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 *

247 related articles for article (PubMed ID: 30157177)

  • 1. Grxcr2 is required for stereocilia morphogenesis in the cochlea.
    Avenarius MR; Jung JY; Askew C; Jones SM; Hunker KL; Azaiez H; Rehman AU; Schraders M; Najmabadi H; Kremer H; Smith RJH; Géléoc GSG; Dolan DF; Raphael Y; Kohrman DC
    PLoS One; 2018; 13(8):e0201713. PubMed ID: 30157177
    [TBL] [Abstract][Full Text] [Related]  

  • 2. GRXCR2 Regulates Taperin Localization Critical for Stereocilia Morphology and Hearing.
    Liu C; Luo N; Tung CY; Perrin BJ; Zhao B
    Cell Rep; 2018 Oct; 25(5):1268-1280.e4. PubMed ID: 30380417
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Murine GRXCR1 Has a Different Function Than GRXCR2 in the Morphogenesis of Stereocilia.
    Liu C; Zhao B
    Front Cell Neurosci; 2021; 15():714070. PubMed ID: 34366792
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutations in Grxcr1 are the basis for inner ear dysfunction in the pirouette mouse.
    Odeh H; Hunker KL; Belyantseva IA; Azaiez H; Avenarius MR; Zheng L; Peters LM; Gagnon LH; Hagiwara N; Skynner MJ; Brilliant MH; Allen ND; Riazuddin S; Johnson KR; Raphael Y; Najmabadi H; Friedman TB; Bartles JR; Smith RJ; Kohrman DC
    Am J Hum Genet; 2010 Feb; 86(2):148-60. PubMed ID: 20137774
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Reducing Taperin Expression Restores Hearing in Grxcr2 Mutant Mice.
    Liu C; Luo N; Zhao B
    Neuroscience; 2022 Aug; 498():85-92. PubMed ID: 35752427
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A frameshift mutation in GRXCR2 causes recessively inherited hearing loss.
    Imtiaz A; Kohrman DC; Naz S
    Hum Mutat; 2014 May; 35(5):618-24. PubMed ID: 24619944
    [TBL] [Abstract][Full Text] [Related]  

  • 7. N-Terminus of GRXCR2 Interacts With CLIC5 and Is Essential for Auditory Perception.
    Li J; Liu C; Zhao B
    Front Cell Dev Biol; 2021; 9():671364. PubMed ID: 34026762
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Grxcr1 regulates hair bundle morphogenesis and is required for normal mechanoelectrical transduction in mouse cochlear hair cells.
    Lorente-Cánovas B; Eckrich S; Lewis MA; Johnson SL; Marcotti W; Steel KP
    PLoS One; 2022; 17(3):e0261530. PubMed ID: 35235570
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Stereocilia fusion pathology in the cochlear outer hair cells at the nanoscale level.
    Ikäheimo K; Leinonen S; Lankinen T; Lindahl M; Saarma M; Pirvola U
    J Physiol; 2024 Aug; 602(16):3995-4025. PubMed ID: 39037943
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Disruption of SorCS2 reveals differences in the regulation of stereociliary bundle formation between hair cell types in the inner ear.
    Forge A; Taylor RR; Dawson SJ; Lovett M; Jagger DJ
    PLoS Genet; 2017 Mar; 13(3):e1006692. PubMed ID: 28346477
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Methionine sulfoxide reductase B3 deficiency causes hearing loss due to stereocilia degeneration and apoptotic cell death in cochlear hair cells.
    Kwon TJ; Cho HJ; Kim UK; Lee E; Oh SK; Bok J; Bae YC; Yi JK; Lee JW; Ryoo ZY; Lee SH; Lee KY; Kim HY
    Hum Mol Genet; 2014 Mar; 23(6):1591-601. PubMed ID: 24191262
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Whole exome sequencing reveals a biallelic frameshift mutation in GRXCR2 in hearing impairment in Cameroon.
    Wonkam A; Lebeko K; Mowla S; Noubiap JJ; Chong M; Pare G
    Mol Genet Genomic Med; 2021 Mar; 9(3):e1609. PubMed ID: 33528103
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Stereocilia morphogenesis and maintenance through regulation of actin stability.
    McGrath J; Roy P; Perrin BJ
    Semin Cell Dev Biol; 2017 May; 65():88-95. PubMed ID: 27565685
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Multiple PDZ domain protein maintains patterning of the apical cytoskeleton in sensory hair cells.
    Jarysta A; Tarchini B
    Development; 2021 Jul; 148(14):. PubMed ID: 34228789
    [TBL] [Abstract][Full Text] [Related]  

  • 15. PKHD1L1 is a coat protein of hair-cell stereocilia and is required for normal hearing.
    Wu X; Ivanchenko MV; Al Jandal H; Cicconet M; Indzhykulian AA; Corey DP
    Nat Commun; 2019 Aug; 10(1):3801. PubMed ID: 31444330
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Coupling between the Stereocilia of Rat Sensory Inner-Hair-Cell Hair Bundles Is Weak, Shaping Their Sensitivity to Stimulation.
    Scharr AL; Ó Maoiléidigh D; Ricci AJ
    J Neurosci; 2023 Mar; 43(12):2053-2074. PubMed ID: 36746628
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutation of the novel gene Tmie results in sensory cell defects in the inner ear of spinner, a mouse model of human hearing loss DFNB6.
    Mitchem KL; Hibbard E; Beyer LA; Bosom K; Dootz GA; Dolan DF; Johnson KR; Raphael Y; Kohrman DC
    Hum Mol Genet; 2002 Aug; 11(16):1887-98. PubMed ID: 12140191
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Daple deficiency causes hearing loss in adult mice by inducing defects in cochlear stereocilia and apical microtubules.
    Ozono Y; Tamura A; Nakayama S; Herawati E; Hanada Y; Ohata K; Takagishi M; Takahashi M; Imai T; Ohta Y; Oshima K; Sato T; Inohara H; Tsukita S
    Sci Rep; 2021 Oct; 11(1):20224. PubMed ID: 34642354
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Sustained cadherin 23 expression in young and adult cochlea of normal and hearing-impaired mice.
    Rzadzinska AK; Derr A; Kachar B; Noben-Trauth K
    Hear Res; 2005 Oct; 208(1-2):114-21. PubMed ID: 16005171
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Compound heterozygosity of the functionally null Cdh23(v-ngt) and hypomorphic Cdh23(ahl) alleles leads to early-onset progressive hearing loss in mice.
    Miyasaka Y; Suzuki S; Ohshiba Y; Watanabe K; Sagara Y; Yasuda SP; Matsuoka K; Shitara H; Yonekawa H; Kominami R; Kikkawa Y
    Exp Anim; 2013; 62(4):333-46. PubMed ID: 24172198
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.