СИНДРОМЫ.
НАСЛЕДСТВЕННЫЕ БОЛЕЗНИ


H


HAEMOPHILIA A
  • Mutations and Therapy


    • HAJDU-CHENEY SYNDROME
  • Mutations in NOTCH2


    • HEARING LOSS
  • Extensive unexplored genetic landscape for auditory dysfunction


    • HEART FAILURE
  • GENETIC CONTROL
      ◊Cdk8 induces eccentric hypertrophy and heart failure*
      ◊ Desmin Phosphorylation Triggers Preamyloid Oligomers Formation and Myocyte Dysfunction
      ◊ The Genetics of Neurodevelopment in Congenital Heart Disease
  • β1-ADRENERGIC RECEPTOR
      ◊Alterations in signal transduction*
      ◊ Polymorphisms
  • HEART ATTACK
      ◊Air temperature is external trigger for heart attack
  • GENETIC FACTORS
      ◊p53-induced inhibition of Hif-1
      ◊TGF-β signaling
      ◊TGF-β signaling.htm"target="frame_b">TGF-β signaling
      ◊The Roles of Histone Lysine Methyltransferases in Heart Development and Disease
  • RISK
      ◊Nut Consumption and Risk of Cardiovascular Disease


  • HEART DYSFUNCTION
      ◊Cardiac macrophages promote diastolic dysfunction
      ◊ Detecting structural heart disease from electrocardiograms using AI
      ◊Molecular Mechanisms of L-Type Calcium Channel Dysregulation in Heart Failure
    • HAEMATOPOIESIS
  • MUTANT CLONAL HAEMATOPOIESIS
      ◊ Mitochondrial metabolism


    • HETEROTAXIAS
  • Genetics


  • PKC-α
  • SECOND HEART FIELD

    •   ◊ On the involvement of the second heart field in congenital heart defects



    HEPATITIS C
  • Danger


    • HEPATOCELLULAR CARCINOMA
  • ETHNIC DIFFERENCES
      ◊Ethnic differences in hepatocellular carcinoma preSHAREvalence and therapeutic outcomes
    • HH-ANOMALIES
  • Signaling pathway


    • HIRSCHSPRUNG's DISEASE
  • GENETICS
      ◊Multigenic disorder
      ◊ Developmental genetics
  • GENES CANDIDATES
      ◊ PMX2B
      ◊ Arhgef3 и Ctnnal1
  • Description

    • HIV Infection
  • enfuvirtide


    • HHT

    HGPS


    HOLOPROSENCEPHALY
  • Description
  • MECHNISMS
      ◊ Patterning forces

  • GENETICS
      ◊ Tgif


    • Holt-Oram (Холта-Орама синдром)

    HOX DISEASEs
  • Non-segmental Organs


    • HUNTINGTON's DESEASE
  • CONVERSION
      ◊ Skin cells into brain cells sheds light on disease
  • DESCRIPTION
      ◊ Description
      ◊ Huntingin

    •   ◊ A developmental component to Huntington's disease
  • GENETIC CONTROL
      ◊ MicroRNAs in Hox Gene Clusters
  • PERSONALIZED THERAPEUTICS
      ◊ Gene silencing


    • HYDATIDIFORM MOLE
  • Genetics


    • HYDROCEPHALUS
  • mTORC1 signaling and primary cilia for brain ventricle morphogenesis


    • HYPERCHOLESTEROLEMIA
  • Description
  • Ezetimibe
  • AUTOSOMAL DOMINANT HYPERCHOLESTEROLEMIA
      ◊Genetic heterogeneity


    • HYPERTENSION
  • PULMONARY HYPERTENSION
      ◊ Unravel biological roots of pulmonary hypertension


    • HYPERTHERMIA
  • MALIGNANT
      ◊ Type 1 ryanodine receptor (RYR1)


    • Hypodontia(oligodontia) second premolars and third molars