Biology:ROBO3
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 Generic protein structure example |
Roundabout homolog 3 is a protein that in humans is encoded by the ROBO3 gene.[1][2]
References
- ↑ "Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesis". Science 304 (5676): 1509–13. Jun 2004. doi:10.1126/science.1096437. PMID 15105459.
- ↑ "Entrez Gene: ROBO3 roundabout, axon guidance receptor, homolog 3 (Drosophila)". https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=64221.
Further reading
- "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides.". Gene 138 (1–2): 171–4. 1994. doi:10.1016/0378-1119(94)90802-8. PMID 8125298.
- "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library.". Gene 200 (1–2): 149–56. 1997. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149.
- "Cloning and functional studies of a novel gene aberrantly expressed in RB-deficient embryos.". Dev. Biol. 207 (1): 62–75. 1999. doi:10.1006/dbio.1998.9141. PMID 10049565.
- "Familial horizontal gaze palsy with progressive scoliosis maps to chromosome 11q23-25.". Neurology 59 (3): 432–5. 2002. doi:10.1212/wnl.59.3.432. PMID 12177379.
- "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.
- "Complete sequencing and characterization of 21,243 full-length human cDNAs.". Nat. Genet. 36 (1): 40–5. 2004. doi:10.1038/ng1285. PMID 14702039.
- "Neurologic features of horizontal gaze palsy and progressive scoliosis with mutations in ROBO3.". Neurology 64 (7): 1196–203. 2006. doi:10.1212/01.WNL.0000156349.01765.2B. PMID 15824346.
- "Evidence for the existence of two Robo3 isoforms with divergent biochemical properties.". Mol. Cell. Neurosci. 30 (4): 485–93. 2006. doi:10.1016/j.mcn.2005.07.014. PMID 16226035.
- "Horizontal gaze palsy with progressive scoliosis can result from compound heterozygous mutations in ROBO3.". J. Med. Genet. 43 (3): e11. 2006. doi:10.1136/jmg.2005.035436. PMID 16525029.
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