[1] Martinez-Castellano F. Non-specific X-linked mental re-tardation. Rev Neurol, 2006, 42(1): 77–83.

[2] Ellison J, Passage M, Yu LC, Yen P, Mohandas TK, Shapiro L. Directed isolation of human genes that escape X inactivation. Somat Cell Mol Genet, 1992, 18(3): 259–268.

[3] Wu J, Ellison J, Salido E, Yen P, Mohandas T, Shapiro LJ. Isolation and characterization of XE169, a novel human gene that escapes X-inactivation. Hum Mol Genet, 1994, 3(1): 153–160.

[4] Agulnik AI, Mitchell MJ, Mattei MG, Borsani G, Avner PA, Lerner JL, Bishop CE. A novel X gene with a widely transcribed Y-linked homologue escapes X-inactivation in mouse and human. Hum Mol Genet, 1994, 3(6): 879–884.

[5] Brown CJ, Miller AP, Carrel L, Rupert JL, Davies KE, Willard HF. The DXS423E gene in Xp11.21 escapes X chromosome inactivation. Hum Mol Genet, 1995, 4(2): 251–255.

[6] Miller AP, Gustashaw K, Wolff DJ, Rider SH, Monaco AP, Eble B, Schlessinger D, Gorski JL, van Ommen GJ, Weissenbach J, Willard HF. Three genes that escape X chromosome inactivation are clustered within a 6 Mb YAC contig and STS map in Xp11.21-p11.22. Hum Mol Genet, 1995, 4(4): 731–739.

[7] Laval SH, Glenister PH, Rasberry C, Thornton CE, Ma-hadevaiah SK, Cooke HJ, Burgoyne PS, Cattanach BM. Y chromosome short arm-Sxr recombination in XSxr/Y males causes deletion of Rbm and XY female sex reversal. Proc Natl Acad Sci USA, 1995, 92(22): 10403–10407.

[8] Yi L, Hao Z, Yang T, Wang S, Xing B, Xu Y. cDNA cloning, bioinformatic and tissue-specific expression analysis of porcine JARID1C gene. J Genet Genomics, 2007, 34(12): 1088–1096.

[9] Wu J, Salido EC, Yen PH, Mohandas TK, Heng HH, Tsui LC, Park J, Chapman VM, Shapiro LJ. The murine Xe169 gene escapes X-inactivation like its human homologue. Nat Genet, 1994, 7(4): 491–496.

[10] Takeuchi T, Yamazaki Y, Katoh-Fukui Y, Tsuchiya R, Kondo S, Motoyama J, Higashinakagawa T. Gene trap capture of a novel mouse gene, jumonji, required for neu-ral tube formation. Genes Dev, 1995, 9(10): 1211–1222.

[11] Iwase S, Lan F, Bayliss P, de la Torre-Ubieta L, Huarte M, Qi HH, Whetstine JR, Bonni A, Roberts TM, Shi Y. The X-linked mental retardation gene SMCX/JARID1C de-fines a family of histone H3 lysine 4 demethylases. Cell, 2007, 128(6): 1077–1088.

[12] Klose RJ, Kallin EM, Zhang Y. JmjC-domain-containing proteins and histone demethylation. Nat Rev Genet, 2006, 7(9): 715–727.

[13] Defeo-Jones D, Huang PS, Jones RE, Haskell KM, Vuo-colo GA, Hanobik MG, Huber HE, Oliff A. Cloning of cDNAs for cellular proteins that bind to the retinoblas-toma gene product. Nature, 1991, 352(6332): 251–254.

[14] Benevolenskaya EV, Murray HL, Branton P, Young RA, Kaelin WG, Jr. Binding of pRB to the PHD protein RBP2 promotes cellular differentiation. Mol Cell, 2005, 18(6): 623–635.

[15] Ahmed S, Palermo C, Wan S, Walworth NC. A novel protein with similarities to Rb binding protein 2 compen-sates for loss of Chk1 function and affects histone modi-fication in fission yeast. Mol Cell Biol, 2004, 24(9): 3660–3669.

[16] Lu PJ, Sundquist K, Baeckstrom D, Poulsom R, Hanby A, Meier-Ewert S, Jones T, Mitchell M, Pitha-Rowe P, Freemont P, Taylor-Papadimitriou J. A novel gene (PLU-1) containing highly conserved putative DNA/chromatin binding motifs is specifically up-regulated in breast cancer. J Biol Chem, 1999, 274(22): 15633–15645.

[17] Tan K, Shaw AL, Madsen B, Jensen K, Taylor-Pa- padimitriou J, Freemont PS. Human PLU-1 Has transcrip-tional repression properties and interacts with the devel-opmental transcription factors BF-1 and PAX9. J Biol Chem, 2003, 278(23): 20507–20513.

[18] Agulnik AI, Mitchell MJ, Lerner JL, Woods DR, Bishop CE. A mouse Y chromosome gene encoded by a region essential for spermatogenesis and expression of male- specific minor histocompatibility antigens. Hum Mol Genet, 1994, 3(6): 873–878.

