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29 results
  • TEM gut cell undergoing secondary necrosis
  • Nesidioblastosis in the neonatal pancreas
  • Normal bone, SEM
  • Type I diabetes, islets of Langerhans glucagon secretion
  • Human bronchus, normal. SEM
  • Detecting colon cancer in human tissues, LM
  • Normal gut cell
  • Somatostatin secretion in pancreas islets
  • Foetal cells in amniotic fluid, + colchicine
  • TWM of gut cell undergoing necrosis
  • Development of islet cells from pancreatic ducts
  • Detecting cancer in human tissues, LM
  • Gut cells undergoing apoptosis
  • Alpha cells secreting glucagon, human pancreas
  • Duchenne muscular dystrophy - normal female, chromosomes have been highlighted by a fluorescent probe for exon 45/47 (note the double yellow band). This disorder is caused by a recessive gene on the X chromosome, so is normally shown only by males, who lack a second X chromosome. The condition starts with difficulty in walking and climbing stairs in early childhood, usually resulting in confinement to a wheelchair by the age of 10, with death from respiratory infection or cardiac failure by about the age of 20.
  • Normal female 46,XX human karyotype
  • SEM bronchial surface of healthy lung
  • TEM Gut cell undergoing apoptosis, with capped chromatin
  • Mother with baby, Zambia
  • Normal human male metaphase, Y banding
  • Formation of islets from ductal cells in foetal pancreas
  • Secretion of pancreatic polypeptide in human pancreas
  • Foetal cells in amniotic fluid, low power LM
  • 3D-printed reconstruction of a healthy adult human brain
  • Beta cells secreting insulin in human pancreas
  • SEM normal bone above trabecular surface
  • Bronchus, normal. SEM
  • Normal male 46,XY human karyotype
  • Insulin secretion in islets of Langerhans, pancreas