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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2002 | 1 |
2003 | 1 |
2005 | 2 |
2007 | 1 |
2011 | 1 |
2012 | 1 |
2024 | 0 |
PubMed (RefSeq) for id: 2678878738
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Smith-Magenis syndrome results in disruption of CLOCK gene transcription and reveals an integral role for RAI1 in the maintenance of circadian rhythmicity.
Am J Hum Genet. 2012 Jun 8;90(6):941-9. doi: 10.1016/j.ajhg.2012.04.013. Epub 2012 May 10.
Am J Hum Genet. 2012.
PMID: 22578325
Free PMC article.
Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium.
Gaudet P, Livstone MS, Lewis SE, Thomas PD.
Gaudet P, et al.
Brief Bioinform. 2011 Sep;12(5):449-62. doi: 10.1093/bib/bbr042. Epub 2011 Aug 27.
Brief Bioinform. 2011.
PMID: 21873635
Free PMC article.
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Penetrance of craniofacial anomalies in mouse models of Smith-Magenis syndrome is modified by genomic sequence surrounding Rai1: not all null alleles are alike.
Yan J, Bi W, Lupski JR.
Yan J, et al.
Am J Hum Genet. 2007 Mar;80(3):518-25. doi: 10.1086/512043. Epub 2007 Jan 18.
Am J Hum Genet. 2007.
PMID: 17273973
Free PMC article.
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Inactivation of Rai1 in mice recapitulates phenotypes observed in chromosome engineered mouse models for Smith-Magenis syndrome.
Bi W, Ohyama T, Nakamura H, Yan J, Visvanathan J, Justice MJ, Lupski JR.
Bi W, et al.
Hum Mol Genet. 2005 Apr 15;14(8):983-95. doi: 10.1093/hmg/ddi085. Epub 2005 Mar 3.
Hum Mol Genet. 2005.
PMID: 15746153
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Gene and alternative splicing annotation with AIR.
Florea L, Di Francesco V, Miller J, Turner R, Yao A, Harris M, Walenz B, Mobarry C, Merkulov GV, Charlab R, Dew I, Deng Z, Istrail S, Li P, Sutton G.
Florea L, et al.
Genome Res. 2005 Jan;15(1):54-66. doi: 10.1101/gr.2889405.
Genome Res. 2005.
PMID: 15632090
Free PMC article.
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Mutations in RAI1 associated with Smith-Magenis syndrome.
Slager RE, Newton TL, Vlangos CN, Finucane B, Elsea SH.
Slager RE, et al.
Nat Genet. 2003 Apr;33(4):466-8. doi: 10.1038/ng1126. Epub 2003 Mar 24.
Nat Genet. 2003.
PMID: 12652298
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Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.
Strausberg RL, Feingold EA, Grouse LH, Derge JG, Klausner RD, Collins FS, Wagner L, Shenmen CM, Schuler GD, Altschul SF, Zeeberg B, Buetow KH, Schaefer CF, Bhat NK, Hopkins RF, Jordan H, Moore T, Max SI, Wang J, Hsieh F, Diatchenko L, Marusina K, Farmer AA, Rubin GM, Hong L, Stapleton M, Soares MB, Bonaldo MF, Casavant TL, Scheetz TE, Brownstein MJ, Usdin TB, Toshiyuki S, Carninci P, Prange C, Raha SS, Loquellano NA, Peters GJ, Abramson RD, Mullahy SJ, Bosak SA, McEwan PJ, McKernan KJ, Malek JA, Gunaratne PH, Richards S, Worley KC, Hale S, Garcia AM, Gay LJ, Hulyk SW, Villalon DK, Muzny DM, Sodergren EJ, Lu X, Gibbs RA, Fahey J, Helton E, Ketteman M, Madan A, Rodrigues S, Sanchez A, Whiting M, Madan A, Young AC, Shevchenko Y, Bouffard GG, Blakesley RW, Touchman JW, Green ED, Dickson MC, Rodriguez AC, Grimwood J, Schmutz J, Myers RM, Butterfield YS, Krzywinski MI, Skalska U, Smailus DE, Schnerch A, Schein JE, Jones SJ, Marra MA; Mammalian Gene Collection Program Team.
Strausberg RL, et al.
Proc Natl Acad Sci U S A. 2002 Dec 24;99(26):16899-903. doi: 10.1073/pnas.242603899. Epub 2002 Dec 11.
Proc Natl Acad Sci U S A. 2002.
PMID: 12477932
Free PMC article.
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