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Randall J Roper

Showing results (41-50 of 49) with videos related to

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G3 (Bethesda, Md.)|March 6, 2026
Genetic analysis of triplicated genes affecting sex-specific skeletal deficits in Down syndrome model miceKourtney Sloan, Kristina M Piner, Pathum Randunu Nawarathna Kandedura Arachchige, et al.
Journal of Immunology (Baltimore, Md. : 1950)|June 10, 2003
Aod1 controlling day 3 thymectomy-induced autoimmune ovarian dysgenesis in mice encompasses two linked quantitative trait loci with opposing allelic effects on disease susceptibilityRandall J Roper, Ryan D McAllister, Julia E Biggins, et al.
Human Molecular Genetics|March 7, 2007
Trisomy for the Down syndrome 'critical region' is necessary but not sufficient for brain phenotypes of trisomic miceLisa E Olson, Randall J Roper, Crystal L Sengstaken, et al.
Bone|April 20, 2020
Interaction of sexual dimorphism and gene dosage imbalance in skeletal deficits associated with Down syndromeJared R Thomas, Jonathan LaCombe, Rachel Long, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 29, 2011
Molecular characterization of the translocation breakpoints in the Down syndrome mouse model Ts65DnLaura G Reinholdt, Yueming Ding, Griffith J Gilbert, et al.
American Journal of Medical Genetics. Part A|December 28, 2018
Clinical identification of feeding and swallowing disorders in 0-6 month old infants with Down syndromeMaria A Stanley, Nicole Shepherd, Nichole Duvall, et al.
Disease Models & Mechanisms|March 20, 2023
Genetic dissection of triplicated chromosome 21 orthologs yields varying skeletal traits in Down syndrome model miceKourtney Sloan, Jared Thomas, Matthew Blackwell, et al.
American Journal of Medical Genetics. Part A|July 12, 2013
Non-trisomic homeobox gene expression during craniofacial development in the Ts65Dn mouse model of Down syndromeCherie N Billingsley, Jared R Allen, Douglas D Baumann, et al.
Nature Communications|October 26, 2022
Rescue of deficits by Brwd1 copy number restoration in the Ts65Dn mouse model of Down syndromeSasha L Fulton, Wendy Wenderski, Ashley E Lepack, et al.
Pageof 5

Showing results (41-50 of 49) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 49 results.
G3 (Bethesda, Md.)|March 6, 2026
Genetic analysis of triplicated genes affecting sex-specific skeletal deficits in Down syndrome model miceKourtney Sloan, Kristina M Piner, Pathum Randunu Nawarathna Kandedura Arachchige, et al.
Journal of Immunology (Baltimore, Md. : 1950)|June 10, 2003
Aod1 controlling day 3 thymectomy-induced autoimmune ovarian dysgenesis in mice encompasses two linked quantitative trait loci with opposing allelic effects on disease susceptibilityRandall J Roper, Ryan D McAllister, Julia E Biggins, et al.
Human Molecular Genetics|March 7, 2007
Trisomy for the Down syndrome 'critical region' is necessary but not sufficient for brain phenotypes of trisomic miceLisa E Olson, Randall J Roper, Crystal L Sengstaken, et al.
Bone|April 20, 2020
Interaction of sexual dimorphism and gene dosage imbalance in skeletal deficits associated with Down syndromeJared R Thomas, Jonathan LaCombe, Rachel Long, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 29, 2011
Molecular characterization of the translocation breakpoints in the Down syndrome mouse model Ts65DnLaura G Reinholdt, Yueming Ding, Griffith J Gilbert, et al.
American Journal of Medical Genetics. Part A|December 28, 2018
Clinical identification of feeding and swallowing disorders in 0-6 month old infants with Down syndromeMaria A Stanley, Nicole Shepherd, Nichole Duvall, et al.
Disease Models & Mechanisms|March 20, 2023
Genetic dissection of triplicated chromosome 21 orthologs yields varying skeletal traits in Down syndrome model miceKourtney Sloan, Jared Thomas, Matthew Blackwell, et al.
American Journal of Medical Genetics. Part A|July 12, 2013
Non-trisomic homeobox gene expression during craniofacial development in the Ts65Dn mouse model of Down syndromeCherie N Billingsley, Jared R Allen, Douglas D Baumann, et al.
Nature Communications|October 26, 2022
Rescue of deficits by Brwd1 copy number restoration in the Ts65Dn mouse model of Down syndromeSasha L Fulton, Wendy Wenderski, Ashley E Lepack, et al.
Pageof 5