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transitional cell carcinoma (tcc)
Objective: This study was designed to investigate differential pattern of G1-cyclins (D1 and E) in transitional cell carcinoma (TCC) of human urinary bladder with or without human papillomavirus-18 (HPV-18) infection.
      
Prostatic adenocarcinoma(PAC) with transitional cell carcinoma(TCC) of the bladder and prostate is a rare clinicopathological entity, presentation is usually late.
      
Ten patients with transitional cell carcinoma (TCC) of the bladder received 3-6 mCi of HMFG1 monoclonal antibody (MAb) intravesically.
      
We previously reported the presence of aFGF in the urine of patients with transitional cell carcinoma (TCC).
      
Histologically, the initial passages of the RBT323 and 157 tumors are grade II transitional cell carcinoma (TCC).
      
The growth patterns of established cell lines from bladder transitional cell carcinoma (TCC) were compared with early passage cell lines.
      
To examine the excretion of urinary epidermal growth factor (EGF) in urological diseases and the relationship of EGF urine levels with transitional cell carcinoma (TCC), we measured the concentration of EGF by radioimmunoassay.
      
This study describes ultrastructural alterations in the basement membrane (BM) of rat bladder with invasive transitional cell carcinoma (TCC) induced by N-butyl-N-(4-hydroxybutyl)nitrosamine.
      
Recent investigations have demonstrated p53 and Rb alterations in a subset of transitional cell carcinoma (TCC).
      
We evaluated flow cytometric (FCM) analysis of transferrin receptor (TFR) expression as a marker for the malignant potential in transitional cell carcinoma (TCC).
      
An intercellular adhesion molecule-1 (ICAM-1)-negative RT4 transitional cell carcinoma (TCC) cell line was transducted with full-length ICAM-1 cDNA via a retroviral vector.
      
This study was designed to investigate c-myc overexpression in transitional cell carcinoma (TCC).
      
In recent years, significant information has been accumulated on the molecular alterations that take place during development of transitional cell carcinoma (TCC).
      
This in vitro study aimed to investigate the cytotoxic activity of 7-N-(2-([2-(gamma-l-glutamylamino)ethyl]dithio)ethyl)-mitomycin C (KW-2149) versus mitomycin C (MMC) against cell lines from human transitional cell carcinoma (TCC).
      
This review focuses on the main oncogenes studied in transitional cell carcinoma (TCC) in order to describe their mechanisms of action and investigate their possible prognostic value.
      
Various tumor markers for transitional cell carcinoma (TCC) of the bladder have been described, but none of them are used in clinical routine.
      
The expression of two of the NOS isoforms, the endothelial and inducible isoforms (eNOS and iNOS, respectively), were evaluated in bladder tissue from patients with transitional cell carcinoma (TCC).
      
A comprehensive review of the literature was performed on the molecular alterations associated with transitional cell carcinoma (TCC) of the bladder.
      
A 44-hour incubation microcytotoxicity assay (MA) was used to titrate the lymphocyte-mediated cytotoxicity in 47 transitional cell carcinoma (TCC) bladder cancer patients and 65 clinical control patients.
      
MHC nonrestricted cytotoxic T cell clones with selective specificity from patients with transitional cell carcinoma (TCC) of the
      
 

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