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Crystel Bonnet

Showing results (11-20 of 72) with videos related to

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Journal De La Societe De Biologie|September 1, 2007
[mRNA localization to the mitochondrial surface: a tool to treat retinal pathologies due to mitochondrial DNA mutations]Crystel Bonnet, Valérie Kaltimbacher, Sami Ellouze, et al.
International Journal of Pediatric Otorhinolaryngology|June 15, 2019
The spectrum of GJB2 gene mutations in Algerian families with nonsyndromic hearing loss from Sahara and Kabylie regionsSonia Talbi, Crystel Bonnet, Farid Boudjenah, et al.
BMC Bioinformatics|April 15, 2021
Phylogenetic analysis of Harmonin homology domainsBaptiste Colcombet-Cazenave, Karen Druart, Crystel Bonnet, et al.
Genes|December 11, 2019
Clinical and Haplotypic Variability of Slovenian <i>USH2A</i> Patients Homozygous for the c. 11864G>A Nonsense MutationAndrej Zupan, Ana Fakin, Saba Battelino, et al.
International Journal of Pediatric Otorhinolaryngology|November 17, 2019
ATP6V1B1 recurrent mutations in Algerian deaf patients associated with renal tubular acidosisMalika Dahmani, Sonia Talbi, Fatima Ammar-Khodja, et al.
Molecular Biology Reports|November 4, 2023
Novel pathogenic WHRN variant causing hearing loss in a moroccan familyImane AitRaise, Ghita Amalou, Salaheddine Redouane, et al.
Molecular Biology Reports|July 25, 2024
Exome sequencing reveals pathogenic mutations in the LARS2 and HSD17B4 genes associated with Perrault syndrome and D-bifunctional protein deficiency in Moroccan familiesAssia Idyahia, Salaheddine Redouan, Ghita Amalou, et al.
Human Heredity|December 5, 2019
Further Evidence for the Implication of the MET Gene in Non-Syndromic Autosomal Recessive DeafnessAmale Bousfiha, Zied Riahi, Lamiae Elkhattabi, et al.
Human Genome Variation|April 28, 2017
A novel <i>PEX1</i> mutation in a Moroccan family with Zellweger spectrum disordersAmale Bousfiha, Amina Bakhchane, Hicham Charoute, et al.
Biochimica Et Biophysica Acta|June 3, 2008
The optimized allotopic expression of ND1 or ND4 genes restores respiratory chain complex I activity in fibroblasts harboring mutations in these genesCrystel Bonnet, Sébastien Augustin, Sami Ellouze, et al.
Pageof 8

Showing results (11-20 of 72) with videos related to

Sort By:
Pageof 8
Journal De La Societe De Biologie|September 1, 2007
[mRNA localization to the mitochondrial surface: a tool to treat retinal pathologies due to mitochondrial DNA mutations]Crystel Bonnet, Valérie Kaltimbacher, Sami Ellouze, et al.
International Journal of Pediatric Otorhinolaryngology|June 15, 2019
The spectrum of GJB2 gene mutations in Algerian families with nonsyndromic hearing loss from Sahara and Kabylie regionsSonia Talbi, Crystel Bonnet, Farid Boudjenah, et al.
BMC Bioinformatics|April 15, 2021
Phylogenetic analysis of Harmonin homology domainsBaptiste Colcombet-Cazenave, Karen Druart, Crystel Bonnet, et al.
Genes|December 11, 2019
Clinical and Haplotypic Variability of Slovenian <i>USH2A</i> Patients Homozygous for the c. 11864G>A Nonsense MutationAndrej Zupan, Ana Fakin, Saba Battelino, et al.
International Journal of Pediatric Otorhinolaryngology|November 17, 2019
ATP6V1B1 recurrent mutations in Algerian deaf patients associated with renal tubular acidosisMalika Dahmani, Sonia Talbi, Fatima Ammar-Khodja, et al.
Molecular Biology Reports|November 4, 2023
Novel pathogenic WHRN variant causing hearing loss in a moroccan familyImane AitRaise, Ghita Amalou, Salaheddine Redouane, et al.
Molecular Biology Reports|July 25, 2024
Exome sequencing reveals pathogenic mutations in the LARS2 and HSD17B4 genes associated with Perrault syndrome and D-bifunctional protein deficiency in Moroccan familiesAssia Idyahia, Salaheddine Redouan, Ghita Amalou, et al.
Human Heredity|December 5, 2019
Further Evidence for the Implication of the MET Gene in Non-Syndromic Autosomal Recessive DeafnessAmale Bousfiha, Zied Riahi, Lamiae Elkhattabi, et al.
Human Genome Variation|April 28, 2017
A novel <i>PEX1</i> mutation in a Moroccan family with Zellweger spectrum disordersAmale Bousfiha, Amina Bakhchane, Hicham Charoute, et al.
Biochimica Et Biophysica Acta|June 3, 2008
The optimized allotopic expression of ND1 or ND4 genes restores respiratory chain complex I activity in fibroblasts harboring mutations in these genesCrystel Bonnet, Sébastien Augustin, Sami Ellouze, et al.
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