177 related articles for article (PubMed ID: 24446963)
1. A reduction in Ptprq associated with specific features of the deafness phenotype of the miR-96 mutant mouse diminuendo.
Chen J; Johnson SL; Lewis MA; Hilton JM; Huma A; Marcotti W; Steel KP
Eur J Neurosci; 2014 Mar; 39(5):744-56. PubMed ID: 24446963
[TBL] [Abstract][Full Text] [Related]
2. A receptor-like inositol lipid phosphatase is required for the maturation of developing cochlear hair bundles.
Goodyear RJ; Legan PK; Wright MB; Marcotti W; Oganesian A; Coats SA; Booth CJ; Kros CJ; Seifert RA; Bowen-Pope DF; Richardson GP
J Neurosci; 2003 Oct; 23(27):9208-19. PubMed ID: 14534255
[TBL] [Abstract][Full Text] [Related]
3. Hair bundle defects and loss of function in the vestibular end organs of mice lacking the receptor-like inositol lipid phosphatase PTPRQ.
Goodyear RJ; Jones SM; Sharifi L; Forge A; Richardson GP
J Neurosci; 2012 Feb; 32(8):2762-72. PubMed ID: 22357859
[TBL] [Abstract][Full Text] [Related]
4. Exploring regulatory networks of miR-96 in the developing inner ear.
Lewis MA; Buniello A; Hilton JM; Zhu F; Zhang WI; Evans S; van Dongen S; Enright AJ; Steel KP
Sci Rep; 2016 Mar; 6():23363. PubMed ID: 26988146
[TBL] [Abstract][Full Text] [Related]
5. A C-terminal nonsense mutation links PTPRQ with autosomal-dominant hearing loss, DFNA73.
Eisenberger T; Di Donato N; Decker C; Delle Vedove A; Neuhaus C; Nürnberg G; Toliat M; Nürnberg P; Mürbe D; Bolz HJ
Genet Med; 2018 Jun; 20(6):614-621. PubMed ID: 29309402
[TBL] [Abstract][Full Text] [Related]
6. An ENU-induced mutation of miR-96 associated with progressive hearing loss in mice.
Lewis MA; Quint E; Glazier AM; Fuchs H; De Angelis MH; Langford C; van Dongen S; Abreu-Goodger C; Piipari M; Redshaw N; Dalmay T; Moreno-Pelayo MA; Enright AJ; Steel KP
Nat Genet; 2009 May; 41(5):614-8. PubMed ID: 19363478
[TBL] [Abstract][Full Text] [Related]
7. Identification of a novel compound heterozygous mutation in PTPRQ in a DFNB84 family with prelingual sensorineural hearing impairment.
Sang Q; Mei H; Kuermanhan A; Feng R; Guo L; Qu R; Xu Y; Li H; Jin L; He L; Wang L
Mol Genet Genomics; 2015 Jun; 290(3):1135-9. PubMed ID: 25557914
[TBL] [Abstract][Full Text] [Related]
8. First confirmatory study on PTPRQ as an autosomal dominant non-syndromic hearing loss gene.
Oziębło D; Sarosiak A; Leja ML; Budde BS; Tacikowska G; Di Donato N; Bolz HJ; Nürnberg P; Skarżyński H; Ołdak M
J Transl Med; 2019 Oct; 17(1):351. PubMed ID: 31655630
[TBL] [Abstract][Full Text] [Related]
9. Delayed progressive sensorineural hearing loss due to a novel compound heterozygous PTPRQ mutation in a Chinese patient.
Qin Y; Ma Y; Zeng Z; Zhong Z; Qi Y; Liu Y
J Clin Lab Anal; 2023 Apr; 37(7):e24886. PubMed ID: 37106574
[TBL] [Abstract][Full Text] [Related]
10. Evidence for multiple, developmentally regulated isoforms of Ptprq on hair cells of the inner ear.
Nayak G; Goodyear RJ; Legan PK; Noda M; Richardson GP
Dev Neurobiol; 2011 Feb; 71(2):129-41. PubMed ID: 20715155
[TBL] [Abstract][Full Text] [Related]
11. miR-96 regulates the progression of differentiation in mammalian cochlear inner and outer hair cells.
