СИНДРОМЫ.
НАСЛЕДСТВЕННЫЕ БОЛЕЗНИ

FARBER DISEASE
  • ACID CERAMIDASE DEFICIENCY
      ◊ Farber disease and SMA-PME disease

    • FABRY'S DISEASE
  • KIDNEY
      ◊ Enzyme replacement therapy
    • FACIAL DYSOSTOSES
  • Forms and genetics
    • FACIOSCAPULOHUMORAL MUSCULAR DYSTROPHY
  • Epigenetic Regulator SMCHD1
  • FHC

    • Familial combined hyperlipidaema
  • USF1

    •   ◊FH
      ◊ FALS and copper

    FANCONI ANEMIE
  • Description
  • & Bllom


    • FATTY LIVER DISEASE
  • MATERNAL OBESITY TRIGGERS Kupffer cell programming by maternal obesity triggers fatty liver disease
    • FERROPTOSIS
  • FERROPTOSIS and ACUTE KIDNEY INJURY
      ◊ Multiple oestradiol functions inhibit ferroptosis and acute kidney injury


    • FERTILIZATION
  • INTERACTION OF SPERMATOZOA AND OOCYTE


    • FETAL ALCOHOL SYNDROME (FAS)
  • Alcohol exposure on body systems


    • FIBRILLATION OF ATRIAL
  • ECGs
      ◊ Origins of re-entry and ectopic foci in the atria


    • FIBROMYALGIA
  • CAUSES
      ◊ Unpicking the genetics of fibromyalgia sheds new light on its causes


    • FIBROTIC SKELETAL MUSCLE
  • EXTRACELLULAR MATRIX
      ◊ Reconstruction of fibrotic skeletal muscle extracellular matrix


    • FRAGILE X SYNDROME

  •   ◊ Description
      ◊ Genetics, Neurodevelopmental, Behavioral and Psychiatric Associations
      ◊ Astrocytes Fuel Erratic Firing in Fragile X Neurons
  • GENETIC CONTROL
      ◊ Fragile X Syndrome Is Alleviated by Brd4 Inhibition
      ◊ Loss of fragile X protein FMRP impairs homeostatic synaptic downscaling through tumor suppressor p53 and ubiquitin E3 ligase Nedd4-2
  • MODELLING
      ◊ Drosophila
      ◊ Mouse
       • Role of glutamate signalling (mGluRs)