Related Experiment Videos
Mouse coat colour mutations: a molecular genetic resource which spans the centuries
1MRC Human Genetics Unit, Western General Hospital, Edinburgh, UK.
Summary
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Assessing the welfare of genetically altered mice.
Laboratory animals·2006
Functional variation of MC1R alleles from red-haired individuals.
Human molecular genetics·2001
Mouse mutagenesis on target.
Nature genetics·2001
Genetic and environmental factors modify bovine spongiform encephalopathy incubation period in mice.
Proceedings of the National Academy of Sciences of the United States of America·2001
Mouse genomics: making sense of the sequence.
Current biology : CB·2001
Mechanisms That Govern Recombinase Fidelity Control During Eukaryotic Homologous Recombination.
BioEssays : news and reviews in molecular, cellular and developmental biology·2026
Quantifying Evolutionary Dynamics of Arthropodization and Arthrodization.
BioEssays : news and reviews in molecular, cellular and developmental biology·2026
Flower Delivery: The Emergence of FLOWER (FWE) as a Multifunctional Regulator of Endo-Lysosome-Related Organelle Trafficking Across Cell Types.
BioEssays : news and reviews in molecular, cellular and developmental biology·2026
The Single-Stranded DNA Platform: A Potential Broad-Spectrum Vector for Editing Genes in Prokaryotes: ssDNA May Break Through the Difficulties of Genetic Manipulation on Non-Model Bacteria.
BioEssays : news and reviews in molecular, cellular and developmental biology·2026
Why a Chloroplast Needs Its Own Genome Tethered to the Thylakoid Membrane-Co-Location for Redox Regulation.
BioEssays : news and reviews in molecular, cellular and developmental biology·2026
Condensates on the Move: Midbody Remnants as Large, Translation-Competent Extracellular Vesicles.
BioEssays : news and reviews in molecular, cellular and developmental biology·2026
Whole-genome resequencing with multidimensional annotation revealed pathogenic networks in sirenomelia.
Italian journal of pediatrics·2026
The ZBTB16/CUL3/ROC1 ubiquitin ligase drives the degradation of pathogenic pendrin (SLC26A4) protein variants.
Journal of biomedical science·2026
The first 25 years of the NICHD Structural Birth Defects Initiative.
Developmental biology·2026