220 related articles for article (PubMed ID: 34828323)
1. The Expression of RAAS Key Receptors,
Punapart M; Seppa K; Jagomäe T; Liiv M; Reimets R; Kirillov S; Kaasik A; Moons L; De Groef L; Terasmaa A; Vasar E; Plaas M
Genes (Basel); 2021 Oct; 12(11):. PubMed ID: 34828323
[TBL] [Abstract][Full Text] [Related]
2. Chronic Stress Alters Hippocampal Renin-Angiotensin-Aldosterone System Component Expression in an Aged Rat Model of Wolfram Syndrome.
Punapart M; Reimets R; Seppa K; Kirillov S; Gaur N; Eskla KL; Jagomäe T; Vasar E; Plaas M
Genes (Basel); 2023 Mar; 14(4):. PubMed ID: 37107585
[TBL] [Abstract][Full Text] [Related]
3. GLP-1 receptor agonist liraglutide has a neuroprotective effect on an aged rat model of Wolfram syndrome.
Seppa K; Toots M; Reimets R; Jagomäe T; Koppel T; Pallase M; Hasselholt S; Krogsbæk Mikkelsen M; Randel Nyengaard J; Vasar E; Terasmaa A; Plaas M
Sci Rep; 2019 Oct; 9(1):15742. PubMed ID: 31673100
[TBL] [Abstract][Full Text] [Related]
4. Early Intervention and Lifelong Treatment with GLP1 Receptor Agonist Liraglutide in a Wolfram Syndrome Rat Model with an Emphasis on Visual Neurodegeneration, Sensorineural Hearing Loss and Diabetic Phenotype.
Jagomäe T; Seppa K; Reimets R; Pastak M; Plaas M; Hickey MA; Kukker KG; Moons L; De Groef L; Vasar E; Kaasik A; Terasmaa A; Plaas M
Cells; 2021 Nov; 10(11):. PubMed ID: 34831417
[TBL] [Abstract][Full Text] [Related]
5. Liraglutide, 7,8-DHF and their co-treatment prevents loss of vision and cognitive decline in a Wolfram syndrome rat model.
Seppa K; Jagomäe T; Kukker KG; Reimets R; Pastak M; Vasar E; Terasmaa A; Plaas M
Sci Rep; 2021 Jan; 11(1):2275. PubMed ID: 33500541
[TBL] [Abstract][Full Text] [Related]
6. Effect of 4-phenylbutyrate and valproate on dominant mutations of WFS1 gene in Wolfram syndrome.
Batjargal K; Tajima T; Jimbo EF; Yamagata T
J Endocrinol Invest; 2020 Sep; 43(9):1317-1325. PubMed ID: 32219690
[TBL] [Abstract][Full Text] [Related]
7. Preventive treatment with liraglutide protects against development of glucose intolerance in a rat model of Wolfram syndrome.
Toots M; Seppa K; Jagomäe T; Koppel T; Pallase M; Heinla I; Terasmaa A; Plaas M; Vasar E
Sci Rep; 2018 Jul; 8(1):10183. PubMed ID: 29976929
[TBL] [Abstract][Full Text] [Related]
8. Calpain inhibitor and ibudilast rescue β cell functions in a cellular model of Wolfram syndrome.
Nguyen LD; Fischer TT; Abreu D; Arroyo A; Urano F; Ehrlich BE
Proc Natl Acad Sci U S A; 2020 Jul; 117(29):17389-17398. PubMed ID: 32632005
[TBL] [Abstract][Full Text] [Related]
9. Wfs1- deficient rats develop primary symptoms of Wolfram syndrome: insulin-dependent diabetes, optic nerve atrophy and medullary degeneration.
Plaas M; Seppa K; Reimets R; Jagomäe T; Toots M; Koppel T; Vallisoo T; Nigul M; Heinla I; Meier R; Kaasik A; Piirsoo A; Hickey MA; Terasmaa A; Vasar E
Sci Rep; 2017 Aug; 7(1):10220. PubMed ID: 28860598
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. 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]
13. 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]
14. A novel heterozygous mutation of the WFS1 gene leading to constitutive endoplasmic reticulum stress is the cause of Wolfram syndrome.
Morikawa S; Tajima T; Nakamura A; Ishizu K; Ariga T
Pediatr Diabetes; 2017 Dec; 18(8):934-941. PubMed ID: 28271591
[TBL] [Abstract][Full Text] [Related]
15. Wolfram syndrome 1 gene negatively regulates ER stress signaling in rodent and human cells.
Fonseca SG; Ishigaki S; Oslowski CM; Lu S; Lipson KL; Ghosh R; Hayashi E; Ishihara H; Oka Y; Permutt MA; Urano F
J Clin Invest; 2010 Mar; 120(3):744-55. PubMed ID: 20160352
[TBL] [Abstract][Full Text] [Related]
16. Novel mutations in the WFS1 gene are associated with Wolfram syndrome and systemic inflammation.
Panfili E; Mondanelli G; Orabona C; Belladonna ML; Gargaro M; Fallarino F; Orecchini E; Prontera P; Proietti E; Frontino G; Tirelli E; Iacono A; Vacca C; Puccetti P; Grohmann U; Esposito S; Pallotta MT
Hum Mol Genet; 2021 Apr; 30(3-4):265-276. PubMed ID: 33693650
[TBL] [Abstract][Full Text] [Related]
17. Identification of novel mutations of the WFS1 gene in Brazilian patients with Wolfram syndrome.
Gasparin MR; Crispim F; Paula SL; Freire MB; Dalbosco IS; Manna TD; Salles JE; Gasparin F; Guedes A; Marcantonio JM; Gambini M; Salim CP; Moisés RS
Eur J Endocrinol; 2009 Feb; 160(2):309-16. PubMed ID: 19042979
[TBL] [Abstract][Full Text] [Related]
18. Clinical and genetic analysis of two wolfram syndrome families with high occurrence of wolfram syndrome and diabetes type II: a case report.
Sobhani M; Tabatabaiefar MA; Ghafouri-Fard S; Rajab A; Hojjat A; Kajbafzadeh AM; Noori-Daloii MR
BMC Med Genet; 2020 Jan; 21(1):13. PubMed ID: 31937257
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]
