All Stories

  1. Mutation in the SR6 region of desmoplakin is associated with pustular psoriasiform rash and left ventricular dysfunction
  2. SLURP-1 is mutated in Mal de Meleda, a potential molecular signature for melanoma and a putative squamous lineage tumor suppressor gene
  3. Erythropoietic protoporphyria a clinical and molecular study from Lebanon: Ferrochelatase a potential tumor suppressor gene in colon cancer
  4. Premature Valvular Heart Disease in Homozygous Familial Hypercholesterolemia
  5. Retinoids: a journey from the molecular structures and mechanisms of action to clinical uses in dermatology and adverse effects
  6. Hereditary vitamin D-resistant rickets in Lebanese patients: the p.R391S and p.H397P variants have different phenotypes
  7. Variable expressivity and co‐occurrence of LDLR and LDLRAP1 mutations in familial hypercholesterolemia: failure of the dominant and recessive dichotomy
  8. GATA5 Homozygous Mutation in a DORV patient
  9. T-box factors: Insights into the evolutionary emergence of the complex heart
  10. Tbx5 et l’adaptation du cœur à la vie sur terre
  11. GATA4 in Heart Development and Disease
  12. Distinct Expression and Function of Alternatively Spliced Tbx5 Isoforms in Cell Growth and Differentiation
  13. The Kruppel-like transcription factor KLF13 is a novel regulator of heart development
  14. A novel mutation in theGATA4 gene in patients with Tetralogy of Fallot
  15. Transcriptional activation of BMP-4 and regulation of mammalian organogenesis by GATA-4 and -6
  16. Regulation of heart development and function through combinatorial interactions of transcription factors
  17. Cooperative Interaction between GATA-4 and GATA-6 Regulates Myocardial Gene Expression