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acyl-Coenzyme A dehydrogenase, C-2 to C-3 short chain
This gene encodes a a tetrameric mitochondrial flavoprotein, which is a member of the acyl-CoA dehydrogenase family. This enzyme catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. Mutations in this gene have been associated with Short Chain Acyl-CoA Dehydrogenase Deficiency. [provided by RefSeq]
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|---|---|---|---|
| Cecum |
100
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| Fat body |
98
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| Mesenteric lymph nod… |
95
|
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| Adrenal gland |
95
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| Skeletal muscle tiss… |
95
|
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| Trigeminal ganglion |
93
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|
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|---|---|---|---|
| Bemegride |
100
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| Aminophylline |
86
|
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| Oxymetholone |
83
|
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| Isoxicam |
80
|
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| Proteoglycan |
79
|
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| D-galactosamine |
77
|
|
|
|
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|---|---|---|---|
| Deficiency of butyry… |
100
|
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| Colonic polyp |
46
|
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| Bordetella |
44
|
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| Placental insufficie… |
43
|
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| Fetal growth retarda… |
43
|
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| Hypoxia |
42
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Individual Studies |
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Authors: Thomas Illig, Christian Gieger, Guangju Zhai, Werner Römisch-Margl, Rui Wang-Sattler, Cornelia Prehn, Elisabeth Altmaier, Gabi Kastenmüller, Bernet S Kato, Hans-Werner Mewes,…
Nature genetics 2010 FebAuthors: Christina B Pedersen, Steen Kølvraa, Agnete Kølvraa, Vibeke Stenbroen, Margrethe Kjeldsen, Regina Ensenauer, Ingrid Tein, Dietrich Matern, Piero Rinaldo, Christine Vianey-Saban,…
Human genetics 2008 AugThought leaders and organizations working on research involving ACADS.
conditions: Attention Deficit Disorder With Hyperactivity
interventions: Methylphenidate
conditions: Chronic Plaque Psoriasis
interventions: CDP870 (Certolizumab pegol)