BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

147 related articles for article (PubMed ID: 33614666)

  • 21. Retrospective Review of Otic Capsule Contour and Thickness in Patients with Otosclerosis and Individuals with Normal Hearing on CT.
    Sanghan N; Chansakul T; Kozin ED; Juliano AF; Curtin HD; Reinshagen KL
    AJNR Am J Neuroradiol; 2018 Dec; 39(12):2350-2355. PubMed ID: 30467217
    [TBL] [Abstract][Full Text] [Related]  

  • 22. CT assessment of bone remodeling in the otic capsule in chronic renal failure: association with hearing loss.
    Erkoç MF; Bulut S; İmamoğlu H; Gümüş C; Kayataş M
    AJR Am J Roentgenol; 2013 Feb; 200(2):396-9. PubMed ID: 23345363
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Current research in otosclerosis.
    Stankovic KM; McKenna MJ
    Curr Opin Otolaryngol Head Neck Surg; 2006 Oct; 14(5):347-51. PubMed ID: 16974150
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Auditory and vestibular defects in the circling (ci2) rat mutant.
    Kaiser A; Fedrowitz M; Ebert U; Zimmermann E; Hedrich HJ; Wedekind D; Löscher W
    Eur J Neurosci; 2001 Oct; 14(7):1129-42. PubMed ID: 11683905
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Single unit recordings in the auditory nerve of congenitally deaf white cats: morphological correlates in the cochlea and cochlear nucleus.
    Ryugo DK; Rosenbaum BT; Kim PJ; Niparko JK; Saada AA
    J Comp Neurol; 1998 Aug; 397(4):532-48. PubMed ID: 9699914
    [TBL] [Abstract][Full Text] [Related]  

  • 26. MPZL2, Encoding the Epithelial Junctional Protein Myelin Protein Zero-like 2, Is Essential for Hearing in Man and Mouse.
    Wesdorp M; Murillo-Cuesta S; Peters T; Celaya AM; Oonk A; Schraders M; Oostrik J; Gomez-Rosas E; Beynon AJ; Hartel BP; Okkersen K; Koenen HJPM; Weeda J; Lelieveld S; Voermans NC; Joosten I; Hoyng CB; Lichtner P; Kunst HPM; Feenstra I; de Bruijn SE; ; Admiraal RJC; Yntema HG; van Wijk E; Del Castillo I; Serra P; Varela-Nieto I; Pennings RJE; Kremer H
    Am J Hum Genet; 2018 Jul; 103(1):74-88. PubMed ID: 29961571
    [TBL] [Abstract][Full Text] [Related]  

  • 27. MAP3K1 function is essential for cytoarchitecture of the mouse organ of Corti and survival of auditory hair cells.
    Yousaf R; Meng Q; Hufnagel RB; Xia Y; Puligilla C; Ahmed ZM; Riazuddin S
    Dis Model Mech; 2015 Dec; 8(12):1543-53. PubMed ID: 26496772
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [A case of Paget's disease with progressive sensorineural hearing loss involved in the bilateral bony labyrinths].
    Kokai H; Oohasi M; Kikuchi H; Iida K; Ishikawa K; Kobashi M; Takizawa M; Ootani H; Terayama Y
    Nihon Jibiinkoka Gakkai Kaiho; 1996 Jun; 99(6):910-7. PubMed ID: 8753076
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [A follow-up study of abnormal mutation in neonatal deafness gene screening].
    Liu QM; Tian Y; Yu JJ; He QQ; Peng L; Guo XQ; Li DY; Chen T
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2019 Dec; 54(12):881-887. PubMed ID: 31887812
    [No Abstract]   [Full Text] [Related]  

  • 30. Absence of hearing loss in a mouse model for DFNA17 and MYH9-related disease: the use of public gene-targeted ES cell resources.
    Parker LL; Gao J; Zuo J
    Brain Res; 2006 May; 1091(1):235-42. PubMed ID: 16630581
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Syndromic Deafness Gene
    Qiu S; Zhao W; Gao X; Li D; Wang W; Gao B; Han W; Yang S; Dai P; Cao P; Yuan Y
    Front Cell Dev Biol; 2021; 9():742714. PubMed ID: 34746137
    [No Abstract]   [Full Text] [Related]  

  • 32. Auditory development in progressive motor neuronopathy mouse mutants.
    Volkenstein S; Brors D; Hansen S; Berend A; Mlynski R; Aletsee C; Dazert S
    Neurosci Lett; 2009 Nov; 465(1):45-9. PubMed ID: 19735697
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Anatomical, metabolic and genetic aspects of age-related hearing loss in mice.
    McFadden SL; Ding D; Salvi R
    Audiology; 2001; 40(6):313-21. PubMed ID: 11781044
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Transgenic expression of a dominant-negative connexin26 causes degeneration of the organ of Corti and non-syndromic deafness.
    Kudo T; Kure S; Ikeda K; Xia AP; Katori Y; Suzuki M; Kojima K; Ichinohe A; Suzuki Y; Aoki Y; Kobayashi T; Matsubara Y
    Hum Mol Genet; 2003 May; 12(9):995-1004. PubMed ID: 12700168
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Genetics of otosclerosis.
    Thys M; Van Camp G
    Otol Neurotol; 2009 Dec; 30(8):1021-32. PubMed ID: 19546831
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Otosclerosis and sensorineural hearing loss: a histopathologic study.
    Hinojosa R; Marion M
    Am J Otolaryngol; 1987; 8(5):296-307. PubMed ID: 3324782
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Studies on congenital osteopetrosis in microphthalmic mice using organ cultures: impairment of bone resorption in response to physiologic stimulators.
    Raisz LG; Simmons HA; Gworek SC; Eilon G
    J Exp Med; 1977 Apr; 145(4):857-65. PubMed ID: 870607
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Pathology of otosclerosis: a review.
    Davis GL
    Am J Otolaryngol; 1987; 8(5):273-81. PubMed ID: 3324781
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Pathophysiology of otosclerosis.
    Chole RA; McKenna M
    Otol Neurotol; 2001 Mar; 22(2):249-57. PubMed ID: 11300278
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Association of Hearing Loss and Otologic Outcomes With Fibrous Dysplasia.
    Boyce AM; Brewer C; DeKlotz TR; Zalewski CK; King KA; Collins MT; Kim HJ
    JAMA Otolaryngol Head Neck Surg; 2018 Feb; 144(2):102-107. PubMed ID: 29192304
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.