E-LIB Suche - Ergebnisse für: Bonnet, Crystel

1

Biallelic variants in TMIE and PDE6B genes mimic Usher synd..:

Abdi, Samia ; Makrelouf, Mohamed ; Rous, Issa Nazim...
Gene Reports. 36 (2024) - p. 101954 , 2024

Link: https://doi.org/10.1016/..

2

Genetic variation of TLR3 gene is associated with the outco..:

Soumbara, Tetou ; Bonnet, Crystel ; Hamed, Cheikh Tijani...
BMC Infectious Diseases. 24 (2024) 1 - p. , 2024

Link: https://doi.org/10.1186/..

3

Current phenotypic and genetic spectrum of syndromic deafne..:

Mkaouar, Rahma ; Riahi, Zied ; Marrakchi, Jihene...
Frontiers in Genetics. 15 (2024) - p. , 2024

Link: https://doi.org/10.3389/..

4

Corrigendum: Current phenotypic and genetic spectrum of syn..:

Mkaouar, Rahma ; Riahi, Zied ; Marrakchi, Jihene...
Frontiers in Genetics. 15 (2024) - p. , 2024

Link: https://doi.org/10.3389/..

5

Single-cell transcriptomic profiling of the mouse cochlea: ..:

Jean, Philippe ; Wong Jun Tai, Fabienne ; Singh-Estivalet, Amrit...
Proceedings of the National Academy of Sciences. 120 (2023) 26 - p. , 2023

Link: https://doi.org/10.1073/..

6

Deafness: from genetic architecture to gene therapy:

Petit, Christine ; Bonnet, Crystel ; Safieddine, Saaïd
Nature Reviews Genetics. 24 (2023) 10 - p. 665-686 , 2023

Link: https://doi.org/10.1038/..

7

Novel pathogenic WHRN variant causing hearing loss in a mor..:

AitRaise, Imane ; Amalou, Ghita ; Redouane, Salaheddine...
Molecular Biology Reports. 50 (2023) 12 - p. 10663-10669 , 2023

Link: https://doi.org/10.1007/..

8

Identification a novel pathogenic LRTOMT mutation in Maurit..:

Salame, Malak ; Bonnet, Crystel ; Moctar, Ely Cheikh Mohamed...
European Archives of Oto-Rhino-Laryngology. 280 (2023) 9 - p. 4057-4063 , 2023

Link: https://doi.org/10.1007/..

9

Homozygous Missense Variants in FOXI1 and TMPRSS3 Genes Ass..:

AitRaise, Imane ; Amalou, Ghita ; Bakhchane, Amina...
Biochemical Genetics. 62 (2023) 3 - p. 1914-1924 , 2023

Link: https://doi.org/10.1007/..

10

Identification a novel pathogenic LRTOMT mutation in Maurit..:

Salame, Malak ; Bonnet, Crystel ; Moctar, Ely Cheikh Mohamed...
info:eu-repo/semantics/altIdentifier/doi/10.1007/s00405-023-07907-z. , 2023

Link: https://pasteur.hal.scie..

11

Deafness: from genetic architecture to gene therapy:

Petit, Christine ; Bonnet, Crystel ; Safieddine, Saaïd
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41576-023-00597-7. , 2023

Link: https://pasteur.hal.scie..

12

Identification a novel pathogenic LRTOMT mutation in Maurit..:

Salame, Malak ; Bonnet, Crystel ; Moctar, Ely Cheikh Mohamed...
info:eu-repo/semantics/altIdentifier/doi/10.1007/s00405-023-07907-z. , 2023

Link: https://pasteur.hal.scie..

13

Identification a novel pathogenic LRTOMT mutation in Maurit..:

Salame, Malak ; Bonnet, Crystel ; Moctar, Ely Cheikh Mohamed...
info:eu-repo/semantics/altIdentifier/doi/10.1007/s00405-023-07907-z. , 2023

Link: https://pasteur.hal.scie..

14

Single-cell transcriptomic profiling of the mouse cochlea: ..:

Jean, Philippe ; Wong Jun Tai, Fabienne ; Singh-Estivalet, Amrit...
info:eu-repo/semantics/altIdentifier/doi/10.1073/pnas.2221744120. , 2023

Link: https://pasteur.hal.scie..

15

Single-cell transcriptomic profiling of the mouse cochlea: ..:

Jean, Philippe ; Wong Jun Tai, Fabienne ; Singh-Estivalet, Amrit...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10293812/. , 2023

Link: http://www.ncbi.nlm.nih...