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For each case, two tissue sections cut at different levels of the histological block were processed to control for tissue heterogeneity.
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The craniofacial block was processed to examine the nasal mucosa.
A portion of the frozen tissue block was processed to create a paraffin-embedded tissue block that was matched and oriented relative to the remaining frozen block.
Formalin-fixed and paraffin-embedded cell blocks were processed to obtain seriate tissue sections for both morphologic analysis and phenotypic studies.
Samples were processed to paraffin blocks.
The excised mouse organs were processed to cryo-blocks using cryo-preservant medium (optimal cutting temperature [OCT] medium; Tissue-Tek, Sakura, the Netherlands) into 10 μm tissue sections.
Tissues were processed to paraffin blocks using an ASP300S dehydration machine (Leica, Wetzlar, Germany) and an EG1160 tissue embedding system (Leica, Wetzlar, Germany).
Pools of 3 to 5 sections of each block were processed.
To find frequency column clusters in the BLOCKS database [ 26], each block from BLOCKS was processed to give a new multiple alignment.
The blocks were processed histologically to obtain slices 4 μm thick and stained with routine hematoxylin and eosin (HE).
In embryonic stem cells, LIN28 selectively blocks let-7 precursor from being processed to mature microRNA [7], [8].
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