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    Results: 1 to 20 of 101

    1.

    NFIX--one gene, two knockouts, multiple effects.

    Pekarik V, Izpisua Belmonte JC.

    J Biol. 2008 Oct 23;7(8):29. Review.

    PMID:
    18983696
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    2.

    Nuclear factor I X deficiency causes brain malformation and severe skeletal defects.

    Driller K, Pagenstecher A, Uhl M, Omran H, Berlis A, Gründer A, Sippel AE.

    Mol Cell Biol. 2007 May;27(10):3855-3867.

    PMID:
    17353270
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    3.

    The transcription factor Nfix is essential for normal brain development.

    Campbell CE, Piper M, Plachez C, Yeh YT, Baizer JS, Osinski JM, Litwack ED, Richards LJ, Gronostajski RM.

    BMC Dev Biol. 2008 May 13;8:52.

    PMID:
    18477394
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    4.

    Disruption of the murine nuclear factor I-A gene (Nfia) results in perinatal lethality, hydrocephalus, and agenesis of the corpus callosum.

    das Neves L, Duchala CS, Tolentino-Silva F, Haxhiu MA, Colmenares C, Macklin WB, Campbell CE, Butz KG, Gronostajski RM.

    Proc Natl Acad Sci U S A. 1999 Oct 12;96(21):11946-51. Erratum in: Proc Natl Acad Sci U S A 2001 Mar 27;98(7):4276. Godinho F [corrected to Tolentino-Silva F].

    PMID:
    10518556
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    5.

    Nuclear factor one transcription factors in CNS development.

    Mason S, Piper M, Gronostajski RM, Richards LJ.

    Mol Neurobiol. 2009 Feb;39(1):10-23. Epub 2008 Dec 5.

    PMID:
    19058033
    [PubMed - indexed for MEDLINE]
    6.

    Abnormal development of forebrain midline glia and commissural projections in Nfia knock-out mice.

    Shu T, Butz KG, Plachez C, Gronostajski RM, Richards LJ.

    J Neurosci. 2003 Jan 1;23(1):203-12.

    PMID:
    12514217
    [PubMed - indexed for MEDLINE]
    Free Article
    7.

    NFIA haploinsufficiency is associated with a CNS malformation syndrome and urinary tract defects.

    Lu W, Quintero-Rivera F, Fan Y, Alkuraya FS, Donovan DJ, Xi Q, Turbe-Doan A, Li QG, Campbell CG, Shanske AL, Sherr EH, Ahmad A, Peters R, Rilliet B, Parvex P, Bassuk AG, Harris DJ, Ferguson H, Kelly C, Walsh CA, Gronostajski RM, Devriendt K, Higgins A, Ligon AH, Quade BJ, Morton CC, Gusella JF, Maas RL.

    PLoS Genet. 2007 May 25;3(5):e80.

    PMID:
    17530927
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    8.

    Distinct effects of allelic NFIX mutations on nonsense-mediated mRNA decay engender either a Sotos-like or a Marshall-Smith syndrome.

    Malan V, Rajan D, Thomas S, Shaw AC, Louis Dit Picard H, Layet V, Till M, van Haeringen A, Mortier G, Nampoothiri S, Puseljić S, Legeai-Mallet L, Carter NP, Vekemans M, Munnich A, Hennekam RC, Colleaux L, Cormier-Daire V.

    Am J Hum Genet. 2010 Aug 13;87(2):189-98. Epub 2010 Jul 30.

    PMID:
    20673863
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    9.

    Switch NFix developmental myogenesis.

    Palacios D, Puri PL.

    Dev Cell. 2010 Mar 16;18(3):340-1.

    PMID:
    20230743
    [PubMed - indexed for MEDLINE]
    10.

    Gene expression analysis of nuclear factor I-A deficient mice indicates delayed brain maturation.

    Wong YW, Schulze C, Streichert T, Gronostajski RM, Schachner M, Tilling T.

    Genome Biol. 2007;8(5):R72.

    PMID:
    17475010
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    12.

    Absence of the transcription factor Nfib delays the formation of the basilar pontine and other mossy fiber nuclei.

    Kumbasar A, Plachez C, Gronostajski RM, Richards LJ, Litwack ED.

    J Comp Neurol. 2009 Mar 1;513(1):98-112.

    PMID:
    19107796
    [PubMed - indexed for MEDLINE]
    13.

    Nfix regulates fetal-specific transcription in developing skeletal muscle.

    Messina G, Biressi S, Monteverde S, Magli A, Cassano M, Perani L, Roncaglia E, Tagliafico E, Starnes L, Campbell CE, Grossi M, Goldhamer DJ, Gronostajski RM, Cossu G.

    Cell. 2010 Feb 19;140(4):554-66.

    PMID:
    20178747
    [PubMed - indexed for MEDLINE]
    14.

    Multiple non-cell-autonomous defects underlie neocortical callosal dysgenesis in Nfib-deficient mice.

    Piper M, Moldrich RX, Lindwall C, Little E, Barry G, Mason S, Sunn N, Kurniawan ND, Gronostajski RM, Richards LJ.

    Neural Dev. 2009 Dec 4;4:43.

    PMID:
    19961580
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    15.

    Essential role for NFI-C/CTF transcription-replication factor in tooth root development.

    Steele-Perkins G, Butz KG, Lyons GE, Zeichner-David M, Kim HJ, Cho MI, Gronostajski RM.

    Mol Cell Biol. 2003 Feb;23(3):1075-84.

    PMID:
    12529411
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    16.

    Emx and Nfi genes regulate cortical development and axon guidance in the telencephalon.

    Piper M, Dawson AL, Lindwall C, Barry G, Plachez C, Richards LJ.

    Novartis Found Symp. 2007;288:230-242; discussion 242-5, 276-81. Review.

    PMID:
    18494262
    [PubMed - indexed for MEDLINE]
    17.

    MHox and vertebrate skeletogenesis: the long and the short of it.

    Brickell PM.

    Bioessays. 1995 Sep;17(9):750-3. Review.

    PMID:
    8763826
    [PubMed - indexed for MEDLINE]
    18.

    Nuclear factor I gene expression in the developing forebrain.

    Plachez C, Lindwall C, Sunn N, Piper M, Moldrich RX, Campbell CE, Osinski JM, Gronostajski RM, Richards LJ.

    J Comp Neurol. 2008 May 20;508(3):385-401.

    PMID:
    18335562
    [PubMed - indexed for MEDLINE]
    19.

    The forkhead/winged helix gene Mf1 is disrupted in the pleiotropic mouse mutation congenital hydrocephalus.

    Kume T, Deng KY, Winfrey V, Gould DB, Walter MA, Hogan BL.

    Cell. 1998 Jun 12;93(6):985-96.

    PMID:
    9635428
    [PubMed - indexed for MEDLINE]
    20.

    Targets of the nuclear factor I regulon involved in early and late development of postmitotic cerebellar granule neurons.

    Wang W, Crandall JE, Litwack ED, Gronostajski RM, Kilpatrick DL.

    J Neurosci Res. 2010 Feb 1;88(2):258-65.

    PMID:
    19658195
    [PubMed - indexed for MEDLINE]

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