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syndrome
It is an essential enzyme required for replication of the acquired immunodeficiency syndrome (AIDS) virus.
      
Detection of a new mutation (T1140C) in a patient with Hunter syndrome from Guangdong, China
      
This study identified mutations of the idurnate-2-sulfatase (IDS) gene in a patient with Hunter syndrome, and established a basis for the diagnosis of the prenatal gene of Hunter syndrome.
      
It is possible that this mutation severely impairs enzymatic activity and is the underlying basis for the pathology seen in this patient with Hunter syndrome.
      
Association of metabolic syndrome with arterial compliance in children and adolescents
      
The association of metabolic syndrome (MS) with arterial compliance in children and adolescents was explored.
      
To restrict indication for stenting of the inferior vena cava and liver transplantation in patients with Budd-Chiari syndrome
      
The Budd-Chiari syndrome (BCS) used to be a very rare disorder and lacked a means of relieving.
      
Within three months after transplantation, four recipients (7.14%) died due to small-for-size syndrome (one case), renal failure (one case) and multiple organ failure (two cases).
      
Differential diagnosis of cervical nerve compression syndrome of the external intervertebral foramen
      
The aim of the present research is to study the mechanism of cervical nerve compression syndrome of the external intervertebral foramen and its differential diagnosis with cervical spondylosis.
      
Fifteen cases with cervical nerve compression syndrome of the external intervertebral foramen were healed by the diagnostic treatment.
      
Diagnostic treatment was propitious to differentiate cervical nerve compression syndrome of the external intervertebral foramen from cervical spondylosis.
      
Mutation analysis of KCNQ1, KCNH2, SCN5A, KCNE1 and KCNE2 genes in Chinese patients with long QT syndrome
      
Long QT syndrome (LQTS) is the prototype of the cardiac ion channelopathies, which cause syncope and sudden death.
      
Inherited LQTS is represented by the autosomal dominant Romano-ward syndrome (RWS), which is not accompanied by congenital deafness, and the autosomal recessive Jervell and Lange-Nielsen syndrome (JLNS), which is accompanied by congenital deafness.
      
Our data provide useful information for the identification of polymorphisms and mutations related to LQTS and the Brugada Syndrome (BS) in Chinese populations.
      
The aim of this research was to investigate the blood coagulation function in the patients with avascular necrosis of the femoral head (ANFH) after severe acute respiratory syndrome (SARS).
      
Site-directed mutagenesis of long QT syndrome KCNQ1 gene in vitro
      
To construct a polymerase chain reaction (PCR) site-directed mutagenesis of the long QT syndrome KCNQ1 gene in vitro, two sets of primers were designed according to the sequence of KCNQ1 cDNA and a mismatch was introduced into primers.
      
 

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