duchenne

是什么意思
  • 网络进行性肌营养不良;杜兴;杜氏
  • 学习怎么用

    双语例句

    1.
    In essence,thenon-Duchennesmileiscontrived,whereasthegenuinesmileseemstoemanatefromadeeper connection to one'sjoy.
    事实上,非杜兴式微笑是做作的,然而,一份真诚的微笑像是从一个人的内心深处的快乐散发出来。
    2.
    DuchenneMuscularDystrophy(DMD)isone of the mostcommonfatalgeneticdisorderstoaffectchildren around the world.
    杜氏肌营养不良(DMD)是最常见的致命的遗传疾病之一,影响到世界各地的儿童。
    www.jingcai.org
    3.
    DuchenneMuscularDystrophyisafatalgeneticmutation in about oneofevery3,500boys.
    杜氏肌萎缩症是一种致死性的基因突变疾病,平均每3500个男孩中就有一个罹患此病。
    4.
    Theyfound that out ofthedeadplayers,Duchennesmilershad tended to livethelongest,followedbynon-Duchennesmilers.
    他们发现在已死亡球员中,杜兴微笑者寿命最长,非杜兴微笑者其次。
    5.
    Thedrug,known as PTC124, has already had encouraging resultsinpatientswithDuchennemusculardystrophyandcysticfibrosis.
    被称为PTC124的药物,已经在治疗Duchenne肌营养不良和囊性纤维化的病人中获得了激动人心的成果。
    news.dxy.cn
    6.
    GenuinesmilesareknownasDuchennesmilesafterthe19th-centuryneurologistwhodefinedthemindetail.
    真实的微笑被称为杜兴微笑。19世纪的神经学家杜兴对其进行了详细定义。
    7.
    ThebehavioralinvestigationonDuchenne muscular dystrophy animalmodelaftermarrowtransplantation.
    型肌营养不良模型鼠骨髓移植后的行为学观察。
    www.ilib.cn
    8.
    ABSTRACT:ObjectiveToinvestigatetheclinicalandlabfeatures of sibling brotherandsisterbothwithDuchennemusculardystrophy(DMD).
    摘要:目的探讨同患假肥大型肌营养不良症(DMD)兄妹的临床以及实验室检查特点。
    www.actacams.com
    9.
    AVI'sleaddrugcandidate,AVI-4658,isinclinicaldevelopmentforDuchenneMuscularDystrophy.
    的AVI的领先候选药物,为AVI-4658,是杜氏肌营养不良症在临床开发。
    www.jingcai.org
    10.
    Theresearchersclassifiedthem as non-smilers, Duchennesmilersornon-Duchennesmilers.
    研究者们把这些微笑分为非微笑、杜兴微笑和非杜兴微笑。
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    权威例句

    A Tensor-Based Algorithm for High-Order Graph Matching.
    A tensor-based algorithm for high-order graph matching
    A graph-matching kernel for object categorization
    Segmentation by transduction
    Respiratory Care of the Patient with Duchenne Muscular Dystrophy
    The Duchenne smile: Emotional expression and brain physiology: II.
    The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion.
    Characterization of dystrophin in muscle-biopsy specimens from patients with Duchenne's or Becker's muscular dystrophy.
    Systemic administration of PRO051 in Duchenne's muscular dystrophy.
    Intracellular calcium accumulation in Duchenne dystrophy and other myopathies: a study of 567,000 muscle fibers in 114 biopsies.
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