| 释义 |
- References
- Further reading
{{Infobox_gene}}Roundabout homolog 3 is a protein that in humans is encoded by the ROBO3 gene.[1][2]{{PBB_Summary
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}}References1. ^{{cite journal | vauthors = Jen JC, Chan WM, Bosley TM, Wan J, Carr JR, Rub U, Shattuck D, Salamon G, Kudo LC, Ou J, Lin DD, Salih MA, Kansu T, Al Dhalaan H, Al Zayed Z, MacDonald DB, Stigsby B, Plaitakis A, Dretakis EK, Gottlob I, Pieh C, Traboulsi EI, Wang Q, Wang L, Andrews C, Yamada K, Demer JL, Karim S, Alger JR, Geschwind DH, Deller T, Sicotte NL, Nelson SF, Baloh RW, Engle EC | title = Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesis | journal = Science | volume = 304 | issue = 5676 | pages = 1509–13 |date=Jun 2004 | pmid = 15105459 | pmc = 1618874 | doi = 10.1126/science.1096437 }}
2. ^{{cite web | title = Entrez Gene: ROBO3 roundabout, axon guidance receptor, homolog 3 (Drosophila)| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=64221| accessdate = }}
Further reading{{refbegin | 2}}- {{cite journal | vauthors=Maruyama K, Sugano S |title=Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides. |journal=Gene |volume=138 |issue= 1-2 |pages= 171–4 |year= 1994 |pmid= 8125298 |doi=10.1016/0378-1119(94)90802-8 }}
- {{cite journal |vauthors=Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, etal |title=Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library. |journal=Gene |volume=200 |issue= 1-2 |pages= 149–56 |year= 1997 |pmid= 9373149 |doi=10.1016/S0378-1119(97)00411-3 }}
- {{cite journal | vauthors=Yuan SS, Cox LA, Dasika GK, Lee EY |title=Cloning and functional studies of a novel gene aberrantly expressed in RB-deficient embryos. |journal=Dev. Biol. |volume=207 |issue= 1 |pages= 62–75 |year= 1999 |pmid= 10049565 |doi= 10.1006/dbio.1998.9141 }}
- {{cite journal |vauthors=Jen J, Coulin CJ, Bosley TM, etal |title=Familial horizontal gaze palsy with progressive scoliosis maps to chromosome 11q23-25. |journal=Neurology |volume=59 |issue= 3 |pages= 432–5 |year= 2002 |pmid= 12177379 |doi= 10.1212/wnl.59.3.432}}
- {{cite journal |vauthors=Strausberg RL, Feingold EA, Grouse LH, etal |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 | pmc=139241 }}
- {{cite journal |vauthors=Ota T, Suzuki Y, Nishikawa T, etal |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285 }}
- {{cite journal |vauthors=Bosley TM, Salih MA, Jen JC, etal |title=Neurologic features of horizontal gaze palsy and progressive scoliosis with mutations in ROBO3. |journal=Neurology |volume=64 |issue= 7 |pages= 1196–203 |year= 2006 |pmid= 15824346 |doi= 10.1212/01.WNL.0000156349.01765.2B }}
- {{cite journal |vauthors=Camurri L, Mambetisaeva E, Davies D, etal |title=Evidence for the existence of two Robo3 isoforms with divergent biochemical properties. |journal=Mol. Cell. Neurosci. |volume=30 |issue= 4 |pages= 485–93 |year= 2006 |pmid= 16226035 |doi= 10.1016/j.mcn.2005.07.014 }}
- {{cite journal |vauthors=Chan WM, Traboulsi EI, Arthur B, etal |title=Horizontal gaze palsy with progressive scoliosis can result from compound heterozygous mutations in ROBO3. |journal=J. Med. Genet. |volume=43 |issue= 3 |pages= e11 |year= 2006 |pmid= 16525029 |doi= 10.1136/jmg.2005.035436 | pmc=2563249 }}
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