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Did you mean crystal bonnet (92 results)?
Deafness: from genetic architecture to gene therapy.
Petit C, Bonnet C, Safieddine S. Petit C, et al. Among authors: bonnet c. Nat Rev Genet. 2023 Oct;24(10):665-686. doi: 10.1038/s41576-023-00597-7. Epub 2023 May 12. Nat Rev Genet. 2023. PMID: 37173518 Free article. Review.
Single-cell transcriptomic profiling of the mouse cochlea: An atlas for targeted therapies.
Jean P, Wong Jun Tai F, Singh-Estivalet A, Lelli A, Scandola C, Megharba S, Schmutz S, Roux S, Mechaussier S, Sudres M, Mouly E, Heritier AV, Bonnet C, Mallet A, Novault S, Libri V, Petit C, Michalski N. Jean P, et al. Among authors: bonnet c. Proc Natl Acad Sci U S A. 2023 Jun 27;120(26):e2221744120. doi: 10.1073/pnas.2221744120. Epub 2023 Jun 20. Proc Natl Acad Sci U S A. 2023. PMID: 37339214 Free PMC article.
An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients.
Bonnet C, Riahi Z, Chantot-Bastaraud S, Smagghe L, Letexier M, Marcaillou C, Lefèvre GM, Hardelin JP, El-Amraoui A, Singh-Estivalet A, Mohand-Saïd S, Kohl S, Kurtenbach A, Sliesoraityte I, Zobor D, Gherbi S, Testa F, Simonelli F, Banfi S, Fakin A, Glavač D, Jarc-Vidmar M, Zupan A, Battelino S, Martorell Sampol L, Claveria MA, Catala Mora J, Dad S, Møller LB, Rodriguez Jorge J, Hawlina M, Auricchio A, Sahel JA, Marlin S, Zrenner E, Audo I, Petit C. Bonnet C, et al. Eur J Hum Genet. 2016 Dec;24(12):1730-1738. doi: 10.1038/ejhg.2016.99. Epub 2016 Jul 27. Eur J Hum Genet. 2016. PMID: 27460420 Free PMC article.
Usher Syndrome and Color Vision.
Kurtenbach A, Hahn G, Kernstock C, Hipp S, Zobor D, Stingl K, Kohl S, Bonnet C, Mohand-Saïd S, Sliesoraityte I, Sahel JA, Audo I, Fakin A, Hawlina M, Testa F, Simonelli F, Petit C, Zrenner E. Kurtenbach A, et al. Among authors: bonnet c. Curr Eye Res. 2018 Oct;43(10):1295-1301. doi: 10.1080/02713683.2018.1501804. Epub 2018 Jul 30. Curr Eye Res. 2018. PMID: 30012035
Phylogenetic analysis of Harmonin homology domains.
Colcombet-Cazenave B, Druart K, Bonnet C, Petit C, Spérandio O, Guglielmini J, Wolff N. Colcombet-Cazenave B, et al. Among authors: bonnet c. BMC Bioinformatics. 2021 Apr 14;22(1):190. doi: 10.1186/s12859-021-04116-5. BMC Bioinformatics. 2021. PMID: 33853521 Free PMC article.
Specific aspects of consanguinity: some examples from the Tunisian population.
Romdhane L, Ben Halim N, Rejeb I, Kefi R, Bouyacoub Y, Ben Rekaya M, Messai H, Messaoud O, Riahi Z, Bonnet C, Ben Rhouma F, Nagara M, Petit C, McElreavey K, Romeo G, Abdelhak S. Romdhane L, et al. Among authors: bonnet c. Hum Hered. 2014;77(1-4):167-74. doi: 10.1159/000362167. Epub 2014 Jul 29. Hum Hered. 2014. PMID: 25060280 Free article. Review.
Screening of BRCA1/2 variants in Mauritanian breast cancer patients.
Brahim SM, Zein EE, Bonnet C, Hamed CT, Salame M, Zein MV, Khyatti M, Tolba A, Houmeida A. Brahim SM, et al. Among authors: bonnet c. BMC Cancer. 2022 Jul 20;22(1):802. doi: 10.1186/s12885-022-09903-8. BMC Cancer. 2022. PMID: 35858847 Free PMC article.
Double Hyperautofluorescent Rings in Patients with USH2A-Retinopathy.
Fakin A, Šuštar M, Brecelj J, Bonnet C, Petit C, Zupan A, Glavač D, Jarc-Vidmar M, Battelino S, Hawlina M. Fakin A, et al. Among authors: bonnet c. Genes (Basel). 2019 Nov 21;10(12):956. doi: 10.3390/genes10120956. Genes (Basel). 2019. PMID: 31766479 Free PMC article.
Novel pathogenic WHRN variant causing hearing loss in a moroccan family.
AitRaise I, Amalou G, Redouane S, Charoute H, Snoussi K, Abdelghaffar H, Bonnet C, Petit C, Barakat A. AitRaise I, et al. Among authors: bonnet c. Mol Biol Rep. 2023 Dec;50(12):10663-10669. doi: 10.1007/s11033-023-08901-8. Epub 2023 Nov 4. Mol Biol Rep. 2023. PMID: 37924449
64 results