СИНДРОМЫ.
НАСЛЕДСТВЕННЫЕ БОЛЕЗНИ



И

IDIOPATHIC PULMONARY FIBROSIS
  • FIBROGENESIS
      ◊ FoxO3 an important player in fibrogenesis for idiopathic pulmonary fibrosis. IMPRINTING IN HUMAN DISEASE
  • DYSREGULATION IMPRINTED GENE
      ◊ Disease
      ◊ Advances in Imprinting Disorders


    • INFARCTION of MYOCARDE
  • RISK
      ◊ Factors
      ◊ Role of ALOX5AP
      ◊ Role of Period 2
      ◊ ‘telomerasing’ for cardioprotection


    • INFANTILE-ONSET MULTISYSTEM NEUROLOGIC ENDOCRINE AND PANCREATIC DISEASE (IMNEPD)
  • PTRH2 GENE
      ◊PTRH2 Gene Variants: infantile-onset multisystem neurologic endocrine and pancreatic disease (IMNEPD) INFERTILITY
  • GENES
      ◊ Loss-of-function mutations in CEP78 cause male infertility in humans and mice
      ◊ heritable gain-of-function chk1 mutations impair human fertility
  • MALES
      ◊ Role of Endoplasmic Reticulum Stress in The Male Reproductive System

    INFLAMMATION DISEASE
  • Neutrophilic Inflammation
      ◊Dampen Neutrophilic Inflammation with MicroRNA-223


    • INFLAMMATORY BOWEL DISEASE
  • INNATE IMMUNE RESPONSE GENES
      ◊Genes polymorphisms
  • MITOCHONDRIAL DNA
      ◊Mitochondrial DNA Is a Pro-Inflammatory Damage-Associated During Active IBD

    monogenic INTESTINAL EPITHELIAL DISORDERS
  • GENETICS
      ◊The genetics of monogenic intestinal epithelial disorders
    • INTELLECTUAL DISABILITY
  • NEW GENES
      ◊ 26 novel candidate genes


    • Intestinal Neuronal Dysplasia B

    INTRAUTERINE DEVELOPMENTAL ABNORMALITIES
  • MATERNAL ENVIRONMENT
      ◊ Glucose and oxygen in the early intrauterine environment and their role in developmental abnormalities


    • IRON DISABILITY
  • NEURODEGENERATIONS
      ◊ Iron Accumulation: neurodegenerations
  • IRON-DEFICIENCY ANEMIA
      ◊ Scribble-mediated control of the erythropoietin receptor
    IVF