[19] Jensen LR, Amende M, Gurok U, Moser B, Gimmel V, Tzschach A, Janecke AR, Tariverdian G, Chelly J, Fryns JP, Van Esch H, Kleefstra T, Hamel B, Moraine C, Gecz J, Turner G, Reinhardt R, Kalscheuer VM, Ropers HH, Lenzner S. Mutations in the JARID1C gene, which is in-volved in transcriptional regulation and chromatin remod-eling, cause X-linked mental retardation. Am J Hum Genet, 2005, 76(2): 227–236.

[20] Marchler-Bauer A, Anderson JB, Cherukuri PF, DeWeese-Scott C, Geer LY, Gwadz M, He S, Hurwitz DI, Jackson JD, Ke Z, Lanczycki CJ, Liebert CA, Liu C, Lu F, Marchler GH, Mullokandov M, Shoemaker BA, Simonyan V, Song JS, Thiessen PA, Yamashita RA, Yin JJ, Zhang D, Bryant SH. CDD: a conserved domain database for protein classification. Nucleic Acids Res, 2005, 33(Database is-sue): D192–196.

[21] Cloosen S, Gratama J, van Leeuwen EB, Senden-Gijsbers BL, Oving EB, von Mensdorff-Pouilly S, Tarp MA, Mandel U, Clausen H, Germeraad WT, Bos GM. Cancer specific Mucin-1 glycoforms are expressed on multiple myeloma. Br J Haematol, 2006, 135(4): 513–516.

[22] Klose C, Matteucci-Gothe R, Linden M. Pre- and post- treatment in inpatient psychosomatic rehabilitation. Reha-bilitation (Stuttg), 2006, 45(6): 359–368.

[23] Whetstine JR, Nottke A, Lan F, Huarte M, Smolikov S, Chen Z, Spooner E, Li E, Zhang G, Colaiacovo M, Shi Y. Reversal of histone lysine trimethylation by the JMJD2 family of histone demethylases. Cell, 2006, 125(3): 467–481.

[24] Wilsker D, Patsialou A, Dallas PB, Moran E. ARID pro-teins: a diverse family of DNA binding proteins implicated in the control of cell growth, differentiation, and devel-opment. Cell Growth Differ, 2002, 13(3): 95–106.

[25] Santos C, Rodriguez-Revenga L, Madrigal I, Badenas C, Pineda M, Mila M. A novel mutation in JARID1C gene associated with mental retardation. Eur J Hum Genet, 2006, 14(5): 583–586.

[26] Tzschach A, Lenzner S, Moser B, Reinhardt R, Chelly J, Fryns JP, Kleefstra T, Raynaud M, Turner G, Ropers HH, Kuss A, Jensen LR. Novel JARID1C/SMCX mutations in patients with X-linked mental retardation. Hum Mutat, 2006, 27(4): 389.

[27] Adegbola A, Gao H, Sommer S, Browning M. A novel mutation in JARID1C/SMCX in a patient with autism spectrum disorder (ASD). Am J Med Genet A, 2008, 146A(4): 505–511.

[28] Abidi F, Holloway L, Moore CA, Weaver DD, Simensen RJ, Stevenson RE, Rogers RC, Schwartz CE. Novel hu-man pathological mutations. Gene symbol: JARID1C. Disease: Mental retardation, X-linked. Hum Genet, 2009, 125(3): 345.

[29] Laumonnier F, Holbert S, Ronce N, Faravelli F, Lenzner S, Schwartz CE, Lespinasse J, Van Esch H, Lacombe D, Go-izet C, Phan-Dinh Tuy F, van Bokhoven H, Fryns JP, Chelly J, Ropers HH, Moraine C, Hamel BC, Briault S. Mutations in PHF8 are associated with X linked mental retardation and cleft lip/cleft palate. J Med Genet, 2005, 42(10): 780–786.

[30] Lower KM, Turner G, Kerr BA, Mathews KD, Shaw MA, Gedeon AK, Schelley S, Hoyme HE, White SM, Delatycki MB, Lampe AK, Clayton-Smith J, Stewart H, van Ravenswaay CM, de Vries BB, Cox B, Grompe M, Ross S, Thomas P, Mulley JC, Gecz J. Mutations in PHF6 are as-sociated with Borjeson-Forssman-Lehmann syndrome. Nat Genet, 2002, 32(4): 661–665.

[31] Tahiliani M, Mei P, Fang R, Leonor T, Rutenberg M, Shimizu F, Li J, Rao A, Shi Y. The histone H3K4 de-methylase SMCX links REST target genes to X-linked mental retardation. Nature, 2007, 447(7144): 601–605.

[32] Akbarian S, Huang HS. Epigenetic regulation in human brain-focus on histone lysine methylation. Biol Psychiatry, 2009, 65(3): 198–203.

[33] Fiala JC, Spacek J, Harris KM. Dendritic spine pathology: cause or consequence of neurological disorders? Brain Res Brain Res Rev, 2002, 39(1): 29–54.

[34] Ropers HH, Hamel BC. X-linked mental retardation. Nat Rev Genet, 2005, 6(1): 46–57.

[35] Xu J, Deng X, Disteche CM. Sex-specific expression of the X-linked histone demethylase gene Jarid1c in brain. PLoS ONE, 2008, 3(7): e2553.