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Longer titles found: Acyl-CoA dehydrogenase (NADP+) (view), Short-chain acyl-CoA dehydrogenase (view), Long-chain acyl-CoA dehydrogenase (view), Medium-chain acyl-CoA dehydrogenase (view), Very-long-chain acyl-CoA dehydrogenase (view), 2-methylacyl-CoA dehydrogenase (view)

searching for Acyl-CoA dehydrogenase 35 found (83 total)

alternate case: acyl-CoA dehydrogenase

2-Methylbutyryl-CoA dehydrogenase deficiency (500 words) [view diff] exact match in snippet view article find links to article

dehydrogenase deficiency Other names 2-Methylbutyryl glycinuria or Short/branched-chain acyl-CoA dehydrogenase deficiency (SBCADD), 2-Methylbutyryl-CoA

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

Acyl-CoA dehydrogenase family member 9, mitochondrial is an enzyme that in humans is encoded by the ACAD9 gene. Mitochondrial Complex I Deficiency with

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

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

ACAD8 (704 words) [view diff] exact match in snippet view article find links to article

protein encoded by ACAD8 is a mitochondrial protein belongs to the acyl-CoA dehydrogenase family of enzymes, which function to catalyze the dehydrogenation

ACAD10 (847 words) [view diff] exact match in snippet view article find links to article

Acyl-CoA dehydrogenase family, member 10 is a protein that in humans is encoded by the ACAD10 gene. This gene encodes a member of the acyl-CoA dehydrogenase

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

disease Mcquarrie type infantile idiopathic hypoglycemia Medium chain acyl-CoA dehydrogenase deficiency Mesothelioma Methylmalonic acidemia Mitiglinide Mitochondrial

List of diseases (A) (1,929 words) [view diff] exact match in snippet view article

tubular necrosis Acyl-CoA dehydrogenase, medium chain, deficiency of Acyl-CoA dehydrogenase, short chain, deficiency of Acyl-CoA dehydrogenase, very long chain

Nitroalkane oxidase (287 words) [view diff] exact match in snippet view article find links to article

oxidase from Fusarium oxysporum identifies a new member of the acyl-CoA dehydrogenase superfamily". Proc. Natl. Acad. Sci. U.S.A. 99 (5): 2702–7. doi:10

ACOX3 (577 words) [view diff] exact match in snippet view article find links to article

signaling receptor binding pristanoyl-CoA oxidase activity FAD binding acyl-CoA dehydrogenase activity flavin adenine dinucleotide binding fatty acid binding

ACOX1 (886 words) [view diff] exact match in snippet view article find links to article

the CH-CH group of donors acyl-CoA oxidase activity FAD binding acyl-CoA dehydrogenase activity flavin adenine dinucleotide binding fatty acid binding

Mitochondrial folate transporter (385 words) [view diff] exact match in snippet view article find links to article

since. The phenotype of the patients is reminiscent of multiple acyl-CoA dehydrogenase deficiency (MADD). According to a review published in 2020, mutations

Butyryl-CoA (2,448 words) [view diff] exact match in snippet view article find links to article

orthologous to each other, including butyryl-CoA dehydrogenase, acyl-CoA dehydrogenase, acyl-CoA oxidase, and short-chain 2-methylacyl-CoA dehydrogenase

Newborn screening (8,018 words) [view diff] exact match in snippet view article find links to article

Germany for 12, the United Kingdom for 2 (PKU and medium chain acyl-CoA dehydrogenase deficiency (MCADD)), while France and Hong Kong only screened for

Global developmental delay (1,038 words) [view diff] exact match in snippet view article find links to article

that no permanent damage occurs.[citation needed] Medium-chain acyl-CoA dehydrogenase deficiency Homocystinuria Congenital hypothyroidism Isovaleric acidemia

Β-Hydroxybutyryl-CoA (260 words) [view diff] exact match in snippet view article find links to article

L-3-hydroxybutyrate: Implications for the treatment of multiple acyl-CoA dehydrogenase deficiency". Journal of Inherited Metabolic Disease. 44 (4): 926–938

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

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

Stylissa massa (241 words) [view diff] exact match in snippet view article find links to article

Shibata T, Sasaki K, Isoda H, Kigoshi H, Kita M (August 2020). "Acyl-CoA dehydrogenase long chain (ACADL) is a target protein of stylissatin A, an anti-inflammatory

List of OMIM disorder codes (18,877 words) [view diff] exact match in snippet view article find links to article

SCARB2 Acyl-CoA dehydrogenase, long chain, deficiency of; 201460; ACADL Acyl-CoA dehydrogenase, medium chain, deficiency of; 201450; ACADM Acyl-CoA dehydrogenase

