Biology:SHFM3P1
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Split hand/foot malformation (ectrodactyly) type 3 pseudogene 1, also known as SHFM3P1, is a human gene.[1]
References
Further reading
- "Combinatorial control in ubiquitin-dependent proteolysis: don't Skp the F-box hypothesis". Trends Genet. 14 (6): 236–43. 1998. doi:10.1016/S0168-9525(98)01473-5. PMID 9635407.
- "M-phase kinases induce phospho-dependent ubiquitination of somatic Wee1 by SCFβ-TrCP". Proc. Natl. Acad. Sci. U.S.A. 101 (13): 4419–24. 2004. doi:10.1073/pnas.0307700101. PMID 15070733. Bibcode: 2004PNAS..101.4419W.
- "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. 2004. doi:10.1038/ng1285. PMID 14702039.
- "A family of mammalian F-box proteins". Curr. Biol. 9 (20): 1180–2. 1999. doi:10.1016/S0960-9822(00)80021-4. PMID 10531037.
- "Identification of a family of human F-box proteins". Curr. Biol. 9 (20): 1177–9. 1999. doi:10.1016/S0960-9822(00)80020-2. PMID 10531035.
- "A novel human gene encoding an F-box/WD40 containing protein maps in the SHFM3 critical region on 10q24". Biochem. Biophys. Res. Commun. 261 (1): 64–70. 1999. doi:10.1006/bbrc.1999.0963. PMID 10405324.
- "Sequence and analysis of the human ABL gene, the BCR gene, and regions involved in the Philadelphia chromosomal translocation". Genomics 27 (1): 67–82. 1995. doi:10.1006/geno.1995.1008. PMID 7665185.
- "Philadelphia chromosomal breakpoints are clustered within a limited region, bcr, on chromosome 22". Cell 36 (1): 93–9. 1984. doi:10.1016/0092-8674(84)90077-1. PMID 6319012.
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