168 related articles for article (PubMed ID: 10356317)
1. Splicing variants in sheep CLN3, the gene underlying juvenile neuronal ceroid lipofuscinosis.
Oswald MJ; Palmer DN; Damak S
Mol Genet Metab; 1999 Jun; 67(2):169-75. PubMed ID: 10356317
[TBL] [Abstract][Full Text] [Related]
2. Immunochemical localization of the Batten disease (CLN3) protein in retina.
Katz ML; Gao CL; Prabhakaram M; Shibuya H; Liu PC; Johnson GS
Invest Ophthalmol Vis Sci; 1997 Oct; 38(11):2375-86. PubMed ID: 9344361
[TBL] [Abstract][Full Text] [Related]
3. Genomic structure and complete nucleotide sequence of the Batten disease gene, CLN3.
Mitchison HM; Munroe PB; O'Rawe AM; Taschner PE; de Vos N; Kremmidiotis G; Lensink I; Munk AC; D'Arigo KL; Anderson JW; Lerner TJ; Moyzis RK; Callen DF; Breuning MH; Doggett NA; Gardiner RM; Mole SE
Genomics; 1997 Mar; 40(2):346-50. PubMed ID: 9119403
[TBL] [Abstract][Full Text] [Related]
4. Structure of the CLN3 gene and predicted structure, location and function of CLN3 protein.
Mitchison HM; Taschner PE; Kremmidiotis G; Callen DF; Doggett NA; Lerner TJ; Janes RB; Wallace BA; Munroe PB; O'Rawe AM; Gardiner RM; Mole SE
Neuropediatrics; 1997 Feb; 28(1):12-4. PubMed ID: 9151311
[TBL] [Abstract][Full Text] [Related]
5. Neural and extraneural expression of the neuronal ceroid lipofuscinoses genes CLN1, CLN2, and CLN3: functional implications for CLN3.
Chattopadhyay S; Pearce DA
Mol Genet Metab; 2000; 71(1-2):207-11. PubMed ID: 11001812
[TBL] [Abstract][Full Text] [Related]
6. CLN3L, a novel protein related to the Batten disease protein, is overexpressed in Cln3-/- mice and in Batten disease.
Narayan SB; Pastor JV; Mitchison HM; Bennett MJ
Brain; 2004 Aug; 127(Pt 8):1748-54. PubMed ID: 15240430
[TBL] [Abstract][Full Text] [Related]
7. A novel c.1135_1138delCTGT mutation in CLN3 leads to juvenile neuronal ceroid lipofuscinosis.
Drack AV; Miller JN; Pearce DA
J Child Neurol; 2013 Sep; 28(9):1112-6. PubMed ID: 23877479
[TBL] [Abstract][Full Text] [Related]
8. Isolation and chromosomal mapping of a mouse homolog of the Batten disease gene CLN3.
Lee RL; Johnson KR; Lerner TJ
Genomics; 1996 Aug; 35(3):617-9. PubMed ID: 8812504
[TBL] [Abstract][Full Text] [Related]
9. Tissue expression and subcellular localization of CLN3, the Batten disease protein.
Margraf LR; Boriack RL; Routheut AA; Cuppen I; Alhilali L; Bennett CJ; Bennett MJ
Mol Genet Metab; 1999 Apr; 66(4):283-9. PubMed ID: 10191116
[TBL] [Abstract][Full Text] [Related]
10. Altered gene expression in the eye of a mouse model for batten disease.
Chattopadhyay S; Kingsley E; Serour A; Curran TM; Brooks AI; Pearce DA
Invest Ophthalmol Vis Sci; 2004 Sep; 45(9):2893-905. PubMed ID: 15326100
[TBL] [Abstract][Full Text] [Related]
11. Gene symbol: CLN3. Disease: Juvenile neuronal ceroid lipofuscinosis (Batten disease).
Leman AR; Pearce DA; Rothberg PG
Hum Genet; 2005 May; 116(6):544. PubMed ID: 15991331
[No Abstract] [Full Text] [Related]
12. Retinal pathology and function in a Cln3 knockout mouse model of juvenile Neuronal Ceroid Lipofuscinosis (batten disease).
Seigel GM; Lotery A; Kummer A; Bernard DJ; Greene ND; Turmaine M; Derksen T; Nussbaum RL; Davidson B; Wagner J; Mitchison HM
Mol Cell Neurosci; 2002 Apr; 19(4):515-27. PubMed ID: 11988019
[TBL] [Abstract][Full Text] [Related]
13. Coding sequence and exon/intron organization of the canine CLN3 (Batten disease) gene and its exclusion as the locus for ceroid-lipofuscinosis in English setter dogs.
Shibuya H; Liu PC; Katz ML; Siakotos AN; Nonneman DJ; Johnson GS
J Neurosci Res; 1998 May; 52(3):268-75. PubMed ID: 9590435
[TBL] [Abstract][Full Text] [Related]
14. Altered arginine metabolism in the central nervous system (CNS) of the Cln3-/- mouse model of juvenile Batten disease.
Chan CH; Ramirez-Montealegre D; Pearce DA
Neuropathol Appl Neurobiol; 2009 Apr; 35(2):189-207. PubMed ID: 19284480
[TBL] [Abstract][Full Text] [Related]
15. Gene symbol: CLN3. Disease: juvenile neuronal ceroid lipofuscinosis (Batten disease).
Leman AR; Pearce DA; Rothberg PG
Hum Genet; 2005 Feb; 116(3):236. PubMed ID: 15818814
[No Abstract] [Full Text] [Related]
16. Mitochondrial ATP synthase subunit c storage in the ceroid-lipofuscinoses (Batten disease).
Palmer DN; Fearnley IM; Walker JE; Hall NA; Lake BD; Wolfe LS; Haltia M; Martinus RD; Jolly RD
Am J Med Genet; 1992 Feb; 42(4):561-7. PubMed ID: 1535179
[TBL] [Abstract][Full Text] [Related]
17. Role of subunit-9 of mitochondrial ATP synthase in Batten disease.
Johnson DW; Speier S; Qian WH; Lane S; Cook A; Suzuki K; Daniel P; Boustany RM
Am J Med Genet; 1995 Jun; 57(2):350-60. PubMed ID: 7668362
[TBL] [Abstract][Full Text] [Related]
18. Cross-species homology of the CLN3 gene.
Taschner PE; de Vos N; Breuning MH
Neuropediatrics; 1997 Feb; 28(1):18-20. PubMed ID: 9151313
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Batten disease and the ATP synthase subunit c turnover pathway: raising antibodies to subunit c.
Palmer DN; Bayliss SL; Westlake VJ
Am J Med Genet; 1995 Jun; 57(2):260-5. PubMed ID: 7668342
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]