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mutations in the phenylalanine hydroxylase ( PAH ) gene , characterized by intellectual deficit and neuropsychiatric complications in untreated patients with estimated frequency of about one in 10,000 to 15,000 live births(passive) caused byamino acid metabolism
deficiency of the mitochondrial branched - chain alpha - ketoacid dehydrogenase complex ( BCKDC ) resulting in the accumulation of branched - chain amino acids ( BCAA ) ( isoleucine , leucine , and valine(passive) caused byamino acid metabolism
a deficiency of liver specific argininosuccinate synthetase activity(passive) caused byamino acid metabolism
deficiency of the enzyme phenylalanine hydroxylase ( PAH(passive) caused byamino acid metabolism
phenylalanine hydroxylase ( pah ) deficiency dietary treatment(passive) caused byamino acid metabolism
the progression of liver diseasesinfluenceamino acid metabolism
MSUD)- Definition , Causes , and Treatment DiseasesDic Genetic Disorders , M 6 Comments Maple syrup urine disease ( MSUD ... in whichcausesirregular amino acid metabolism
phenylalanine hydroxylase ( pah ) deficiency due to the difficulties in adhering to diet therapy in the treatment of pku(passive) caused byamino acid metabolism
a defect in the glycine cleavage multienzyme complex resulting in high concentrations of glycine within the brain and spinal cord(passive) caused byamino acid metabolism
deficiency of histidase activity in liver and skin with consequent accumulation of histidine in plasma and tissues(passive) caused bymetabolism of amino acids
From a functional point of view , the infection seemsto have influencedthe amino acids metabolism
Glycine loadinginfluencedintermediate amino acid metabolism
TTA and fish oilmay influenceamino acid metabolism
increased 2-aminobutyric acid - ophtalmate compensatory pathway activationoriginatedfrom amino acids metabolism
Cd treatment(passive) influenced byamino acids metabolism
the level of ammonia increases in the bloodleadsto amino acid metabolism
6-azauridine(passive) caused byamino acid metabolism
conditionsinfluencethe amino acid metabolism
the acidosisresultingfrom the metabolism of amino acids
hyperammonaemiaresultingfrom amino acids metabolism
pathways from acetyl - CoAleadingto amino acid metabolism
gut - derived microbial metabolitesresultingfrom metabolism of amino acids
long - term lysine restrictioninfluencedamino acid metabolism
the higher acid levelsresultfrom amino acid metabolism
Molybdenumcontributesto normal amino - acid metabolism
a variety of factors , which can be investigated directly at the amino acid level or at the related metabolite level in the corresponding amino acid pathway(passive) is therefore influenced byAmino acid metabolism
also(passive) was ... influencedAmino acid metabolism
the action of the alleles at these loci(passive) is apparently influenced byAmino acid metabolism
blood flowinfluencedHQ amino acid metabolism
As steroid hormones are knownto influenceamino acid metabolism
the deficiency of argininiosuccinate synthase ( ASS1 ) , which performs the third enzymatic step in the urea cycle , condensing citrulline and aspartic acid to form argininosuccinic acid(passive) caused byamino acid metabolism
Select itemcontributes2393373316.Impaired amino acid metabolism
the kidneycontributingto amino acid metabolism
N lossresultingfrom amino acid metabolism
a deficiency of propionyl - CoA carboxylase(1–3(passive) caused byamino acid metabolism
deficient activity of propionyl coenzyme A carboxylase(passive) caused byamino acid metabolism
E. acervulina infection extended beyond reduced amino acid digestibility(passive) caused byamino acid metabolism
that contained 10 μg / ml antimycin Ato preventoxidative metabolism of amino acids
BCKD ) enzymecausesirregular amino acid metabolism
Academic Service ziassignmentpbbf.sgoods4.me Physiological statesinfluencethe body 's amino acid metabolism
in severe mental retardation if not treated early and appropriatelyresultsin severe mental retardation if not treated early and appropriately
from a defect in the enzyme HOMOGENTISATE 1,2-DIOXYGENASE , an enzyme involved in the breakdown of PHENYLALANINE and TYROSINEresultingfrom a defect in the enzyme HOMOGENTISATE 1,2-DIOXYGENASE , an enzyme involved in the breakdown of PHENYLALANINE and TYROSINE
specific labelling of amino acids that would be useful in multidimensional NMR spectroscopypreventingspecific labelling of amino acids that would be useful in multidimensional NMR spectroscopy
as a result of deficiency in phenylalanine hydroxylase , an enzyme that converts phenylalanine to tyrosinecausedas a result of deficiency in phenylalanine hydroxylase , an enzyme that converts phenylalanine to tyrosine
in the build - up of phenylalanine in the bloodresultsin the build - up of phenylalanine in the blood
in an excess of phenylalanine ( Phe ) in the brain and plasmaresultsin an excess of phenylalanine ( Phe ) in the brain and plasma
