[cite web | title = Entrez Gene: RAB11FIP4 RAB11 family interacting protein 4 (class II)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=84440| accessdate = ] ] PBB_Summary
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References
Further reading
PBB_Further_reading
citations =
*cite journal | author=Jenne DE, Tinschert S, Stegmann E, "et al." |title=A common set of at least 11 functional genes is lost in the majority of NF1 patients with gross deletions. |journal=Genomics |volume=66 |issue= 1 |pages= 93–7 |year= 2000 |pmid= 10843809 |doi= 10.1006/geno.2000.6179
*cite journal | author=Nagase T, Nakayama M, Nakajima D, "et al." |title=Prediction of the coding sequences of unidentified human genes. XX. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro. |journal=DNA Res. |volume=8 |issue= 2 |pages= 85–95 |year= 2001 |pmid= 11347906 |doi=
*cite journal | author=Jenne DE, Tinschert S, Reimann H, "et al." |title=Molecular characterization and gene content of breakpoint boundaries in patients with neurofibromatosis type 1 with 17q11.2 microdeletions. |journal=Am. J. Hum. Genet. |volume=69 |issue= 3 |pages= 516–27 |year= 2001 |pmid= 11468690 |doi=
*cite journal | author=Wallace DM, Lindsay AJ, Hendrick AG, McCaffrey MW |title=Rab11-FIP4 interacts with Rab11 in a GTP-dependent manner and its overexpression condenses the Rab11 positive compartment in HeLa cells. |journal=Biochem. Biophys. Res. Commun. |volume=299 |issue= 5 |pages= 770–9 |year= 2003 |pmid= 12470645 |doi=
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |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
*cite journal | author=Jenne DE, Tinschert S, Dorschner MO, "et al." |title=Complete physical map and gene content of the human NF1 tumor suppressor region in human and mouse. |journal=Genes Chromosomes Cancer |volume=37 |issue= 2 |pages= 111–20 |year= 2003 |pmid= 12696059 |doi= 10.1002/gcc.10206
*cite journal | author=Ota T, Suzuki Y, Nishikawa T, "et al." |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 | author=Gerhard DS, Wagner L, Feingold EA, "et al." |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504
*cite journal | author=Fielding AB, Schonteich E, Matheson J, "et al." |title=Rab11-FIP3 and FIP4 interact with Arf6 and the exocyst to control membrane traffic in cytokinesis. |journal=EMBO J. |volume=24 |issue= 19 |pages= 3389–99 |year= 2006 |pmid= 16148947 |doi= 10.1038/sj.emboj.7600803
*cite journal | author=Lim J, Hao T, Shaw C, "et al." |title=A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration. |journal=Cell |volume=125 |issue= 4 |pages= 801–14 |year= 2006 |pmid= 16713569 |doi= 10.1016/j.cell.2006.03.032
*cite journal | author=Douglas J, Cilliers D, Coleman K, "et al." |title=Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth. |journal=Nat. Genet. |volume=39 |issue= 8 |pages= 963–5 |year= 2007 |pmid= 17632510 |doi= 10.1038/ng2083
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