All Stories

  1. High Burden of Non-Clonal Chromosome Aberrations Before Onset of Detectable Neoplasia in Fanconi Anemia Bone Marrow
  2. A Molecular Characterization of the Allelic Expression of the BRCA1 Founder Δ9–12 Pathogenic Variant and Its Potential Clinical Relevance in Hereditary Cancer
  3. Reversion from basal histone H4 hypoacetylation at the replication fork increases DNA damage in FANCA deficient cells
  4. A Boolean network model of the double-strand break repair pathway choice
  5. Anemia de Fanconi, Parte 2. Estrategia metodológica para el diagnóstico molecular en pacientes con anemia de Fanconi
  6. Frequent copy number variants in a cohort of Mexican-Mestizo individuals
  7. Fanconi Anemia Patients from an Indigenous Community in Mexico Carry a New Founder Pathogenic Variant in FANCG
  8. Fanconi Anemia Patients from an Indigenous Community in Mexico Carry a New Founder Pathogenic Variant in FANCG
  9. MYC Promotes Bone Marrow Stem Cell Dysfunction in Fanconi Anemia
  10. WIP1 Contributes to the Adaptation of Fanconi Anemia Cells to DNA Damage as Determined by the Regulatory Network of the Fanconi Anemia and Checkpoint Recovery Pathways
  11. FANCCDutch founder mutation in a Mennonite family from Tamaulipas, México
  12. Low bone mineral density and renal malformation in Mexican patients with Turner syndrome are associated with single nucleotide variants in vitamin D-metabolism genes
  13. Paraptosis in human glioblastoma cell line induced by curcumin
  14. Derivative chromosomes involving 5p large rearranged segments went unnoticed with the use of conventional cytogenetics
  15. Microarray analysis of microRNA expression in mouse fetus at 13.5 and 14.5 days post - coitum in ear and back skin tissues
  16. A Boolean network model of human gonadal sex determination
  17. Fanconi anemia cells with unrepaired DNA damage activate components of the checkpoint recovery process
  18. Hydroxyurea induces chromosomal damage in G2 and enhances the clastogenic effect of mitomycin C in Fanconi anemia cells
  19. Interstitial deletion of 2q24.2: Further delineation of an emerging syndrome associated with intellectual disability, severe hypotonia and moderate intrauterine growth restriction
  20. A Boolean network model of the FA/BRCA pathway
  21. Clinical traits and molecular findings in 46,XX males
  22. Disturbed Expression of Sox9 in Pre-Sertoli Cells Underlies Sex-Reversal in Mice B6.Ytir1
  23. Expression profiles of Dax1, Dmrt1, and Sox9 during temperature sex determination in gonads of the sea turtle Lepidochelys olivacea
  24. Timing of SOX9 downregulation and female sex determination in gonads of the sea turtleLepidochelys olivacea
  25. Scant XYqh− testicular cells with normal SRY was enough to differentiate bilateral testes in a 45,X/46,XYqh− patient
  26. An atypical contiguous gene syndrome: molecular studies in a family with X-linked Kallmann's syndrome and X-linked ichthyosis
  27. SRY alone can induce normal male sexual differentiation