in most patients from phenylalanine hydroxylase ( PAH ) deficiencyresultsin most patients from phenylalanine hydroxylase ( PAH ) deficiency
from a deficiency in the liver enzyme phenylalanine hydroxylase ( PAHresultingfrom a deficiency in the liver enzyme phenylalanine hydroxylase ( PAH
in decreased metabolism of the amino acid phenylalanine due to the deficiency of enzyme , phenylalanine hydroxylaseresultsin decreased metabolism of the amino acid phenylalanine due to the deficiency of enzyme , phenylalanine hydroxylase
to the consumption of oxygencan ... contributeto the consumption of oxygen
from the digestion of dietary protein and glucose resulting from the digestion of carbohydrateresultingfrom the digestion of dietary protein and glucose resulting from the digestion of carbohydrate
an excess of methylmalonic acid in the urine and bloodcausingan excess of methylmalonic acid in the urine and blood
from defects either in the synthesis of or the breakdown of amino acids or in the body s ability to get the amino acids into cellsresultfrom defects either in the synthesis of or the breakdown of amino acids or in the body s ability to get the amino acids into cells
to elevated ATP and protein levelsleadingto elevated ATP and protein levels
to increased ammonia / by - product productionleadingto increased ammonia / by - product production
to elevated levels of glutamate , histamine , and nitrate as well as elevated ammonia ( from nitrate ) , which , due to enzyme deficienciesleadsto elevated levels of glutamate , histamine , and nitrate as well as elevated ammonia ( from nitrate ) , which , due to enzyme deficiencies
to alterations of biology and function of the vascular wall , anorexia and endocrine dysfunctionpotentially leadingto alterations of biology and function of the vascular wall , anorexia and endocrine dysfunction
to mobilization of both C and N resources and recycling of cell wall componentsleadsto mobilization of both C and N resources and recycling of cell wall components
a hereditary disease(passive) is caused bya hereditary disease
from a significant increase in the content of essential amino acidsresultingfrom a significant increase in the content of essential amino acids
in partial oxidationresultingin partial oxidation
macrophage responses by generating catabolites with immunomodulatory propertiescan influencemacrophage responses by generating catabolites with immunomodulatory properties
the activity of the enzymes involved in it via structural analogy to the particular carboxylic acids or by the transition state imitationinfluencingthe activity of the enzymes involved in it via structural analogy to the particular carboxylic acids or by the transition state imitation
to protein formationleadsto protein formation
to toxic elevations of one or more amino acids that can have significant neurodevelopmental impairment as a consequenceleadingto toxic elevations of one or more amino acids that can have significant neurodevelopmental impairment as a consequence
to substantial amounts of biogenic amines in either spontaneously fermented or spoiled foodsmay leadto substantial amounts of biogenic amines in either spontaneously fermented or spoiled foods
to glutathione biosynthesisleadingto glutathione biosynthesis
to decreased pyruvate formation via catalysis of aminotransferasesleadsto decreased pyruvate formation via catalysis of aminotransferases
in low levels of branched chain amino acids such as leucine , isoleucine and valineresultingin low levels of branched chain amino acids such as leucine , isoleucine and valine
elevated amounts of homocysteine in the bloodcauseselevated amounts of homocysteine in the blood
alsomight ... influencealso
hypoglycemia result in organic acidemias with an anion gapcausinghypoglycemia result in organic acidemias with an anion gap
to collagen synthesis through proline and hydroxyproline.8 Metabolomicsleadingto collagen synthesis through proline and hydroxyproline.8 Metabolomics
to our understanding of normal metabolic processeshas ... contributedto our understanding of normal metabolic processes
in an increased mobilization from skeletal muscle protein [ 23–25resultingin an increased mobilization from skeletal muscle protein [ 23–25
in worsening of encephalopathy ( ammoniacan resultin worsening of encephalopathy ( ammonia
other amino acid species(passive) caused byother amino acid species
the excessive water lossalso preventsthe excessive water loss
a high ATP production in the pancreatic tissue that may cause mitochondrial initiation of cell deathcausesa high ATP production in the pancreatic tissue that may cause mitochondrial initiation of cell death
to increased BUN levels , which negatively affect both your kidneys and your liver " , Evidence pleaseleadsto increased BUN levels , which negatively affect both your kidneys and your liver " , Evidence please