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R Wilcox

Showing results (591-600 of 627) with videos related to

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Human Molecular Genetics|August 13, 2003
Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degenerationTamar Ben-Yosef, Inna A Belyantseva, Thomas L Saunders, et al.
Nature Genetics|July 1, 2008
Gain-of-function mutations in TRPV4 cause autosomal dominant brachyolmiaMatthew J Rock, Jean Prenen, Vincent A Funari, et al.
Molecular Genetics and Metabolism|November 27, 2007
Females with Fabry disease frequently have major organ involvement: lessons from the Fabry RegistryWilliam R Wilcox, João Paulo Oliveira, Robert J Hopkin, et al.
Human Mutation|August 21, 2019
De novo GRIN variants in NMDA receptor M2 channel pore-forming loop are associated with neurological diseasesJia Li, Jin Zhang, Weiting Tang, et al.
Oecologia|July 14, 2022
Richness, not evenness, varies across water availability gradients in grassy biomes on five continentsMelinda D Smith, Sally E Koerner, Meghan L Avolio, et al.
Ecology|December 30, 2021
Do trade-offs govern plant species' responses to different global change treatments?J Adam Langley, Emily Grman, Kevin R Wilcox, et al.
Oecologia|November 1, 2020
Temporal variability in production is not consistently affected by global change drivers across herbaceous-dominated ecosystemsMeghan L Avolio, Kevin R Wilcox, Kimberly J Komatsu, et al.
Journal of Medical Genetics|April 5, 2003
Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafnessH-J Park, S Shaukat, X-Z Liu, et al.
Advances in Therapy|October 26, 2023
Vosoritide Therapy in Children with Achondroplasia: Early Experience and Practical Considerations for Clinical PracticeOliver Semler, Valérie Cormier-Daire, Ekkehart Lausch, et al.
Human Genetics|July 8, 1998
Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutationsA L DeStefano, L A Cupples, K S Arnos, et al.
Pageof 63

Showing results (591-600 of 627) with videos related to

Sort By:
Pageof 63
Human Molecular Genetics|August 13, 2003
Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degenerationTamar Ben-Yosef, Inna A Belyantseva, Thomas L Saunders, et al.
Nature Genetics|July 1, 2008
Gain-of-function mutations in TRPV4 cause autosomal dominant brachyolmiaMatthew J Rock, Jean Prenen, Vincent A Funari, et al.
Molecular Genetics and Metabolism|November 27, 2007
Females with Fabry disease frequently have major organ involvement: lessons from the Fabry RegistryWilliam R Wilcox, João Paulo Oliveira, Robert J Hopkin, et al.
Human Mutation|August 21, 2019
De novo GRIN variants in NMDA receptor M2 channel pore-forming loop are associated with neurological diseasesJia Li, Jin Zhang, Weiting Tang, et al.
Oecologia|July 14, 2022
Richness, not evenness, varies across water availability gradients in grassy biomes on five continentsMelinda D Smith, Sally E Koerner, Meghan L Avolio, et al.
Ecology|December 30, 2021
Do trade-offs govern plant species' responses to different global change treatments?J Adam Langley, Emily Grman, Kevin R Wilcox, et al.
Oecologia|November 1, 2020
Temporal variability in production is not consistently affected by global change drivers across herbaceous-dominated ecosystemsMeghan L Avolio, Kevin R Wilcox, Kimberly J Komatsu, et al.
Journal of Medical Genetics|April 5, 2003
Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafnessH-J Park, S Shaukat, X-Z Liu, et al.
Advances in Therapy|October 26, 2023
Vosoritide Therapy in Children with Achondroplasia: Early Experience and Practical Considerations for Clinical PracticeOliver Semler, Valérie Cormier-Daire, Ekkehart Lausch, et al.
Human Genetics|July 8, 1998
Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutationsA L DeStefano, L A Cupples, K S Arnos, et al.
Pageof 63