512 related articles for article (PubMed ID: 19363479)
1. Mutations in the seed region of human miR-96 are responsible for nonsyndromic progressive hearing loss.
Mencía A; Modamio-Høybjør S; Redshaw N; Morín M; Mayo-Merino F; Olavarrieta L; Aguirre LA; del Castillo I; Steel KP; Dalmay T; Moreno F; Moreno-Pelayo MA
Nat Genet; 2009 May; 41(5):609-13. PubMed ID: 19363479
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Gain-of-function mutation of microRNA-140 in human skeletal dysplasia.
Grigelioniene G; Suzuki HI; Taylan F; Mirzamohammadi F; Borochowitz ZU; Ayturk UM; Tzur S; Horemuzova E; Lindstrand A; Weis MA; Grigelionis G; Hammarsjö A; Marsk E; Nordgren A; Nordenskjöld M; Eyre DR; Warman ML; Nishimura G; Sharp PA; Kobayashi T
Nat Med; 2019 Apr; 25(4):583-590. PubMed ID: 30804514
[TBL] [Abstract][Full Text] [Related]
4. MicroRNAs and epigenetic regulation in the mammalian inner ear: implications for deafness.
Friedman LM; Avraham KB
Mamm Genome; 2009; 20(9-10):581-603. PubMed ID: 19876605
[TBL] [Abstract][Full Text] [Related]
5. A splice-site mutation and overexpression of MYO6 cause a similar phenotype in two families with autosomal dominant hearing loss.
Hilgert N; Topsakal V; van Dinther J; Offeciers E; Van de Heyning P; Van Camp G
Eur J Hum Genet; 2008 May; 16(5):593-602. PubMed ID: 18212818
[TBL] [Abstract][Full Text] [Related]
6. Individual microRNAs (miRNAs) display distinct mRNA targeting "rules".
Wang WX; Wilfred BR; Xie K; Jennings MH; Hu YH; Stromberg AJ; Nelson PT
RNA Biol; 2010; 7(3):373-80. PubMed ID: 20421741
[TBL] [Abstract][Full Text] [Related]
7. MicroRNAs: effective elements in ear-related diseases and hearing loss.
Mahmoudian-Sani MR; Mehri-Ghahfarrokhi A; Ahmadinejad F; Hashemzadeh-Chaleshtori M; Saidijam M; Jami MS
Eur Arch Otorhinolaryngol; 2017 Jun; 274(6):2373-2380. PubMed ID: 28224282
[TBL] [Abstract][Full Text] [Related]
8. miRNA mutations are not a common cause of deafness.
Hildebrand MS; Witmer PD; Xu S; Newton SS; Kahrizi K; Najmabadi H; Valle D; Smith RJ
Am J Med Genet A; 2010 Mar; 152A(3):646-52. PubMed ID: 20186779
[TBL] [Abstract][Full Text] [Related]
9. Role of microRNAs in inner ear development and hearing loss.
Mittal R; Liu G; Polineni SP; Bencie N; Yan D; Liu XZ
Gene; 2019 Feb; 686():49-55. PubMed ID: 30389561
[TBL] [Abstract][Full Text] [Related]
10. A novel mutation within the MIR96 gene causes non-syndromic inherited hearing loss in an Italian family by altering pre-miRNA processing.
Soldà G; Robusto M; Primignani P; Castorina P; Benzoni E; Cesarani A; Ambrosetti U; Asselta R; Duga S
Hum Mol Genet; 2012 Feb; 21(3):577-85. PubMed ID: 22038834
[TBL] [Abstract][Full Text] [Related]
11. MicroRNA-183 family members regulate sensorineural fates in the inner ear.
Li H; Kloosterman W; Fekete DM
J Neurosci; 2010 Mar; 30(9):3254-63. PubMed ID: 20203184
[TBL] [Abstract][Full Text] [Related]
12. A rare novel mutation in TECTA causes autosomal dominant nonsyndromic hearing loss in a Mongolian family.
Bai H; Yang X; Temuribagen ; Guilan ; Suyalatu ; Narisu ; Wu H; Chen Y; Liu Y; Wu Q
BMC Med Genet; 2014 Mar; 15():34. PubMed ID: 25008054
[TBL] [Abstract][Full Text] [Related]
13. Role of pri-miRNA tertiary structure in miR-17~92 miRNA biogenesis.
Chaulk SG; Thede GL; Kent OA; Xu Z; Gesner EM; Veldhoen RA; Khanna SK; Goping IS; MacMillan AM; Mendell JT; Young HS; Fahlman RP; Glover JN
RNA Biol; 2011; 8(6):1105-14. PubMed ID: 21955497
[TBL] [Abstract][Full Text] [Related]
14. MicroRNAs in inner ear biology and pathogenesis.
Patel M; Hu BH
Hear Res; 2012 May; 287(1-2):6-14. PubMed ID: 22484222
[TBL] [Abstract][Full Text] [Related]
15. Target identification of microRNAs expressed highly in human embryonic stem cells.
Li SS; Yu SL; Kao LP; Tsai ZY; Singh S; Chen BZ; Ho BC; Liu YH; Yang PC
J Cell Biochem; 2009 Apr; 106(6):1020-30. PubMed ID: 19229866
[TBL] [Abstract][Full Text] [Related]
16. Loop nucleotides control primary and mature miRNA function in target recognition and repression.
Yue SB; Trujillo RD; Tang Y; O'Gorman WE; Chen CZ
RNA Biol; 2011; 8(6):1115-23. PubMed ID: 22142974
[TBL] [Abstract][Full Text] [Related]
17. Nonsense mutations in SMPX, encoding a protein responsive to physical force, result in X-chromosomal hearing loss.
Huebner AK; Gandia M; Frommolt P; Maak A; Wicklein EM; Thiele H; Altmüller J; Wagner F; Viñuela A; Aguirre LA; Moreno F; Maier H; Rau I; Giesselmann S; Nürnberg G; Gal A; Nürnberg P; Hübner CA; del Castillo I; Kurth I
Am J Hum Genet; 2011 May; 88(5):621-7. PubMed ID: 21549336
[TBL] [Abstract][Full Text] [Related]
18. Identification and characteristics of microRNAs from Bombyx mori.
He PA; Nie Z; Chen J; Chen J; Lv Z; Sheng Q; Zhou S; Gao X; Kong L; Wu X; Jin Y; Zhang Y
BMC Genomics; 2008 May; 9():248. PubMed ID: 18507836
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. MicroRNA-142 is mutated in about 20% of diffuse large B-cell lymphoma.
Kwanhian W; Lenze D; Alles J; Motsch N; Barth S; Döll C; Imig J; Hummel M; Tinguely M; Trivedi P; Lulitanond V; Meister G; Renner C; Grässer FA
Cancer Med; 2012 Oct; 1(2):141-55. PubMed ID: 23342264
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
