304 related articles for article (PubMed ID: 32219690)
21. 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]
22. Efficacy of GLP-1 Agonist Therapy in Autosomal Dominant WFS1-Related Disorder: A Case Report.
Scully KJ; Wolfsdorf JI
Horm Res Paediatr; 2020; 93(6):409-414. PubMed ID: 33075784
[TBL] [Abstract][Full Text] [Related]
23. Dominant ER Stress-Inducing
De Franco E; Flanagan SE; Yagi T; Abreu D; Mahadevan J; Johnson MB; Jones G; Acosta F; Mulaudzi M; Lek N; Oh V; Petz O; Caswell R; Ellard S; Urano F; Hattersley AT
Diabetes; 2017 Jul; 66(7):2044-2053. PubMed ID: 28468959
[TBL] [Abstract][Full Text] [Related]
24. Metabolomics of the Wolfram Syndrome 1 Gene (Wfs1) Deficient Mice.
Porosk R; Terasmaa A; Mahlapuu R; Soomets U; Kilk K
OMICS; 2017 Dec; 21(12):721-732. PubMed ID: 29257731
[TBL] [Abstract][Full Text] [Related]
25. Valproate Attenuates Endoplasmic Reticulum Stress-Induced Apoptosis in SH-SY5Y Cells via the AKT/GSK3β Signaling Pathway.
Li Z; Wu F; Zhang X; Chai Y; Chen D; Yang Y; Xu K; Yin J; Li R; Shi H; Wang Z; Li X; Xiao J; Zhang H
Int J Mol Sci; 2017 Feb; 18(2):. PubMed ID: 28208696
[TBL] [Abstract][Full Text] [Related]
26. WFS1 is a novel component of the unfolded protein response and maintains homeostasis of the endoplasmic reticulum in pancreatic beta-cells.
Fonseca SG; Fukuma M; Lipson KL; Nguyen LX; Allen JR; Oka Y; Urano F
J Biol Chem; 2005 Nov; 280(47):39609-15. PubMed ID: 16195229
[TBL] [Abstract][Full Text] [Related]
27. [Wolfram syndrome: from definition to molecular bases].
Ribeiro MR; Crispim F; Vendramini MF; Moisés RS
Arq Bras Endocrinol Metabol; 2006 Oct; 50(5):839-44. PubMed ID: 17160206
[TBL] [Abstract][Full Text] [Related]
28. Autosomal-dominant WFS1-related disorder-Report of a novel WFS1 variant and review of the phenotypic spectrum of autosomal recessive and dominant forms.
Abu-El-Haija A; McGowan C; Vanderveen D; Bodamer O
Am J Med Genet A; 2021 Feb; 185(2):528-533. PubMed ID: 33179441
[TBL] [Abstract][Full Text] [Related]
29. [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]
30. Wolfram Syndrome 1: From Genetics to Therapy.
Rigoli L; Caruso V; Salzano G; Lombardo F
Int J Environ Res Public Health; 2022 Mar; 19(6):. PubMed ID: 35328914
[TBL] [Abstract][Full Text] [Related]
31. Congenital central diabetes insipidus and optic atrophy in a Wolfram newborn: is there a role for WFS1 gene in neurodevelopment?
Ghirardello S; Dusi E; Castiglione B; Fumagalli M; Mosca F
Ital J Pediatr; 2014 Sep; 40():76. PubMed ID: 25255707
[TBL] [Abstract][Full Text] [Related]
32. [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]
33. Identification of p.A684V missense mutation in the WFS1 gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment.
Rendtorff ND; Lodahl M; Boulahbel H; Johansen IR; Pandya A; Welch KO; Norris VW; Arnos KS; Bitner-Glindzicz M; Emery SB; Mets MB; Fagerheim T; Eriksson K; Hansen L; Bruhn H; Möller C; Lindholm S; Ensgaard S; Lesperance MM; Tranebjaerg L
Am J Med Genet A; 2011 Jun; 155A(6):1298-313. PubMed ID: 21538838
[TBL] [Abstract][Full Text] [Related]
34. Sodium 4-phenylbutyrate protects against liver ischemia reperfusion injury by inhibition of endoplasmic reticulum-stress mediated apoptosis.
Vilatoba M; Eckstein C; Bilbao G; Smyth CA; Jenkins S; Thompson JA; Eckhoff DE; Contreras JL
Surgery; 2005 Aug; 138(2):342-51. PubMed ID: 16153446
[TBL] [Abstract][Full Text] [Related]
35. A novel mutation of WFS1 gene in a Chinese patient with Wolfram syndrome: a case report.
Li M; Liu J; Yi H; Xu L; Zhong X; Peng F
BMC Pediatr; 2018 Mar; 18(1):116. PubMed ID: 29549887
[TBL] [Abstract][Full Text] [Related]
36. Vacuolar-type H+-ATPase V1A subunit is a molecular partner of Wolfram syndrome 1 (WFS1) protein, which regulates its expression and stability.
Gharanei S; Zatyka M; Astuti D; Fenton J; Sik A; Nagy Z; Barrett TG
Hum Mol Genet; 2013 Jan; 22(2):203-17. PubMed ID: 23035048
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. 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]
39. [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]
40. Novel missense
Mair H; Fowler N; Papatzanaki ME; Sudhakar P; Maldonado RS
Ophthalmic Genet; 2022 Aug; 43(4):567-572. PubMed ID: 35450504
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
