Citations for
1RPL10, RPL10L
RPL10L Is Required for Male Meiotic Division by Compensating for RPL10 during Meiotic Sex Chromosome Inactivation in Mice
Jiang L, Li T, Zhang X, Zhang B, Yu C, Li Y, Fan S, Jiang X, Khan T, Hao Q, Xu P, Nadano D, Huleihel M, Lunenfeld E, Wang PJ, Zhang Y, Shi Q.
Curr Biol. May 22;27(10):1498-1505.e6. doi: 10.1016/j.cub.2017.04.017. Epub 2017 May 11. 2017
2RPL10, RPL11, RPL22, RPL5, RPS15, RPS20
Role of ribosomal protein mutations in tumor development (Review)
Goudarzi KM, Lindström MS.
Int J Oncol. Apr;48(4):1313-24. doi: 10.3892/ijo.2016.3387. Epub 2016 Feb 9. 2016
3MRXS35, RPL10
A Novel Mutation in RPL10 (Ribosomal Protein L10) Causes X-Linked Intellectual Disability, Cerebellar Hypoplasia, and Spondylo-Epiphyseal Dysplasia.
Zanni G, Kalscheuer VM, Friedrich A, Barresi S, Alfieri P, Di Capua M, Haas SA, Piccini G, Karl T, Klauck SM, Bellacchio E, Emma F, Cappa M, Bertini E, Breitenbach-Koller L.
Hum Mutat 36(12):1155-8. doi: 10.1002/humu.22860. Epub 2015 Sep 14. 2015
4MRXS35, RPL10
RPL10 mutation segregating in a family with X-linked syndromic Intellectual Disability.
Thevenon J, Michot C, Bole C, Nitschke P, Nizon M, Faivre L, Munnich A, Lyonnet S, Bonnefont JP, Portes VD, Amiel J.
Am J Med Genet A 167A(8):1908-12. doi: 10.1002/ajmg.a.37094. Epub 2015 Apr 6. 2015
5MRXS35, RPL10
A novel ribosomopathy caused by dysfunction of RPL10 disrupts neurodevelopment and causes X-linked microcephaly in humans.
Brooks SS, Wall AL, Golzio C, Reid DW, Kondyles A, Willer JR, Botti C, Nicchitta CV, Katsanis N, Davis EE.
Genetics 198(2):723-33. doi: 10.1534/genetics.114.168211. 2014
6CNOT3, RPL10, RPL5
Exome sequencing identifies mutation in CNOT3 and ribosomal genes RPL5 and RPL10 in T-cell acute lymphoblastic leukemia.
De Keersmaecker K, Atak ZK, Li N, Vicente C, Patchett S, Girardi T, Gianfelici V, Geerdens E, Clappier E, Porcu M, Lahortiga I, Lucà R, Yan J, Hulselmans G, Vranckx H, Vandepoel R, Sweron B, Jacobs K, Mentens N, Wlodarska I, Cauwelier B, Cloos J, Soulier J, Uyttebroeck A, Bagni C, Hassan BA, Vandenberghe P, Johnson AW, Aerts S, Cools J.
Nat Genet 45(2):186-90. doi: 10.1038/ng.2508. Epub 2012 Dec 23. 2013
7AUTSX5, RPL10
Mutation and expression analyses of the ribosomal protein gene RPL10 in an extended German sample of patients with autism spectrum disorder.
Chiocchetti A, Pakalapati G, Duketis E, Wiemann S, Poustka A, Poustka F, Klauck SM.
Am J Med Genet A 155A(6):1472-5. doi: 10.1002/ajmg.a.33977. Epub 2011 May 12. No abstract available. 2011
8AUTSX5, RPL10
An investigation of ribosomal protein L10 gene in autism spectrum disorders.
Gong X, Delorme R, Fauchereau F, Durand CM, Chaste P, Betancur C, Goubran-Botros H, Nygren G, Anckarsäter H, Rastam M, Gillberg IC, Kopp S, Mouren-Simeoni MC, Gillberg C, Leboyer M, Bourgeron T.
BMC Med Genet 10:7. doi: 10.1186/1471-2350-10-7. 2009
9RPL10
Crystal structure of human ribosomal protein L10 core domain reveals eukaryote-specific motifs in addition to the conserved fold.
Nishimura M, Kaminishi T, Takemoto C, Kawazoe M, Yoshida T, Tanaka A, Sugano S, Shirouzu M, Ohkubo T, Yokoyama S, Kobayashi Y.
J Mol Biol 377(2):421-30. doi: 10.1016/j.jmb.2008.01.003. Epub 2008 Jan 11. 2008
10AUTS20, NLGN, NLGN4X, NRXN1, RPL10, SHANK3
Contribution of SHANK3 Mutations to Autism Spectrum Disorder.
