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For the Acc1 and rDNA ITS regions, PCR programs were as previously described (references listed in Table 2).
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Details about the validation of the proposed model using the described reference case are found in Silpngarmlert et al. (2012).
Additionally, all sequences were manually aligned with the above described reference database using PAUP* 4.0b10 [55].
Specificity of autoantibodies was determined using previously described reference sera.
Specificities were determined using previously described reference sera.
Specificity of the autoantibodies was determined using previously described reference sera.
Specificity of autoantibodies was determined using previously described reference sera [ 7].
Different authors have described reference equations and tables to predict the 6MWT-distance in healthy elderly subjects.
We described reference intervals for normal segmental mobility, prevalence of LSMDs under each model, and the association of LSMDs with pain and disability.
Specificities such as anti-U1RNP, Sm, ribosomal P, Ro, La, Ku, argonaute 2 (Ago2)/Su, and RNA polymerase II (RNAP II) were verified using previously described reference sera.
We also used the described reference set of human tissue-specific splicing events for comparative analyses of the performance of our method with 3 other previously published methods.
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