نتایج جستجو برای: copper accumulation

تعداد نتایج: 230041  

Journal: :The EMBO journal 2007
Kuppusamy Balamurugan Dieter Egli Haiqing Hua Rama Rajaram Gerhard Seisenbacher Oleg Georgiev Walter Schaffner

Copper is an essential but potentially toxic trace element. In Drosophila, the metal-responsive transcription factor (MTF-1) plays a dual role in copper homeostasis: at limiting copper concentrations, it induces the Ctr1B copper importer gene, whereas at high copper concentrations, it mainly induces the metallothionein genes. Here we find that, despite the downregulation of the Ctr1B gene at hi...

Journal: :International Journal of Advances in Medicine 2022

Wilson's disease is an inborn error of copper metabolism that characterized by deficiency ceruloplasmin, the serum transport protein for copper. Copper collected in liver, and after hepatic binding sites are saturated, it released. Systemic then develops there abnormal accumulation brain, particularly putamen globus pallidus. Presenting this case a 32-year-old male patient who presented with pe...

Journal: :The Journal of biological chemistry 2008
Salah E Abdel-Ghany Marinus Pilon

In plants, copper is an essential micronutrient required for photosynthesis. Two of the most abundant copper proteins, plastocyanin and copper/zinc superoxide dismutase, are found in chloroplasts. Whereas plastocyanin is essential for photo-autotrophic growth, copper/zinc superoxide dismutase is dispensable and in plastids can be replaced by an iron superoxide dismutase when copper is limiting....

Journal: :Hepatology 1987
G M Hill G J Brewer A S Prasad C R Hydrick D E Hartmann

The standard therapy for preventing copper accumulation in Wilson's disease, D-penicillamine, has been a life-saving drug, but it has many side effects and some patients are completely intolerant. We have been using oral zinc as another approach to the therapy for Wilson's disease, with copper balance studies as the key initial assessment of the adequacy of a given dose or regimen of zinc thera...

Journal: :Archives of disease in childhood 1980
I Blumenthal G T Lealman P P Franklyn

A preterm baby boy with blood and bone changes of copper deficiency is described. Copper deficiency was suspected after fracture of the left femur during examination of the hip joint. A low serum copper concentration (2.7 mumol/l; 17.2 micrograms/100 ml) and caeruloplasmin (0.04 g/l; 0.004 g/100 ml) confirmed the diagnosis. Despite the introduction of solids at 18 weeks the copper concentration...

Journal: :Food chemistry 2017
Eduardo Vela Purificación Hernández-Orte Ernesto Franco-Luesma Vicente Ferreira

Three different red wines with reductive character have been treated with two different doses of copper sulfate (0.06 and 0.5mg/L) and with a commercial copper-containing product at the recommended dose (0.6mg/L). Wines were in contact with copper one week, centrifuged and stored at 50°C in strict anoxia for 2weeks (up to 7 in one case). Brine-releasable (BR-) and free fractions of Volatile Sul...

ژورنال: مجله علمی پژوهان 2014
رماوندی, بهمن , شمسی, مریم , عبدالهی, نسیبه ,

Introduction: The increasing environmental pollution by heavy metals caused serious concern due to the carcinogenicity non biodegradability, and biological accumulation properties. The purpose of this study was to investigate the removal of copper as a heavy metal by using camel bone powder from wastewater. Methods: The process of copper absorption by powdered camel bone was performed in l...

B. Falahatkar F. Bagherzadeh Lakani M.A. Yazdani Sadati S. Meshkini

Copper (Cu) is an essential element required by all living organisms, since at least 30 enzymes are known to use Cu as a cofactor. Cu is also toxic in excess and liver and gills are known to be target organs for it. In the present study, 240 Siberian sturgeon juvenile (with initial weight 29.2 ± 3.1 g and initial length 21.8 ± 1.4 cm) were randomly distributed in 12 fiberglass tanks at 4 differ...

Journal: :Comparative Hepatology 2003
I Carmen Fuentealba Enrique M Aburto

Recent advances in molecular biology have made possible the identification of genetic defects responsible for Wilson's disease, Indian childhood cirrhosis and copper toxicosis in Long Evans Cinnamon rats, toxic milk mice, and Bedlington terriers. The Wilson's disease gene is localized on human chromosome 13 and codes for ATP7B, a copper transporting P-type ATPase. A genetic defect similar to th...

Journal: :Genetics 2004
Mats Eriksson Jeffrey L Moseley Stephen Tottey Jose A Del Campo Jeanette Quinn Youngbae Kim Sabeeha Merchant

A genetic screen for Chlamydomonas reinhardtii mutants with copper-dependent growth or nonphotosynthetic phenotypes revealed three loci, COPPER RESPONSE REGULATOR 1 (CRR1), COPPER RESPONSE DEFECT 1 (CRD1), and COPPER RESPONSE DEFECT 2 (CRD2), distinguished as regulatory or target genes on the basis of phenotype. CRR1 was shown previously to be required for transcriptional activation of target g...

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