170 related articles for article (PubMed ID: 18613120)
1. Wolfram syndrome 1 (Wfs1) gene expression in the normal mouse visual system.
Kawano J; Tanizawa Y; Shinoda K
J Comp Neurol; 2008 Sep; 510(1):1-23. PubMed ID: 18613120
[TBL] [Abstract][Full Text] [Related]
2. Wolfram syndrome 1 (WFS1) protein expression in retinal ganglion cells and optic nerve glia of the cynomolgus monkey.
Yamamoto H; Hofmann S; Hamasaki DI; Yamamoto H; Kreczmanski P; Schmitz C; Parel JM; Schmidt-Kastner R
Exp Eye Res; 2006 Nov; 83(5):1303-6. PubMed ID: 16928372
[TBL] [Abstract][Full Text] [Related]
3. Wolfram syndrome 1 (Wfs1) mRNA expression in the normal mouse brain during postnatal development.
Kawano J; Fujinaga R; Yamamoto-Hanada K; Oka Y; Tanizawa Y; Shinoda K
Neurosci Res; 2009 Jun; 64(2):213-30. PubMed ID: 19428703
[TBL] [Abstract][Full Text] [Related]
4. Distribution of Wfs1 protein in the central nervous system of the mouse and its relation to clinical symptoms of the Wolfram syndrome.
Luuk H; Koks S; Plaas M; Hannibal J; Rehfeld JF; Vasar E
J Comp Neurol; 2008 Aug; 509(6):642-60. PubMed ID: 18551525
[TBL] [Abstract][Full Text] [Related]
5. Expressional and functional studies of Wolframin, the gene function deficient in Wolfram syndrome, in mice and patient cells.
Philbrook C; Fritz E; Weiher H
Exp Gerontol; 2005; 40(8-9):671-8. PubMed ID: 16087305
[TBL] [Abstract][Full Text] [Related]
6. Expression of the diabetes risk gene wolframin (WFS1) in the human retina.
Schmidt-Kastner R; Kreczmanski P; Preising M; Diederen R; Schmitz C; Reis D; Blanks J; Dorey CK
Exp Eye Res; 2009 Oct; 89(4):568-74. PubMed ID: 19523951
[TBL] [Abstract][Full Text] [Related]
7. Behavioral and gene expression analyses of Wfs1 knockout mice as a possible animal model of mood disorder.
Kato T; Ishiwata M; Yamada K; Kasahara T; Kakiuchi C; Iwamoto K; Kawamura K; Ishihara H; Oka Y
Neurosci Res; 2008 Jun; 61(2):143-58. PubMed ID: 18343518
[TBL] [Abstract][Full Text] [Related]
8. Growth hormone and its receptor in projection neurons of the chick visual system: retinofugal and tectobulbar tracts.
Baudet ML; Rattray D; Harvey S
Neuroscience; 2007 Aug; 148(1):151-63. PubMed ID: 17618059
[TBL] [Abstract][Full Text] [Related]
9. Wolfram syndrome: new pathophysiological insights and therapeutic strategies.
Mishra R; Chen BS; Richa P; Yu-Wai-Man P
Ther Adv Rare Dis; 2021; 2():26330040211039518. PubMed ID: 37181110
[TBL] [Abstract][Full Text] [Related]
10. Wolfram syndrome 1 gene (WFS1) product localizes to secretory granules and determines granule acidification in pancreatic beta-cells.
Hatanaka M; Tanabe K; Yanai A; Ohta Y; Kondo M; Akiyama M; Shinoda K; Oka Y; Tanizawa Y
Hum Mol Genet; 2011 Apr; 20(7):1274-84. PubMed ID: 21199859
[TBL] [Abstract][Full Text] [Related]
11. The spatial and temporal expression patterns of netrin receptors, DCC and neogenin, in the developing mouse retina.
Gad JM; Keeling SL; Shu T; Richards LJ; Cooper HM
Exp Eye Res; 2000 Jun; 70(6):711-22. PubMed ID: 10843775
[TBL] [Abstract][Full Text] [Related]
12. Mutational spectrum of the WFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric disease.
Cryns K; Sivakumaran TA; Van den Ouweland JM; Pennings RJ; Cremers CW; Flothmann K; Young TL; Smith RJ; Lesperance MM; Van Camp G
Hum Mutat; 2003 Oct; 22(4):275-87. PubMed ID: 12955714
[TBL] [Abstract][Full Text] [Related]
13. Wolfram syndrome and WFS1 gene.
Rigoli L; Lombardo F; Di Bella C
Clin Genet; 2011 Feb; 79(2):103-17. PubMed ID: 20738327
[TBL] [Abstract][Full Text] [Related]
14. [From gene to disease; mutations in the WFS1-gene as the cause of juvenile type I diabetes mellitus with optic atrophy (Wolfram syndrome)].
Pennings RJ; Dikkeschei LD; Cremers CW; van den Ouweland JM
Ned Tijdschr Geneeskd; 2002 May; 146(21):985-7. PubMed ID: 12058630
[TBL] [Abstract][Full Text] [Related]
15. WFS1-deficiency increases endoplasmic reticulum stress, impairs cell cycle progression and triggers the apoptotic pathway specifically in pancreatic beta-cells.
Yamada T; Ishihara H; Tamura A; Takahashi R; Yamaguchi S; Takei D; Tokita A; Satake C; Tashiro F; Katagiri H; Aburatani H; Miyazaki J; Oka Y
Hum Mol Genet; 2006 May; 15(10):1600-9. PubMed ID: 16571599
[TBL] [Abstract][Full Text] [Related]
16. Wolfram syndrome-associated mutations lead to instability and proteasomal degradation of wolframin.
Hofmann S; Bauer MF
FEBS Lett; 2006 Jul; 580(16):4000-4. PubMed ID: 16806192
[TBL] [Abstract][Full Text] [Related]
17. Tenascin protein and mRNA in the avian visual system: distribution and potential contribution to retinotectal development.
Perez RG; Halfter W
Perspect Dev Neurobiol; 1994; 2(1):75-87. PubMed ID: 7530146
[TBL] [Abstract][Full Text] [Related]
18. [Genetic diagnosis of diabetes mellitus: Wolfram syndrome--from positional cloning to DNA diagnosis].
Tanizawa Y
Rinsho Byori; 2003 Jun; 51(6):544-9. PubMed ID: 12884741
[TBL] [Abstract][Full Text] [Related]
19. First prenatal diagnosis for Wolfram syndrome by molecular analysis of the WFS1 gene.
Domènech E; Kruyer H; Gómez C; Calvo MT; Nunes V
Prenat Diagn; 2004 Oct; 24(10):787-9. PubMed ID: 15503287
[TBL] [Abstract][Full Text] [Related]
20. WFS1 (Wolfram syndrome 1) gene product: predominant subcellular localization to endoplasmic reticulum in cultured cells and neuronal expression in rat brain.
Takeda K; Inoue H; Tanizawa Y; Matsuzaki Y; Oba J; Watanabe Y; Shinoda K; Oka Y
Hum Mol Genet; 2001 Mar; 10(5):477-84. PubMed ID: 11181571
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
