126 related articles for article (PubMed ID: 16802712)
1. Does ASPA gene mutation in Canavan disease alter oligodendrocyte development? A tissue culture study of ASPA KO mice brain.
Kumar S; Sowmyalakshmi R; Daniels SL; Chang R; Surendran S; Matalon R; de Vellis J
Adv Exp Med Biol; 2006; 576():175-82; discussion 361-3. PubMed ID: 16802712
[No Abstract] [Full Text] [Related]
2. Lack of aspartoacylase activity disrupts survival and differentiation of neural progenitors and oligodendrocytes in a mouse model of Canavan disease.
Kumar S; Biancotti JC; Matalon R; de Vellis J
J Neurosci Res; 2009 Nov; 87(15):3415-27. PubMed ID: 19739253
[TBL] [Abstract][Full Text] [Related]
3. Aspartoacylase gene knockout in the mouse: impact on reproduction.
Surendran S; Szucs S; Tyring SK; Matalon R
Reprod Toxicol; 2005; 20(2):281-3. PubMed ID: 15907664
[TBL] [Abstract][Full Text] [Related]
4. Restoration of aspartoacylase activity in CNS neurons does not ameliorate motor deficits and demyelination in a model of Canavan disease.
Klugmann M; Leichtlein CB; Symes CW; Serikawa T; Young D; During MJ
Mol Ther; 2005 May; 11(5):745-53. PubMed ID: 15851013
[TBL] [Abstract][Full Text] [Related]
5. Canavan disease: genomic organization and localization of human ASPA to 17p13-ter and conservation of the ASPA gene during evolution.
Kaul R; Balamurugan K; Gao GP; Matalon R
Genomics; 1994 May; 21(2):364-70. PubMed ID: 8088831
[TBL] [Abstract][Full Text] [Related]
6. Aspartoacylase gene transfer to the mammalian central nervous system with therapeutic implications for Canavan disease.
Leone P; Janson CG; Bilaniuk L; Wang Z; Sorgi F; Huang L; Matalon R; Kaul R; Zeng Z; Freese A; McPhee SW; Mee E; During MJ
Ann Neurol; 2000 Jul; 48(1):27-38. PubMed ID: 10894213
[TBL] [Abstract][Full Text] [Related]
7. Nur7 is a nonsense mutation in the mouse aspartoacylase gene that causes spongy degeneration of the CNS.
Traka M; Wollmann RL; Cerda SR; Dugas J; Barres BA; Popko B
J Neurosci; 2008 Nov; 28(45):11537-49. PubMed ID: 18987190
[TBL] [Abstract][Full Text] [Related]
8. Adeno-associated virus-mediated aspartoacylase gene transfer to the brain of knockout mouse for canavan disease.
Matalon R; Surendran S; Rady PL; Quast MJ; Campbell GA; Matalon KM; Tyring SK; Wei J; Peden CS; Ezell EL; Muzyczka N; Mandel RJ
Mol Ther; 2003 May; 7(5 Pt 1):580-7. PubMed ID: 12718900
[TBL] [Abstract][Full Text] [Related]
9. Canavan disease: studies on the knockout mouse.
Matalon R; Michals-Matalon K; Surendran S; Tyring SK
Adv Exp Med Biol; 2006; 576():77-93; discussion 361-3. PubMed ID: 16802706
[TBL] [Abstract][Full Text] [Related]
10. Mutation analysis of the aspartoacylase gene in non-Jewish patients with Canavan disease.
Zeng BJ; Pastores GM; Leone P; Raghavan S; Wang ZH; Ribeiro LA; Torres P; Ong E; Kolodny EH
Adv Exp Med Biol; 2006; 576():165-73; discussion 361-3. PubMed ID: 16802711
[No Abstract] [Full Text] [Related]
11. Identification and characterization of novel mutations of the aspartoacylase gene in non-Jewish patients with Canavan disease.
Zeng BJ; Wang ZH; Ribeiro LA; Leone P; De Gasperi R; Kim SJ; Raghavan S; Ong E; Pastores GM; Kolodny EH
J Inherit Metab Dis; 2002 Nov; 25(7):557-70. PubMed ID: 12638939
[TBL] [Abstract][Full Text] [Related]
12. A novel aspartoacylase (ASPA) gene mutation in Canavan disease.
Durmaz AA; Akin H; Onay H; Vahabi A; Ozkinay F
Fetal Pediatr Pathol; 2012 Aug; 31(4):236-9. PubMed ID: 22468686
[TBL] [Abstract][Full Text] [Related]
13. Two novel aspartoacylase gene (ASPA) missense mutations specific to Norwegian and Swedish patients with Canavan disease.
Olsen TR; Tranebjaerg L; Kvittingen EA; Hagenfeldt L; Møller C; Nilssen O
J Med Genet; 2002 Sep; 39(9):e55. PubMed ID: 12205125
[No Abstract] [Full Text] [Related]
14. Knock-out mouse for Canavan disease: a model for gene transfer to the central nervous system.
Matalon R; Rady PL; Platt KA; Skinner HB; Quast MJ; Campbell GA; Matalon K; Ceci JD; Tyring SK; Nehls M; Surendran S; Wei J; Ezell EL; Szucs S
J Gene Med; 2000; 2(3):165-75. PubMed ID: 10894262
[TBL] [Abstract][Full Text] [Related]
15. Loss of central auditory processing in a mouse model of Canavan disease.
von Jonquieres G; Froud KE; Klugmann CB; Wong AC; Housley GD; Klugmann M
PLoS One; 2014; 9(5):e97374. PubMed ID: 24826990
[TBL] [Abstract][Full Text] [Related]
16. A benign polymorphism in the aspartoacylase gene may cause misinterpretation of Canavan gene testing.
Propheta O; Magal N; Shohat M; Eyal N; Navot N; Horowitz M
Eur J Hum Genet; 1998; 6(6):635-7. PubMed ID: 9887384
[TBL] [Abstract][Full Text] [Related]
17. Aspartoacylase gene knockout results in severe vacuolation in the white matter and gray matter of the spinal cord in the mouse.
Surendran S; Campbell GA; Tyring SK; Matalon R
Neurobiol Dis; 2005 Mar; 18(2):385-9. PubMed ID: 15686967
[TBL] [Abstract][Full Text] [Related]
18. A mutation of aspartoacylase gene in a Turkish patient with Canavan disease.
Eke GH; Iscan A; Cece H; Calik M
Genet Couns; 2012; 23(1):9-12. PubMed ID: 22611636
[TBL] [Abstract][Full Text] [Related]
19. The impact of structural biology on neurobiology.
Viola RE
Proc Natl Acad Sci U S A; 2007 Jan; 104(2):399-400. PubMed ID: 17213329
[No Abstract] [Full Text] [Related]
20. A missense mutation (p.G274R) in gene ASPA causes Canavan disease in a Pakistani family.
Hussain R; Daud S; Kakar N; Ahmad A; Baloch AH; Tareen AM; Kakar MA; Ahmad J
Mol Biol Rep; 2012 May; 39(5):6197-201. PubMed ID: 22219087
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]