-
trisomy Xq25 X
fragile site
folic acid type
Xanthic urolithiasis Xanthine oxydase deficiency Xanthinuria Xanthomatosis cerebrotendinous Xerocytosis, hereditary...
-
Monoamine oxidases (MAO) (EC 1.4.3.4) are a
family of
enzymes that
catalyze the
oxidation of monoamines,
employing oxygen to clip off
their amine group...
- Xanthinuria, also
known as
xanthine oxidase deficiency, is a rare
genetic disorder causing the ac****ulation of xanthine. It is
caused by a
deficiency of...
-
analysis of
Crested Serpent Eagle (Spilornis cheela)
based on cytochrome-c
oxydase subunit I (COI): a
stepping stone towards genetic conservation of raptors...
- 1016/0005-2744(68)90102-2. PMID 4295160.
Thoai NV,
Olomucki A (1962). "Arginine decarboxy-
oxydase. I.
Caracteres et
nature de l'enzyme". Biochim. Biophys. Acta. 59 (3):...
-
Sugarman syndrome Sulfatidosis juvenile,
Austin type
Sulfite and
xanthine oxydase deficiency Sulfite oxidase deficiency Summitt syndrome Superior mesenteric...
- Christian, W. (1938). "Isolation of the
prosthetic group of the
amino acid
oxydase".
Biochemische Zeitschrift. 298: 150–68. Christie, S. M. H.; Kenner, G...
-
pigment in
terms of
chromogen (genes were
responsible for the chromogen) and
oxydase (enzyme). John
Cairns as
recently as 2003
credited Lucien Cuénot with the...
-
collected at
Bouharoune off the
Algerian coast. The
analysis of the
cytochrome oxydase 1 gene of
Microcotyle visa
revealed only
minor intraspecific variation...
- DNA
barcode markers to
identify diets are the
mitochondrial cytochrome C
oxydase (COI) and
cytochrome b (cytb). When the diet is
broad and diverse, DNA...
