |volume=62 |issue= 1 |pages= 33–41 |year= 1997 |pmid= 9373945 |doi=
*cite journal | author=Stamataki D, Kastrinaki M, Mankoo BS, "et al." |title=Homeodomain proteins Mox1 and Mox2 associate with Pax1 and Pax3 transcription factors. |journal=FEBS Lett. |volume=499 |issue= 3 |pages= 274–8 |year= 2001 |pmid= 11423130 |doi=
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
*cite journal | author=Petropoulos H, Gianakopoulos PJ, Ridgeway AG, Skerjanc IS |title=Disruption of Meox or Gli activity ablates skeletal myogenesis in P19 cells. |journal=J. Biol. Chem. |volume=279 |issue= 23 |pages= 23874–81 |year= 2004 |pmid= 15039437 |doi= 10.1074/jbc.M312612200
*cite journal | author=Gerhard DS, Wagner L, Feingold EA, "et al." |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504
*cite journal | author=Gianakopoulos PJ, Skerjanc IS |title=Hedgehog signaling induces cardiomyogenesis in P19 cells. |journal=J. Biol. Chem. |volume=280 |issue= 22 |pages= 21022–8 |year= 2005 |pmid= 15793308 |doi= 10.1074/jbc.M502977200
*cite journal | author=Wissmüller S, Kosian T, Wolf M, "et al." |title=The high-mobility-group domain of Sox proteins interacts with DNA-binding domains of many transcription factors. |journal=Nucleic Acids Res. |volume=34 |issue= 6 |pages= 1735–44 |year= 2006 |pmid= 16582099 |doi= 10.1093/nar/gkl105

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