| 1 | CD36, CUL7, IRS1
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| Ubiquitinated CD36 sustains insulin-stimulated Akt activation by stabilizing insulin receptor substrate 1 in myotubes.
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| Sun S, Tan P, Huang X, Zhang W, Kong C, Ren F, Su X.
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| J Biol Chem 293(7):2383-2394. doi: 10.1074/jbc.M117.811471. Epub 2017 Dec 21.
2018
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| 2 | CCDC8, CUL7, GFS, GFS2, GFS3, OBSL1
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| 3M Syndrome: An Easily Recognizable yet Underdiagnosed Cause of Proportionate Short Stature.
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| Al-Dosari MS, Al-Shammari M, Shaheen R, Faqeih E, Alghofely MA, Boukai A, Alkuraya FS.
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| J Pediatr Pediatr. 2012 Feb 9. [Epub ahead of print]
2012
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| 3 | CCDC8, CUL7, GFS, GFS2, GFS3, OBSL1
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| Exome sequencing identifies CCDC8 mutations in 3-M syndrome, suggesting that CCDC8 contributes in a pathway with CUL7 and OBSL1 to control human growth.
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| Hanson D, Murray PG, O'Sullivan J, Urquhart J, Daly S, Bhaskar SS, Biesecker LG, Skae M, Smith C, Cole T, Kirk J, Chandler K, Kingston H, Donnai D, Clayton PE, Black GC.
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| Am J Hum Genet 89(1):148-53. Epub 2011 Jul 7.
2011
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| 4 | CCDC8, CUL7, GFS, GFS2, GFS3, OBSL1, SRS17
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| Is autosomal recessive Silver-Russel syndrome a separate entity or is it part of the 3-M syndrome spectrum?
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| Akawi NA, Ali BR, Hamamy H, Al-Hadidy A, Al-Gazali L.
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| Am J Med Genet A 155A(6):1236-45. doi: 10.1002/ajmg.a.34009. Epub 2011 May 5.
2011
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| 5 | CCDC8, CUL7, GFS, GFS2, GFS3, OBSL1, SRS17
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| The genetics of 3-m syndrome: unravelling a potential new regulatory growth pathway.
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| Hanson D, Murray PG, Black GC, Clayton PE.
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| Horm Res Paediatr 76(6):369-78. doi: 10.1159/000334392. Epub 2011 Nov 29.
2011
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| 6 | CUL7, FBXW8, OBSL1
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| An OBSL1-Cul7Fbxw8 ubiquitin ligase signaling mechanism regulates Golgi morphology and dendrite patterning.
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| Litterman N, Ikeuchi Y, Gallardo G, O'Connell BC, Sowa ME, Gygi SP, Harper JW, Bonni A.
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| PLoS Biol 9(5):e1001060. Epub 2011 May 10.
2011
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| 7 | CUL7, GFS
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| A large-scale mutation search reveals genetic heterogeneity in 3M syndrome.
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| Huber C, Delezoide AL, Guimiot F, Baumann C, Malan V, Le Merrer M, Da Silva DB, Bonneau D, Chatelain P, Chu C, Clark R, Cox H, Edery P, Edouard T, Fano V, Gibson K, Gillessen-Kaesbach G, Giovannucci-Uzielli ML, Graul-Neumann LM, van Hagen JM, van Hest L, Horovitz D, Melki J, Partsch CJ, Plauchu H, Rajab A, Rossi M, Sillence D, Steichen-Gersdorf E, Stewart H, Unger S, Zenker M, Munnich A, Cormier-Daire V.
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| Eur J Hum Genet 17(3):395-400. Epub 2008 Oct 29.PMID: 19225462 2009
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| 8 | CUL7, FBXW7
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| Disruption of the Fbxw8 gene results in pre- and postnatal growth retardation in mice.
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| Tsutsumi T, Kuwabara H, Arai T, Xiao Y, Decaprio JA.
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| Mol Cell Biol 28(2):743-51. Epub 2007 Nov 12.PMID: 17998335 2008
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| 9 | CUL7, FBXW8, SKP1
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| The cullin7 E3 ubiquitin ligase: a novel player in growth control.
