Citations for
1CCDC8, CUL7, GFS, GFS2, GFS3, OBSL1
3M Syndrome: An Easily Recognizable yet Underdiagnosed Cause of Proportionate Short Stature.
Al-Dosari MS, Al-Shammari M, Shaheen R, Faqeih E, Alghofely MA, Boukai A, Alkuraya FS.
J Pediatr Pediatr. 2012 Feb 9. [Epub ahead of print] 2012
2CCDC8, CUL7, GFS, GFS2, GFS3, OBSL1
Exome sequencing identifies CCDC8 mutations in 3-M syndrome, suggesting that CCDC8 contributes in a pathway with CUL7 and OBSL1 to control human growth.
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.
Am J Hum Genet 89(1):148-53. Epub 2011 Jul 7. 2011
3CCDC8, CUL7, GFS, GFS2, GFS3, OBSL1, SRS17
Is autosomal recessive Silver-Russel syndrome a separate entity or is it part of the 3-M syndrome spectrum?
Akawi NA, Ali BR, Hamamy H, Al-Hadidy A, Al-Gazali L.
Am J Med Genet A 155A(6):1236-45. doi: 10.1002/ajmg.a.34009. Epub 2011 May 5. 2011
4CCDC8, CUL7, GFS, GFS2, GFS3, OBSL1, SRS17
The genetics of 3-m syndrome: unravelling a potential new regulatory growth pathway.
Hanson D, Murray PG, Black GC, Clayton PE.
Horm Res Paediatr 76(6):369-78. doi: 10.1159/000334392. Epub 2011 Nov 29. 2011
5CCDC8
Differential effects on p53-mediated cell cycle arrest vs. apoptosis by p90.
Dai C, Tang Y, Jung SY, Qin J, Aaronson SA, Gu W.
Proc Natl Acad Sci U S A 108(47):18937-42. Epub 2011 Nov 14. 2011
6ATP5G2, CCDC8, CORO6, FBN2, KLHL35, PCDH8, QPCT, SCUBE3, ZSCAN18
Genome-wide methylation analysis identifies epigenetically inactivated candidate tumour suppressor genes in renal cell carcinoma.
Morris MR, Ricketts CJ, Gentle D, McRonald F, Carli N, Khalili H, Brown M, Kishida T, Yao M, Banks RE, Clarke N, Latif F, Maher ER.
Oncogene ncogene. 2010 Dec 6. [Epub ahead of print]PMID: 21132003 2010
7ABHD12, ABHD12B, ABTB2, ADCK4, AGBL3, AMMECR1L, ANAPC15, ANKMY1, ANKRD16, ANKRD22, ANKRD29, ANKRD36, ANKRD40, ANKRD43, ANKRD44, APOPT1, ARHGAP30, ARL16, ARL17, ARL17P1, ARMC1, ATAD1, BRD9, C10orf126, C10orf132, C10orf57, C10orf58, C10orf84, C10orf85, C10orf88, C10orf90, C10orf91, C10orf92, C10orf93, C10orf95, C11orf10, C11orf36, C11orf41, C11orf42, C11orf45, C11orf46, C11orf52, C11orf53, C11orf57, C11orf58, C11orf61, C11orf63, C11orf64, C11orf66, C11orf70, C11orf71, C11orf72, C11orf76, C12orf23, C12orf26, C12orf28, C12orf32, C12orf33, C12orf34, C12orf36, C12orf45, C12orf48, C12orf54, C12orf60, C12orf62, C13orf16, C13orf26, C13orf27, C13orf28, C13orf29, C13orf30, C13orf33, C14orf101, C14orf109, C14orf126, C14orf128, C14orf138, C14orf148, C14orf152, C14orf177, C14orf178, C15orf24, C15orf26, C15orf32, C15orf33, C15orf34, C15orf40, C15orf43, C16orf58, C16orf61, C16orf63, C16orf74, C16orf78, C17orf44, C17orf50, C17orf54, C17orf57, C17orf58, C18orf16, C18orf18, C18orf22, C19orf18, C19orf22, C19orf23, C19orf28, C19orf30, C19orf36, C19orf48, C19orf52, C1orf106, C1orf109, C1orf57, C20orf103, C20orf106, C20orf108, C20