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Integrated Histology and Molecular Profiling of Postmortem Human Auditory and Vestibular Organs via a Poly (Methyl Methacrylate)-Based Workflow. [PDF]
Bächinger D +19 more
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Unveiling the role of perineural telocytes in mechanosensation, structural insights into their association with herbst and ruffini corpuscles in the quail beak. [PDF]
Soliman SA.
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Advances in multiscale myelin imaging: from classical histology to functional insights. [PDF]
Okuyama K +13 more
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Histo-LOOP: A Novel Embedding Tool for Standardizing, Simplifying, and Advancing Histological Tissue Preparation. [PDF]
Nilcham P +7 more
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Chemical Dehydration for Rapid Paraffin Embedding
Biotechnic and Histochemistry, 1994We describe chemical dehydration with 2,2-dimethoxypropane (DMP) for rapid paraffin embedding using a mixture of DMP and mineral oil followed by mineral oil as clearing intermediates. This method is useful for classical histological techniques as well as for histochemistry and immunocytochemistry.
Gabriele Möller
exaly +3 more sources
Decalcifying Tissues for Paraffin Embedding
Cold Spring Harbor Protocols, 2008INTRODUCTIONParaffin sections of bone usually require a decalcification step after fixation before sectioning. This protocol describes a method for decalcifying fixed tissue.
Fischer, Andrew H. +3 more
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Improvement of the Butyl Methacrylate-Paraffin Embedment
Stain Technology, 1983The excellent butyl methacrylate-paraffin method as an embedment for light microscopy has been technically improved. More uniform and reproducible polymerization has been obtained by using a vacuum oven to degas the polymerizing mixture and to replace the air with nitrogen at 650 Torr. The amount of benzoyl peroxide required must be determined for each
P J, McMillan +3 more
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A Sample-Grouping Technique for Paraffin Embedments
Stain Technology, 1983A technique is described which facilitates histological preparation of multiple tissue specimens for light microscopy. The procedure enables the investigator to separate and label identifiable subgroups from a larger number of specimens in one histological section. After standard fixation, murine esophagi were arranged longitudinally and secured within
N H, Rubin, P S, Baur
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