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.
211 related articles for article (PubMed ID: 9450775)
21. Cln3(Deltaex7/8) knock-in mice with the common JNCL mutation exhibit progressive neurologic disease that begins before birth. Cotman SL; Vrbanac V; Lebel LA; Lee RL; Johnson KA; Donahue LR; Teed AM; Antonellis K; Bronson RT; Lerner TJ; MacDonald ME Hum Mol Genet; 2002 Oct; 11(22):2709-21. PubMed ID: 12374761 [TBL] [Abstract][Full Text] [Related]
22. Deletion of the Caenorhabditis elegans homologues of the CLN3 gene, involved in human juvenile neuronal ceroid lipofuscinosis, causes a mild progeric phenotype. de Voer G; van der Bent P; Rodrigues AJ; van Ommen GJ; Peters DJ; Taschner PE J Inherit Metab Dis; 2005; 28(6):1065-80. PubMed ID: 16435200 [TBL] [Abstract][Full Text] [Related]
23. Molecular genetic analysis of neuronal ceroid lipofuscinosis. Mole SE; Gardiner M Int J Neurol; 1991-1992; 25-26():52-9. PubMed ID: 11980063 [TBL] [Abstract][Full Text] [Related]
24. Clinical and molecular characterization of non-syndromic retinal dystrophy due to c.175G>A mutation in ceroid lipofuscinosis neuronal 3 (CLN3). Chen FK; Zhang X; Eintracht J; Zhang D; Arunachalam S; Thompson JA; Chelva E; Mallon D; Chen SC; McLaren T; Lamey T; De Roach J; McLenachan S Doc Ophthalmol; 2019 Feb; 138(1):55-70. PubMed ID: 30446867 [TBL] [Abstract][Full Text] [Related]
27. Juvenile neuronal ceroid lipofuscinosis (Batten disease) CLN3 mutation (Chrom 16p11.2) with different phenotypes in a sibling pair and low intensity in vivo autofluorescence. Mantel I; Brantley MA; Bellmann C; Robson AG; Holder GE; Taylor A; Anderson G; Moore AT Klin Monbl Augenheilkd; 2004 May; 221(5):427-30. PubMed ID: 15162299 [TBL] [Abstract][Full Text] [Related]
28. Spectrum of CLN6 mutations in variant late infantile neuronal ceroid lipofuscinosis. Sharp JD; Wheeler RB; Parker KA; Gardiner RM; Williams RE; Mole SE Hum Mutat; 2003 Jul; 22(1):35-42. PubMed ID: 12815591 [TBL] [Abstract][Full Text] [Related]
33. DNA diagnosis and identification of carriers of infantile and juvenile neuronal ceroid lipofuscinoses. Syvänen AC; Järvelä I; Paunio T; Vesa J Neuropediatrics; 1997 Feb; 28(1):63-6. PubMed ID: 9151326 [TBL] [Abstract][Full Text] [Related]
34. Strategy for mutation detection in CLN3: characterisation of two Finnish mutations. Munroe PB; O'Rawe AM; Mitchison HM; Järvelä IE; Santavuori P; Lerner TJ; Taschner PE; Gardiner RM; Mole SE Neuropediatrics; 1997 Feb; 28(1):15-7. PubMed ID: 9151312 [TBL] [Abstract][Full Text] [Related]
35. A function retained by the common mutant CLN3 protein is responsible for the late onset of juvenile neuronal ceroid lipofuscinosis. Kitzmüller C; Haines RL; Codlin S; Cutler DF; Mole SE Hum Mol Genet; 2008 Jan; 17(2):303-12. PubMed ID: 17947292 [TBL] [Abstract][Full Text] [Related]
36. Current Insights in Elucidation of Possible Molecular Mechanisms of the Juvenile Form of Batten Disease. Shematorova EK; Shpakovski GV Int J Mol Sci; 2020 Oct; 21(21):. PubMed ID: 33137890 [TBL] [Abstract][Full Text] [Related]
37. Spectrum of mutations in the Batten disease gene, CLN3. Munroe PB; Mitchison HM; O'Rawe AM; Anderson JW; Boustany RM; Lerner TJ; Taschner PE; de Vos N; Breuning MH; Gardiner RM; Mole SE Am J Hum Genet; 1997 Aug; 61(2):310-6. PubMed ID: 9311735 [TBL] [Abstract][Full Text] [Related]
38. Genetic heterogeneity of neuronal ceroid lipofuscinosis in The Netherlands. Taschner PE; Franken PF; van Berkel L; Breuning MH Mol Genet Metab; 1999 Apr; 66(4):339-43. PubMed ID: 10191126 [TBL] [Abstract][Full Text] [Related]
39. Novel interactions of CLN3 protein link Batten disease to dysregulation of fodrin-Na+, K+ ATPase complex. Uusi-Rauva K; Luiro K; Tanhuanpää K; Kopra O; Martín-Vasallo P; Kyttälä A; Jalanko A Exp Cell Res; 2008 Sep; 314(15):2895-905. PubMed ID: 18621045 [TBL] [Abstract][Full Text] [Related]
40. Late onset neurodegeneration in the Cln3-/- mouse model of juvenile neuronal ceroid lipofuscinosis is preceded by low level glial activation. Pontikis CC; Cella CV; Parihar N; Lim MJ; Chakrabarti S; Mitchison HM; Mobley WC; Rezaie P; Pearce DA; Cooper JD Brain Res; 2004 Oct; 1023(2):231-42. PubMed ID: 15374749 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]