BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

153 related articles for article (PubMed ID: 36134655)

  • 1. Multidimensional analysis and therapeutic development using patient iPSC-derived disease models of Wolfram syndrome.
    Kitamura RA; Maxwell KG; Ye W; Kries K; Brown CM; Augsornworawat P; Hirsch Y; Johansson MM; Weiden T; Ekstein J; Cohen J; Klee J; Leslie K; Simeonov A; Henderson MJ; Millman JR; Urano F
    JCI Insight; 2022 Sep; 7(18):. PubMed ID: 36134655
    [TBL] [Abstract][Full Text] [Related]  

  • 2. GLP-1R agonists demonstrate potential to treat Wolfram syndrome in human preclinical models.
    Gorgogietas V; Rajaei B; Heeyoung C; Santacreu BJ; Marín-Cañas S; Salpea P; Sawatani T; Musuaya A; Arroyo MN; Moreno-Castro C; Benabdallah K; Demarez C; Toivonen S; Cosentino C; Pachera N; Lytrivi M; Cai Y; Carnel L; Brown C; Urano F; Marchetti P; Gilon P; Eizirik DL; Cnop M; Igoillo-Esteve M
    Diabetologia; 2023 Jul; 66(7):1306-1321. PubMed ID: 36995380
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular characterization of WFS1 in patients with Wolfram syndrome.
    van ven Ouweland JM; Cryns K; Pennings RJ; Walraven I; Janssen GM; Maassen JA; Veldhuijzen BF; Arntzenius AB; Lindhout D; Cremers CW; Van Camp G; Dikkeschei LD
    J Mol Diagn; 2003 May; 5(2):88-95. PubMed ID: 12707373
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. Next generation sequencing identifies a pathogenic mutation of WFS1 gene in a Moroccan family with Wolfram syndrome: a case report.
    Sahli M; Zrhidri A; Boualaoui I; Cherkaoui Jaouad I; El Kadiri Y; Nouini Y; Sefiani A
    J Med Case Rep; 2023 Sep; 17(1):409. PubMed ID: 37752530
    [TBL] [Abstract][Full Text] [Related]  

  • 7. WFS1 protein expression correlates with clinical progression of optic atrophy in patients with Wolfram syndrome.
    Hu K; Zatyka M; Astuti D; Beer N; Dias RP; Kulkarni A; Ainsworth J; Wright B; Majander A; Yu-Wai-Man P; Williams D; Barrett T
    J Med Genet; 2022 Jan; 59(1):65-74. PubMed ID: 34006618
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Depletion of WFS1 compromises mitochondrial function in hiPSC-derived neuronal models of Wolfram syndrome.
    Zatyka M; Rosenstock TR; Sun C; Palhegyi AM; Hughes GW; Lara-Reyna S; Astuti D; di Maio A; Sciauvaud A; Korsgen ME; Stanulovic V; Kocak G; Rak M; Pourtoy-Brasselet S; Winter K; Varga T; Jarrige M; Polvèche H; Correia J; Frickel EM; Hoogenkamp M; Ward DG; Aubry L; Barrett T; Sarkar S
    Stem Cell Reports; 2023 May; 18(5):1090-1106. PubMed ID: 37163979
    [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. 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]  

  • 11. Genomics of Wolfram Syndrome 1 (WFS1).
    Kõks S
    Biomolecules; 2023 Sep; 13(9):. PubMed ID: 37759745
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Early Diagnosis of Wolfram Syndrome by Ophthalmologic Screening in a Patient with Type 1B Diabetes Mellitus: A Case Report.
    Kokumai T; Suzuki S; Nishikawa N; Yamamura H; Mukai T; Tanahashi Y; Takahashi S
    J Clin Res Pediatr Endocrinol; 2024 Mar; 16(1):102-105. PubMed ID: 35983751
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Wolfram syndrome type 1: a case series.
    Du D; Tuhuti A; Ma Y; Abuduniyimu M; Li S; Ma G; Zynat J; Guo Y
    Orphanet J Rare Dis; 2023 Nov; 18(1):359. PubMed ID: 37974252
    [TBL] [Abstract][Full Text] [Related]  

  • 14. ISR inhibition reverses pancreatic β-cell failure in Wolfram syndrome models.
    Hu R; Chen X; Su Q; Wang Z; Wang X; Gong M; Xu M; Le R; Gao Y; Dai P; Zhang ZN; Shao L; Li W
    Cell Death Differ; 2024 Mar; 31(3):322-334. PubMed ID: 38321214
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel
    Bouhouche A; Sefiani S; Charoute H; Houyam T; Bouslam N; El Yousfi FZ; Bnouhana W; Benomar A; Ouadghiri FZ; Regragui W
    Genet Test Mol Biomarkers; 2024 Jun; 28(6):257-262. PubMed ID: 38721948
    [No Abstract]   [Full Text] [Related]  

  • 16. Genotype and clinical characteristics of patients with Wolfram syndrome and WFS1-related disorders.
    Lee EM; Verma M; Palaniappan N; Pope EM; Lee S; Blacher L; Neerumalla P; An W; Campbell T; Brown C; Hurst S; Marshall B; Hershey T; Nunes V; López de Heredia M; Urano F
    Front Genet; 2023; 14():1198171. PubMed ID: 37415600
    [No Abstract]   [Full Text] [Related]  

  • 17. A mutant wfs1 zebrafish model of Wolfram syndrome manifesting visual dysfunction and developmental delay.
    Cairns G; Burté F; Price R; O'Connor E; Toms M; Mishra R; Moosajee M; Pyle A; Sayer JA; Yu-Wai-Man P
    Sci Rep; 2021 Oct; 11(1):20491. PubMed ID: 34650143
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The miR-668 binding site variant rs1046322 on
    Hammad MM; Abu-Farha M; Hebbar P; Anoop E; Chandy B; Melhem M; Channanath A; Al-Mulla F; Thanaraj TA; Abubaker J
    Front Endocrinol (Lausanne); 2023; 14():1185956. PubMed ID: 37859980
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Variants of
    Tang Y; Shao X; Ying B; Qiu J; Zheng S; Liu Y; Zhang X; Li Y
    Biomed Rep; 2023 Oct; 19(4):68. PubMed ID: 37719678
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Case Report: Off-Label Liraglutide Use in Children With Wolfram Syndrome Type 1: Extensive Characterization of Four Patients.
    Frontino G; Raouf T; Canarutto D; Tirelli E; Di Tonno R; Rigamonti A; Cascavilla ML; Baldoli C; Scotti R; Leocani L; Huang SC; Meschi F; Barera G; Broccoli V; Rossi G; Torchio S; Chimienti R; Bonfanti R; Piemonti L
    Front Pediatr; 2021; 9():755365. PubMed ID: 34970515
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.