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 *

180 related articles for article (PubMed ID: 24702843)

  • 21. Usher syndrome: Hearing loss, retinal degeneration and associated abnormalities.
    Mathur P; Yang J
    Biochim Biophys Acta; 2015 Mar; 1852(3):406-20. PubMed ID: 25481835
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A core cochlear phenotype in USH1 mouse mutants implicates fibrous links of the hair bundle in its cohesion, orientation and differential growth.
    Lefèvre G; Michel V; Weil D; Lepelletier L; Bizard E; Wolfrum U; Hardelin JP; Petit C
    Development; 2008 Apr; 135(8):1427-37. PubMed ID: 18339676
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Usher Syndrome: Genetics of a Human Ciliopathy.
    Fuster-García C; García-Bohórquez B; Rodríguez-Muñoz A; Aller E; Jaijo T; Millán JM; García-García G
    Int J Mol Sci; 2021 Jun; 22(13):. PubMed ID: 34201633
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss.
    Ebermann I; Scholl HP; Charbel Issa P; Becirovic E; Lamprecht J; Jurklies B; Millán JM; Aller E; Mitter D; Bolz H
    Hum Genet; 2007 Apr; 121(2):203-11. PubMed ID: 17171570
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Usher syndrome: hearing loss with vision loss.
    Friedman TB; Schultz JM; Ahmed ZM; Tsilou ET; Brewer CC
    Adv Otorhinolaryngol; 2011; 70():56-65. PubMed ID: 21358186
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells.
    Adato A; Lefèvre G; Delprat B; Michel V; Michalski N; Chardenoux S; Weil D; El-Amraoui A; Petit C
    Hum Mol Genet; 2005 Dec; 14(24):3921-32. PubMed ID: 16301217
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A New Mouse Model for Usher Syndrome Crossing Kunming Mice with CBA/J Mice.
    Li S; Jiang Y; Zhang L; Yan W; Wei D; Zhang M; Zhu B; Chen T; Wang X; Zhang Z; Su Y
    Gene; 2024 Sep; 922():148562. PubMed ID: 38754567
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Evidence for impaired olfactory function and structural brain integrity in a disorder of ciliary function, Usher syndrome.
    Ramos JN; Ribeiro JC; Pereira AC; Ferreira S; Duarte IC; Castelo-Branco M
    Neuroimage Clin; 2019; 22():101757. PubMed ID: 30897432
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The genetic and phenotypic landscapes of Usher syndrome: from disease mechanisms to a new classification.
    Delmaghani S; El-Amraoui A
    Hum Genet; 2022 Apr; 141(3-4):709-735. PubMed ID: 35353227
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Accelerated age-related olfactory decline among type 1 Usher patients.
    Ribeiro JC; Oliveiros B; Pereira P; António N; Hummel T; Paiva A; Silva ED
    Sci Rep; 2016 Jun; 6():28309. PubMed ID: 27329700
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Usher syndrome type 1-associated gene, pcdh15b, is required for photoreceptor structural integrity in zebrafish.
    Miles A; Blair C; Emili A; Tropepe V
    Dis Model Mech; 2021 Dec; 14(12):. PubMed ID: 34668518
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Distinct expression and function of whirlin isoforms in the inner ear and retina: an insight into pathogenesis of USH2D and DFNB31.
    Mathur PD; Zou J; Zheng T; Almishaal A; Wang Y; Chen Q; Wang L; Vashist D; Brown S; Park A; Yang J
    Hum Mol Genet; 2015 Nov; 24(21):6213-28. PubMed ID: 26307081
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Genetics and pathological mechanisms of Usher syndrome.
    Yan D; Liu XZ
    J Hum Genet; 2010 Jun; 55(6):327-35. PubMed ID: 20379205
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Inframe deletion of human
    Ahmed ZM; Jaworek TJ; Sarangdhar GN; Zheng L; Gul K; Khan SN; Friedman TB; Sisk RA; Bartles JR; Riazuddin S; Riazuddin S
    J Med Genet; 2018 Jul; 55(7):479-488. PubMed ID: 29572253
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Hiding in plain sight: genetic deaf-blindness is not always Usher syndrome.
    Medina G; Perry J; Oza A; Kenna M
    Cold Spring Harb Mol Case Stud; 2021 Aug; 7(4):. PubMed ID: 34021019
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Therapy strategies for Usher syndrome Type 1C in the retina.
    Nagel-Wolfrum K; Baasov T; Wolfrum U
    Adv Exp Med Biol; 2014; 801():741-7. PubMed ID: 24664766
    [TBL] [Abstract][Full Text] [Related]  

  • 37. SANS (USH1G) expression in developing and mature mammalian retina.
    Overlack N; Maerker T; Latz M; Nagel-Wolfrum K; Wolfrum U
    Vision Res; 2008 Feb; 48(3):400-12. PubMed ID: 17923142
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Ush1c gene expression levels in the ear and eye suggest different roles for Ush1c in neurosensory organs in a new Ush1c knockout mouse.
    Tian C; Liu XZ; Han F; Yu H; Longo-Guess C; Yang B; Lu C; Yan D; Zheng QY
    Brain Res; 2010 Apr; 1328():57-70. PubMed ID: 20211154
    [TBL] [Abstract][Full Text] [Related]  

  • 39. CLINICAL PRESENTATION AND DISEASE COURSE OF USHER SYNDROME BECAUSE OF MUTATIONS IN MYO7A OR USH2A.
    Testa F; Melillo P; Bonnet C; Marcelli V; de Benedictis A; Colucci R; Gallo B; Kurtenbach A; Rossi S; Marciano E; Auricchio A; Petit C; Zrenner E; Simonelli F
    Retina; 2017 Aug; 37(8):1581-1590. PubMed ID: 27828912
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Usher Syndrome and Color Vision.
    Kurtenbach A; Hahn G; Kernstock C; Hipp S; Zobor D; Stingl K; Kohl S; Bonnet C; Mohand-Saïd S; Sliesoraityte I; Sahel JA; Audo I; Fakin A; Hawlina M; Testa F; Simonelli F; Petit C; Zrenner E
    Curr Eye Res; 2018 Oct; 43(10):1295-1301. PubMed ID: 30012035
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.