E-LIB Suche - Ergebnisse für: Bonnet, Crystel

1

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/..

2

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/..

3

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/..

4

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/..

5

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/..

6

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/..

7

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/..

8

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/..

9

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/..

10

Screening of BRCA1/2 variants in Mauritanian breast cancer ..:

Brahim, Selma Mohamed ; Zein, Ekht Elbenina ; Bonnet, Crystel...
BMC Cancer. 22 (2022) 1 - p. , 2022

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

11

Retinal Phenotype of Patients withCLRN1-Associated Usher 3A..:

Smirnov, Vasily M. ; Nassisi, Marco ; Mohand-Saïd, Saddek...
Investigative Opthalmology & Visual Science. 63 (2022) 4 - p. 25 , 2022

Link: https://doi.org/10.1167/..

12

Genetic heterogeneity in GJB2, COL4A3, ATP6V1B1 and EDNRB v..:

AitRaise, Imane ; Amalou, Ghita ; Bousfiha, Amale...
Molecular Biology Reports. 49 (2022) 5 - p. 3949-3954 , 2022

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

13

Phylogenetic analysis of Harmonin homology domains:

Colcombet-Cazenave, Baptiste ; Druart, Karen ; Bonnet, Crystel...
BMC Bioinformatics. 22 (2021) 1 - p. , 2021

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

14

Mutated CCDC51 Coding for a Mitochondrial Protein, MITOK Is..:

Zeitz, Christina ; Méjécase, Cécile ; Michiels, Christelle...
International Journal of Molecular Sciences. 22 (2021) 15 - p. 7875 , 2021

Link: https://doi.org/10.3390/..

15

Characteristics of Retinitis Pigmentosa Associated with ADG..:

Fakin, Ana ; Bonnet, Crystel ; Kurtenbach, Anne...
International Journal of Molecular Sciences. 22 (2021) 19 - p. 10352 , 2021

Link: https://doi.org/10.3390/..