Results 81 to 90 of about 184 (130)

From Phenotype to Molecules: Unveiling the Genetic and Immunological Bridges Between Autoimmune Diseases and Vitiligo

Clinical, Cosmetic and Investigational Dermatology
Yuan Hu,1,* Shao-Bo Wang,1,* Kun Wang,2 Ming-Jie He2 1Suining Central Hospital, Suining, Sichuan, People’s Republic of China; 2First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, People’s Republic of China*These authors ...
Hu Y, Wang SB, Wang K, He MJ
doaj  

Very early neuroimages of sulfite oxidase deficiency mimicing severe hypoxic ischemic encephalopathy in a neonate

Pediatrics and Neonatology, 2021
Zhuxiao Ren, Jianlan Wang, Runqiang Liang, Yingyi Lin, Fang Xu, Xuaner Zheng, Yang Haoming, Jie Yang   +7 more
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Purification and Properties of Hepatic Sulfite Oxidase

Journal of Biological Chemistry, 1961
R M, MACLEOD, W, FARKAS, I, FRIDOVICH, P, HANDLER   +3 more
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Isolated Sulfite Oxidase Deficiency

Neuropediatrics, 1996
Isolated sulfite oxidase (SO) deficiency is an autosomal recessively inherited inborn error of sulfur metabolism. In this report of a ninth patient the clinical history, laboratory results, neuropathological findings and a mutation in the sulfite oxidase gene are described.
K V Rajagopalan
exaly   +3 more sources

Molecular cloning of human liver sulfite oxidase

Biochimica Et Biophysica Acta Gene Regulatory Mechanisms, 1995
A 2.4 kilobase cDNA clone of human sulfite oxidase was isolated from a human liver cDNA library in lambda gt10. Comparison of three sulfite oxidase sequences to several plant and fungal nitrate reductase sequences reveals a single conserved cysteine with highly conserved flanking sequences.
K V Rajagopalan, Robert M Garrett, K V Rajagopalan   +2 more
exaly   +3 more sources

Sulfite oxidase deficiency and the detection of urinary sulfite

European Journal of Pediatrics, 1983
S K Wadman
exaly   +2 more sources

Isolated sulfite oxidase deficiency

Journal of Inherited Metabolic Disease, 2017
AbstractIsolated sulfite oxidase deficiency (ISOD) is a life‐threatening, autosomal recessive disease characterized by severe neurological impairment. As no long‐term effective treatment is available, distinction from other treatable diseases, such as molybdenum cofactor deficiency (MoCD) type A, should be made.
Helena, Claerhout, Peter, Witters, Luc, Régal, Katrien, Jansen, Marie-Rose, Van Hoestenberghe, Jeroen, Breckpot, Pieter, Vermeersch   +6 more
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Screening for sulfite oxidase deficiency

Clinica Chimica Acta, 1969
Abstract Two screening methods for mass detection of sulfite oxidase deficiency are described. The assay of the rather labile sulfite is performed as bed-side test using a commercially available test paper. For the assay of S- sulfo- l -cysteine a Chromatographic technique on thin-layer cellulose is described. Good stability of S- sulfo-
D, Kutter, R, Humbel
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Significance of Plant Sulfite Oxidase

Plant Biology, 2007
Abstract: Sulfite oxidizing activities are known since years in animals, microorganisms, and also plants. Among plants, the only enzyme well characterized on molecular and biochemical level is the molybdoenzyme sulfite oxidase (SO). It oxidizes sulfite using molecular oxygen as electron acceptor, leading to the production of sulfate and hydrogen ...
Hänsch, Robert, Lang, Christina, Rennenberg, Heinz, Mendel, Ralf-Rainer   +3 more
openaire   +3 more sources

Isolated sulfite oxidase deficiency

Journal of Neonatal-Perinatal Medicine, 2015
Abstract BACKGROUND: Sulfite oxidase deficiency is an uncommon metabolic disease. Only few cases of its isolated form have been reported in the literature. CASE PRESENTATION: We report a case of severe neonatal onset. A newborn baby of 41 weeks gestational age, weighted at birth of 3240 grams and had an Apgar score of 6-10-10.
B, Relinque, L, Bardallo, M, Granero, P J, Jiménez, S, Luna   +4 more
openaire   +2 more sources