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

144 related items for PubMed ID: 26092248

  • 1.
    ; . PubMed ID:
    [No 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. Accumulation of bis(monoacylglycero)phosphate and gangliosides in mouse models of neuronal ceroid lipofuscinosis.
    Jabs S, Quitsch A, Käkelä R, Koch B, Tyynelä J, Brade H, Glatzel M, Walkley S, Saftig P, Vanier MT, Braulke T.
    J Neurochem; 2008 Aug; 106(3):1415-25. PubMed ID: 18498441
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Cathepsin D deficiency underlies congenital human neuronal ceroid-lipofuscinosis.
    Siintola E, Partanen S, Strömme P, Haapanen A, Haltia M, Maehlen J, Lehesjoki AE, Tyynelä J.
    Brain; 2006 Jun; 129(Pt 6):1438-45. PubMed ID: 16670177
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Early infantile neuronal ceroid lipofuscinosis (CLN10 disease) associated with a novel mutation in CTSD.
    Doccini S, Sartori S, Maeser S, Pezzini F, Rossato S, Moro F, Toldo I, Przybylski M, Santorelli FM, Simonati A.
    J Neurol; 2016 May; 263(5):1029-1032. PubMed ID: 27072142
    [No Abstract] [Full Text] [Related]

  • 14. Genetic modifiers of degeneration in the cathepsin D deficient Drosophila model for neuronal ceroid lipofuscinosis.
    Kuronen M, Talvitie M, Lehesjoki AE, Myllykangas L.
    Neurobiol Dis; 2009 Dec; 36(3):488-93. PubMed ID: 19761846
    [Abstract] [Full Text] [Related]

  • 15. Melancholic-Like behaviors and circadian neurobiological abnormalities in melatonin MT1 receptor knockout mice.
    Comai S, Ochoa-Sanchez R, Dominguez-Lopez S, Bambico FR, Gobbi G.
    Int J Neuropsychopharmacol; 2015 Jan 31; 18(3):. PubMed ID: 25638817
    [Abstract] [Full Text] [Related]

  • 16. Prenatal-onset of congenital neuronal ceroid lipofuscinosis with a novel CTSD mutation.
    Chartier S, Boutaud L, Le Guillou E, Alby C, Billon C, Millischer AE, Caillaud C, Galmiche L, Mechler C, Sonigo P, Boddaert N, Lyonnet S, Rondeau S, Bole-Feysot C, Masson C, Ville Y, Roth P, Desguerre I, Encha-Razavi F, Attie-Bitach T.
    Birth Defects Res; 2021 Nov 31; 113(18):1324-1332. PubMed ID: 34491000
    [Abstract] [Full Text] [Related]

  • 17. Purkinje Cells Are More Vulnerable to the Specific Depletion of Cathepsin D Than to That of Atg7.
    Koike M, Shibata M, Sunabori T, Yamaguchi J, Sakimura K, Komatsu M, Tanaka K, Uchiyama Y.
    Am J Pathol; 2017 Jul 31; 187(7):1586-1600. PubMed ID: 28502476
    [Abstract] [Full Text] [Related]

  • 18. The c.863A>G (p.Glu288Gly) variant of the CTSD gene is not associated with CLN10 disease.
    Yang J, Ding X, Meng S, Cai J, Zhou W.
    Mol Genet Genomic Med; 2021 Oct 31; 9(10):e1777. PubMed ID: 34331747
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Amphetamine sensitization in mice is sufficient to produce both manic- and depressive-related behaviors as well as changes in the functional connectivity of corticolimbic structures.
    Pathak G, Ibrahim BA, McCarthy SA, Baker K, Kelly MP.
    Neuropharmacology; 2015 Aug 31; 95():434-47. PubMed ID: 25959066
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.