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MACULAR DEGENERATION
  • PATHOGENESIS
      ◊cGAS drives noncanonical-inflammasome activation in macular degeneration
      ◊ Cell Transplantation Attenuates Müller Glial Reactivity

    • MALARIA Resistens
    MALFORMATION
  • VASCULAR
      ◊ genetics

    • MABRY SYNDROME
  • CAUSES
      ◊ Mabry Syndrome (MIM 239300) Index Cases and Glycophosphatidylinositol (GPI) Disorders

    • MARFAN SYNDROME
  • CARDIOVASCULAR MANIFESTATIONS
      ◊ Multiple genes

    • MAYER�ROKITANSKY�KUSTER�HAUSER �������
  • GENE CANDIDATE
      ◊ GREB1L as a candidate gene of Mayer�Rokitansky�Küster�Hauser Syndrome
  • PROTEIN�PROTEIN INTERACTION NETWORK
      ◊ DNA copy number profiling suggests new perspectives on the aetiology of Mayer�Rokitansky�Kuster�Hauser syndrome

    • MEDICINE
  • Home Handbook of Medicine and Health


    • MEDULLOBLASTOMA
  • CAUSES Failure of human rhombic lip differentiation underlies medulloblastoma formation


    • MEGACYSTIS-MICROCOLON-INTESTINAL HYPOPERISTALSIS SYNDROME
  • MUTATIONS Mutations in the Smooth Muscle Actin (ACTG2)


    • MEIER-GORLIN SYNDROME
  • GENETICS
      ◊ Mutations in origin recognition complex gene ORC4

    • MELANOMA
  • NOCICEPTOR NEURONS
      ◊ Nociceptor neurons affect cancer immunosurveillance
  • SINGLE-CELL ANALYSIS OF A MUTANT
      ◊ Mutant library generated using CRISPR-guided deaminase in human melanoma cells

    • MENKES DISEASE
  • GENETICS
      ◊Menkes Disease and Other Disorders Related to ATP7A
    • MENTAL RETARDATION
  • GENETICS
      ◊ Role of Noncoding RNAs
      ◊ Role de novo mutations

    • METABOLIC SYNDROME
  • Genetics
      ◊ AMP kinase and Malonyl-CoA   ◊ Using developmental biology to gain insight into human metabolic diseases

    • METASTASIS
  • CELL MOTILITY
      ◊ RSK2 drives cell motility

    • MICROCEPHALY
  • GENETIC CONTROL
      ◊ Condensin complex proteins cause microcephaly
  • HAPLOINSUFFICIENCY
      ◊ Haploinsufficiency for Core Exon Junction Complex Components

    • MICROGLIAIA
  • SIGNATURES
      ◊ Microglia Signatures: A Cause or Consequence of Microglia-Related Brain Disorders?

    • MICROPHTHALMIA
  • Genetics
      ◊ Mutation SIX6

    • MIGRAINE
  • with Aura
      ◊ Susceptibility: C677T of MTHFR
  • Origin, therapy
  • Susceptibility


    • MITOCHONDRIAL DISEASE
  • ANTIOXIDANTS Oxidative stress in pre-clinical models of mitochondrial complex I disease
  • LIPID PROCESSING IN ENTEROCYTES Mitochondrial dysfunction abrogates dietary lipid processing in enterocytes
  • MITOCHONDRIAL NEUROGASTROINTESTINAL ENCEPHALOPATHY (MNGIE) Gastrointestinal Dysmotility in MNGIE from thymidine phosphorylase enzyme deficiency
  • ORGANELLE STRESS RESPONSES TO PATHOLOGY
      ◊ Mitochondrial diseases: the contribution of organelle stress responses to pathology
  • PRO-MITOCHONDRIAL FUSION PROTEIN MSTO1 is a cytoplasmic pro-mitochondrial fusion protein, whose mutation induces myopathy and ataxia in humans


    • MITRAL VALVE PROLAPSE
  • Linkage


    • Moebius synd
    Misfolding proteins Deseases

    Motor Neuron Degeneration 2
  • role of Omi


    • MUCOVISCIDOSIS
  • CFTR genetics
  • Description
  • Therapy


    • MULTIPLE DISEASES
  • MUTATIONS of GENE XPD HELICASE
      ◊ ◊Mechanisms


    • MULTIPLE SCLEROSIS
  • Description
  • Antibody to Lipids
  • DIAGNOSIS
      ◊Tear fluid: new biomarkers
  • GENETIC CONTROL
      ◊Candidate genes

    •   ◊Role acid-sensing ion channel-1 (ASIC1)
      ◊LncRNA GAS5 inhibits microglial M2 polarization and exacerbates demyelination
      ◊Expression of the Factor TOX Promotes the Encephalitogenic Potential of Microbe-Induced Autoreactive CD8 T Cells.
  • IMMUNE CELLS
      ◊Tracking Down Innate Immune Cells in Multiple Sclerosis


    • MUSCULAR DYSTROPHIES
  • MECHANISMS
      ◊ Molecular mechanisms
      ◊ Fibrotic skeletal muscle extracellular matrix
  • CONGENITAL MUSCULAR DYSTROPHIES
      ◊ α-dystroglycan glycosylation defects


    • MYELOPROLIFERATIVE GROUP of DISORDERS
  • Mutation JAK2 V617F


    • MYOPATHIES CONGENITAL
  • ACTIN-RELATED
      ◊ Rescue of skeletal muscle α-actin-null mice
  • DESMIN-RELATED
      ◊ Description
  • INFLAMMATION MYOPATHIES
      ◊ muscle inflammation upon Opa1 deficiency




    • MYELODYSPLASIAS
  • SPLICEOSOME
      ◊ Insights from Spliceosome Structures
    • MYELOID LEUKAEMIA
  • ACUTE MYELOID LEUKAEMIA
      ◊ Promoter-bound METTL3 maintains myeloid leukaemia
    • MYOPIA
  • GENETIC CONTROL
      ◊ Meta-analysis highlights light-induced signaling as a driver for refractive error
    • MYOTONIC DYSTROPHY
  • SUBTYPES
      ◊ Distinct pathological signatures in human cellular models of myotonic dystrophy