نتایج جستجو برای: acid maltase deficiency

تعداد نتایج: 868406  

Journal: :Journal of bacteriology 1992
A Geber P R Williamson J H Rex E C Sweeney J E Bennett

In order to isolate the structural gene involved in sucrose utilization, we screened a sucrose-induced Candida albicans cDNA library for clones expressing alpha-glucosidase activity. The C. albicans maltase structural gene (CAMAL2) was isolated. No other clones expressing alpha-glucosidase activity. were detected. A genomic CAMAL2 clone was obtained by screening a size-selected genomic library ...

2016
B. L. Nichols M. Diaz-Sotomayor S. E. Avery S. K. Chacko D. L. Hadsell S. S. Baker B. R. Hamaker L. K. Yan H. M. Lin R. Quezada-Calvillo

UNLABELLED ᅟ: Starch requires six enzymes for digestion to free glucose: two amylases (salivary and pancreatic) and four mucosal maltase activities; sucrase-isomaltase and maltase-glucoamylase. All are deficient in suckling rodents. OBJECTIVE The objective of this study is to test (13)C-starch digestion before weaning by measuring enrichment of blood (13)C-glucose in maltase-glucoamylase-null...

2017
Hassan A.H. Ibrahim M. Nasr

In vitroantimicrobial activity, DNA cleavage, anti-diabetic, antioxidant, anti-inflammotary and antihaemolytic of some synthesized Metallocephradines and Metallocefepimes were examined. In a broadspectrum of antibacterial and antifungal property, it was found that nickel (1:1) and copper (1:2) complexes were more active than cephradine against all tested bacteria except S.pyogenes and E.fecalis...

Journal: :iranian journal of pediatric hematology and oncology 0
mehran karimi hematology research center, shiraz university of medical sciences, shiraz, iran nader cohan hematology research center, shiraz university of medical sciences, shiraz, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی شیراز (shiraz university of medical sciences) vincenzo de sanctis pediatric and adolescent outpatient clinic, quisisana hospital, ferrara, italyسازمان اصلی تایید شده: دانشگاه علوم پزشکی شیراز (shiraz university of medical sciences)

this study presented a mini review on folic acid deficiency and recommendations for its supplementation in thalassemia intermedia (ti). ti is a clinical condition which lies between thalassemia major and thalassemia minor. although ti patients may not need regular blood transfusion, precise diagnosis and management are critical for the prevention of clinical complications and quality of life im...

Journal: :Applied and environmental microbiology 1982
E J Schaefer C L Cooney

The production of maltase, an inducible and repressible catabolic enzyme in Saccharomyces italicus, was studied and compared in batch, fed-batch, and continuous fermentations. Tight genetic controls on maltase synthesis limited the effect of environmental manipulations such as fed-batch or continuous culture in enhancement of maltase synthesis, and neither approach was able to improve the perfo...

2012
Yi-Na Huang Dong-Dong Zhao Bo Gao Kai Zhong Rui-Xue Zhu Yan Zhang Wang-Jun Xie Li-Rong Jia Hong Gao

In the present study, we firstly compared rat intestinal α-glucosidase inhibitory activity by different ethanol-aqueous extractions from the dried fruits of Terminalia chebula Retz. The enzymatic assay showed that the 80% ethanol extract was more potent against maltase activity than both 50% and 100% ethanol extracts. By HPLC analysis, it was determined that the 80% ethanol extract had a higher...

Journal: :Blood 1983
P J Philip J Giudicelli P Delqué J P Cassuto P Sudaka N Ayraud

Neutral maltase activity (alpha-D-glucoside glucohydrolase; EC: 3.2.1.20) was measured in B and T lymphocytes from peripheral blood of normal subjects and patients suffering from chronic or acute lymphoid leukemias. Neutral maltase activity is undetectable in T cells from normal subjects as well as in patients with chronic or acute T-lymphoid leukemias. Conversely, whereas this enzyme activity ...

Journal: :Journal of the Institute of Brewing 1926

Journal: :Molecular genetics and metabolism 2007
Toshika Okumiya Marian A Kroos Laura Van Vliet Hiroaki Takeuchi Ans T Van der Ploeg Arnold J J Reuser

Glycogen storage disease type II (GSDII; Pompe disease or acid maltase deficiency) is an autosomal recessive disorder caused by lysosomal acid alpha-glucosidase (AalphaGlu) deficiency and manifests predominantly as skeletal muscle weakness. Defects in post-translational modification and transport of mutant AalphaGlu species are frequently encountered and may potentially be corrected with chaper...

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