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Barbara Vona

Showing results (21-30 of 101) with videos related to

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Human Genomics|October 14, 2023
FGFR1 variants contributed to families with tooth agenesisSiyue Yao, Xi Zhou, Min Gu, et al.
Ear and Hearing|June 12, 2018
Recommendations on Collecting and Storing Samples for Genetic Studies in Hearing and Tinnitus ResearchAgnieszka J Szczepek, Lidia Frejo, Barbara Vona, et al.
International Journal of Molecular Sciences|September 23, 2022
Skeletal Class III Malocclusion Is Associated with <i>ADAMTS2</i> Variants and Reduced Expression in a Familial CaseSiyue Yao, Xi Zhou, Barbara Vona, et al.
Molecular Genetics & Genomic Medicine|June 11, 2020
A novel missense variant in MYO3A is associated with autosomal dominant high-frequency hearing loss in a German familyJulia Doll, Michaela A H Hofrichter, Paulina Bahena, et al.
Ear and Hearing|February 6, 2016
Confirmation of PDZD7 as a Nonsyndromic Hearing Loss GeneBarbara Vona, Stanislav Lechno, Michaela A H Hofrichter, et al.
Cell Death & Disease|March 21, 2024
METTL3-dependent m<sup>6</sup>A modification of PSEN1 mRNA regulates craniofacial development through the Wnt/β-catenin signaling pathwayLan Ma, Xi Zhou, Siyue Yao, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|December 12, 2018
Phenotypic Characterization of DFNB16-associated Hearing LossDaniela Back, Wafaa Shehata-Dieler, Barbara Vona, et al.
European Journal of Medical Genetics|July 18, 2019
Exome-wide copy number variation analysis identifies a COL9A1 in frame deletion that is associated with hearing lossMichaela A H Hofrichter, Julia Doll, Haleh Habibi, et al.
Cell Reports|October 1, 2025
Genetic regulation of ARID3B confers cleft lip with/without cleft palate susceptibility through LLPS-mediated transcriptional programXiaofeng Li, Dandan Li, Shu Lou, et al.
BMC Medical Genomics|June 9, 2019
Unbalanced segregation of a paternal t(9;11)(p24.3;p15.4) translocation causing familial Beckwith-Wiedemann syndrome: a case reportCaroline Lekszas, Indrajit Nanda, Barbara Vona, et al.
Pageof 11

Showing results (21-30 of 101) with videos related to

Sort By:
Pageof 11
Human Genomics|October 14, 2023
FGFR1 variants contributed to families with tooth agenesisSiyue Yao, Xi Zhou, Min Gu, et al.
Ear and Hearing|June 12, 2018
Recommendations on Collecting and Storing Samples for Genetic Studies in Hearing and Tinnitus ResearchAgnieszka J Szczepek, Lidia Frejo, Barbara Vona, et al.
International Journal of Molecular Sciences|September 23, 2022
Skeletal Class III Malocclusion Is Associated with <i>ADAMTS2</i> Variants and Reduced Expression in a Familial CaseSiyue Yao, Xi Zhou, Barbara Vona, et al.
Molecular Genetics & Genomic Medicine|June 11, 2020
A novel missense variant in MYO3A is associated with autosomal dominant high-frequency hearing loss in a German familyJulia Doll, Michaela A H Hofrichter, Paulina Bahena, et al.
Ear and Hearing|February 6, 2016
Confirmation of PDZD7 as a Nonsyndromic Hearing Loss GeneBarbara Vona, Stanislav Lechno, Michaela A H Hofrichter, et al.
Cell Death & Disease|March 21, 2024
METTL3-dependent m<sup>6</sup>A modification of PSEN1 mRNA regulates craniofacial development through the Wnt/β-catenin signaling pathwayLan Ma, Xi Zhou, Siyue Yao, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|December 12, 2018
Phenotypic Characterization of DFNB16-associated Hearing LossDaniela Back, Wafaa Shehata-Dieler, Barbara Vona, et al.
European Journal of Medical Genetics|July 18, 2019
Exome-wide copy number variation analysis identifies a COL9A1 in frame deletion that is associated with hearing lossMichaela A H Hofrichter, Julia Doll, Haleh Habibi, et al.
Cell Reports|October 1, 2025
Genetic regulation of ARID3B confers cleft lip with/without cleft palate susceptibility through LLPS-mediated transcriptional programXiaofeng Li, Dandan Li, Shu Lou, et al.
BMC Medical Genomics|June 9, 2019
Unbalanced segregation of a paternal t(9;11)(p24.3;p15.4) translocation causing familial Beckwith-Wiedemann syndrome: a case reportCaroline Lekszas, Indrajit Nanda, Barbara Vona, et al.
Pageof 11