Publications by authors named "Gene Elliot"

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A murine model lacking Lyst recapitulates Chediak-Higashi syndrome with an earlier-onset neurodegenerative phenotype.
Sunny Greene, Mackenzie L Talbert, F Graeme Frost, Patricia M Zerfas, Danielle Springer, Gene Elliot

Commun Biol· July 2025

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Variants in , a component of the WASH complex, cause short stature, variable neurodevelopmental abnormalities, and distinctive facial dysmorphism.
Youn Hee Jee, Julian C Lui, Dana Marafi, Zhi-Jie Xia, Ruchika Bhatia, Gene Elliot

Genet Med Open· December 2024

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The RAD51 S181P mutation shortens lifespan of female mice.
Sherry G Dodds, Gene Hubbard, Yong Jun Choi, Kyungjae Myung, Gene Elliot

Mutat Res· November 2024

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Genetic background modifies phenotypic severity and longevity in a mouse model of Niemann-Pick disease type C1.
Jorge L Rodriguez-Gil, Dawn E Watkins-Chow, Laura L Baxter, Gene Elliot, Ursula L Harper

Dis Model Mech· March 2020

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A mouse model of Proteus syndrome.
Marjorie J Lindhurst, Lauren R Brinster, Hannah C Kondolf, Jasmine J Shwetar, Miranda R Yourick, Gene Elliot

Hum Mol Genet· September 2019

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Disruption of Visc-2, a Brain-Expressed Conserved Long Noncoding RNA, Does Not Elicit an Overt Anatomical or Behavioral Phenotype.
Peter L Oliver, Rebecca A Chodroff, Amrit Gosal, Benjamin Edwards, Amanda F P Cheung, Gene Elliot

Cereb Cortex· October 2015

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Predisposition to cancer caused by genetic and functional defects of mammalian Atad5.
Daphne W Bell, Nilabja Sikdar, Kyoo-Young Lee, Jessica C Price, Raghunath Chatterjee, Gene Elliot

PLoS Genet· August 2011

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Wnt signaling gradients establish planar cell polarity by inducing Vangl2 phosphorylation through Ror2.
Bo Gao, Hai Song, Kevin Bishop, Gene Elliot, Lisa Garrett

Dev Cell· February 2011

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Identification of neural crest and glial enhancers at the mouse Sox10 locus through transgenesis in zebrafish.
Anthony Antonellis, Jimmy L Huynh, Shih-Queen Lee-Lin, Ryan M Vinton, Gabriel Renaud, Gene Elliot

PLoS Genet· September 2008

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