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    Similar articles for PubMed (Select 21287218)

    1.

    C4ORF48, a gene from the Wolf-Hirschhorn syndrome critical region, encodes a putative neuropeptide and is expressed during neocortex and cerebellar development.

    Endele S, Nelkenbrecher C, Bördlein A, Schlickum S, Winterpacht A.

    Neurogenetics. 2011 May;12(2):155-63. doi: 10.1007/s10048-011-0275-8. Epub 2011 Feb 2.

    PMID:
    21287218
    2.

    Comparative analysis of a novel gene from the Wolf-Hirschhorn/Pitt-Rogers-Danks syndrome critical region.

    Wright TJ, Costa JL, Naranjo C, Francis-West P, Altherr MR.

    Genomics. 1999 Jul 15;59(2):203-12.

    PMID:
    10409432
    3.

    DSCAM: a novel member of the immunoglobulin superfamily maps in a Down syndrome region and is involved in the development of the nervous system.

    Yamakawa K, Huot YK, Haendelt MA, Hubert R, Chen XN, Lyons GE, Korenberg JR.

    Hum Mol Genet. 1998 Feb;7(2):227-37.

    4.

    WHSC1, a 90 kb SET domain-containing gene, expressed in early development and homologous to a Drosophila dysmorphy gene maps in the Wolf-Hirschhorn syndrome critical region and is fused to IgH in t(4;14) multiple myeloma.

    Stec I, Wright TJ, van Ommen GJ, de Boer PA, van Haeringen A, Moorman AF, Altherr MR, den Dunnen JT.

    Hum Mol Genet. 1998 Jul;7(7):1071-82. Erratum in: Hum Mol Genet 1998 Sep;7(9):1527.

    5.

    Identification of Nepro, a gene required for the maintenance of neocortex neural progenitor cells downstream of Notch.

    Muroyama Y, Saito T.

    Development. 2009 Dec;136(23):3889-93. doi: 10.1242/dev.039180.

    6.

    Transmembrane protein 50b (C21orf4), a candidate for Down syndrome neurophenotypes, encodes an intracellular membrane protein expressed in the rodent brain.

    Moldrich RX, Lainé J, Visel A, Beart PM, Laffaire J, Rossier J, Potier MC.

    Neuroscience. 2008 Jul 17;154(4):1255-66. doi: 10.1016/j.neuroscience.2008.01.089. Epub 2008 Mar 4.

    PMID:
    18541381
    7.

    Isolation of human and murine homologues of the Drosophila minibrain gene: human homologue maps to 21q22.2 in the Down syndrome "critical region".

    Song WJ, Sternberg LR, Kasten-Sportès C, Keuren ML, Chung SH, Slack AC, Miller DE, Glover TW, Chiang PW, Lou L, Kurnit DM.

    Genomics. 1996 Dec 15;38(3):331-9.

    PMID:
    8975710
    8.

    LRRN6A/LERN1 (leucine-rich repeat neuronal protein 1), a novel gene with enriched expression in limbic system and neocortex.

    Carim-Todd L, Escarceller M, Estivill X, Sumoy L.

    Eur J Neurosci. 2003 Dec;18(12):3167-82.

    PMID:
    14686891
    9.

    A microdeletion proximal of the critical deletion region is associated with mild Wolf-Hirschhorn syndrome.

    Hannes F, Hammond P, Quarrell O, Fryns JP, Devriendt K, Vermeesch JR.

    Am J Med Genet A. 2012 May;158A(5):996-1004. doi: 10.1002/ajmg.a.35299. Epub 2012 Mar 21.

    PMID:
    22438245
    10.
    11.

    LETM1, a gene deleted in Wolf-Hirschhorn syndrome, encodes an evolutionarily conserved mitochondrial protein.

    Schlickum S, Moghekar A, Simpson JC, Steglich C, O'Brien RJ, Winterpacht A, Endele SU.

    Genomics. 2004 Feb;83(2):254-61.

    PMID:
    14706454
    12.

    Duplication of the Wolf-Hirschhorn syndrome critical region causes neurodevelopmental delay.

    Hannes F, Drozniewska M, Vermeesch JR, Haus O.

    Eur J Med Genet. 2010 May-Jun;53(3):136-40. doi: 10.1016/j.ejmg.2010.02.004. Epub 2010 Mar 1.

    PMID:
    20197130
    13.

    Molecular cloning and distinct developmental expression pattern of spliced forms of a novel zinc finger gene wiz in the mouse cerebellum.

    Matsumoto K, Ishii N, Yoshida S, Shiosaka S, Wanaka A, Tohyama M.

    Brain Res Mol Brain Res. 1998 Oct 30;61(1-2):179-89.

    PMID:
    9795207
    14.

    Molecular markers of neuronal progenitors in the embryonic cerebellar anlage.

    Morales D, Hatten ME.

    J Neurosci. 2006 Nov 22;26(47):12226-36.

    15.

    Genomic organisation and nervous system expression of radial spoke protein 3.

    Koukoulas I, Augustine C, Silkenbeumer N, Gunnersen JM, Scott HS, Tan SS.

    Gene. 2004 Jul 7;336(1):15-23.

    PMID:
    15225872
    16.

    A novel transverse expression domain in the mouse cerebellum revealed by a neurofilament-associated antigen.

    Marzban H, Kim CT, Doorn D, Chung SH, Hawkes R.

    Neuroscience. 2008 Jun 2;153(4):1190-201. doi: 10.1016/j.neuroscience.2008.02.036. Epub 2008 Feb 29.

    PMID:
    18455884
    17.

    The mammalian single-minded (SIM) gene: mouse cDNA structure and diencephalic expression indicate a candidate gene for Down syndrome.

    Yamaki A, Noda S, Kudoh J, Shindoh N, Maeda H, Minoshima S, Kawasaki K, Shimizu Y, Shimizu N.

    Genomics. 1996 Jul 1;35(1):136-43.

    PMID:
    8661114
    18.
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    20.

    Characterisation of Fmrp in zebrafish: evolutionary dynamics of the fmr1 gene.

    van 't Padje S, Engels B, Blonden L, Severijnen LA, Verheijen F, Oostra BA, Willemsen R.

    Dev Genes Evol. 2005 Apr;215(4):198-206. Epub 2005 Jan 27.

    PMID:
    15818485
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