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| Sarikas A, Xu X, Field LJ, Pan ZQ.
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| Cell Cycle 7(20):3154-61. Epub 2008 Oct 4. Review.PMID: 18927510 2008
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| 10 | CUL7, IRS1, SKP1
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| The CUL7 E3 ubiquitin ligase targets insulin receptor substrate 1 for ubiquitin-dependent degradation.
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| Xu X, Sarikas A, Dias-Santagata DC, Dolios G, Lafontant PJ, Tsai SC, Zhu W, Nakajima H, Nakajima HO, Field LJ, Wang R, Pan ZQ.
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| Mol Cell 30(4):403-14.PMID: 18498745 2008
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| 11 | CUL7, GFS
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| Clinical, molecular and histopathological features of short stature syndrome with novel CUL7 mutation in Yakuts: new population isolate in Asia.
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| Maksimova N, Hara K, Miyashia A, Nikolaeva I, Shiga A, Nogovicina A, Sukhomyasova A, Argunov V, Shvedova A, Ikeuchi T, Nishizawa M, Kuwano R, Onodera O.
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| J Med Genet 44(12):772-8. Epub 2007 Aug 3. 2007
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| 12 | CUL7
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| CUL7 is a novel antiapoptotic oncogene.
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| Kim SS, Shago M, Kaustov L, Boutros PC, Clendening JW, Sheng Y, Trentin GA, Barsyte-Lovejoy D, Mao DY, Kay R, Jurisica I, Arrowsmith CH, Penn LZ.
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| Cancer Res 67(20):9616-22.PMID: 17942889 2007
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| 13 | CUL7
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| A novel p53-binding domain in CUL7.
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| Kasper JS, Arai T, DeCaprio JA.
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| Biochem Biophys Res Commun 348(1):132-8. Epub 2006 Jul 13. 2006
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| 14 | CUL7
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| Cytoplasmic localized ubiquitin ligase cullin 7 binds to p53 and promotes cell growth by antagonizing p53 function.
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| Andrews P, He YJ, Xiong Y.
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| Oncogene 25(33):4534-48. Epub 2006 Mar 20. 2006
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| 15 | CUL7, GFS
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| Identification of mutations in CUL7 in 3-M syndrome.
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| Huber C, Dias-Santagata D, Glaser A, O'sullivan J, Brauner R, Wu K, Xu X, Pearce K, Wang R, Uzielli ML, Dagoneau N, Chemaitilly W, Superti-Furga A, Santos HD, Megarbane A, Morin G, Gillessen-Kaesbach G, Hennekam R, Burgt IV, Black GC, Clayton PE, Read A, Merrer ML, Scambler PJ, Munnich A, Pan ZQ, Winter R, Cormier-Daire V.
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| Nat Genet 37(10):1119-24. Epub 2005 Sep 4. 2005
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| 16 | CUL7
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| CUL7: A DOC domain-containing cullin selectively binds Skp1.Fbx29 to form an SCF-like complex.
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| Dias DC, Dolios G, Wang R, Pan ZQ.
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| Proc Natl Acad Sci U S A 99(26):16601-6. Epub 2002 Dec 12. 2002
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| 17 | ARHGAP11A, ARHGAP25, CCT8, CD302, CLTC, CUL7, EFTUD2, HELZ, HERC3, IQCB1, JOSD1, KIAA0020, KIAA0040, KIF14, LRRC14, MORF4L2, MTFR1, MTREX, POLD3, PPM1F, PPWD1, PSME4, R3HDM1, SETDB1, SF3B3, SNX17, TOMM20, TRIP12, UBE3C, USP6NL
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| Prediction of the coding sequences of unidentified human genes. I. The coding sequences of 40 new genes (KIAA0001-KIAA0040) deduced by analysis of randomly sampled cDNA clones from human immature myeloid cell line KG-1 (supplement).
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| Nomura N, Miyajima N, Sazuka T, Tanaka A, Kawarabayasi Y, Sato S, NagaseT, Seki N, Ishikawa K, Tabata S.
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| DNA Res 1(5):223-9. 1994
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