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 *

270 related articles for article (PubMed ID: 23666531)

  • 1. GATA3 controls the specification of prosensory domain and neuronal survival in the mouse cochlea.
    Luo XJ; Deng M; Xie X; Huang L; Wang H; Jiang L; Liang G; Hu F; Tieu R; Chen R; Gan L
    Hum Mol Genet; 2013 Sep; 22(18):3609-23. PubMed ID: 23666531
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Limited inner ear morphogenesis and neurosensory development are possible in the absence of GATA3.
    Duncan JS; Lim KC; Engel JD; Fritzsch B
    Int J Dev Biol; 2011; 55(3):297-303. PubMed ID: 21553382
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Gata3 is required for the functional maturation of inner hair cells and their innervation in the mouse cochlea.
    Bardhan T; Jeng JY; Waldmann M; Ceriani F; Johnson SL; Olt J; Rüttiger L; Marcotti W; Holley MC
    J Physiol; 2019 Jul; 597(13):3389-3406. PubMed ID: 31069810
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Continued expression of GATA3 is necessary for cochlear neurosensory development.
    Duncan JS; Fritzsch B
    PLoS One; 2013; 8(4):e62046. PubMed ID: 23614009
    [TBL] [Abstract][Full Text] [Related]  

  • 5. GATA3 maintains the quiescent state of cochlear supporting cells by regulating p27
    Xu J; Yu D; Dong X; Xie X; Xu M; Guo L; Huang L; Tang Q; Gan L
    Sci Rep; 2021 Aug; 11(1):15779. PubMed ID: 34349220
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The role of Pax2 in mouse inner ear development.
    Burton Q; Cole LK; Mulheisen M; Chang W; Wu DK
    Dev Biol; 2004 Aug; 272(1):161-75. PubMed ID: 15242798
    [TBL] [Abstract][Full Text] [Related]  

  • 7. HDR syndrome with a novel mutation in GATA3 mimicking a congenital X-linked stapes gusher: a case report.
    Yang A; Kim J; Ki CS; Hong SH; Cho SY; Jin DK
    BMC Med Genet; 2017 Oct; 18(1):121. PubMed ID: 29073906
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Comparative analysis of Gata3 and Gata2 expression during chicken inner ear development.
    Lilleväli K; Haugas M; Pituello F; Salminen M
    Dev Dyn; 2007 Jan; 236(1):306-13. PubMed ID: 17103399
    [TBL] [Abstract][Full Text] [Related]  

  • 9. GATA3 haploinsufficiency causes a rapid deterioration of distortion product otoacoustic emissions (DPOAEs) in mice.
    van Looij MA; van der Burg H; van der Giessen RS; de Ruiter MM; van der Wees J; van Doorninck JH; De Zeeuw CI; van Zanten GA
    Neurobiol Dis; 2005 Dec; 20(3):890-7. PubMed ID: 15994092
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical Auditory Phenotypes Associated with
    Wang L; Lin QF; Wang HY; Guan J; Lan L; Xie LY; Yu L; Yang J; Zhao C; Liang JL; Zhou HL; Yang HM; Xiong WP; Zhang QJ; Wang DY; Wang QJ
    Chin Med J (Engl); 2017 Mar; 130(6):703-709. PubMed ID: 28303854
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Familial congenital choanal atresia with GATA3 associated hypoparathyroidism-deafness-renal dysplasia syndrome unidentified on auditory brainstem response.
    Kita M; Kuwata Y; Usui T
    Auris Nasus Larynx; 2019 Oct; 46(5):808-812. PubMed ID: 30396722
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel GATA3 nonsense mutation in a newly diagnosed adult patient of hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome.
    Nanba K; Usui T; Nakamura M; Toyota Y; Hirota K; Tamanaha T; Kawashima ST; Nakao K; Yuno A; Tagami T; Naruse M; Shimatsu A
    Endocr Pract; 2013; 19(1):e17-20. PubMed ID: 23186964
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Gata3 is required in late proneurosensory development for proper sensory cell formation and organization.
    Blinkiewicz PV; Long MR; Stoner ZA; Ketchum EM; Sheltz-Kempf SN; Duncan JS
    Sci Rep; 2023 Aug; 13(1):12573. PubMed ID: 37537240
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Defects in sensory organ morphogenesis and generation of cochlear hair cells in Gata3-deficient mouse embryos.
    Haugas M; Lilleväli K; Salminen M
    Hear Res; 2012 Jan; 283(1-2):151-61. PubMed ID: 22094003
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Unusual Proliferative Glomerulonephritis in a Patient Diagnosed to Have Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia (HDR) Syndrome with a Novel Mutation in the GATA3 Gene.
    Kamezaki M; Kusaba T; Adachi T; Yamashita N; Nakata M; Ota N; Shiotsu Y; Ishida M; Usui T; Tamagaki K
    Intern Med; 2017; 56(11):1393-1397. PubMed ID: 28566604
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Making connections in the inner ear: recent insights into the development of spiral ganglion neurons and their connectivity with sensory hair cells.
    Coate TM; Kelley MW
    Semin Cell Dev Biol; 2013 May; 24(5):460-9. PubMed ID: 23660234
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Ahsa1 and Hsp90 activity confers more severe craniofacial phenotypes in a zebrafish model of hypoparathyroidism, sensorineural deafness and renal dysplasia (HDR).
    Sheehan-Rooney K; Swartz ME; Zhao F; Liu D; Eberhart JK
    Dis Model Mech; 2013 Sep; 6(5):1285-91. PubMed ID: 23720234
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel dominant-negative mutant of GATA3 in HDR syndrome.
    Ohta M; Eguchi-Ishimae M; Ohshima M; Iwabuki H; Takemoto K; Murao K; Chisaka T; Yamamoto E; Higaki T; Isoyama K; Eguchi M; Ishii E
    J Mol Med (Berl); 2011 Jan; 89(1):43-50. PubMed ID: 21120445
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Neonatal diagnosis of a patient with hypoparathyroidism, sensorineural deafness and renal dysplasia (HDR) syndrome associated with cerebral infarction.
    Mejia JD; Cervantes L; Puerta H; Bauer M; Diaz A
    J Pediatr Endocrinol Metab; 2014 Sep; 27(9-10):961-5. PubMed ID: 24859509
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Partially overlapping expression of Gata2 and Gata3 during inner ear development.
    Lilleväli K; Matilainen T; Karis A; Salminen M
    Dev Dyn; 2004 Dec; 231(4):775-81. PubMed ID: 15499560
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.