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    Results: 1 to 20 of 167

    1.

    XACT, a long noncoding transcript coating the active X chromosome in human pluripotent cells.

    Vallot C, Huret C, Lesecque Y, Resch A, Oudrhiri N, Bennaceur-Griscelli A, Duret L, Rougeulle C.

    Nat Genet. 2013 Mar;45(3):239-41. doi: 10.1038/ng.2530. Epub 2013 Jan 20.

    PMID:
    23334669
    [PubMed - indexed for MEDLINE]
    2.

    The WSTF-ISWI chromatin remodeling complex transiently associates with the human inactive X chromosome during late S-phase prior to BRCA1 and γ-H2AX.

    Culver-Cochran AE, Chadwick BP.

    PLoS One. 2012;7(11):e50023. doi: 10.1371/journal.pone.0050023. Epub 2012 Nov 14.

    PMID:
    23166813
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    3.

    High resolution X chromosome-specific array-CGH detects new CNVs in infertile males.

    Krausz C, Giachini C, Lo Giacco D, Daguin F, Chianese C, Ars E, Ruiz-Castane E, Forti G, Rossi E.

    PLoS One. 2012;7(10):e44887. doi: 10.1371/journal.pone.0044887. Epub 2012 Oct 9.

    PMID:
    23056185
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    4.

    Serum levels of perfluorinated compounds and sperm Y:X chromosome ratio in two European populations and in Inuit from Greenland.

    Kvist L, Giwercman YL, Jönsson BA, Lindh CH, Bonde JP, Toft G, Strucinski P, Pedersen HS, Zvyezday V, Giwercman A.

    Reprod Toxicol. 2012 Dec;34(4):644-50. doi: 10.1016/j.reprotox.2012.09.007. Epub 2012 Oct 5.

    PMID:
    23044208
    [PubMed - indexed for MEDLINE]
    5.

    Comparative evaluation of alternative batteries of genetic markers to complement autosomal STRs in kinship investigations: autosomal indels vs. X-chromosome STRs.

    Gomes C, Magalhães M, Alves C, Amorim A, Pinto N, Gusmão L.

    Int J Legal Med. 2012 Nov;126(6):917-21. doi: 10.1007/s00414-012-0768-5. Epub 2012 Sep 1.

    PMID:
    22940765
    [PubMed - indexed for MEDLINE]
    6.

    Vulnerability for autism traits in boys and men with an extra X chromosome (47,XXY): the mediating role of cognitive flexibility.

    van Rijn S, Bierman M, Bruining H, Swaab H.

    J Psychiatr Res. 2012 Oct;46(10):1300-6. doi: 10.1016/j.jpsychires.2012.06.004. Epub 2012 Aug 11.

    PMID:
    22884425
    [PubMed - indexed for MEDLINE]
    7.
    8.

    X chromosome gene methylation in peripheral lymphocytes from monozygotic twins discordant for scleroderma.

    Selmi C, Feghali-Bostwick CA, Lleo A, Lombardi SA, De Santis M, Cavaciocchi F, Zammataro L, Mitchell MM, Lasalle JM, Medsger T Jr, Gershwin ME.

    Clin Exp Immunol. 2012 Sep;169(3):253-62. doi: 10.1111/j.1365-2249.2012.04621.x.

    PMID:
    22861365
    [PubMed - indexed for MEDLINE]
    9.

    Human MECP2 gene at Q28 arm of X chromosome as a suitable target for monitoring PCR inhibition in a nested, multiplexed HIV-1 DNA detection protocol.

    Acharya A, Chavan YG, Mukhopadhyaya PN, Nagee A, Kunjadia P, Misra RN.

    Roum Arch Microbiol Immunol. 2012 Jan-Mar;71(1):29-38.

    PMID:
    22838217
    [PubMed - indexed for MEDLINE]
    10.

    Interpretation of clinical relevance of X-chromosome copy number variations identified in a large cohort of individuals with cognitive disorders and/or congenital anomalies.

    Willemsen MH, de Leeuw N, de Brouwer AP, Pfundt R, Hehir-Kwa JY, Yntema HG, Nillesen WM, de Vries BB, van Bokhoven H, Kleefstra T.

    Eur J Med Genet. 2012 Nov;55(11):586-98. doi: 10.1016/j.ejmg.2012.05.001. Epub 2012 Jul 14.

    PMID:
    22796527
    [PubMed - indexed for MEDLINE]
    11.

    Association study of X chromosome SNPs in attempted suicide.

    Jancic D, Seifuddin F, Zandi PP, Potash JB, Willour VL.

