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Rosan Kenana

Showing results (1-10 of 13) with videos related to

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Genes|February 25, 2023
Towards a Cure for HARS DiseaseSarah D P Wilhelm, Rosan Kenana, Yi Qiu, et al.
Experimental & Molecular Medicine|October 8, 2016
A novel anti-IL4Rα nanoparticle efficiently controls lung inflammation during asthmaRabih Halwani, Asma Sultana Shaik, Elaref Ratemi, et al.
The Journal of Asthma : Official Journal of the Association for the Care of Asthma|December 7, 2017
Association of IL-13 rs20541 and rs1295686 variants with symptomatic asthma in a Saudi Arabian populationRabih Halwani, Alejandro Vazquez-Tello, Rosan Kenana, et al.
Nucleic Acids Research|November 12, 2024
Transfer RNA supplementation rescues HARS deficiency in a humanized yeast model of Charcot-Marie-Tooth diseaseSarah D P Wilhelm, Jenica H Kakadia, Aruun Beharry, et al.
Genes|March 29, 2019
The Role of 3' to 5' Reverse RNA Polymerization in tRNA Fidelity and RepairAllan W Chen, Malithi I Jayasinghe, Christina Z Chung, et al.
Human Molecular Genetics|September 27, 2022
Histidine supplementation can escalate or rescue HARS deficiency in a Charcot-Marie-Tooth disease modelYi Qiu, Rosan Kenana, Aruun Beharry, et al.
NAR Molecular Medicine|February 25, 2026
Inhibition of the integrated stress response rescues a histidyl-tRNA synthetase variant associated with Charcot-Marie-Tooth diseaseMaria Mahmood, Sarah D P Wilhelm, Marisa I Mendes, et al.
Clinical Dysmorphology|February 27, 2024
Novel UBE3B mutations: report of eight patients with Kaufman oculocerebrofacial syndrome with additional clinical findings from a highly consanguineous populationAlBandary Albakheet, Duaa Almuallami, Rawan Almass, et al.
American Journal of Medical Genetics. Part A|March 27, 2014
Novel homozygous DEAF1 variant suspected in causing white matter disease, intellectual disability, and microcephalyEissa A Faqeih, Mohammed Al-Owain, Dilek Colak, et al.
American Journal of Human Genetics|October 1, 2013
Mutations in NALCN cause an autosomal-recessive syndrome with severe hypotonia, speech impairment, and cognitive delayMoeenaldeen D Al-Sayed, Hamad Al-Zaidan, Albandary Albakheet, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Genes|February 25, 2023
Towards a Cure for HARS DiseaseSarah D P Wilhelm, Rosan Kenana, Yi Qiu, et al.
Experimental & Molecular Medicine|October 8, 2016
A novel anti-IL4Rα nanoparticle efficiently controls lung inflammation during asthmaRabih Halwani, Asma Sultana Shaik, Elaref Ratemi, et al.
The Journal of Asthma : Official Journal of the Association for the Care of Asthma|December 7, 2017
Association of IL-13 rs20541 and rs1295686 variants with symptomatic asthma in a Saudi Arabian populationRabih Halwani, Alejandro Vazquez-Tello, Rosan Kenana, et al.
Nucleic Acids Research|November 12, 2024
Transfer RNA supplementation rescues HARS deficiency in a humanized yeast model of Charcot-Marie-Tooth diseaseSarah D P Wilhelm, Jenica H Kakadia, Aruun Beharry, et al.
Genes|March 29, 2019
The Role of 3' to 5' Reverse RNA Polymerization in tRNA Fidelity and RepairAllan W Chen, Malithi I Jayasinghe, Christina Z Chung, et al.
Human Molecular Genetics|September 27, 2022
Histidine supplementation can escalate or rescue HARS deficiency in a Charcot-Marie-Tooth disease modelYi Qiu, Rosan Kenana, Aruun Beharry, et al.
NAR Molecular Medicine|February 25, 2026
Inhibition of the integrated stress response rescues a histidyl-tRNA synthetase variant associated with Charcot-Marie-Tooth diseaseMaria Mahmood, Sarah D P Wilhelm, Marisa I Mendes, et al.
Clinical Dysmorphology|February 27, 2024
Novel UBE3B mutations: report of eight patients with Kaufman oculocerebrofacial syndrome with additional clinical findings from a highly consanguineous populationAlBandary Albakheet, Duaa Almuallami, Rawan Almass, et al.
American Journal of Medical Genetics. Part A|March 27, 2014
Novel homozygous DEAF1 variant suspected in causing white matter disease, intellectual disability, and microcephalyEissa A Faqeih, Mohammed Al-Owain, Dilek Colak, et al.
American Journal of Human Genetics|October 1, 2013
Mutations in NALCN cause an autosomal-recessive syndrome with severe hypotonia, speech impairment, and cognitive delayMoeenaldeen D Al-Sayed, Hamad Al-Zaidan, Albandary Albakheet, et al.
Pageof 2