"MAN on FIRE”

PATHOGENESIS
  ◊Man on Fire” Syndrome, Ion Channels, and the Quest for Safer Pain Treatments

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

MAMMARY GLAND

CANCEROGENESIS
  ◊Fetal Mammary Gland Development and Offspring’s Breast Cancer Risk in Adulthood

MARFAN SYNDROME

CARDIOVASCULAR MANIFESTATIONS
  ◊ Multiple genes

MAYER–ROKITANSKY–KUSTER–HAUSER СИНДРОМ

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

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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

ORGANELLE STRESS RESPONSES TO PATHOLOGY
  ◊ Mitochondrial diseases: the contribution of organelle stress responses to pathology 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
  ◊EBV induces CNS homing of B cells attracting inflammatory T cells

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