СИНДРОМЫ.
НАСЛЕДСТВЕННЫЕ БОЛЕЗНИ

C



CANCER
  • MAMMARY
      ◊Mammary
  • COLON
      ◊DNA repair defects

      ◊Non-Canonical Hedgehog Signaling Is Required for the Survival of Colon Cancer Stem Cells
  • BREAST CANCER
      ◊Risk
       •Apicobasal Polarization
      ◊Specific gene repositioning
  • GENETIC AND EPIGENETIC ALTERATIONS
      ◊ Genetic and Epigenetic Alterations in Cancer

      ◊ Epigenetic Changes Drive Cancer
  • GENES EMBRYONIC CELLS
      ◊ The Developmental Origins of Cancer: Role of the Genes Expressed in Embryonic Cells with Implications for Tumorigenesis
  • LUNG CANCER
      ◊Role of Estrogens in Pathogenesis, Progression and Therapy of Lung Cancer
  • MALES CANCERS
      ◊ X Chromosome Silenced in Some Cancers in Males
  • OROPHARYNGEAL
      ◊Human papilloma viruses
  • PROSTATE
      ◊Androgen receptor & cell cycle
      ◊Molecular genetics
      ◊developmental epigenomic programs during metastatic progression


    • CANCEROGENESIS
  • ENDOMETRIAL
      ◊Hypomethylation-linked activation of PAX2
  • ROLE
      ◊How cancer hijacks the nervous system to grow and spread
  • role of EMSY
  • Antagonists XIAP
  • Cancer Cells Spread When They Stop Recycling Waste
  • TETRAPLOIDY
      ◊role of tetraploidy


    • CARDIAC HYPERTROPHY
  • MECHANISMS
      ◊Signalling Pathways


    • CARDIOVASCULAR DISEASES
  • CARDIO-FACIO-CUTANEOUS SYNDROME
      ◊ Tooth anomaly
  • CARDIOMYOPATHY
      ◊ Desmoplakin mutations
      ◊ δ-sarcoglycan deficiency
  • CHEMOKINES
      ◊Targets in atherosclerosis
  • MicroRNA
      ◊MicroRNA therapeutics
  • MUTATIONS
      ◊Cardiovascular connexin genes
  • HIGH-DENSITY LIPOPROTEIN
      ◊Molecular mechanisms
  • SYNDROMIC CONGENITAL CARDIOVASCULAR DISEASE
      ◊ syndromic congenital cardiovascular disease and LPM. Descendant lineages


    • CATARACTS
  • GENETICS
      ◊Genetics of human cataract
      ◊DOMINANT CONGENITAL
       •Connexin mutation


    • CATCH22.Группа синдомов
    Cell CardioMyocite Plastics
    CEREBRAL SMALL-VESSEL DISEASE
  • Mechanisms


    • CHANNELOPATHY
  • Mechanisms


    • Chlamidiosis
    Chordoma
    CHARCOT-MARIE-TOOTH NEUROPATHY
  • AXONAL TRANSPORT DEFICITS Aberrant GlyRS-HDAC6 interaction


    • CHOLESTEROL METABOLISM DEFECTS
  • EFFECTS ON DEVELOPMENT
      ◊ Activation of WNT signaling restores the facial deficits
      ◊ Medication effects on developmental sterol biosynthesis


    • CHONDRODYSPLASIA
  • Endoplasmic reticulum stress


    • CHRONIC GRANULOMATOUS DISEASE

  •   ◊ Genetics


    • CHRONIC OBSTRUCTIVE PULMONARY DISEASE (COPD)

  •   ◊ genetics
      ◊ Blockade of RAGE ameliorates


    • CILIOPATHY
  • Cell biological basis
  • PRIMARY CILIARY DYSKINESIA
      ◊ Mutations in CCDC114
  • GENETIC CONTROL
      ◊Role of KIF14
      ◊Role of Odal6/Wdr69
      ◊A CRISPR-based screen for Hedgehog signaling provides insights into ciliary function and ciliopathies


    • Clonal Desease
    COHESINOPATHY
  • COHESIN IN DEVELOPMENT AND DISEASE
      ◊ Mechnisms
    • COLOBOMA OCULAR
  • An update on the genetics of ocular coloboma


    • COLORECTAL ADENOMATOUS POLYPOSIS
  • Gene MYH


    • COLORECTAL CANCER
  • RESEARCH PROGRESS
      ◊ Tumor-suppressive roles of miR-487b in colorectal cancer
      ◊ Wnt/β-catenin signaling pathway in colorectal cancer


    • Complex III deficit
    CONGENITAL MUSCULAR DYSTROPHY
  • GENETIC
      ◊ Mutations in INPP5K
    • CONNEXINOPATHIES
  • STRUCTURAL AND FUNCTIONAL GLIMPSE
      ◊ Human genetic disease


    • СONGENITAL INSENSITIVITY TO PAIN
  • WITH ANHIDROSIS (CIPA)
      ◊Nerve growth factor


    • СONGENITAL HEART MALFORMATION
  • Description Developmental screening and assessment in congenital heart disease of neural Defects
  • GENETIC FACTORS
      ◊ Genetic factors
      ◊ Using Patient-Derived Induced Pluripotent Stem Cells (iPSCs)
      ◊ hiPSCs in predictive modeling of heart development and disease

  • Exome Sequencing
  • MUTATIONS
      ◊ de novo variants mutations
      ◊ SORBS2 is a genetic factor contributing to 4q deletion syndrome
      ◊ A Non-coding HES1 Variant Predisposes Children to Congenital Heart Disease
  • ROLE FOLIC ACID
      ◊ role Folic acid
      ◊ Role Folate, Homocysteine and the Cardiac Neural Crest


    • CONDUCTION SYSTEM ERRORS
  • role Nkx2-5


    • COORDINATION DISORDER in CHILDREN
  • Advances in Genetics and Epigenetics of Developmental Coordination Disorder in Children


    • CORNELIA DE LANGE SYNDROME (CdLS)
  • Mutations


    • CORNEAL
  • DYSTROPHY
      ◊ Genetics


    • СORONARY ARTERY DISEASE (coronary heart disease)
  • GENETIC SUSCEPTIBILITY
      ◊Genome-wide approaches
  • role MEF2A
  • RISK FACTORS
      ◊ Biomarkers
      ◊ Lipoprotein-associated phospholipase A2
      ◊ carbohydrates

    • COVID-19
  • GENE THERAPY
      ◊CRISPR/Cas9 gene editing technology

  • VACCINES
      ◊Development of Next Generation Vaccines against SARS-CoV-2 and Variants of Concern

    • Сranio-Сerebello-Сardiac synd.(3C)
    Crohn disease
    CTAF
    CMT2A
    CMTX
    CP Ventricular Tachycardia
    Craniosynostosis (Boston type)

    CUSHING
  • PITUITARY ACTH
      ◊ Genetics


    • CYSTIC KIDNEY DISEASES
  • CYSTIC KIDNEY AND LIVER DISORDERS
      ◊ Polycystin-1 is a key player
  • PLANAR CELL POLARITY
      ◊ Genetics


    • CYSTIC FIBROSIS
  • CFTR genetics
  • Description
  • Therapy
  • Ferreting Out the Causes of Cystic Fibrosis