68 related articles for article (PubMed ID: 8833154)
21. Increased expression of lysosomal acid phosphatase in CLN3-defective cells and mouse brain tissue.
Pohl S; Mitchison HM; Kohlschütter A; van Diggelen O; Braulke T; Storch S
J Neurochem; 2007 Dec; 103(6):2177-88. PubMed ID: 17868323
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. 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]
24. Mapping of the mouse hyh gene to a YAC/BAC contig on proximal Chromosome 7.
Chae TH; Allen KM; Davisson MT; Sweet HO; Walsh CA
Mamm Genome; 2002 May; 13(5):239-44. PubMed ID: 12016511
[TBL] [Abstract][Full Text] [Related]
25. A mouse gene knockout model for juvenile ceroid-lipofuscinosis (Batten disease).
Katz ML; Shibuya H; Liu PC; Kaur S; Gao CL; Johnson GS
J Neurosci Res; 1999 Aug; 57(4):551-6. PubMed ID: 10440905
[TBL] [Abstract][Full Text] [Related]
26. Genetic localization of Cd63, a member of the transmembrane 4 superfamily, reveals two distinct loci in the mouse genome.
Gwynn B; Eicher EM; Peters LL
Genomics; 1996 Jul; 35(2):389-91. PubMed ID: 8661157
[TBL] [Abstract][Full Text] [Related]
27. Genetic and physical maps of the stargazer locus on mouse chromosome 15.
Letts VA; Valenzuela A; Kirley JP; Sweet HO; Davisson MT; Frankel WN
Genomics; 1997 Jul; 43(1):62-8. PubMed ID: 9226373
[TBL] [Abstract][Full Text] [Related]
28. Transcript mapping of the human chromosome 11q12-q13.1 gene-rich region identifies several newly described conserved genes.
Cooper PR; Nowak NJ; Higgins MJ; Church DM; Shows TB
Genomics; 1998 May; 49(3):419-29. PubMed ID: 9615227
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. Ultrafine mapping of Dyscalc1 to an 80-kb chromosomal segment on chromosome 7 in mice susceptible for dystrophic calcification.
Aherrahrou Z; Doehring LC; Kaczmarek PM; Liptau H; Ehlers EM; Pomarino A; Wrobel S; Götz A; Mayer B; Erdmann J; Schunkert H
Physiol Genomics; 2007 Jan; 28(2):203-12. PubMed ID: 16926270
[TBL] [Abstract][Full Text] [Related]
31. Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease.
Le Ber I; Camuzat A; Berger E; Hannequin D; Laquerrière A; Golfier V; Seilhean D; Viennet G; Couratier P; Verpillat P; Heath S; Camu W; Martinaud O; Lacomblez L; Vercelletto M; Salachas F; Sellal F; Didic M; Thomas-Anterion C; Puel M; Michel BF; Besse C; Duyckaerts C; Meininger V; Campion D; Dubois B; Brice A;
Neurology; 2009 May; 72(19):1669-76. PubMed ID: 19433740
[TBL] [Abstract][Full Text] [Related]
32. Retrovirally transduced bone marrow has a therapeutic effect on brain in the mouse model of mucopolysaccharidosis IIIB.
Zheng Y; Ryazantsev S; Ohmi K; Zhao HZ; Rozengurt N; Kohn DB; Neufeld EF
Mol Genet Metab; 2004 Aug; 82(4):286-95. PubMed ID: 15308126
[TBL] [Abstract][Full Text] [Related]
33. The protein kinase N (PKN) gene PRKCL1/Prkcl1 maps to human chromosome 19p12-p13.1 and mouse chromosome 8 with close linkage to the myodystrophy (myd) mutation.
Bartsch JW; Mukai H; Takahashi N; Ronsiek M; Fuchs S; Jockusch H; Ono Y
Genomics; 1998 Apr; 49(1):129-32. PubMed ID: 9570957
[TBL] [Abstract][Full Text] [Related]
34. A high-resolution genetic and physical map of a mouse coat abnormality locus (Uncv).
Shi YZ; Wang DP; Hu LD; Zhao GP; Wang YZ; Kong XY; Li SR
Sheng Wu Hua Xue Yu Sheng Wu Wu Li Xue Bao (Shanghai); 2003 May; 35(5):397-402. PubMed ID: 12766798
[TBL] [Abstract][Full Text] [Related]
35. Mapping of the alpha-tectorin gene (TECTA) to mouse chromosome 9 and human chromosome 11: a candidate for human autosomal dominant nonsyndromic deafness.
Hughes DC; Legan PK; Steel KP; Richardson GP
Genomics; 1998 Feb; 48(1):46-51. PubMed ID: 9503015
[TBL] [Abstract][Full Text] [Related]
36. Developmental impairments of select neurotransmitter systems in brains of Cln3(Deltaex7/8) knock-in mice, an animal model of juvenile neuronal ceroid lipofuscinosis.
Herrmann P; Druckrey-Fiskaaen C; Kouznetsova E; Heinitz K; Bigl M; Cotman SL; Schliebs R
J Neurosci Res; 2008 Jun; 86(8):1857-70. PubMed ID: 18265413
[TBL] [Abstract][Full Text] [Related]
37. An ENU-induced mutation in Rs1h causes disruption of retinal structure and function.
Jablonski MM; Dalke C; Wang X; Lu L; Manly KF; Pretsch W; Favor J; Pardue MT; Rinchik EM; Williams RW; Goldowitz D; Graw J
Mol Vis; 2005 Jul; 11():569-81. PubMed ID: 16088326
[TBL] [Abstract][Full Text] [Related]
38. Evidence that lysosomal storage of proteolipids is a cell autonomous process in the motor neuron degeneration (mnd) mouse, a model of neuronal ceroid lipofuscinosis.
Lipman RD; Donohue LR; Hoppe P; Bronson RT
Neurosci Lett; 1996 Nov; 219(2):111-4. PubMed ID: 8971792
[TBL] [Abstract][Full Text] [Related]
39. The kinesin light chain gene: its mapping and exclusion in mouse and human forms of inherited motor neuron degeneration.
Hafezparast M; Witherden A; Nicholson S; Bermingham N; Mackin J; ten Asbroek A; Ball S; Peters J; Baas F; Martin JE; Fisher EM
Neurosci Lett; 1999 Sep; 273(1):49-52. PubMed ID: 10505649
[TBL] [Abstract][Full Text] [Related]
40. Mapping functional chicken genes: an alternative approach.
Smith EJ; Cheng HH; Vallejo RL
Poult Sci; 1996 May; 75(5):642-7. PubMed ID: 8722913
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]