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Longer titles found: Very-long-chain acyl-CoA dehydrogenase (view)

searching for Long-chain acyl-CoA dehydrogenase 14 found (18 total)

alternate case: long-chain acyl-CoA dehydrogenase

Very long-chain acyl-coenzyme A dehydrogenase deficiency (1,061 words) [view diff] no match in snippet view article find links to article

mutations in DNA. A change of the gene that codes for very long-chain-acyl-CoA-dehydrogenase (VLCAD) results in a deficiency or malfunction of the produced

Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (399 words) [view diff] no match in snippet view article find links to article

Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency is a rare autosomal recessive fatty acid oxidation disorder that prevents the body from converting

ACADL (1,610 words) [view diff] exact match in snippet view article find links to article

activation, and hepatic insulin resistance. In animals with very long-chain acyl-CoA dehydrogenase deficiency, LCAD and MCAD work to compensate for the reduced

ACADVL (986 words) [view diff] exact match in snippet view article find links to article

(Nov 1995). "Molecular basis of human mitochondrial very-long-chain acyl-CoA dehydrogenase deficiency causing cardiomyopathy and sudden death in childhood"

List of disorders included in newborn screening programs (716 words) [view diff] exact match in snippet view article find links to article

acyl-CoA dehydrogenase deficiency (MCAD) > 1 in 25,000 Very-long-chain acyl-CoA dehydrogenase deficiency (VLCAD) > 1 in 75,000 Trifunctional protein deficiency

ACAD9 (1,710 words) [view diff] exact match in snippet view article find links to article

FA (July 2006). "Acyl-CoA dehydrogenase 9 (ACAD 9) is the long-chain acyl-CoA dehydrogenase in human embryonic and fetal brain". Biochemical and Biophysical

List of causes of hypoglycemia (1,265 words) [view diff] exact match in snippet view article find links to article

Tumors Tyrosinaemia type 1 Urea cycle disorder Uremia Very-long-chain acyl-CoA dehydrogenase deficiency Visceral leishmaniasis Wiedemann-Beckwith syndrome

Mitochondrial trifunctional protein (589 words) [view diff] no match in snippet view article find links to article

deficiency LCHAD deficiency Acute fatty liver of pregnancy "Long-Chain Acyl CoA Dehydrogenase Deficiency: eMedicine Pediatrics: Genetics and Metabolic Disease"

Very long chain fatty acid (445 words) [view diff] exact match in snippet view article find links to article

web}}: CS1 maint: multiple names: authors list (link) "Very long-chain acyl-CoA dehydrogenase deficiency". Genetics Home Reference, National Institutes

TECR (454 words) [view diff] no match in snippet view article find links to article

acting on the CH-CH group of donors protein binding very-long-chain-acyl-CoA dehydrogenase activity oxidoreductase activity very-long-chain enoyl-CoA

Erucic acid (1,140 words) [view diff] no match in snippet view article find links to article

into shorter-chain fatty acids in the human liver by the long-chain acyl CoA dehydrogenase enzyme. Studies done on laboratory animals in the early 1970s

ACADM (955 words) [view diff] exact match in snippet view article find links to article

Tyurina YY, Kagan VE, Mallampalli RK, Vockley J (Apr 2014). "Long-chain acyl-CoA dehydrogenase deficiency as a cause of pulmonary surfactant dysfunction"

ETFA (2,140 words) [view diff] exact match in snippet view article find links to article

decreased thermal stability and is overrepresented in very-long-chain acyl-CoA dehydrogenase-deficient patients with mild childhood presentation". Molecular

ETFB (2,257 words) [view diff] exact match in snippet view article find links to article

decreased thermal stability and is overrepresented in very-long-chain acyl-CoA dehydrogenase-deficient patients with mild childhood presentation". Molecular