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Barbara Vona

Showing results (11-20 of 101) with videos related to

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Pflugers Archiv : European Journal of Physiology|December 18, 2020
Age-related hearing loss pertaining to potassium ion channels in the cochlea and auditory pathwayBarbara Peixoto Pinheiro, Barbara Vona, Hubert Löwenheim, et al.
Hearing Research|February 18, 2020
Small fish, big prospects: using zebrafish to unravel the mechanisms of hereditary hearing lossBarbara Vona, Julia Doll, Michaela A H Hofrichter, et al.
American Journal of Medical Genetics. Part A|December 17, 2024
A Homozygous MYH1 Variant Underlies Autosomal Recessive Isolated Recurrent RhabdomyolysisEyyup Uctepe, Hanifenur Mancılar, Fatma Nisa Esen, et al.
BMC Research Notes|June 16, 2018
Hereditary hearing loss SNP-microarray pilot studyBarbara Vona, Michaela A H Hofrichter, Jörg Schröder, et al.
STAR Protocols|June 19, 2025
Protocol for a minigene splice assay using the pET01 vectorHannah Andreae, Marialessandra Curcio, Daniel Owrang, et al.
BMC Medical Genetics|June 26, 2014
Terminal chromosome 4q deletion syndrome in an infant with hearing impairment and moderate syndromic features: review of literatureBarbara Vona, Indrajit Nanda, Cordula Neuner, et al.
Journal of Cellular and Molecular Medicine|March 27, 2024
Autosomal recessive non-syndromic hearing loss genes in Pakistan during the previous three decadesMadiha Shadab, Ansar Ahmed Abbasi, Ahsan Ejaz, et al.
Life (Basel, Switzerland)|September 28, 2023
mRNA Abundance of Neurogenic Factors Correlates with Hearing Capacity in Auditory Brainstem Nuclei of the RatJonas Engert, Julia Doll, Barbara Vona, et al.
EMBO Molecular Medicine|July 14, 2022
Is there an unmet medical need for improved hearing restoration?Bettina Julia Wolf, Kathrin Kusch, Victoria Hunniford, et al.
Molecular Syndromology|December 10, 2015
A Novel de novo Mutation in CEACAM16 Associated with Postlingual Hearing ImpairmentMichaela A H Hofrichter, Indrajit Nanda, Jens Gräf, et al.
Pageof 11

Showing results (11-20 of 101) with videos related to

Sort By:
Pageof 11
Pflugers Archiv : European Journal of Physiology|December 18, 2020
Age-related hearing loss pertaining to potassium ion channels in the cochlea and auditory pathwayBarbara Peixoto Pinheiro, Barbara Vona, Hubert Löwenheim, et al.
Hearing Research|February 18, 2020
Small fish, big prospects: using zebrafish to unravel the mechanisms of hereditary hearing lossBarbara Vona, Julia Doll, Michaela A H Hofrichter, et al.
American Journal of Medical Genetics. Part A|December 17, 2024
A Homozygous MYH1 Variant Underlies Autosomal Recessive Isolated Recurrent RhabdomyolysisEyyup Uctepe, Hanifenur Mancılar, Fatma Nisa Esen, et al.
BMC Research Notes|June 16, 2018
Hereditary hearing loss SNP-microarray pilot studyBarbara Vona, Michaela A H Hofrichter, Jörg Schröder, et al.
STAR Protocols|June 19, 2025
Protocol for a minigene splice assay using the pET01 vectorHannah Andreae, Marialessandra Curcio, Daniel Owrang, et al.
BMC Medical Genetics|June 26, 2014
Terminal chromosome 4q deletion syndrome in an infant with hearing impairment and moderate syndromic features: review of literatureBarbara Vona, Indrajit Nanda, Cordula Neuner, et al.
Journal of Cellular and Molecular Medicine|March 27, 2024
Autosomal recessive non-syndromic hearing loss genes in Pakistan during the previous three decadesMadiha Shadab, Ansar Ahmed Abbasi, Ahsan Ejaz, et al.
Life (Basel, Switzerland)|September 28, 2023
mRNA Abundance of Neurogenic Factors Correlates with Hearing Capacity in Auditory Brainstem Nuclei of the RatJonas Engert, Julia Doll, Barbara Vona, et al.
EMBO Molecular Medicine|July 14, 2022
Is there an unmet medical need for improved hearing restoration?Bettina Julia Wolf, Kathrin Kusch, Victoria Hunniford, et al.
Molecular Syndromology|December 10, 2015
A Novel de novo Mutation in CEACAM16 Associated with Postlingual Hearing ImpairmentMichaela A H Hofrichter, Indrajit Nanda, Jens Gräf, et al.
Pageof 11