304 related articles for article (PubMed ID: 32219690)
41. Mutation update and uncommon phenotypes in a French cohort of 96 patients with WFS1-related disorders.
Chaussenot A; Rouzier C; Quere M; Plutino M; Ait-El-Mkadem S; Bannwarth S; Barth M; Dollfus H; Charles P; Nicolino M; Chabrol B; Vialettes B; Paquis-Flucklinger V
Clin Genet; 2015 May; 87(5):430-9. PubMed ID: 24890733
[TBL] [Abstract][Full Text] [Related]
42. Valproate, a mood stabilizer, induces WFS1 expression and modulates its interaction with ER stress protein GRP94.
Kakiuchi C; Ishigaki S; Oslowski CM; Fonseca SG; Kato T; Urano F
PLoS One; 2009; 4(1):e4134. PubMed ID: 19125190
[TBL] [Abstract][Full Text] [Related]
43. Wolfram syndrome, a rare neurodegenerative disease: from pathogenesis to future treatment perspectives.
Pallotta MT; Tascini G; Crispoldi R; Orabona C; Mondanelli G; Grohmann U; Esposito S
J Transl Med; 2019 Jul; 17(1):238. PubMed ID: 31337416
[TBL] [Abstract][Full Text] [Related]
44. A novel nonsense mutation in the WFS1 gene causes the Wolfram syndrome.
Noorian S; Savad S; Mohammadi DS
J Pediatr Endocrinol Metab; 2016 May; 29(5):607-9. PubMed ID: 26943604
[TBL] [Abstract][Full Text] [Related]
45. 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]
46. 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]
47. Genetic and clinical aspects of Wolfram syndrome 1, a severe neurodegenerative disease.
Rigoli L; Bramanti P; Di Bella C; De Luca F
Pediatr Res; 2018 May; 83(5):921-929. PubMed ID: 29774890
[TBL] [Abstract][Full Text] [Related]
48. [A novel mutation of WFS1 gene in Chinese patients with Wolfram syndrome].
Fang QC; Jia WP; Zhang R; Li Q; Hu C; Shao XY; Chai HQ; Lu HJ; Xiang KS
Zhonghua Yi Xue Za Zhi; 2005 Sep; 85(35):2468-71. PubMed ID: 16321270
[TBL] [Abstract][Full Text] [Related]
49. 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]
50. WFS1 autosomal dominant variants linked with hearing loss: update on structural analysis and cochlear implant outcome.
Lim HD; Lee SM; Yun YJ; Lee DH; Lee JH; Oh SH; Lee SY
BMC Med Genomics; 2023 Apr; 16(1):79. PubMed ID: 37041640
[TBL] [Abstract][Full Text] [Related]
51. 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]
52. Developmental hypomyelination in Wolfram syndrome: new insights from neuroimaging and gene expression analyses.
Samara A; Rahn R; Neyman O; Park KY; Samara A; Marshall B; Dougherty J; Hershey T
Orphanet J Rare Dis; 2019 Dec; 14(1):279. PubMed ID: 31796109
[TBL] [Abstract][Full Text] [Related]
53. Endoplasmic reticulum stress inhibition ameliorated WFS1 expression alterations and reduced pancreatic islets' insulin secretion induced by high-fat diet in rats.
Binayi F; Fahanik-Babaei J; Salimi M; Eskandari F; Sahraei M; Ghorbani Ranjbary A; Ghasemi R; Hedayati M; Khodagholi F; Eliassi A; Zardooz H
Sci Rep; 2023 Feb; 13(1):1860. PubMed ID: 36725880
[TBL] [Abstract][Full Text] [Related]
54. Segregation of two variants suggests the presence of autosomal dominant and recessive forms of
Lusk L; Black E; Vengoechea J
J Med Genet; 2020 Feb; 57(2):121-123. PubMed ID: 31363008
[TBL] [Abstract][Full Text] [Related]
55. Wolfram syndrome 1 gene regulates pathways maintaining beta-cell health and survival.
Abreu D; Asada R; Revilla JMP; Lavagnino Z; Kries K; Piston DW; Urano F
Lab Invest; 2020 Jun; 100(6):849-862. PubMed ID: 32060407
[TBL] [Abstract][Full Text] [Related]
56. Wolfram syndrome 1b mutation suppresses Mauthner-cell axon regeneration via ER stress signal pathway.
Wang Z; Wang X; Shi L; Cai Y; Hu B
Acta Neuropathol Commun; 2022 Dec; 10(1):184. PubMed ID: 36527091
[TBL] [Abstract][Full Text] [Related]
57. 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]
58. Rapidly progressive renal disease as part of Wolfram syndrome in a large inbred Turkish family due to a novel WFS1 mutation (p.Leu511Pro).
Yuca SA; Rendtorff ND; Boulahbel H; Lodahl M; Tranebjærg L; Cesur Y; Dogan M; Yilmaz C; Akgun C; Acikgoz M
Eur J Med Genet; 2012 Jan; 55(1):37-42. PubMed ID: 21968327
[TBL] [Abstract][Full Text] [Related]
59. Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous missense mutation in the Wolfram syndrome gene WFS1.
Young TL; Ives E; Lynch E; Person R; Snook S; MacLaren L; Cater T; Griffin A; Fernandez B; Lee MK; King MC
Hum Mol Genet; 2001 Oct; 10(22):2509-14. PubMed ID: 11709538
[TBL] [Abstract][Full Text] [Related]
60. Activation of GLP-1 receptor signalling alleviates cellular stresses and improves beta cell function in a mouse model of Wolfram syndrome.
Kondo M; Tanabe K; Amo-Shiinoki K; Hatanaka M; Morii T; Takahashi H; Seino S; Yamada Y; Tanizawa Y
Diabetologia; 2018 Oct; 61(10):2189-2201. PubMed ID: 30054673
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
