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  2. Histidinemia - Wikipedia

    en.wikipedia.org/wiki/Histidinemia

    A typical characteristic of histidinemia is an increase in the blood histidine levels from normal levels (70–120 μM) to an elevated level (290–1420 μM). [3] Further testing includes: observing histidine as well as imidazolepyruvic acid metabolites in the urine. However, neonatal urine testing has been discontinued in most places, with the ...

  3. Histidine - Wikipedia

    en.wikipedia.org/wiki/Histidine

    Histidine ball and stick model spinning. Histidine (symbol His or H) [2] is an essential amino acid that is used in the biosynthesis of proteins.It contains an α-amino group (which is in the protonated –NH 3 + form under biological conditions), a carboxylic acid group (which is in the deprotonated –COO − form under biological conditions), and an imidazole side chain (which is partially ...

  4. Carnosinemia - Wikipedia

    en.wikipedia.org/wiki/Carnosinemia

    Carnosine is a dipeptide composed of beta-alanine and histidine, and is found in skeletal muscle and cells of the nervous system. [6] This disorder results in an excess of carnosine in the urine , cerebrospinal fluid , blood , and nervous tissue . [ 7 ]

  5. Histamine - Wikipedia

    en.wikipedia.org/wiki/Histamine

    Since human blood is slightly basic (with a normal pH range of 7.35 to 7.45) therefore the predominant form of histamine present in human blood is monoprotic at the aliphatic nitrogen. Histamine is a monoamine neurotransmitter .

  6. Signs of multiple sclerosis can be detected in blood 5 years ...

    www.aol.com/lifestyle/signs-multiple-sclerosis...

    A new study found that in about 10% cases of multiple sclerosis, the body begins producing a distinctive set of antibodies against its own proteins years before symptoms emerge. “Multiple ...

  7. Hemoglobin M disease - Wikipedia

    en.wikipedia.org/wiki/Hemoglobin_M_disease

    Hemoglobin M disease is a rare form of hemoglobinopathy, characterized by the presence of hemoglobin M (HbM) and elevated methemoglobin (metHb) level in blood. [1] HbM is an altered form of hemoglobin (Hb) due to point mutation occurring in globin-encoding genes, mostly involving tyrosine substitution for proximal (F8) or distal (E7) histidine residues. [2]

  8. Pope Francis in hospital: How to reduce the chances of ... - AOL

    www.aol.com/reduce-chance-contracting-pneumonia...

    The treatment depends on the type of organism involved. Common causes of bacterial pneumonia include Mycoplasma pneumoniae and Streptococcus pneumoniae . These would be treated with antibiotics.

  9. HFE H63D gene mutation - Wikipedia

    en.wikipedia.org/wiki/HFE_H63D_gene_mutation

    HFE. The HFE H63D is a single-nucleotide polymorphism in the HFE gene (c.187C>G, rs1799945), which results in the substitution of a histidine for an aspartic acid at amino acid position 63 of the HFE protein (p.His63Asp).