词条 | RAI2 |
释义 |
| section_title = | summary_text = Retinoic acid plays a critical role in development, cellular growth, and differentiation. The specific function of this intronless, retinoic acid-induced gene has not yet been determined; however, it has been suggested to play a role in development. Localization of this gene designates it to be a candidate for diseases such as Nance-Horan syndrome, sensorineural deafness, non-specific X-linked mental retardation, oral-facial-digital syndrome, and Fried syndrome.[3] }} References1. ^{{cite journal | vauthors = Walpole SM, Hiriyana KT, Nicolaou A, Bingham EL, Durham J, Vaudin M, Ross MT, Yates JR, Sieving PA, Trump D | title = Identification and characterization of the human homologue (RAI2) of a mouse retinoic acid-induced gene in Xp22 | journal = Genomics | volume = 55 | issue = 3 | pages = 275–83 |date=May 1999 | pmid = 10049581 | pmc = | doi = 10.1006/geno.1998.5667 }} 2. ^{{cite journal | vauthors = Walpole SM, Ronce N, Grayson C, Dessay B, Yates JR, Trump D, Toutain A | title = Exclusion of RAI2 as the causative gene for Nance-Horan syndrome | journal = Hum Genet | volume = 104 | issue = 5 | pages = 410–1 |date=Jul 1999 | pmid = 10394933 | pmc = | doi =10.1007/s004390050976 }} 3. ^1 {{cite web | title = Entrez Gene: RAI2 retinoic acid induced 2| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=10742| accessdate = }} Further reading{{refbegin | 2}}
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