Kuhn S; Johnson SL; Furness DN; Chen J; Ingham N; Hilton JM; Steffes G; Lewis MA; Zampini V; Hackney CM; Masetto S; Holley MC; Steel KP; Marcotti W
Proc Natl Acad Sci U S A; 2011 Feb; 108(6):2355-60. PubMed ID: 21245307
[TBL] [Abstract][Full Text] [Related]
12. A cell type-specific approach to elucidate the role of miR-96 in inner ear hair cells.
Gwilliam K; Sperber M; Perry K; Rose KP; Ginsberg L; Paladugu N; Song Y; Milon B; Elkon R; Hertzano R
Front Audiol Otol; 2024; 2():. PubMed ID: 38826689
[TBL] [Abstract][Full Text] [Related]
13. High PTPRQ Expression and Its Relationship to Expression of PTPRZ1 and the Presence of KRAS Mutations in Colorectal Cancer Tissues.
Laczmanska I; Karpinski P; Gil J; Laczmanski L; Bebenek M; Sasiadek MM
Anticancer Res; 2016 Feb; 36(2):677-81. PubMed ID: 26851024
[TBL] [Abstract][Full Text] [Related]
14. Autosomal Recessive Congenital Sensorineural Hearing Loss due to a Novel Compound Heterozygous PTPRQ Mutation in a Chinese Family.
Wu X; Wang S; Chen S; Wen YY; Liu B; Xie W; Li D; Liu L; Huang X; Sun Y; Kong WJ
Neural Plast; 2018; 2018():9425725. PubMed ID: 29849575
[TBL] [Abstract][Full Text] [Related]
15. Mutations in PTPRQ are a cause of autosomal-recessive nonsyndromic hearing impairment DFNB84 and associated with vestibular dysfunction.
Schraders M; Oostrik J; Huygen PL; Strom TM; van Wijk E; Kunst HP; Hoefsloot LH; Cremers CW; Admiraal RJ; Kremer H
Am J Hum Genet; 2010 Apr; 86(4):604-10. PubMed ID: 20346435
[TBL] [Abstract][Full Text] [Related]
16. Dynamic compartmentalization of protein tyrosine phosphatase receptor Q at the proximal end of stereocilia: implication of myosin VI-based transport.
Sakaguchi H; Tokita J; Naoz M; Bowen-Pope D; Gov NS; Kachar B
Cell Motil Cytoskeleton; 2008 Jul; 65(7):528-38. PubMed ID: 18412156
[TBL] [Abstract][Full Text] [Related]
17. Null mutation of alpha1D Ca2+ channel gene results in deafness but no vestibular defect in mice.
Dou H; Vazquez AE; Namkung Y; Chu H; Cardell EL; Nie L; Parson S; Shin HS; Yamoah EN
J Assoc Res Otolaryngol; 2004 Jun; 5(2):215-26. PubMed ID: 15357422
[TBL] [Abstract][Full Text] [Related]
18. Protein Tyrosine Phosphatase Receptor-type Q: Structure, Activity, and Implications in Human Disease.
Zhang W; Tang Z; Fan S; Yao D; Zhang Z; Guan C; Deng W; Ying Y
Protein Pept Lett; 2022; 29(7):567-573. PubMed ID: 35546749
[TBL] [Abstract][Full Text] [Related]
19. Deafness and vestibular dysfunction in a Doberman Pinscher puppy associated with a mutation in the PTPRQ gene.
Guevar J; Olby NJ; Meurs KM; Yost O; Friedenberg SG
J Vet Intern Med; 2018 Mar; 32(2):665-669. PubMed ID: 29460419
[TBL] [Abstract][Full Text] [Related]
20. Stereocilia defects in waltzer (Cdh23), shaker1 (Myo7a) and double waltzer/shaker1 mutant mice.
Holme RH; Steel KP
Hear Res; 2002 Jul; 169(1-2):13-23. PubMed ID: 12121736
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
