glycogen storage

美 [ˈglaɪkədʒɪn ˈstɔːrɪdʒ]

网络  贮存糖原

医学



双语例句

  1. Carbohydrates are stored as glycogen, and storage for protein is new muscle.
    碳水化合物则储存为糖元,蛋白质则会作为构建新肌肉的材料。
  2. Objective To develop and evaluate a simple, fast and accurate prenatal diagnosis method for glycogen storage disease Ia ( GSD Ia) in Chinese.
    目的探讨中国人Ia型糖原累积病简便、快速、准确的产前诊断方法。
  3. Objective To study renal involvement in hepatic glycogen storage disease ( GSD) in childhood.
    目的观察儿童期肝糖原贮积症(GSD)的肾脏并发症。
  4. Ultrastructural study on live tissue in a case of glycogen storage disease type ⅰ
    糖原累积病Ⅰ型肝脏组织的超微结构观察
  5. Glycogen storage diseases presenting as hypertrophic cardiomyopathy
    表现为肥厚型心肌病的糖原贮积病
  6. Glycogenosis type ⅴ: A case report Glycogen storage diseases presenting as hypertrophic cardiomyopathy
    糖原贮积症一例报告表现为肥厚型心肌病的糖原贮积病
  7. Glycogen Storage Disease Associated with Lipid Storage Myopathy
    糖原贮积症伴脂质贮积症
  8. Effects of liver glycogen storage on hepatic functional reserve during warm ischemia and reperfusion injury in rats
    肝糖原贮备的变化对热缺血再灌注期大鼠肝储备功能的影响
  9. Clinical and Mutation Analysis of Glycogen Storage Disease Type ⅲ
    糖原累积症-Ⅲ型的临床和糖原脱枝酶基因突变分析
  10. Mutation analysis of glycogen debrancher enzyme gene in five Chinese patients with glycogen storage disease type ⅲ
    糖原贮积症Ⅲ型基因突变的初步研究
  11. Clinical and genomic study of the infant with glycogen storage disease type ⅱ
    糖原累积病Ⅱ型的临床分析和基因学检测
  12. Recent advances of clinical and genomic study of glycogen storage disease type ⅲ
    糖原累积病Ⅲ型临床和基因研究进展
  13. The clinical and pathological features of Chinese patients of type ⅰ glycogen storage disease with renal involvement
    Ⅰ型糖原贮积症肾损害临床表现和病理改变
  14. Neonatal type IV glycogen storage disease associated with null mutations in glycogen branching enzyme 1
    糖原分枝酶1无效突变相关性IV型糖原贮积病新生儿亚型
  15. Results HA lesions were composed of cells arranged in 2-cell-thick plates, with focal fatty change and excessive glycogen storage.
    结果2例HA光镜下细胞排列成条索状,厚约2层,局部伴有脂肪变性及糖原贮积。
  16. Prenatal diagnosis of glycogen storage disease Ia by screening for hot spot mutations in combination with the 1176 nucleotide polymorphism linkage analysis
    葡萄糖6磷酸酶基因热点突变检测结合1176多态位点连锁分析快速产前诊断Ia型糖原累积病
  17. Renal complications of hepatic glycogen storage disease
    肝糖原贮积症肾脏并发症的临床观察
  18. Advances in the Study of Glycogen Storage Disease Type ⅱ
    Ⅱ型糖原累积病的研究进展
  19. Research Advances of Glycogen Storage Disease Type I
    糖原累积病Ⅰ型研究的新进展
  20. Molecular Genetics Analysis of Glycogen Storage Disease Ia in Chinese Family
    糖原累积病Ⅰa型分子遗传学家系研究
  21. Objective To obtain the mutation spectrum of glucose-6-phosphatase ( G6Pase) gene in Chinese patients with glycogen storage disease type ⅰ a ( GSD ⅰ a) and to analyze the relationship of its genotype and phenotype.
    目的了解中国人葡萄糖6磷酸酶(G6Pase)基因突变谱和突变热点,并分析糖原累积病Ⅰa型(GSDⅠa)基因型和临床表型的相关性。
  22. Benign course of glycogen storage disease type IIb in two brothers: Nature or nurture?
    兄弟二人IIb型糖原贮积症的良性病程:自然还是营养的结果?
  23. Objective To investigate the molecular genetic mechanism of a patient with glycogen storage disease la.
    目的研究1例糖原累积病Ⅰa型患者发病的分子遗传学机制。
  24. Glycogen storage can not only slow down the accumulation of VFA, but reduce the production rate of hydrogen, lower hydrogen partial pressure in ASBR, create a good condition for the stable and efficient operation of ASBR.
    ASBR反应器中,糖原的储存不仅能减缓VFA的积累,且能减小产氢速率,降低反应器内的氢分压,从而为ASBR反应器的高效稳定运行创造良好条件。
  25. Higher F/ M led to more glycogen storage, less VFA directly degraded from substrate, and slower hydrogen-producing rate, lower hydrogen partial pressure in reactor.
    F/M越高,储存的糖原量越多,相应地基质直接降解为VFA的份额越少,单糖直接发酵过程的产氢速率则较为缓慢,从而导致反应器中的氢分压较低。
  26. Therefore, physicians must have sufficient recognition for this disease, and be on the alert for hepatic glycogen storage disease, give a right and prompt diagnosis combined with family history, physical examinations and laboratory findings.
    结论肝糖原累积病临床表现多样,要及时准确地诊断本病,需要对本病有充分的认识,结合患者的家族史、临床表现及各种实验室,影像学检查结果正确地加以综合分析。
  27. Accordingly, it mainly divided into three categories: glycogen storage diseases, lipid storage myopathy and mitochondrial diseases caused by the respiratory chain impairment, each type can be divided into many clinical subtypes.
    常见的代谢性肌病主要分为三大类:糖原累积病,脂质沉积性肌病及由于呼吸链氧化磷酸化障碍所导致的的线粒体疾病,每一类型又可分为许多临床亚型。
  28. ( 3) bifidobacteria M13-4 strain have increased body weight in rats fed with high-fat diet. However, it has improved serum TG and TCH and lipidoses in liver, no influence to hepatic glycogen storage and serum glucose and insulin.
    双歧杆菌株M13-4可加速高脂饮食大鼠体重增加,但对血清TG、TCH及肝脏的脂质沉积具有改善作用,而对肝糖原的储存、血糖及INS的调节作用不明显。