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They suffer due to low number of human osteoporotic specimens, use of animal proxies and/or the lack of differentiation between confounding parameters such as gender and state of diseased bone.
These include inadequate specimens, use of proton pump inhibitors and other acid suppressive agents, recent use of antibiotics among others [ 23].
Since delayed time to fixation can alter the phosphorylation status in resection specimens, use of these epitopes in companion diagnostic tests will likely have to be limited to core needle biopsies.
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Four of the biopsy specimens used for determination of H. pylori infection were also used for histological evaluation.
The same ovarian tissue specimens used for determination of proliferation index and DNA content were used for ploidy analysis.
The same formalin-fixed, paraffin-embedded ovarian tissue specimens used for quantitation of the proliferation index (see Results section) were used to determine DNA content.
List of the specimens used for DNA extraction, with accession numbers of the sequences.
The number of specimens used to produce the tensity value is at least 3.
The majority of specimens used for IHC staining did not have DNA or RNA samples available.
Sections of the specimens used for DNA extraction contained a majority proportion of tumour cells.
This could be partly explained by potential limitations of the specimens used for our investigation.
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