orf112, C20orf144, C20orf149, C20orf165, C20orf166, C20orf194, C20orf197, C20orf39, C20orf62, C20orf79, C21orf122, C21orf128, C22orf13, C22orf25, C22orf27, C22orf36, C2orf24, C2orf48, C3orf14, C3orf17, C3orf18, C3orf22, C3orf24, C3orf25, C3orf26, C3orf31, C3orf32, C3orf33, C3orf36, C3orf37, C3orf38, C3orf45, C3orf46, C3orf54, C3orf58, C3orf62, C4orf36, C5orf23, C7orf30, C7orf38, C7orf45, C8orf44, C8orf45, C8orf46, C8orf74, C9orf116, C9orf70, CC2D2B, CCDC101, CCDC102A, CCDC103, CCDC109A, CCDC111, CCDC117, CCDC124, CCDC147, CCDC37, CCDC38, CCDC46, CCDC48, CCDC58, CCDC58P1, CCDC68, CCDC70, CCDC74B, CCDC8, CCDC84, CCDC99, CHCHD5, CLDND2, CXorf21, CXorf38, CXorf42, DDRGK1, DEM1, DEXI, DNAJB8, DNAJC18, DNAJC5G, DPY19L1, DPY19L3, DPY19L4, DUS1L, DUS3L, EFCAB1, EFCAB2, EFCAB3, EFCAB4B, EFHA2, EFHB, EPHX4, FAM100B, FAM106A, FAM162B, FAM168A, FAM81A, FAM81B, HEATR3, HEATR4, HSFX2, IFT43, IL34, KANSL1, KLHL29, KLHL30, KLHL30, KLHL36, LAMTOR1, LRRC20, LRRC24, LRRC34, MARCH9, MT1P3, NACC2, NCRNA00175, NJMUR1, NJMUR1, NKAPL, ODF3L2, OTUD7A, PID1, POMGNT2, PRR11, PRR12, RWDD2A, SKAP, THOC6, TMEM101, TMEM103, TMEM106A, TMEM106C, TMEM107, TMEM108, TMEM109, TMEM110, TMEM111, TMEM116, TMEM217, TMEM229B, TRIM65, TTC17, TTC6, TTPAL, TUBB6, WDR72, WDR85, ZBTB45, ZBTB5, ZBTB9, ZNF385B, ZNF439, ZNF440, ZNF454, ZNF485, ZNF486, ZNF497, ZNF509, ZNF519, ZNF524, ZNF613, ZNF625, ZNF643, ZNRF3, ZSCAN1, ZSCAN23, ZSCAN5A, ZSWIM1, ZSWIM3
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
Gerhard DS, Wagner L, Feingold EA, Shenmen CM, Grouse LH, Schuler G, Klein SL, Old S, Rasooly R, Good P, Guyer M, Peck AM, Derge JG, Lipman D, Collins FS, Jang W, Sherry S, Feolo M, Misquitta L, Lee E, Rotmistrovsky K, Greenhut SF, Schaefer CF, Buetow K, Bonner TI, Haussler D, Kent J, Kiekhaus M, Furey T, Brent M, Prange C, Schreiber K, Shapiro N, Bhat NK, Hopkins RF, Hsie F, Driscoll T, Soares MB, Casavant TL, Scheetz TE, Brown-stein MJ, Usdin TB, Toshiyuki S, Carninci P, Piao Y, Dudekula DB, Ko MS, Kawakami K, Suzuki Y, Sugano S, Gruber CE, Smith MR, Simmons B, Moore T, Waterman R, Johnson SL, Ruan Y, Wei CL, Mathavan S, Gunaratne PH, Wu J, Garcia AM, Hulyk SW, Fuh E, Yuan Y, Sneed A, Kowis C, Hodgson A, Muzny DM, McPherson J, Gibbs RA, Fahey J, Helton E, Ketteman M, Madan A, Rodrigues S, Sanchez A, Whiting M, Madari A, Young AC, Wetherby KD, Granite SJ, Kwong PN, Brinkley CP, Pearson RL, Bouffard GG, Blakesly RW, Green ED, Dickson MC, Rodriguez AC, Grimwood J, Schmutz J, Myers RM, Butterfield YS, Griffith M, Griffith OL, Krzywinski MI, Liao N, Morin R, Palmquist D, Petrescu AS, Skalska U, Smailus DE, Stott JM, Schnerch A, Schein JE, Jones SJ, Holt RA, Baross A, Marra MA, Clifton S, Makowski KA, Bosak S, Malek J; MGC Project Team.
Genome Res 14(10B):2121-7. Erratum in: Genome Res. 2006 Jun;16(6):804. Morrin, Ryan [corrected to Morin, Ryan]. 2004