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Human Molecular Genetics|April 4, 2002
Hyperekplexia associated with compound heterozygote mutations in the beta-subunit of the human inhibitory glycine receptor (GLRB)Mark I Rees, Trevor M Lewis, John B J Kwok, et al.Journal of Animal Science and Biotechnology|February 11, 2022
A Capra hircus chromosome 19 locus linked to milk production influences mammary conformationAndrew Jiang, Alex Ankersmit-Udy, Sally-Anne Turner, et al.Journal of Human Genetics|February 26, 2025
Germline mosaicism in TCF20-associated neurodevelopmental disorders: a case study and literature reviewJessie Poquérusse, Whitney Whitford, Juliet Taylor, et al.Journal of Chemical Neuroanatomy|January 22, 2019
Chemical neuroanatomy of the substantia nigra in the ovine brainSamantha J Murray, Brittney L Black, Suzanne J Reid, et al.BMC Genomics|August 28, 2020
A new mechanism for a familiar mutation - bovine DGAT1 K232A modulates gene expression through multi-junction exon splice enhancementTania Fink, Thomas J Lopdell, Kathryn Tiplady, et al.The Journal of Dairy Research|July 24, 2014
Estimation of genetic and crossbreeding parameters of fatty acid concentrations in milk fat predicted by mid-infrared spectroscopy in New Zealand dairy cattleNicolas Lopez-Villalobos, Richard J Spelman, Janine Melis, et al.Journal of Proteomics|May 5, 2012
Metabolic proteomics of the liver and mammary gland during lactationPisana Rawson, Christine Stockum, Lifeng Peng, et al.Brain Research. Molecular Brain Research|June 15, 2004
TBP, a polyglutamine tract containing protein, accumulates in Alzheimer's diseaseSuzanne J Reid, Willeke M C van Roon-Mom, Phil C Wood, et al.Cold Spring Harbor Molecular Case Studies|July 12, 2017
Compound heterozygous SLC19A3 mutations further refine the critical promoter region for biotin-thiamine-responsive basal ganglia diseaseWhitney Whitford, Isobel Hawkins, Emma Glamuzina, et al.Genes|February 27, 2026
Foundations of an Ovine Model of Fragile X SyndromeVictoria Hawkins, Skye R Rudiger, Clive J McLaughlan, et al.Pageof 8