These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

186 related articles for article (PubMed ID: 19523951)

  • 21. Expressional and functional studies of Wolframin, the gene function deficient in Wolfram syndrome, in mice and patient cells.
    Philbrook C; Fritz E; Weiher H
    Exp Gerontol; 2005; 40(8-9):671-8. PubMed ID: 16087305
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Localization and distribution of wolframin in human tissues.
    De Falco M; Manente L; Lucariello A; Baldi G; Fiore P; Laforgia V; Baldi A; Iannaccone A; De Luca A
    Front Biosci (Elite Ed); 2012 Jan; 4(5):1986-98. PubMed ID: 22202014
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A new structural rearrangement associated to Wolfram syndrome in a child with a partial phenotype.
    Elli FM; Ghirardello S; Giavoli C; Gangi S; Dioni L; Crippa M; Finelli P; Bergamaschi S; Mosca F; Spada A; Beck-Peccoz P
    Gene; 2012 Nov; 509(1):168-72. PubMed ID: 22771918
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [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]  

  • 25. 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]  

  • 26. Wolfram syndrome-associated mutations lead to instability and proteasomal degradation of wolframin.
    Hofmann S; Bauer MF
    FEBS Lett; 2006 Jul; 580(16):4000-4. PubMed ID: 16806192
    [TBL] [Abstract][Full Text] [Related]  

  • 27. High-fat diet associated sensitization to metabolic stress in Wfs1 heterozygous mice.
    Ivask M; Volke V; Raasmaja A; Kõks S
    Mol Genet Metab; 2021; 134(1-2):203-211. PubMed ID: 34312071
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Identification of a novel WFS1 homozygous nonsense mutation in Jordanian children with Wolfram syndrome.
    Bodoor K; Batiha O; Abu-Awad A; Al-Sarihin K; Ziad H; Jarun Y; Abu-Sheikha A; Abu Jalboush S; Alibrahim KS
    Meta Gene; 2016 Sep; 9():219-24. PubMed ID: 27617222
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Modulation of wolframin expression in human placenta during pregnancy: comparison among physiological and pathological states.
    Lucariello A; Perna A; Sellitto C; Baldi A; Iannaccone A; Cobellis L; De Luca A; De Falco M
    Biomed Res Int; 2014; 2014():985478. PubMed ID: 24588001
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A single base-pair deletion in the WFS1 gene causes Wolfram syndrome.
    Pitt K; James C; Kochar IS; Kapoor A; Jain S; Hussain K; Bennett K
    J Pediatr Endocrinol Metab; 2011; 24(5-6):389-91. PubMed ID: 21823543
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. Teaching NeuroImages: a neuroendocrine rarity: Wolfram syndrome.
    Vale TC; Perpétuo FO
    Neurology; 2013 Nov; 81(20):e153. PubMed ID: 24218323
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Familial Wolfram syndrome].
    Bessahraoui M; Paquis V; Rouzier C; Bouziane-Nedjadi K; Naceur M; Niar S; Zennaki A; Boudraa G; Touhami M
    Arch Pediatr; 2014 Nov; 21(11):1229-32. PubMed ID: 25282462
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. Retinal pigment epithelial integrity is compromised in the developing albino mouse retina.
    Iwai-Takekoshi L; Ramos A; Schaler A; Weinreb S; Blazeski R; Mason C
    J Comp Neurol; 2016 Dec; 524(18):3696-3716. PubMed ID: 27097562
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Wolframin expression induces novel ion channel activity in endoplasmic reticulum membranes and increases intracellular calcium.
    Osman AA; Saito M; Makepeace C; Permutt MA; Schlesinger P; Mueckler M
    J Biol Chem; 2003 Dec; 278(52):52755-62. PubMed ID: 14527944
    [TBL] [Abstract][Full Text] [Related]  

  • 37. WFS1 variants in Finnish patients with diabetes mellitus, sensorineural hearing impairment or optic atrophy, and in suicide victims.
    Kytövuori L; Seppänen A; Martikainen MH; Moilanen JS; Kamppari S; Särkioja T; Remes AM; Räsänen P; Rönnemaa T; Majamaa K
    J Hum Genet; 2013 Aug; 58(8):495-500. PubMed ID: 23595122
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A Novel Genetic Variant in the WFS1 Gene in a Patient with Partial Uniparental Mero-Isodisomy of Chromosome 4.
    Delvecchio M; Ortolani F; Palumbo O; Aloi C; Salina A; Susca FC; Palumbo P; Carella M; Resta N; Piccinno E
    Int J Mol Sci; 2021 Jul; 22(15):. PubMed ID: 34360843
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The WFS1 gene, responsible for low frequency sensorineural hearing loss and Wolfram syndrome, is expressed in a variety of inner ear cells.
    Cryns K; Thys S; Van Laer L; Oka Y; Pfister M; Van Nassauw L; Smith RJ; Timmermans JP; Van Camp G
    Histochem Cell Biol; 2003 Mar; 119(3):247-56. PubMed ID: 12649740
    [TBL] [Abstract][Full Text] [Related]  

  • 40. WFS1/wolframin mutations, Wolfram syndrome, and associated diseases.
    Khanim F; Kirk J; Latif F; Barrett TG
    Hum Mutat; 2001 May; 17(5):357-67. PubMed ID: 11317350
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.