| 释义 |
- References
- Further reading
{{Infobox_gene}}Split hand/foot malformation (ectrodactyly) type 3 pseudogene 1, also known as SHFM3P1, is a human gene.[1]{{PBB_Summary
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}}References1. ^{{cite web | title = Entrez Gene: SHFM3P1 split hand/foot malformation (ectrodactyly) type 3 pseudogene 1| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=26226| accessdate = }}
Further reading{{refbegin | 2}}- {{cite journal | vauthors=Patton EE, Willems AR, Tyers M |title=Combinatorial control in ubiquitin-dependent proteolysis: don't Skp the F-box hypothesis |journal=Trends Genet. |volume=14 |issue= 6 |pages= 236–43 |year= 1998 |pmid= 9635407 |doi=10.1016/S0168-9525(98)01473-5 }}
- {{cite journal |vauthors=Watanabe N, Arai H, Nishihara Y, etal |title=M-phase kinases induce phospho-dependent ubiquitination of somatic Wee1 by SCFβ-TrCP |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=101 |issue= 13 |pages= 4419–24 |year= 2004 |pmid= 15070733 |doi= 10.1073/pnas.0307700101 | pmc=384762 }}
- {{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=Winston JT, Koepp DM, Zhu C, etal |title=A family of mammalian F-box proteins |journal=Curr. Biol. |volume=9 |issue= 20 |pages= 1180–2 |year= 1999 |pmid= 10531037 |doi= 10.1016/S0960-9822(00)80021-4 }}
- {{cite journal |vauthors=Cenciarelli C, Chiaur DS, Guardavaccaro D, etal |title=Identification of a family of human F-box proteins |journal=Curr. Biol. |volume=9 |issue= 20 |pages= 1177–9 |year= 1999 |pmid= 10531035 |doi= 10.1016/S0960-9822(00)80020-2 }}
- {{cite journal |vauthors=Ianakiev P, Kilpatrick MW, Dealy C, etal |title=A novel human gene encoding an F-box/WD40 containing protein maps in the SHFM3 critical region on 10q24 |journal=Biochem. Biophys. Res. Commun. |volume=261 |issue= 1 |pages= 64–70 |year= 1999 |pmid= 10405324 |doi= 10.1006/bbrc.1999.0963 }}
- {{cite journal |vauthors=Chissoe SL, Bodenteich A, Wang YF, etal |title=Sequence and analysis of the human ABL gene, the BCR gene, and regions involved in the Philadelphia chromosomal translocation |journal=Genomics |volume=27 |issue= 1 |pages= 67–82 |year= 1995 |pmid= 7665185 |doi=10.1006/geno.1995.1008 }}
- {{cite journal |vauthors=Groffen J, Stephenson JR, Heisterkamp N, etal |title=Philadelphia chromosomal breakpoints are clustered within a limited region, bcr, on chromosome 22 |journal=Cell |volume=36 |issue= 1 |pages= 93–9 |year= 1984 |pmid= 6319012 |doi=10.1016/0092-8674(84)90077-1 }}
{{refend}}{{protein-stub}} 1 : Pseudogenes |