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Elevated level of AMMONIA in the blood. It is a sign of defective CATABOLISM of AMINO ACIDS or ammonia to UREA.

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Individual Studies
  • Identifying targets of MeCP2 during neuronal maturational differentiation

    Homo sapiens Homo sapiens | RNA Expression   RNA Expression

    To control MeCP2 expression and deficiency during neuronal maturation, SH-SY5Y cells were transfected with methylated MeCP2 oligonucleotide decoy to disrupt the binding of MeCP2 to endogenous targets.

    Authors: Peddada Sailaja, Yasui H Dag, LaSalle M Janine

    Organization: University of California, Davis Medical …

  • Mouse Phenotypes - Autosomal recessive hereditary disorder

    Mus musculus Mus musculus | Mutations/Phenotypic   Mutations/Phenotypic

    This study contains curated mouse gene mutation data extracted from the Mouse Genome Database (MGD) at The Jackson Laboratory, Bar Harbor, Maine. Additional computational processing and curation of mouse phenotype data was performed to further organize and group data from related phenotypes into uni…

    Source: NextBio Library/Mutation and Phenotypic data

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Thought leaders and organizations working on research involving hyperammonemia.

  • Vicente Felipo
  • Omar Cauli
  • Regina Rodrigo
  • Pilar Monfort
  • Marta Llansola
  • Hyperion Therapeutics, Inc.
  • National Center for Research Resources (NCRR)
  • Children's Mercy Hospital Kansas City
  • Children's Research Institute
  • University of Utah
  • Centro de Investigacion Principe Felipe
  • Laboratory of Neurobiology
  • Centro de Investigación Príncipe Felipe
  • Boston University School of Medicine
  • Duke University Medical Center

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