Riboflavin-responsive exercise intolerance (429 words) [view diff] exact match in snippet view article find links to article

intolerance was first described in 2016 by Schiff et al. Multiple acyl-CoA dehydrogenase deficiency - similar in biochemical features; responsive to riboflavin

Mitochondrial myopathy (3,236 words) [view diff] exact match in snippet view article find links to article

myopathies affect multiple bioenergetic pathways, for instance multiple acyl-CoA dehydrogenase deficiency (MADD), formerly known as glutaric acidemia type II (GA-II)

Pirinixic acid (675 words) [view diff] exact match in snippet view article find links to article

enzymes: carnitine palmitoyltransferase I (M-CPT I) and medium-chain acyl-CoA dehydrogenase (MCAD). ATGL deficient mice administered pirinixic acid demonstrated

Macrocephaly (1,722 words) [view diff] exact match in snippet view article find links to article

MPS-II Mucopolysaccharidosis, MPS-III-D Muenke syndrome Multiple acyl-CoA dehydrogenase deficiency Multiple congenital anomalies-hypotonia-seizures syndrome

Chromosome 12 (1,735 words) [view diff] exact match in snippet view article find links to article

the link in the infobox on the right. ACAD10: encoding protein Acyl-CoA dehydrogenase family, member 10 ACSS3: encoding protein Acyl-CoA synthetase short-chain

KIAA1257 (884 words) [view diff] no match in snippet view article find links to article

protein Rab-43 and several pseudogenes and on the opposite strand Acyl CoA dehydrogenase family member 9 (ACAD9) and EF-hand and coiled-coil domain containing

Sodium phenylbutyrate (1,661 words) [view diff] exact match in snippet view article find links to article

Mohsen AW (December 2012). "Evidence for involvement of medium chain acyl-CoA dehydrogenase in the metabolism of phenylbutyrate". Molecular Genetics and Metabolism

Reye syndrome (2,301 words) [view diff] exact match in snippet view article find links to article

disorders, particularly a fatty-acid oxidation disorder medium-chain acyl-CoA dehydrogenase deficiency. There is an association between taking aspirin for viral

List of diseases (S) (1,934 words) [view diff] exact match in snippet view article

Short bowel syndrome Short broad great toe macrocranium Short-chain acyl-CoA dehydrogenase deficiency Short limb dwarf lethal Colavita–Kozlowski type Short

List of diseases (M) (2,469 words) [view diff] exact match in snippet view article

sinus tumors Mediastinal syndrome Mediterranean fever Medium-chain Acyl-CoA dehydrogenase deficiency Medrano Roldan syndrome Medullary cystic disease Medullary

Decenoic acid (2,503 words) [view diff] exact match in snippet view article find links to article

"Cis-4-decenoic acid in plasma: a characteristic metabolite in medium-chain acyl-CoA dehydrogenase deficiency". Clinical Chemistry, volume 34, issue 3, pages 548–551

Genetic disorder (3,582 words) [view diff] exact match in snippet view article find links to article

disorder. Examples of this type of disorder are albinism, medium-chain acyl-CoA dehydrogenase deficiency, cystic fibrosis, sickle cell disease, Tay–Sachs disease

Fatty acid (5,037 words) [view diff] case mismatch in snippet view article find links to article

ISBN 978-1-118-16945-2. Roth, Karl S. (2013-12-19). "Medium-Chain Acyl-CoA Dehydrogenase Deficiency". Medscape. Beermann, C.; Jelinek, J.; Reinecker, T.;

Astrocyte (9,291 words) [view diff] exact match in snippet view article find links to article

Bross, P.; Gregersen, N. (June 2010). "Misfolding of short-chain acyl-CoA dehydrogenase leads to mitochondrial fission and oxidative stress". Molecular

Hydrogen (12,426 words) [view diff] exact match in snippet view article find links to article

(1980). "The deuterium isotope effect upon the reaction of fatty acyl-CoA dehydrogenase and butyryl-CoA". J. Biol. Chem. 255 (19): 9093–97. doi:10

Oxidative phosphorylation (9,411 words) [view diff] exact match in snippet view article find links to article

liver mitochondria. Identification of a new 2-methyl branched chain acyl-CoA dehydrogenase". J. Biol. Chem. 258 (2): 1066–76. doi:10.1016/S0021-9258(18)33160-0

Type 2 diabetes (12,151 words) [view diff] exact match in snippet view article find links to article

by a misfolding variant of the mitochondrial protein short-chain acyl-CoA dehydrogenase". Journal of Inherited Metabolic Disease. 34 (2): 465–475. doi:10