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Crystel Bonnet

Showing results (21-30 of 72) with videos related to

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International Journal of Pediatric Otorhinolaryngology|September 4, 2018
Two novel homozygous missense mutations identified in the BSND gene in Moroccan patients with Bartter's syndromeSoukaina Elrharchi, Zied Riahi, Sara Salime, et al.
Molecular Biology Reports|March 18, 2022
Genetic heterogeneity in GJB2, COL4A3, ATP6V1B1 and EDNRB variants detected among hearing impaired families in MoroccoImane AitRaise, Ghita Amalou, Amale Bousfiha, et al.
Biochemical Genetics|October 1, 2023
Homozygous Missense Variants in FOXI1 and TMPRSS3 Genes Associated with Non-syndromic Deafness in Moroccan FamiliesImane AitRaise, Ghita Amalou, Amina Bakhchane, et al.
Molecular Vision|July 22, 2016
Genetic analysis of Tunisian families with Usher syndrome type 1: toward improving early molecular diagnosisImen Ben-Rebeh, Mhamed Grati, Crystel Bonnet, et al.
Orphanet Journal of Rare Diseases|August 19, 2015
EPS8L2 is a new causal gene for childhood onset autosomal recessive progressive hearing lossMalika Dahmani, Fatima Ammar-Khodja, Crystel Bonnet, et al.
Rejuvenation Research|May 24, 2007
Allotopic mRNA localization to the mitochondrial surface rescues respiratory chain defects in fibroblasts harboring mitochondrial DNA mutations affecting complex I or v subunitsCrystel Bonnet, Valérie Kaltimbacher, Sami Ellouze, et al.
American Journal of Human Genetics|September 6, 2008
Optimized allotopic expression of the human mitochondrial ND4 prevents blindness in a rat model of mitochondrial dysfunctionSami Ellouze, Sébastien Augustin, Aicha Bouaita, et al.
Human Heredity|January 24, 2021
Novel Mutation in AIFM1 Gene Associated with X-Linked Deafness in a Moroccan FamilySoukaina Elrharchi, Zied Riahi, Sara Salime, et al.
Genes|November 27, 2019
Double Hyperautofluorescent Rings in Patients with USH2A-RetinopathyAna Fakin, Maja Šuštar, Jelka Brecelj, et al.
International Journal of Pediatric Otorhinolaryngology|November 25, 2020
A homozygous MPZL2 deletion is associated with non syndromic hearing loss in a moroccan familyGhita Amalou, Crystel Bonnet, Zied Riahi, et al.
Pageof 8

Showing results (21-30 of 72) with videos related to

Sort By:
Pageof 8
International Journal of Pediatric Otorhinolaryngology|September 4, 2018
Two novel homozygous missense mutations identified in the BSND gene in Moroccan patients with Bartter's syndromeSoukaina Elrharchi, Zied Riahi, Sara Salime, et al.
Molecular Biology Reports|March 18, 2022
Genetic heterogeneity in GJB2, COL4A3, ATP6V1B1 and EDNRB variants detected among hearing impaired families in MoroccoImane AitRaise, Ghita Amalou, Amale Bousfiha, et al.
Biochemical Genetics|October 1, 2023
Homozygous Missense Variants in FOXI1 and TMPRSS3 Genes Associated with Non-syndromic Deafness in Moroccan FamiliesImane AitRaise, Ghita Amalou, Amina Bakhchane, et al.
Molecular Vision|July 22, 2016
Genetic analysis of Tunisian families with Usher syndrome type 1: toward improving early molecular diagnosisImen Ben-Rebeh, Mhamed Grati, Crystel Bonnet, et al.
Orphanet Journal of Rare Diseases|August 19, 2015
EPS8L2 is a new causal gene for childhood onset autosomal recessive progressive hearing lossMalika Dahmani, Fatima Ammar-Khodja, Crystel Bonnet, et al.
Rejuvenation Research|May 24, 2007
Allotopic mRNA localization to the mitochondrial surface rescues respiratory chain defects in fibroblasts harboring mitochondrial DNA mutations affecting complex I or v subunitsCrystel Bonnet, Valérie Kaltimbacher, Sami Ellouze, et al.
American Journal of Human Genetics|September 6, 2008
Optimized allotopic expression of the human mitochondrial ND4 prevents blindness in a rat model of mitochondrial dysfunctionSami Ellouze, Sébastien Augustin, Aicha Bouaita, et al.
Human Heredity|January 24, 2021
Novel Mutation in AIFM1 Gene Associated with X-Linked Deafness in a Moroccan FamilySoukaina Elrharchi, Zied Riahi, Sara Salime, et al.
Genes|November 27, 2019
Double Hyperautofluorescent Rings in Patients with USH2A-RetinopathyAna Fakin, Maja Šuštar, Jelka Brecelj, et al.
International Journal of Pediatric Otorhinolaryngology|November 25, 2020
A homozygous MPZL2 deletion is associated with non syndromic hearing loss in a moroccan familyGhita Amalou, Crystel Bonnet, Zied Riahi, et al.
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