    Psychiatry Res. 2012 Dec 30;200(2-3):1044-6. doi: 10.1016/j.psychres.2012.06.001. Epub 2012 Jul 4.

    PMID:
    22766010
    [PubMed - indexed for MEDLINE]
    12.

    An X chromosome association scan of the Norfolk Island genetic isolate provides evidence for a novel migraine susceptibility locus at Xq12.

    Maher BH, Lea RA, Benton M, Cox HC, Bellis C, Carless M, Dyer TD, Curran J, Charlesworth JC, Buring JE, Kurth T, Chasman DI, Ridker PM, Schürks M, Blangero J, Griffiths LR.

    PLoS One. 2012;7(5):e37903. doi: 10.1371/journal.pone.0037903. Epub 2012 May 29.

    PMID:
    22666411
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    13.

    Sporadic male patients with intellectual disability: contribution of X-chromosome copy number variants.

    Isrie M, Froyen G, Devriendt K, de Ravel T, Fryns JP, Vermeesch JR, Van Esch H.

    Eur J Med Genet. 2012 Nov;55(11):577-85. doi: 10.1016/j.ejmg.2012.05.005. Epub 2012 May 30.

    PMID:
    22659343
    [PubMed - indexed for MEDLINE]
    14.

    Development of multilocus putatively neutral DNA markers in the X-chromosome for population genetic studies in humans.

    Khan N, Chittoria A, Pande V, Jaiswal YK, Das A.

    Ann Hum Biol. 2012 Jul;39(4):281-9. doi: 10.3109/03014460.2012.689326. Epub 2012 Jun 1.

    PMID:
    22656191
    [PubMed - indexed for MEDLINE]
    15.

    Parental origin of the X-chromosome does not influence growth hormone treatment effect in Turner syndrome.

    Devernay M, Bolca D, Kerdjana L, Aboura A, Gérard B, Tabet AC, Benzacken B, Ecosse E, Coste J, Carel JC.

    J Clin Endocrinol Metab. 2012 Jul;97(7):E1241-8. doi: 10.1210/jc.2011-3488. Epub 2012 May 16.

    PMID:
    22593588
    [PubMed - indexed for MEDLINE]
    16.

    Characterization of six novel patients with MECP2 duplications due to unbalanced rearrangements of the X chromosome.

    Sanmann JN, Bishay DL, Starr LJ, Bell CA, Pickering DL, Stevens JM, Kahler SG, Olney AH, Schaefer GB, Sanger WG.

    Am J Med Genet A. 2012 Jun;158A(6):1285-91. doi: 10.1002/ajmg.a.35347. Epub 2012 May 11.

    PMID:
    22581587
    [PubMed - indexed for MEDLINE]
    17.

    XM: association testing on the X-chromosome in case-control samples with related individuals.

    Thornton T, Zhang Q, Cai X, Ober C, McPeek MS.

    Genet Epidemiol. 2012 Jul;36(5):438-50. doi: 10.1002/gepi.21638. Epub 2012 May 2.

    PMID:
    22552845
    [PubMed - indexed for MEDLINE]
    18.

    Copy number changes on the X chromosome in women with and without highly skewed X-chromosome inactivation.

    Jobanputra V, Levy B, Kinney A, Brown S, Shirazi M, Yu C, Kline J, Warburton D.

    Cytogenet Genome Res. 2012;136(4):264-9. doi: 10.1159/000337920. Epub 2012 Apr 20.

    PMID:
    22516899
    [PubMed - indexed for MEDLINE]
    19.

    Connective tissue diseases. Unravelling aetiology in male SLE--the X chromosome dose effect.

    Zandman-Goddard G, Peeva E.

    Nat Rev Rheumatol. 2012 Apr 17;8(6):310-2. doi: 10.1038/nrrheum.2012.44.

    PMID:
    22508431
    [PubMed - indexed for MEDLINE]
    20.

    Collaborative genetic mapping of 12 forensic short tandem repeat (STR) loci on the human X chromosome.

    Nothnagel M, Szibor R, Vollrath O, Augustin C, Edelmann J, Geppert M, Alves C, Gusmão L, Vennemann M, Hou Y, Immel UD, Inturri S, Luo H, Lutz-Bonengel S, Robino C, Roewer L, Rolf B, Sanft J, Shin KJ, Sim JE, Wiegand P, Winkler C, Krawczak M, Hering S.

    Forensic Sci Int Genet. 2012 Dec;6(6):778-84. doi: 10.1016/j.fsigen.2012.02.015. Epub 2012 Mar 27.

    PMID:
    22459949
    [PubMed - indexed for MEDLINE]

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