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1  expedites the transition from cell lysis to protein electrophoresis.
2 unzel mutants by both immunofluorescence and protein electrophoresis.
3       Blood samples were collected for serum protein electrophoresis.
4                             The gel supports protein electrophoresis after concurrent in situ chemica
5       Appropriate evaluation including serum protein electrophoresis and hematology consultation shou
6 available for proteome analysis including 2D protein electrophoresis and mass spectrometry.
7 cal interaction between Tat and MMP, we used protein electrophoresis and Western blot techniques, and
8  95% confidence interval, 74%-97%); by serum protein electrophoresis and/or immunofixation electropho
9 fferential scanning calorimetry (DSC), serum protein electrophoresis, and free light chain assay.
10 tic antibodies with immunofixation and serum protein electrophoresis assays may lead to underestimati
11 s used include scanning electron microscopy, protein electrophoresis, atomic force microscopy, and te
12                                        While protein electrophoresis conducted in capillaries and mic
13 alyses, reporter assays, and two-dimensional protein electrophoresis data of metabolic genes (includi
14 roportion of polymorphic loci as measured by protein electrophoresis, even when controlling for poten
15  values, injectors), we adapted the original protein electrophoresis format-moving boundary electroph
16  lysis of single cells seated in microwells, protein electrophoresis from those microwells into a sup
17                                        Serum protein electrophoresis, immunofixation electrophoresis,
18              Using assays for monoclonal (M)-proteins (electrophoresis/immunofixation) and kappa-lamb
19                              A new method of protein electrophoresis is described here.
20                               In designing a protein electrophoresis platform composed of a single-in
21  abnormal free light-chain ratio or abnormal protein electrophoresis results from the original study.
22                                              Protein electrophoresis revealed hypergammaglobulinemia
23                                              Protein electrophoresis revealed that the aqueous fracti
24 ands of parallel high-resolution single-cell protein electrophoresis separations for targets accross
25                                              Protein electrophoresis showed multiple clonal paraprote
26                                        Serum protein electrophoresis (SPEP) demonstrated a 3.5 g/dL m
27 FLC, SRM data was more consistent with serum protein electrophoresis than nephelometric data and SRM
28                                 We have used protein electrophoresis through polyacrylamide gels deri
29                       Twenty-four-hour urine protein electrophoresis (UPEP) was normal.
30 al protein (>/=200 mg per 24 hours) in urine protein electrophoresis (UPEP).
31  chip array hybridization, and 2-dimensional protein electrophoresis were used.
32                                        Serum protein electrophoresis with immunofixation and serum fr
33 abolic panel, vitamin B12 measurement, serum protein electrophoresis with immunofixation, fasting glu

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