277 related articles for article (PubMed ID: 32949681)
1. 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]
2. A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca2+ homeostasis and ER-mitochondria interactions.
Rouzier C; Moore D; Delorme C; Lacas-Gervais S; Ait-El-Mkadem S; Fragaki K; Burté F; Serre V; Bannwarth S; Chaussenot A; Catala M; Yu-Wai-Man P; Paquis-Flucklinger V
Hum Mol Genet; 2017 May; 26(9):1599-1611. PubMed ID: 28335035
[TBL] [Abstract][Full Text] [Related]
3. Uniting the divergent Wolfram syndrome-linked proteins WFS1 and CISD2 as modulators of Ca
Loncke J; Vervliet T; Parys JB; Kaasik A; Bultynck G
Sci Signal; 2021 Sep; 14(702):eabc6165. PubMed ID: 34582248
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. A novel mutation of WFS1 gene leading to increase ER stress and cell apoptosis is associated an autosomal dominant form of Wolfram syndrome type 1.
Gong Y; Xiong L; Li X; Su L; Xiao H
BMC Endocr Disord; 2021 Apr; 21(1):76. PubMed ID: 33879153
[TBL] [Abstract][Full Text] [Related]
7. Homozygosity mapping and direct sequencing identify a novel pathogenic variant in the CISD2 gene in an Iranian Wolfram syndrome family.
Pourreza MR; Sobhani M; Rahimi A; Aramideh M; Kajbafzadeh AM; Noori-Daloii MR; Tabatabaiefar MA
Acta Diabetol; 2020 Jan; 57(1):81-87. PubMed ID: 31309279
[TBL] [Abstract][Full Text] [Related]
8. 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]
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. 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]
11. 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]
12. Knockdown of wfs1, a fly homolog of Wolfram syndrome 1, in the nervous system increases susceptibility to age- and stress-induced neuronal dysfunction and degeneration in Drosophila.
Sakakibara Y; Sekiya M; Fujisaki N; Quan X; Iijima KM
PLoS Genet; 2018 Jan; 14(1):e1007196. PubMed ID: 29357349
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Genomics of Wolfram Syndrome 1 (WFS1).
Kõks S
Biomolecules; 2023 Sep; 13(9):. PubMed ID: 37759745
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. 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]
18. Wolfram Syndrome Type 2: A Systematic Review of a Not Easily Identifiable Clinical Spectrum.
Rosanio FM; Di Candia F; Occhiati L; Fedi L; Malvone FP; Foschini DF; Franzese A; Mozzillo E
Int J Environ Res Public Health; 2022 Jan; 19(2):. PubMed ID: 35055657
[TBL] [Abstract][Full Text] [Related]
19. Loss of Function of WFS1 Causes ER Stress-Mediated Inflammation in Pancreatic Beta-Cells.
Morikawa S; Blacher L; Onwumere C; Urano F
Front Endocrinol (Lausanne); 2022; 13():849204. PubMed ID: 35399956
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]