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 *

205 related articles for article (PubMed ID: 25012701)

  • 1. GJB2 c.-23+1G>A mutation is second most common mutation among Iranian individuals with autosomal recessive hearing loss.
    Zeinali S; Davoudi-Dehaghani E; Azadmehr S; DabbaghBagheri S; Bagherian H; Jamali M; Zafarghandimotlagh F; Masoodifard M; BandehiSarhaddi A; Rejali L; Sahebi S
    Eur Arch Otorhinolaryngol; 2015 Sep; 272(9):2255-9. PubMed ID: 25012701
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Finding mutation within non-coding region of GJB2 reveals its importance in genetic testing of hearing loss in Iranian population.
    Kashef A; Nikzat N; Bazzazadegan N; Fattahi Z; Sabbagh-Kermani F; Taghdiri M; Azadeh B; Mojahedi F; Khoshaeen A; Habibi H; Najmabadi H; Kahrizi K
    Int J Pediatr Otorhinolaryngol; 2015 Feb; 79(2):136-8. PubMed ID: 25555641
    [TBL] [Abstract][Full Text] [Related]  

  • 3. First report of prevalence c.IVS1+1G>A and del (GJB6-13S1854) mutations in Syrian families with non-syndromic sensorineural hearing loss.
    Al-Achkar W; Al-Halabi B; Ali B; Moassass F
    Int J Pediatr Otorhinolaryngol; 2017 Jan; 92():82-87. PubMed ID: 28012540
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prevalence of DFNB1 mutations in Argentinean children with non-syndromic deafness. Report of a novel mutation in GJB2.
    Gravina LP; Foncuberta ME; Prieto ME; Garrido J; Barreiro C; Chertkoff L
    Int J Pediatr Otorhinolaryngol; 2010 Mar; 74(3):250-4. PubMed ID: 20022641
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Spectrum and frequency of GJB2 mutations causing deafness in the northwest of Iran.
    Bonyadi MJ; Fotouhi N; Esmaeili M
    Int J Pediatr Otorhinolaryngol; 2014 Apr; 78(4):637-40. PubMed ID: 24529908
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Spectrum of GJB2 (Cx26) gene mutations in Iranian Azeri patients with nonsyndromic autosomal recessive hearing loss.
    Davarnia B; Babanejad M; Fattahi Z; Nikzat N; Bazazzadegan N; Pirzade A; Farajollahi R; Nishimura C; Jalalvand K; Arzhangi S; Kahrizi K; Smith RJ; Najmabadi H
    Int J Pediatr Otorhinolaryngol; 2012 Feb; 76(2):268-71. PubMed ID: 22172221
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prevalence of IVS1+1G>A mutation among Iranian Azeri Turkish patients with autosomal recessive non-syndromic hearing loss (ARNSHL).
    Bonyadi M; Fotouhi N; Esmaeili M
    Int J Pediatr Otorhinolaryngol; 2011 Dec; 75(12):1612-5. PubMed ID: 22000900
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Frequency of GJB2 mutations, GJB6-D13S1830 and GJB6-D13S1854 deletions among patients with non-syndromic hearing loss from the central region of Iran.
    Naddafnia H; Noormohammadi Z; Irani S; Salahshoorifar I
    Mol Genet Genomic Med; 2019 Jul; 7(7):e00780. PubMed ID: 31162818
    [TBL] [Abstract][Full Text] [Related]  

  • 9. GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2-35delG mutation.
    Abidi O; Boulouiz R; Nahili H; Ridal M; Alami MN; Tlili A; Rouba H; Masmoudi S; Chafik A; Hassar M; Barakat A
    Int J Pediatr Otorhinolaryngol; 2007 Aug; 71(8):1239-45. PubMed ID: 17553572
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prevalence of GJB2 Mutations in Affected Individuals from United Arab Emirates with Autosomal Recessive Nonsyndromic Hearing Loss.
    Tlili A; Al Mutery A; Kamal Eddine Ahmad Mohamed W; Mahfood M; Hadj Kacem H
    Genet Test Mol Biomarkers; 2017 Nov; 21(11):686-691. PubMed ID: 29016196
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Distribution and phenotype of GJB2 mutations in 102 Sicilian patients with congenital non syndromic sensorineural hearing loss.
    Salvago P; Martines E; La Mattina E; Mucia M; Sammarco P; Sireci F; Martines F
    Int J Audiol; 2014 Aug; 53(8):558-63. PubMed ID: 24793888
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prevalence of the GJB2 IVS1+1G >A mutation in Chinese hearing loss patients with monoallelic pathogenic mutation in the coding region of GJB2.
    Yuan Y; Yu F; Wang G; Huang S; Yu R; Zhang X; Huang D; Han D; Dai P
    J Transl Med; 2010 Dec; 8():127. PubMed ID: 21122151
    [TBL] [Abstract][Full Text] [Related]  

