СИНДРОМЫ.
НАСЛЕДСТВЕННЫЕ БОЛЕЗНИ


R

RAB8-Diseases

RASOPATHIES
  • RAS MUTATIONS
      ◊ Genetics
  • RAS/MAPK SIGNALING
      ◊RASopathies - what they reveal about RAS/MAPK signaling in skeletal muscle development
    • Approaches to Therapy

    REPRODUCTIVE DISORDERS
  • FEMALE
      ◊ Invisible Hand behind Female Reproductive Disorders: Bisphenols
    • RETINAL ANOMALIES
  • AGE-RELATED MACULAR DEGENERATION
      ◊ Genetics
  • RETINOPATHIES
      ◊ CRX-associated
      ◊ Retinopathy of Prematurity With Low Levels of Arachidonic Acid
      ◊ Identification and Analysis of Genes Associated with Inherited Retinal Diseases
      ◊ Nuclear Receptor Subfamily 2 Group E Member 3 (NR2E3): Role in Retinal Development and Disease

    •   ◊     Hypomorphic variants in inherited retinal and ocular diseases

    RETINITIS PIGMENTOSA
  • GENETICS
      ◊     Alternative splicing
      ◊ Retinitis Pigmentosa
      ◊ Genes and mutations
      ◊ Genes variants
      ◊ Gen WDR19


    • RETINOSCHISIS
  • X-LINKED JUVENILE RETINOSCHISISCRISPR-CAS9
      ◊ Carboxylated nanodiamond-mediated CRISPR-Cas9 delivery of human retinoschisis mutation into human iPSCs and mouse retina RETT SYNDROME
  • ORTHOPAEDIC CONDITIONS
      ◊Prevalence of orthopaedic conditions in Rett syndrome
    • RHEUMATOID ARTRITIS
  • DESCRIPTION
      ◊Description
      ◊Single-cell RNA-seq of rheumatoid arthritis synovial tissue
  • MUTATIONS
      ◊ Mutations ZAP-70

    • Ritscher-Schinzel 3C(cranio-cerebello-cardiac)синдром
    Rolin sequence