These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

110 related items for PubMed ID: 15498463

  • 1. The human LMX1B gene: transcription unit, promoter, and pathogenic mutations.
    Dunston JA, Hamlington JD, Zaveri J, Sweeney E, Sibbring J, Tran C, Malbroux M, O'Neill JP, Mountford R, McIntosh I.
    Genomics; 2004 Sep; 84(3):565-76. PubMed ID: 15498463
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. The LIM-homeodomain transcription factor Lmx1b plays a crucial role in podocytes.
    Rohr C, Prestel J, Heidet L, Hosser H, Kriz W, Johnson RL, Antignac C, Witzgall R.
    J Clin Invest; 2002 Apr; 109(8):1073-82. PubMed ID: 11956245
    [Abstract] [Full Text] [Related]

  • 6. Functional characterization of LMX1B mutations associated with nail-patella syndrome.
    Sato U, Kitanaka S, Sekine T, Takahashi S, Ashida A, Igarashi T.
    Pediatr Res; 2005 Jun; 57(6):783-8. PubMed ID: 15774843
    [Abstract] [Full Text] [Related]

  • 7. Functional mapping of the promoter region of the GNB2L1 human gene coding for RACK1 scaffold protein.
    Del Vecchio I, Zuccotti A, Pisano F, Canneva F, Lenzken SC, Rousset F, Corsini E, Govoni S, Racchi M.
    Gene; 2009 Feb 01; 430(1-2):17-29. PubMed ID: 19000751
    [Abstract] [Full Text] [Related]

  • 8. Twenty-two novel LMX1B mutations identified in nail patella syndrome (NPS) patients.
    Hamlington JD, Jones C, McIntosh I.
    Hum Mutat; 2001 Nov 01; 18(5):458. PubMed ID: 11668639
    [Abstract] [Full Text] [Related]

  • 9. Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndrome.
    Dreyer SD, Zhou G, Baldini A, Winterpacht A, Zabel B, Cole W, Johnson RL, Lee B.
    Nat Genet; 1998 May 01; 19(1):47-50. PubMed ID: 9590287
    [Abstract] [Full Text] [Related]

  • 10. LMX1B, a LIM homeodomain class transcription factor, is necessary for normal development of multiple tissues in the anterior segment of the murine eye.
    Pressman CL, Chen H, Johnson RL.
    Genesis; 2000 Jan 01; 26(1):15-25. PubMed ID: 10660670
    [Abstract] [Full Text] [Related]

  • 11. Genotype-phenotype studies in nail-patella syndrome show that LMX1B mutation location is involved in the risk of developing nephropathy.
    Bongers EM, Huysmans FT, Levtchenko E, de Rooy JW, Blickman JG, Admiraal RJ, Huygen PL, Cruysberg JR, Toolens PA, Prins JB, Krabbe PF, Borm GF, Schoots J, van Bokhoven H, van Remortele AM, Hoefsloot LH, van Kampen A, Knoers NV.
    Eur J Hum Genet; 2005 Aug 01; 13(8):935-46. PubMed ID: 15928687
    [Abstract] [Full Text] [Related]

  • 12. A promoter with bidirectional activity is located between TLX1/HOX11 and a divergently transcribed novel human gene.
    Greene WK, Sontani Y, Sharp MA, Dunn DS, Kees UR, Bellgard MI.
    Gene; 2007 Apr 15; 391(1-2):223-32. PubMed ID: 17303350
    [Abstract] [Full Text] [Related]

  • 13. Transcriptional regulation of the mouse PNRC2 promoter by the nuclear factor Y (NFY) and E2F1.
    Zhou D, Masri S, Ye JJ, Chen S.
    Gene; 2005 Nov 21; 361():89-100. PubMed ID: 16181749
    [Abstract] [Full Text] [Related]

  • 14. A neurological phenotype in nail patella syndrome (NPS) patients illuminated by studies of murine Lmx1b expression.
    Dunston JA, Reimschisel T, Ding YQ, Sweeney E, Johnson RL, Chen ZF, McIntosh I.
    Eur J Hum Genet; 2005 Mar 21; 13(3):330-5. PubMed ID: 15562281
    [Abstract] [Full Text] [Related]

  • 15. Regulation of glomerular basement membrane collagen expression by LMX1B contributes to renal disease in nail patella syndrome.
    Morello R, Zhou G, Dreyer SD, Harvey SJ, Ninomiya Y, Thorner PS, Miner JH, Cole W, Winterpacht A, Zabel B, Oberg KC, Lee B.
    Nat Genet; 2001 Feb 21; 27(2):205-8. PubMed ID: 11175791
    [Abstract] [Full Text] [Related]

  • 16. The LIM-homeodomain transcription factor LMX1B regulates expression of NF-kappa B target genes.
    Rascle A, Neumann T, Raschta AS, Neumann A, Heining E, Kastner J, Witzgall R.
    Exp Cell Res; 2009 Jan 01; 315(1):76-96. PubMed ID: 18996370
    [Abstract] [Full Text] [Related]

  • 17. Limb and kidney defects in Lmx1b mutant mice suggest an involvement of LMX1B in human nail patella syndrome.
    Chen H, Lun Y, Ovchinnikov D, Kokubo H, Oberg KC, Pepicelli CV, Gan L, Lee B, Johnson RL.
    Nat Genet; 1998 May 01; 19(1):51-5. PubMed ID: 9590288
    [Abstract] [Full Text] [Related]

  • 18. Effects of methylation of non-CpG sequence in the promoter region on the expression of human synaptotagmin XI (syt11).
    Inoue S, Oishi M.
    Gene; 2005 Mar 28; 348():123-34. PubMed ID: 15777718
    [Abstract] [Full Text] [Related]

  • 19. Identification of four new PITX2 gene mutations in patients with Axenfeld-Rieger syndrome.
    Vieira V, David G, Roche O, de la Houssaye G, Boutboul S, Arbogast L, Kobetz A, Orssaud C, Camand O, Schorderet DF, Munier F, Rossi A, Delezoide AL, Marsac C, Ricquier D, Dufier JL, Menasche M, Abitbol M.
    Mol Vis; 2006 Dec 01; 12():1448-60. PubMed ID: 17167399
    [Abstract] [Full Text] [Related]

  • 20. [From gene to disease; the nail-patella syndrome and the LMX1B gene].
    Bongers EM, Knoers NV.
    Ned Tijdschr Geneeskd; 2003 Jan 11; 147(2):67-9. PubMed ID: 12602071
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 6.