Scads

Short-chain acyl-CoA dehydrogenase (SCAD) deficiency has been recorded in only a few patients and these show wide variation in clinical presentation. The defect has been seen in infants with a syndrome of psychomotor retardation and failure to thrive. These infants showed abnormal organic aciduria, and drastically decreased SCAD activity was demonstrable in cultured fibroblasts. Muscle symptoms were only part of a wider syndrome in all infants and children so far reported to have SCAD deficiency, but were the sole presenting feature in two adult patients, in whom lipid storage was demonstrable in skeletal muscle. The gene encoding for human SCAD has been mapped to chromosome 12. 

Soot deposited on the chamber wall contained mostly carbonaceous particles, where no MWNTs were contained. The deposits on the cathode consist of two portions the inside is black fragile core and the outside hard shell. The inside include MWNTs scad poljd ral graphitic nanoparticles. The outer-shell part ojnsisted of the crystd of graphite. 

Absolute sum of H-bond acceptor, donor factors/molecular polarizability (HYBOT) [23] also SCad A Sum of H-bond donor factors (HYBOT) [23] also SumCd Sum of H-bond donor factors/molecular polarizability (HYBOT) [23] also SCd A... 

PLA phospholipase A SCAD short chain acyl-CoA dehydrogenase... 

Scadding, S.R. 1990. Effects of tributyltin oxide on the skeletal structures of developing and regenerating limbs of axolotyl larvae, Ambystoma mexicanum. Bull. Environ. Contam. Toxicol. 45 574-581. 

Fig. 11. Distribution of Lp(a) lys+ (A) and lys- (B) levels in plasma of male patients with moderate coronary artery disease (MCAD) and serious coronary artery disease (SCAD). [With permission of Karmansky et al. (K8).]...

Brostoff J, Scadding GK, Male D, Roitt IM, Clinical Immunology. Mosby, London, 1994. 

Fox W, Scadding JG. Medical Research Council comparative trial of surgery and radiotherapy for primary treatment of small-celled or oat-celled carcinoma of bronchus Ten-year follow-up. Lancet 1973 2 63-65. 

MCAD deficiency is more common than SCAD deficiency, which impairs oxidation of shortfatty acids, or LCHAD deficiency, which impairs oxidation of iong-chain (C12-C22) fatty acids. 

Thiansilakul, Y., Benjakul, S., and Shahidi, F. (2007). Antioxidative activity of protein hydrolysate from round scad muscle using alcalase and flavourzyme. ]. Food Biochem. 31, 266-287. 

Krozowski Z. 11 (3-hydroxysteroid dehydrogenase and the short chain alcohol dehydrogenase (SCAD) superfamily. Mol Cell Endocrinol 84 1992 C25-C31. 

Butyrylglycine C4 Butyryl- CoA (FAO) SCAD deficiency Glutaric acidemia type II... 

C4 Butyryl-/ Isobutyryl- SCAD deficiency, IBDH deficiency, GA-2, EE... 

Fig. 3.2.3 Profiles of acylcarnitines as their butyl esters in plasma (precursor of m/z 85 scan) of a normal control (a) and three patients with elevated Gi-acyl carnitine (m/z 288 peak 4) that represents primarily butyrylcarnitine in a patient with short-chain acyl-CoA dehydrogenase (SCAD) deficiency (b), isobutyrylcarnitine in a patient with isobutyryl-CoA dehydrogenase (IBDH) deficiency (c), and a natural isotope of formiminoglutamate (FIGLU m/z 287 peak 3) in a patient with glutamate formimino-transferase deficiency (d). Peak 1 free carnitine (m/z 218), peak 2 acetylcarnitine (C2 m/z 260). The asterisks represent the internal standards (from left to right) d3-acetylcarnitine (C2 m/z 263), d3-propionylcarnitine (C3 m/z 277), d3-butyrylcarnitine (C4 m/z 291), d3-octanoylcarnitine (C8 m/z 347), d3-dodecanoylcarnitine (Ci, m/z 403), and d3-pal-mitoylcarnitine (Ci6 m/z 459)...

Scadding GK, Brostoff J Low dose sublingual therapy in patients with allergic rhinitis and asthma due to house dust mite. Clin Allergy 1986 16 483-491. 

Hore I, Georgalas C, Scadding G. Oral antihistamines for the symptom of nasal obstruction in persistent allergic rhinitis—a systematic review of randomized controlled trials. Clin Exp Allergy. 2005 35 207-212. 

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