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Journal Abstract Search

204 related items for PubMed ID: 20026556

  • 1. A Drosophila mutant of LETM1, a candidate gene for seizures in Wolf-Hirschhorn syndrome.
    McQuibban AG, Joza N, Megighian A, Scorzeto M, Zanini D, Reipert S, Richter C, Schweyen RJ, Nowikovsky K.
    Hum Mol Genet; 2010 Mar 15; 19(6):987-1000. PubMed ID: 20026556
    [Abstract] [Full Text] [Related]

  • 2. Unusual 4p16.3 deletions suggest an additional chromosome region for the Wolf-Hirschhorn syndrome-associated seizures disorder.
    Zollino M, Orteschi D, Ruiter M, Pfundt R, Steindl K, Cafiero C, Ricciardi S, Contaldo I, Chieffo D, Ranalli D, Acquafondata C, Murdolo M, Marangi G, Asaro A, Battaglia D.
    Epilepsia; 2014 Jun 15; 55(6):849-57. PubMed ID: 24738919
    [Abstract] [Full Text] [Related]

  • 3. Cell biology. A revolving door for calcium.
    Demaurex N, Poburko D.
    Science; 2009 Oct 02; 326(5949):57-8. PubMed ID: 19797650
    [No Abstract] [Full Text] [Related]

  • 4. LETM1 haploinsufficiency causes mitochondrial defects in cells from humans with Wolf-Hirschhorn syndrome: implications for dissecting the underlying pathomechanisms in this condition.
    Hart L, Rauch A, Carr AM, Vermeesch JR, O'Driscoll M.
    Dis Model Mech; 2014 May 02; 7(5):535-45. PubMed ID: 24626991
    [Abstract] [Full Text] [Related]

  • 5. Letm1, the mitochondrial Ca2+/H+ antiporter, is essential for normal glucose metabolism and alters brain function in Wolf-Hirschhorn syndrome.
    Jiang D, Zhao L, Clish CB, Clapham DE.
    Proc Natl Acad Sci U S A; 2013 Jun 11; 110(24):E2249-54. PubMed ID: 23716663
    [Abstract] [Full Text] [Related]

  • 6. Characterization of the mitochondrial protein LETM1, which maintains the mitochondrial tubular shapes and interacts with the AAA-ATPase BCS1L.
    Tamai S, Iida H, Yokota S, Sayano T, Kiguchiya S, Ishihara N, Hayashi J, Mihara K, Oka T.
    J Cell Sci; 2008 Aug 01; 121(Pt 15):2588-600. PubMed ID: 18628306
    [Abstract] [Full Text] [Related]

  • 7. LETM1, a novel gene encoding a putative EF-hand Ca(2+)-binding protein, flanks the Wolf-Hirschhorn syndrome (WHS) critical region and is deleted in most WHS patients.
    Endele S, Fuhry M, Pak SJ, Zabel BU, Winterpacht A.
    Genomics; 1999 Sep 01; 60(2):218-25. PubMed ID: 10486213
    [Abstract] [Full Text] [Related]

  • 8. LETM1, deleted in Wolf-Hirschhorn syndrome is required for normal mitochondrial morphology and cellular viability.
    Dimmer KS, Navoni F, Casarin A, Trevisson E, Endele S, Winterpacht A, Salviati L, Scorrano L.
    Hum Mol Genet; 2008 Jan 15; 17(2):201-14. PubMed ID: 17925330
    [Abstract] [Full Text] [Related]

  • 9. 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 15; 83(2):254-61. PubMed ID: 14706454
    [Abstract] [Full Text] [Related]

  • 10. The mitochondrial ribosome-specific MrpL55 protein is essential in Drosophila and dynamically required during development.
    Tselykh TV, Roos C, Heino TI.
    Exp Cell Res; 2005 Jul 15; 307(2):354-66. PubMed ID: 15894314
    [Abstract] [Full Text] [Related]

  • 11. LETM1: Essential for Mitochondrial Biology and Cation Homeostasis?
    Austin S, Nowikovsky K.
    Trends Biochem Sci; 2019 Aug 15; 44(8):648-658. PubMed ID: 31101453
    [Abstract] [Full Text] [Related]

  • 12. Association of LETM1 and MRPL36 contributes to the regulation of mitochondrial ATP production and necrotic cell death.
    Piao L, Li Y, Kim SJ, Byun HS, Huang SM, Hwang SK, Yang KJ, Park KA, Won M, Hong J, Hur GM, Seok JH, Shong M, Cho MH, Brazil DP, Hemmings BA, Park J.
    Cancer Res; 2009 Apr 15; 69(8):3397-404. PubMed ID: 19318571
    [Abstract] [Full Text] [Related]

  • 13. The LETM1/YOL027 gene family encodes a factor of the mitochondrial K+ homeostasis with a potential role in the Wolf-Hirschhorn syndrome.
    Nowikovsky K, Froschauer EM, Zsurka G, Samaj J, Reipert S, Kolisek M, Wiesenberger G, Schweyen RJ.
    J Biol Chem; 2004 Jul 16; 279(29):30307-15. PubMed ID: 15138253
    [Abstract] [Full Text] [Related]

  • 14. Genome-wide RNAi screen identifies Letm1 as a mitochondrial Ca2+/H+ antiporter.
    Jiang D, Zhao L, Clapham DE.
    Science; 2009 Oct 02; 326(5949):144-7. PubMed ID: 19797662
    [Abstract] [Full Text] [Related]

  • 15. Association of mitochondrial letm1 with epileptic seizures.
    Zhang X, Chen G, Lu Y, Liu J, Fang M, Luo J, Cao Q, Wang X.
    Cereb Cortex; 2014 Oct 02; 24(10):2533-40. PubMed ID: 23645710
    [Abstract] [Full Text] [Related]

  • 16. Inverse correlation between expression of the Wolfs Hirschhorn candidate gene Letm1 and mitochondrial volume in C. elegans and in mammalian cells.
    Hasegawa A, van der Bliek AM.
    Hum Mol Genet; 2007 Sep 01; 16(17):2061-71. PubMed ID: 17606466
    [Abstract] [Full Text] [Related]

  • 17. Deletions involving genes WHSC1 and LETM1 may be necessary, but are not sufficient to cause Wolf-Hirschhorn Syndrome.
    Andersen EF, Carey JC, Earl DL, Corzo D, Suttie M, Hammond P, South ST.
    Eur J Hum Genet; 2014 Apr 01; 22(4):464-70. PubMed ID: 23963300
    [Abstract] [Full Text] [Related]

  • 18. Molecular Mechanisms of Leucine Zipper EF-Hand Containing Transmembrane Protein-1 Function in Health and Disease.
    Lin QT, Stathopulos PB.
    Int J Mol Sci; 2019 Jan 12; 20(2):. PubMed ID: 30642051
    [Abstract] [Full Text] [Related]

  • 19. Distinct Epileptogenic Mechanisms Associated with Seizures in Wolf-Hirschhorn Syndrome.
    Corrêa T, Mayndra M, Santos-Rebouças CB.
    Mol Neurobiol; 2022 May 12; 59(5):3159-3169. PubMed ID: 35278209
    [Abstract] [Full Text] [Related]

  • 20. On the nosology and pathogenesis of Wolf-Hirschhorn syndrome: genotype-phenotype correlation analysis of 80 patients and literature review.
    Zollino M, Murdolo M, Marangi G, Pecile V, Galasso C, Mazzanti L, Neri G.
    Am J Med Genet C Semin Med Genet; 2008 Nov 15; 148C(4):257-69. PubMed ID: 18932124
    [Abstract] [Full Text] [Related]

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