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Human Molecular Genetics|May 22, 2024
Single nuclei RNA-seq reveals a medium spiny neuron glutamate excitotoxicity signature prior to the onset of neuronal death in an ovine Huntington's disease modelAndrew Jiang, Linya You, Renee R Handley, et al.Scientific Reports|February 27, 2015
Phenotypic population screen identifies a new mutation in bovine DGAT1 responsible for unsaturated milk fatKlaus Lehnert, Hamish Ward, Sarah D Berry, et al.The New Zealand Medical Journal|August 18, 2018
Genomic medicine must reduce, not compound, health inequities: the case for hauora-enhancing genomic resources for New ZealandStephen P Robertson, Jennie Harre Hindmarsh, Sarah Berry, et al.Nature Communications|September 11, 2020
DNA methylation study of Huntington's disease and motor progression in patients and in animal modelsAke T Lu, Pritika Narayan, Matthew J Grant, et al.Journal of Huntington'S Disease|August 23, 2021
A Multi-Omic Huntington's Disease Transgenic Sheep-Model Database for Investigating Disease PathogenesisEmily R Mears, Renee R Handley, Matthew J Grant, et al.Science Advances|November 14, 2025
Structural and epistatic regulatory variants cause hallmark white spotting in cattleSwati Jivanji, Emma Wilkinson, Lijing Tang, et al.Clinical and Translational Medicine|August 27, 2025
Molecular architecture of language-related cortical areas revealed by integrative proteomic and connectome analysesJinsong Wu, Zixian Wang, Fengjiao Li, et al.Nature Genetics|March 6, 2012
Complex reorganization and predominant non-homologous repair following chromosomal breakage in karyotypically balanced germline rearrangements and transgenic integrationColby Chiang, Jessie C Jacobsen, Carl Ernst, et al.American Journal of Human Genetics|October 23, 2018
De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and DyskinesiasKatherine L Helbig, Robert J Lauerer, Jacqueline C Bahr, et al.Pageof 8