All Stories

  1. The association of novel polymorphisms with stress fracture injury in Elite Athletes: Further insights from the SFEA cohort
  2. SNPs in the vicinity of P2X7R, RANK/RANKL/OPG and Wnt signalling pathways and their association with bone phenotypes in academy footballers
  3. Increased Training Volume Improves Bone Density and Cortical Area in Adolescent Football Players
  4. Functional polymorphisms in the P2X7 receptor gene are associated with stress fracture injury
  5. Athlome Project Consortium: a concerted effort to discover genomic and other “omic” markers of athletic performance
  6. RANK/RANKL/OPG pathway: Genetic associations with stress fracture period prevalence in elite athletes
  7. Rankl/rank/opg Pathway
  8. Single Nucleotide Polymorphisms in the P2X7 Receptor Gene are Associated with Stress Fracture Risk
  9. Identification of novel breast cancer-associated transcripts by uniGene database mining and gene expression analysis in normal and malignant cells
  10. Expression of transglutaminase-2 isoforms in normal human tissues and cancer cell lines: dysregulation of alternative splicing in cancer
  11. Low-Cost QCM Sensor System for Screening Semen Samples
  12. INVESTIGATION OF OPERATING PARAMETERS FOR A SEMEN QUALITY ANALYSIS SYSTEM
  13. ZP genes in avian species illustrate the dynamic evolution of the vertebrate egg envelope
  14. Cracking the egg: increased complexity in the zona pellucida
  15. Four zona pellucida glycoproteins are expressed in the human
  16. Svp1p defines a family of phosphatidylinositol 3,5-bisphosphate effectors
  17. Isolation and mapping the chicken zona pellucida genes: An insight into the evolution of orthologous genes in different species
  18. Analysis of fish ZP1/ZPB homologous genes--evidence for both genome duplication and species-specific amplification models of evolution
  19. Vac14 Controls PtdIns(3,5) P 2 Synthesis and Fab1-Dependent Protein Trafficking to the Multivesicular Body
  20. Functional genomics in reproductive medicine
  21. Alternative Splicing of the Human VEGFGR-3/FLT4 Gene as a Consequence of an Integrated Human Endogenous Retrovirus
  22. MIRs as agents of mammalian gene evolution
  23. A deletion on Chromosome 4 cosegregates with the whirler deafness mutation: exclusion of Orm1 as a candidate
  24. Identification of the true human orthologue of the mouse Zp1 gene: evidence for greater complexity in the mammalian zona pellucida?
  25. Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment
  26. Mapping of the α-Tectorin Gene (TECTA) to Mouse Chromosome 9 and Human Chromosome 11: A Candidate for Human Autosomal Dominant Nonsyndromic Deafness
  27. Cloning and Sequencing of the MouseGli2Gene: Localization to theDominant hemimeliaCritical Region
  28. Paradigms and Paradoxes: Mouse (and Human) Models of Genetic Deafness
  29. A screen for RAS mutations in individuals at risk of secondary leukaemia due to occupational exposure to petrochemicals
  30. Rearrangement of the Human mel Gene, the rab 8 Homologue, in Human Malignant Melanomas
  31. Activation of Ha-ras in human chronic granulocytic and chronic myelomonocytic leukaemia