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 *

94 related articles for article (PubMed ID: 12565131)

  • 1. No association of mutations and mRNA expression of WFS1/wolframin with bipolar disorder in humans.
    Kato T; Iwamoto K; Washizuka S; Mori K; Tajima O; Akiyama T; Nanko S; Kunugi H; Kato N
    Neurosci Lett; 2003 Feb; 338(1):21-4. PubMed ID: 12565131
    [TBL] [Abstract][Full Text] [Related]  

  • 2. WFS1 gene mutation search in depressive patients: detection of five missense polymorphisms but no association with depression or bipolar affective disorder.
    Ohtsuki T; Ishiguro H; Yoshikawa T; Arinami T
    J Affect Disord; 2000 Apr; 58(1):11-7. PubMed ID: 10760554
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Missense variations of the gene responsible for Wolfram syndrome (WFS1/wolframin) in Japanese: possible contribution of the Arg456His mutation to type 1 diabetes as a nonautoimmune genetic basis.
    Awata T; Inoue K; Kurihara S; Ohkubo T; Inoue I; Abe T; Takino H; Kanazawa Y; Katayama S
    Biochem Biophys Res Commun; 2000 Feb; 268(2):612-6. PubMed ID: 10679252
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The Impact of Mutations in Wolframin on Psychiatric Disorders.
    Munshani S; Ibrahim EY; Domenicano I; Ehrlich BE
    Front Pediatr; 2021; 9():718132. PubMed ID: 34746052
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Polymorphisms in wolframin (WFS1) gene are possibly related to increased risk for mood disorders.
    Koido K; Kõks S; Nikopensius T; Maron E; Altmäe S; Heinaste E; Vabrit K; Tammekivi V; Hallast P; Kurg A; Shlik J; Vasar V; Metspalu A; Vasar E
    Int J Neuropsychopharmacol; 2005 Jun; 8(2):235-44. PubMed ID: 15473915
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic variations in the WFS1 gene in Japanese with type 2 diabetes and bipolar disorder.
    Kawamoto T; Horikawa Y; Tanaka T; Kabe N; Takeda J; Mikuni M
    Mol Genet Metab; 2004 Jul; 82(3):238-45. PubMed ID: 15234338
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Behavioral and gene expression analyses of Wfs1 knockout mice as a possible animal model of mood disorder.
    Kato T; Ishiwata M; Yamada K; Kasahara T; Kakiuchi C; Iwamoto K; Kawamura K; Ishihara H; Oka Y
    Neurosci Res; 2008 Jun; 61(2):143-58. PubMed ID: 18343518
    [TBL] [Abstract][Full Text] [Related]  

  • 8. No association between wolframin gene H611R polymorphism and mood disorders: evidence from 2,570 subjects.
    Tang XW; Wang J; Zou YF
    Nord J Psychiatry; 2015 Feb; 69(2):132-7. PubMed ID: 25074416
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of four novel mutations of the WFS1 gene in Iranian Wolfram syndrome pedigrees.
    Ghahraman M; Abbaszadegan MR; Vakili R; Hosseini S; Fardi Golyan F; Ghaemi N; Forghanifard MM
    Acta Diabetol; 2016 Dec; 53(6):899-904. PubMed ID: 27412528
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A rare coding variant within the wolframin gene in bipolar and unipolar affective disorder cases.
    Furlong RA; Ho LW; Rubinsztein JS; Michael A; Walsh C; Paykel ES; Rubinsztein DC
    Neurosci Lett; 1999 Dec; 277(2):123-6. PubMed ID: 10624825
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Wolfram syndrome: structural and functional analyses of mutant and wild-type wolframin, the WFS1 gene product.
    Hofmann S; Philbrook C; Gerbitz KD; Bauer MF
    Hum Mol Genet; 2003 Aug; 12(16):2003-12. PubMed ID: 12913071
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. Molecular genetics of bipolar disorder.
    Kato T
    Neurosci Res; 2001 Jun; 40(2):105-13. PubMed ID: 11377748
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss.
    Bespalova IN; Van Camp G; Bom SJ; Brown DJ; Cryns K; DeWan AT; Erson AE; Flothmann K; Kunst HP; Kurnool P; Sivakumaran TA; Cremers CW; Leal SM; Burmeister M; Lesperance MM
    Hum Mol Genet; 2001 Oct; 10(22):2501-8. PubMed ID: 11709537
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Wolfram syndrome 1 (Wfs1) gene expression in the normal mouse visual system.
    Kawano J; Tanizawa Y; Shinoda K
    J Comp Neurol; 2008 Sep; 510(1):1-23. PubMed ID: 18613120
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutational analysis of the Wolfram syndrome gene in two families with chromosome 4p-linked bipolar affective disorder.
    Evans KL; Lawson D; Meitinger T; Blackwood DH; Porteous DJ
    Am J Med Genet; 2000 Apr; 96(2):158-60. PubMed ID: 10893488
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Wolfram syndrome 1 (Wfs1) mRNA expression in the normal mouse brain during postnatal development.
    Kawano J; Fujinaga R; Yamamoto-Hanada K; Oka Y; Tanizawa Y; Shinoda K
    Neurosci Res; 2009 Jun; 64(2):213-30. PubMed ID: 19428703
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.