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Results 1661 - 1670 of 1730 for Acquired mutation
  • Causes of PKU
    Health - 31 May 2019
    PKU or Phenylketonuria is a genetically inherited condition.PKU occurs due to the lack of an enzyme called phenylalanine hydroxylase. This enzyme is a protein. Consequently, it is synthesized based on...
  • Exploring Epigenetics in Cancer
    White Paper - 11 Mar 2019
    Epigenetic modifications are changes in the chromatin structure and they can alter the accessibility of DNA, influencing gene expression.
  • Onychogryphosis - Ram's Horn Nails
    Health - 27 Feb 2019
    Some people have an overgrown nail on the great toe which can actually begin to curl as it continues to grow without being clipped. Also known as “Ram’s Horn Nails” because of the way it looks,...
  • Lipodystrophy Treatment
    Health - 26 Feb 2019
    Lipodystrophy is a term used to describe a collection of metabolic conditions that disrupt fat storage.
  • Hemolytic Uremic Syndrome: Investigation and Diagnosis
    Health - 26 Feb 2019
    Hemolytic uremic syndrome (HUS) usually occurs in children following an episode of diarrheal infection caused by STEC strain O157:H7, and occasionally following infection with Shigella dysenterieae or...
  • What is the Expanded Genetic Code?
    Life Sciences - 26 Feb 2019
    There are 20 canonical amino acids that are encoded by the genetic code of nearly all known organisms - there are only very few exceptions. In order to add novel building blocks to this existing...
  • Epidermolysis Bullosa Diagnosis
    Health - 26 Feb 2019
    The four main types of epidermolysis bullosa (EB): dystrophic epidermolysis bullosa (DEB), epidermolysis bullosa simplex (EBS), junctional epidermolysis bullosa (JEB) and Kindler syndrome (KS) are...
  • Lichen Striatus (LS) / Linear Lichenoid Dermatosis
    Health - 26 Feb 2019
    Lichen striatus (LS), also known as Blaschko linear acquired inflammatory skin eruption, or linear lichenoid dermatosis, is a benign, rare and self-limiting inflammatory skin condition.
  • Factor H Autoantibodies
    Health - 26 Feb 2019
    Factor H is a soluble complementary glycoprotein present in the blood plasma that serves the primary function of controlling the alternative pathway in blood and maintaining homeostasis. In vitro...
  • CRISPR-Cpf1
    Life Sciences - 26 Feb 2019
    In 2015, scientists at MIT and Harvard identified a novel gene editing system called CRISPR-Cpf1, which was simpler and smaller in size than CRISPR-Cas9.

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