All Stories

  1. A CRISPR/Cas9-generated mutation in the zebrafish orthologue of PPP2R3B causes idiopathic scoliosis
  2. Ciliopathy-associated missense mutations in IFT140 are hypomorphic and have edgetic effects on protein interaction networks
  3. A CRISPR/Cas9-generated mutation in the zebrafish orthologue of PPP2R3B causes idiopathic scoliosis
  4. Diverse species-specific phenotypic consequences of loss of function sorting nexin 14 mutations
  5. Diverse Species-Specific Phenotypic Consequences of Loss of Function Sorting Nexin 14 Mutations
  6. Generating Mutant Renal Cell Lines Using CRISPR Technologies
  7. Analysis of transgenic zebrafish expressing the Lenz-Majewski syndrome gene PTDSS1 in skeletal cell lineages
  8. A CRISPR/Cas9-generated zebrafish mutant implicates PPP2R3B loss in idiopathic scoliosis pathogenesis in Turner syndrome.
  9. An FDA-Approved Drug Screen for Compounds Influencing Craniofacial Skeletal Development and Craniosynostosis
  10. SNX14 mutations affect endoplasmic reticulum-associated neutral lipid metabolism in autosomal recessive spinocerebellar ataxia 20
  11. Dissecting the Transcriptional Regulatory Properties of Human Chromosome 16 Highly Conserved Non-Coding Regions
  12. Functional and Molecular Characterization of Voltage-Gated Sodium Channels in Uteri from Nonpregnant Rats1
  13. A role for tachykinins in the regulation of human sperm motility
  14. Molecular diversity of voltage-gated sodium channel α and β subunit mRNAs in human tissues