  • 13. GJB2 (Cx26) gene mutations in Chinese patients with congenital sensorineural deafness and a report of one novel mutation.
    Xiao ZA; Xie DH
    Chin Med J (Engl); 2004 Dec; 117(12):1797-801. PubMed ID: 15603707
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Autosomal recessive deafness 1A (DFNB1A) in Yakut population isolate in Eastern Siberia: extensive accumulation of the splice site mutation IVS1+1G>A in GJB2 gene as a result of founder effect.
    Barashkov NA; Dzhemileva LU; Fedorova SA; Teryutin FM; Posukh OL; Fedotova EE; Lobov SL; Khusnutdinova EK
    J Hum Genet; 2011 Sep; 56(9):631-9. PubMed ID: 21776002
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Unexpected heterogeneity due to recessive and de novo dominant mutations of GJB2 in an Iranian family with nonsyndromic hearing loss: implication for genetic counseling.
    Mahdieh N; Shirkavand A; Raeisi M; Akbari MT; Tekin M; Zeinali S
    Biochem Biophys Res Commun; 2010 Nov; 402(2):305-7. PubMed ID: 20937258
    [TBL] [Abstract][Full Text] [Related]  

  • 16. GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants.
    Koohiyan M; Hashemzadeh-Chaleshtori M; Salehi M; Abtahi H; Reiisi S; Pourreza MR; Noori-Daloii MR; Tabatabaiefar MA
    Int J Pediatr Otorhinolaryngol; 2018 Apr; 107():121-126. PubMed ID: 29501291
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel frameshift mutation (c.405delC) in the GJB2 gene associated with autosomal recessive hearing loss in two Tunisian families.
    Riahi Z; Chahed H; Jaafoura H; Zainine R; Messaoud O; Naili M; Nagara M; Hammami H; Laroussi N; Bouyacoub Y; Kefi R; Bonnet C; Besbes G; Abdelhak S
    Int J Pediatr Otorhinolaryngol; 2013 Sep; 77(9):1485-8. PubMed ID: 23856379
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prevalence of GJB2 (CX26) gene mutations in south Iranian patients with autosomal recessive nonsyndromic sensorineural hearing loss.
    Hashemi SB; Ashraf MJ; Saboori M; Azarpira N; Darai M
    Mol Biol Rep; 2012 Dec; 39(12):10481-7. PubMed ID: 23073770
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The Analysis of GJB2, GJB3, and GJB6 Gene Mutations in Patients with Hereditary Non-Syndromic Hearing Loss Living in Sivas.
    Küçük Kurtulgan H; Altuntaş EE; Yıldırım ME; Özdemir Ö; Bağcı B; Sezgin İ
    J Int Adv Otol; 2019 Dec; 15(3):373-378. PubMed ID: 31846914
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The spectrum of GJB2 mutations in the Iranian population with non-syndromic hearing loss--a twelve year study.
    Bazazzadegan N; Nikzat N; Fattahi Z; Nishimura C; Meyer N; Sahraian S; Jamali P; Babanejad M; Kashef A; Yazdan H; Sabbagh Kermani F; Taghdiri M; Azadeh B; Mojahedi F; Khoshaeen A; Habibi H; Reyhanifar F; Nouri N; Smith RJ; Kahrizi K; Najmabadi H
    Int J Pediatr Otorhinolaryngol; 2012 Aug; 76(8):1164-74. PubMed ID: 22695344
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.