Biology:SIX2
From HandWiki
Short description: Protein-coding gene in the species Homo sapiens
 Generic protein structure example |
Homeobox protein SIX2 is a protein that in humans is encoded by the SIX2 gene.[1][2]
References
- ↑ "Entrez Gene: SIX2 sine oculis homeobox homolog 2 (Drosophila)". https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=10736.
- ↑ Oliver, Guillermo (1995). "Homeobox genes and connective tissue patterning". Development 121 (3): 693–705. doi:10.1242/dev.121.3.693. PMID 7720577. http://dev.biologists.org/content/121/3/693.full.pdf.
Further reading
- "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. 2003. doi:10.1073/pnas.242603899. PMID 12477932. Bibcode: 2002PNAS...9916899M.
- "Six3 and Six6 activity is modulated by members of the groucho family.". Development 130 (1): 185–95. 2003. doi:10.1242/dev.00185. PMID 12441302.
- "Molecular interaction and synergistic activation of a promoter by Six, Eya, and Dach proteins mediated through CREB binding protein.". Mol. Cell. Biol. 22 (19): 6759–66. 2002. doi:10.1128/MCB.22.19.6759-6766.2002. PMID 12215533.
- "Molecular effects of Eya1 domain mutations causing organ defects in BOR syndrome.". Hum. Mol. Genet. 10 (24): 2775–81. 2002. doi:10.1093/hmg/10.24.2775. PMID 11734542.
- "Structure, mapping and expression of the human gene encoding the homeodomain protein, SIX2.". Gene 247 (1–2): 145–51. 2000. doi:10.1016/S0378-1119(00)00105-0. PMID 10773454.
- "Familial syndromic esophageal atresia maps to 2p23-p24". Am. J. Hum. Genet. 66 (2): 436–44. 2000. doi:10.1086/302779. PMID 10677303.
- "Identification and expression of six family genes in mouse retina". FEBS Lett. 393 (2–3): 259–63. 1996. doi:10.1016/0014-5793(96)00899-X. PMID 8814301.
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