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  2. Hypermethioninemia - Wikipedia

    en.wikipedia.org/wiki/Hypermethioninemia

    People with hypermethioninemia often do not show any symptoms. Some individuals with hypermethioninemia exhibit learning disabilities, mental retardation, and other neurological problems; delays in motor skills such as standing or walking; sluggishness; muscle weakness; liver problems; unusual facial features; and their breath, sweat, or urine may have a smell resembling boiled cabbage.

  3. Methionine - Wikipedia

    en.wikipedia.org/wiki/Methionine

    Methionine (symbol Met or M) [3] (/ m ɪ ˈ θ aɪ ə n iː n /) [4] is an essential amino acid in humans.. As the precursor of other non-essential amino acids such as cysteine and taurine, versatile compounds such as SAM-e, and the important antioxidant glutathione, methionine plays a critical role in the metabolism and health of many species, including humans.

  4. Methionine gamma-lyase - Wikipedia

    en.wikipedia.org/wiki/Methionine_gamma-lyase

    Trifluoromethionine (TFM) is a fluorinated methionine prodrug, which only presents its toxicity after degradation by MGL. Studies show that TFM is toxic to and slows the growth of anaerobic microorganisms (Mycobacterium smegmatis, Mycobacterium phlei, Candida lipolytica) , periodontal bacteria (P. gingivalis, F. nucleatum) , and parasitic ...

  5. Mercury poisoning - Wikipedia

    en.wikipedia.org/wiki/Mercury_poisoning

    Mercury poisoning is a type of metal poisoning due to exposure to mercury. [3] Symptoms depend upon the type, dose, method, and duration of exposure. [3] [4] They may include muscle weakness, poor coordination, numbness in the hands and feet, skin rashes, anxiety, memory problems, trouble speaking, trouble hearing, or trouble seeing. [1]

  6. Homocystinuria - Wikipedia

    en.wikipedia.org/wiki/Homocystinuria

    Homocystinuria (HCU) [2] is an inherited disorder of the metabolism of the amino acid methionine due to a deficiency of cystathionine beta synthase or methionine synthase. [3] It is an inherited autosomal recessive trait, which means a child needs to inherit a copy of the defective gene from both parents to be affected.

  7. This is the best time of day to take vitamin D supplements ...

    www.aol.com/news/best-time-day-vitamin-d...

    In rare cases, vitamin D can reach toxic levels. This can increase calcium absorption, leading to abnormally high levels of calcium in the blood, Zumpano notes. Symptoms of vitamin D toxicity include:

  8. S-Adenosyl methionine - Wikipedia

    en.wikipedia.org/wiki/S-Adenosyl_methionine

    The sulfonium functional group present in S-adenosyl methionine is the center of its peculiar reactivity. Depending on the enzyme, S-adenosyl methionine can be converted into one of three products: adenosyl radical, which converts to deoxyadenosine (AdO): classic rSAM reaction, also cogenerates methionine

  9. What is ‘Disease X’ and why are experts worried? - AOL

    www.aol.com/disease-x-why-experts-worried...

    Health authorities around the world are still grappling with lessons learned at the start of the Covid-19 pandemic and trying to determine the best way to prevent a new one.. Many researchers have ...