257 related articles for article (PubMed ID: 18551525)
21. Sex-related hearing impairment in Wolfram syndrome patients identified by inactivating WFS1 mutations.
Pennings RJ; Huygen PL; van den Ouweland JM; Cryns K; Dikkeschei LD; Van Camp G; Cremers CW
Audiol Neurootol; 2004; 9(1):51-62. PubMed ID: 14676474
[TBL] [Abstract][Full Text] [Related]
22. A new mutation in WFS1 gene (C.1522-1523delTA, Y508fsX421) may be responsible for early appearance of clinical features of Wolfram syndrome and suicidal behaviour.
Aluclu MU; Bahceci M; Tuzcu A; Arikan S; Gokalp D
Neuro Endocrinol Lett; 2006 Dec; 27(6):691-4. PubMed ID: 17187023
[TBL] [Abstract][Full Text] [Related]
23. Wolfram syndrome 1 and Wolfram syndrome 2.
Rigoli L; Di Bella C
Curr Opin Pediatr; 2012 Aug; 24(4):512-7. PubMed ID: 22790102
[TBL] [Abstract][Full Text] [Related]
24. Primary diagnosis of Wolfram syndrome in an adult patient--case report and description of a novel pathogenic mutation.
Waschbisch A; Volbers B; Struffert T; Hoyer J; Schwab S; Bardutzky J
J Neurol Sci; 2011 Jan; 300(1-2):191-3. PubMed ID: 20875904
[TBL] [Abstract][Full Text] [Related]
25. Wolfram/DIDMOAD syndrome, a heterogenic and molecularly complex neurodegenerative disease.
Domenech E; Gomez-Zaera M; Nunes V
Pediatr Endocrinol Rev; 2006 Mar; 3(3):249-57. PubMed ID: 16639390
[TBL] [Abstract][Full Text] [Related]
26. WFS1 mutations in Spanish patients with diabetes mellitus and deafness.
Domènech E; Gómez-Zaera M; Nunes V
Eur J Hum Genet; 2002 Jul; 10(7):421-6. PubMed ID: 12107816
[TBL] [Abstract][Full Text] [Related]
27. Molecular characterization of WFS1 in an Iranian family with Wolfram syndrome reveals a novel frameshift mutation associated with early symptoms.
Sobhani M; Tabatabaiefar MA; Rajab A; Kajbafzadeh AM; Noori-Daloii MR
Gene; 2013 Oct; 528(2):309-13. PubMed ID: 23845777
[TBL] [Abstract][Full Text] [Related]
28. Deletion of the Wolfram syndrome-related gene Wfs1 results in increased sensitivity to ethanol in female mice.
Raud S; Reimets R; Loomets M; Sütt S; Altpere A; Visnapuu T; Innos J; Luuk H; Plaas M; Volke V; Vasar E
Neuropharmacology; 2015 Aug; 95():59-67. PubMed ID: 25725334
[TBL] [Abstract][Full Text] [Related]
29. Genetic variations in the WFS1 gene in Japanese with type 2 diabetes and bipolar disorder.
Kawamoto T; Horikawa Y; Tanaka T; Kabe N; Takeda J; Mikuni M
Mol Genet Metab; 2004 Jul; 82(3):238-45. PubMed ID: 15234338
[TBL] [Abstract][Full Text] [Related]
30. Identification of a novel WFS1 mutation (AFF344-345ins) in Japanese patients with Wolfram syndrome.
Inukai K; Awata T; Inoue K; Kurihara S; Nakashima Y; Watanabe M; Sawa T; Takata N; Katayama S
Diabetes Res Clin Pract; 2005 Aug; 69(2):136-41. PubMed ID: 16005363
[TBL] [Abstract][Full Text] [Related]
31. Wfs1-deficient mice display impaired behavioural adaptation in stressful environment.
Luuk H; Plaas M; Raud S; Innos J; Sütt S; Lasner H; Abramov U; Kurrikoff K; Kõks S; Vasar E
Behav Brain Res; 2009 Mar; 198(2):334-45. PubMed ID: 19041897
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. WFS1 mutations are frequent monogenic causes of juvenile-onset diabetes mellitus in Lebanon.
Zalloua PA; Azar ST; Delépine M; Makhoul NJ; Blanc H; Sanyoura M; Lavergne A; Stankov K; Lemainque A; Baz P; Julier C
Hum Mol Genet; 2008 Dec; 17(24):4012-21. PubMed ID: 18806274
[TBL] [Abstract][Full Text] [Related]
34. c.376G>A mutation in WFS1 gene causes Wolfram syndrome without deafness.
Safarpour Lima B; Ghaedi H; Daftarian N; Ahmadieh H; Jamshidi J; Khorrami M; Noroozi R; Sohrabifar N; Assarzadegan F; Hesami O; Taghavi S; Ahmadifard A; Atakhorrami M; Rahimi-Aliabadi S; Shahmohammadibeni N; Alehabib E; Andarva M; Darvish H; Emamalizadeh B
Eur J Med Genet; 2016 Feb; 59(2):65-9. PubMed ID: 26773575
[TBL] [Abstract][Full Text] [Related]
35. Function of WFS1 and WFS2 in the Central Nervous System: Implications for Wolfram Syndrome and Alzheimer's disease.
Li L; Venkataraman L; Chen S; Fu H
Neurosci Biobehav Rev; 2020 Nov; 118():775-783. PubMed ID: 32949681
[TBL] [Abstract][Full Text] [Related]
36. [Positional cloning of the gene(WFS1) for Wolfram syndrome].
Tanizawa Y; Inoue H; Oka Y
Rinsho Byori; 2000 Oct; 48(10):941-7. PubMed ID: 11215108
[TBL] [Abstract][Full Text] [Related]
37. Identification of four novel mutations of the WFS1 gene in Iranian Wolfram syndrome pedigrees.
Ghahraman M; Abbaszadegan MR; Vakili R; Hosseini S; Fardi Golyan F; Ghaemi N; Forghanifard MM
Acta Diabetol; 2016 Dec; 53(6):899-904. PubMed ID: 27412528
[TBL] [Abstract][Full Text] [Related]
38. Expression of somatostatin and somatostatin receptor subtypes in Apolipoprotein D (ApoD) knockout mouse brain: An immunohistochemical analysis.
Rajput PS; Billova S; Patel SC; Kharmate G; Somvanshi RK; Kumar U
J Chem Neuroanat; 2009 Sep; 38(1):20-33. PubMed ID: 19465111
[TBL] [Abstract][Full Text] [Related]
39. Identification of unsuspected Wolfram syndrome cases through clinical assessment and WFS1 gene screening in type 1 diabetes mellitus patients.
Blanco-Aguirre ME; la Parra DR; Tapia-Garcia H; Gonzalez-Rodriguez J; Welschen D; Arroyo-Yllanes ME; Escudero I; Nuñez-Hernandez JA; Medina-Bravo P; Zenteno JC
Gene; 2015 Jul; 566(1):63-7. PubMed ID: 25895475
[TBL] [Abstract][Full Text] [Related]
40. Phenotype Prediction of Pathogenic Nonsynonymous Single Nucleotide Polymorphisms in WFS1.
Qian X; Qin L; Xing G; Cao X
Sci Rep; 2015 Oct; 5():14731. PubMed ID: 26435059
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]