Moessner R, Marshall CR, Sutcliffe JS, Skaug J, Pinto D, Vincent J, Zwaigenbaum L, Fernandez B, Roberts W, Szatmari P, Scherer SW.
Am J Hum Genet 81(6):1289-97. Epub 2007 Oct 16. 2007
11RPL10
Reduction of QM protein expression correlates with tumor grade in prostatic adenocarcinoma.
Altinok G, Powell IJ, Che M, Hormont K, Sarkar FH, Sakr WA, Grignon D, Liao DJ.
Prostate Cancer Prostatic Dis 9(1):77-82. 2006
12AUTSX3, RPL10
Mutations in the ribosomal protein gene RPL10 suggest a novel modulating disease mechanism for autism.
Klauck SM, Felder B, Kolb-Kokocinski A, Schuster C, Chiocchetti A, Schupp I, Wellenreuther R, Schmštzer G, Poustka F, Breitenbach-Koller L, Poustka A.
Mol Psychiatry 11(12):1073-84. Epub 2006 Aug 29. 2006
13AUTSX5, RPL10
Mutations in the ribosomal protein gene RPL10 suggest a novel modulating disease mechanism for autism.
Klauck SM, Felder B, Kolb-Kokocinski A, Schuster C, Chiocchetti A, Schupp I, Wellenreuther R, Schmötzer G, Poustka F, Breitenbach-Koller L, Poustka A.
Mol Psychiatry 11(12):1073-84. Epub 2006 Aug 29. 2006
14RPL10
QM, a putative tumor suppressor, regulates proto-oncogene c-yes.
Oh HS, Kwon H, Sun SK, Yang CH.
J Biol Chem 277(39):36489-98. 2002
15RP2, RPL10, RPL10A, RPL11, RPL12, RPL13A, RPL15, RPL17, RPL18A, RPL23, RPL24, RPL26, RPL29, RPL3, RPL34, RPL36A, RPL38, RPL4, UBA52, RPL41, RPL7, RPL8, RPLP0, RPS10, RPS11, RPS12, RPS13, RPS14, RPS15, RPS15A, RPS16, RPS17, RPS18, RPS2, RPS20, RPS21, RPS23, RPS24, RPS25, RPS26, RPS27, RPS27A, RPS28, RPS29, RPS3A, RPS4L, RPS5, RPS9
A map of 75 human ribosomal protein genes.
Kenmochi N, Kawaguchi T, Rozen S, Davis E, Goodman N, Hudson TJ, Tanaka T, Page DC.
Genome Res 8(5):509-23. 1998
16RPL10
QM is a novel zinc-binding transcription regulatory protein : its binding to c-Jun is regulated by zinc ions and phosphorylation by protein kinase C.
Inada H, et al.
Biochem Biophys Res Commun 230 : 331-334. 1997
17RPL10
Isolation and characterization of the QM promoter.
Farmer AA, et al.
Nucleic Acids Res 24 : 2158-2165. 1996
18BGN, RPL10
Use of a radiation-reduced hybrid panel for the localization of seven markers in the Xq28 region of the human genome.
Smahi A, et al.
Ann Genet 37 : 11-13. 1994
19QMR1, RPL10
Extreme evolutionary conservation of QM, a novel c-Jun associated transcription factor.
Farmer AA, et al.
Hum Mol Genet 3 : 723-728. 1994
20ATP6AP1, DNASE1L1, DXS253E, DXS254E, EMD, FLNA, G6PD, GDI1, RGCP@, RPL10, UBL4A
Transcriptional organization of a 450-kb region of the human X chromosome in Xq28.
Bione S, et al.
Proc Natl Acad Sci U S A 90 : 10977-10981. 1993
21RPL10
Identification and characterization of a new gene in the human Xq28 region.
van den Ouweland AMW, et al.
Hum Mol Genet 1 : 269-273. 1992
22RPL10
Genomic organization of a cDNA (QM) demonstrating an altered mRNA level in nontumorigenic Wilms' microcell hybrid cells and its localization to Xq28.
Kaneko K, et al.
Hum Mol Genet 1 : 529-533. 1992
23RPL10
The QM gene is X-linked and therefore not involved in suppression of tumorigenesis in Wilms' tumor.
van den Ouweland AMW, et al.
Hum Genet 90 : 144-146. 1992
24FRAXA, L1CAM, RPL10
A strategy for the selection of transcribed sequences in the Xq28 region.
Korn B, et al.
Hum Mol Genet 1 : 235-242. 1992
25QMR1, RPL10
The isolation and characterization of a novel cDNA demonstrating an altered mRNA level in nontumorigenic Wilms' microcell hybrid cells.
Dowdy SF, et al.
Nucleic Acids Res 19 : 5763-5769. 1991