A team of scientists from Sweden and India has recently conducted a study to evaluate type I interferon (IFN-I) responses in cells infected with severe
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Newborns who are diagnosed with phenylalanine hydroxylase deficiency may show no initial symptoms or signs. Over time they may develop symptoms of phenylalanine build-up in
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Hypotonia or weakness of muscles and lack of muscle tone is a symptom of an underlying condition rather than a disease entity in itself. Therapy
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Histone deacetylases are enzymes involved in the modification of histones in order to allow DNA to wrap around them tightly. The enzymes achieve this through
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Hepatitis B virus (HBV) is a common cause for liver disease and accounts for approximately one million deaths worldwide every year. This virus is of
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Sleep is essential for physical and mental health. Approximately 8 hours of sleep is adequate to feel good and to function optimally for most people.
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NOTICE: This Consumer Medicine Information (CMI) is intended for persons living in Australia. ZIAGEN TABLETS 300 mg tablets Abacavir (as sulfate) Consumer Medicine Information PATIENTS
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There are many different types of Charcot-Marie-Tooth disease (CMT), which are classified according to the gene mutation that causes the disease. The main types (CMT1,
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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.
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Micromanipulation uses microsurgical techniques to study and alter the structure or composition of single living cells or a group of cells under a microscope. It
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