ライフサイエンスコーパス: immunofixation

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1 as confirmed to be immunoglobulin Mlambda at immunofixation.

2 ells in addition to negative serum and urine immunofixation.

3 discrete or localized band were subjected to immunofixation.

4 0 years and subjected to electrophoresis and immunofixation.

5 ht to have a localized band was subjected to immunofixation.

6 whom myeloma protein was detectable only by immunofixation.

7 lobulin G and lambda light chain detected on immunofixation.

8 ic plasma cell levels is more sensitive than immunofixation and can identify which patients may benef

9 Pre-beta-1 HDL levels were quantified by immunofixation and nondenaturing 2-dimensional gel elect

10 Serum protein electrophoresis with immunofixation and serum free light chain (FLC) analysis

11 interference of therapeutic antibodies with immunofixation and serum protein electrophoresis assays

12 for monoclonal (M)-proteins (electrophoresis/immunofixation) and kappa-lambda free light chains (FLCs

13 ete responses (CRs), four near CRs (positive immunofixation), and 12 partial responses; six patients

14 These additional protein bands, detected by immunofixation electrophoresis (IFE), could be due to al

15 ore the relationship between SFLCR and serum immunofixation electrophoresis (SIFE).

16 espectively), whereas positive UPEP or urine immunofixation electrophoresis (uIFE) did not.

17 7%); by serum protein electrophoresis and/or immunofixation electrophoresis in 21 patients (77.8%), a

18 r plasma cell dyscrasias were evaluated with immunofixation electrophoresis of serum and urine specim

19 samples with sufficient serum remaining, and immunofixation electrophoresis was done for all samples

20 Serum protein electrophoresis, immunofixation electrophoresis, and serum free light-cha

21 ission (CR) or near-CR (nCR; defined as only immunofixation electrophoresis-positive).

22 y the presence of two distinct M proteins in immunofixation electrophoresis.

23 myositis (IBM) was subjected to agarose gel immunofixation electrophoresis.

24 surement, serum protein electrophoresis with immunofixation, fasting glucose measurement, and glucose

25 Immunofixation, genomic restriction fragment length poly

26 MGUS was detected in 55 (6%) relatives, and immunofixation identified 28 additional relatives for an

27 with multiple myeloma who achieved negative immunofixation in the serum and urine after therapy and

28 001, respectively) and in patients achieving immunofixation-negative complete response (CR; PFS, P =

29 ma cells were detectable in 27% (9 of 33) of immunofixation-negative complete-remission patients.

30 atients had a significantly shorter PFS than immunofixation-negative patients with no detectable neop

31 We also found that, on achieving immunofixation-negative status, patients with less than

32 atients (68%), including two CRs (6%), three immunofixation-positive CRs (9%), 11 PRs (32%), and seve

33 the serum-free light chain ratio to negative immunofixation studies did not negate the need for BM st

34 ormal FLC ratio and negative serum and urine immunofixation), very good partial response (difference

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