2019
DOI: 10.3892/mmr.2019.10417
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Differential expression of claudin‑4, occludin, SOX2 and proliferating cell nuclear antigen between basaloid squamous cell carcinoma and squamous cell carcinoma

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Cited by 7 publications
(15 citation statements)
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“…Ten 4 μm serial sections were prepared for staining and incubated with primary antibodies for 2 h. Immunohistochemistry was performed using a Discovery Auto-Stainer with automated protocols (Ventana Medical Systems, Inc., Tucson, AZ, USA; Roche, Mannheim, Germany) as previously described [ 37 , 38 ]. The intensities of DEC1, DEC2, SOX2, c-MYC and vimentin were determined by qualitative assessment of three levels: weak (1), moderate (2) and strong (3), as previously described [ 38 ].…”
Section: Methodsmentioning
confidence: 99%
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“…Ten 4 μm serial sections were prepared for staining and incubated with primary antibodies for 2 h. Immunohistochemistry was performed using a Discovery Auto-Stainer with automated protocols (Ventana Medical Systems, Inc., Tucson, AZ, USA; Roche, Mannheim, Germany) as previously described [ 37 , 38 ]. The intensities of DEC1, DEC2, SOX2, c-MYC and vimentin were determined by qualitative assessment of three levels: weak (1), moderate (2) and strong (3), as previously described [ 38 ].…”
Section: Methodsmentioning
confidence: 99%
“…The cells were lysed using M-PER protein lysis buffer (Thermo Fisher Scientific, Inc.). Protein determination was performed using the bicinchoninic method [ 38 ], and the 40 µg proteins of the total cell lysates were run on SDS-polyacrylamide gels followed by western blotting using standard procedures. A WesternBright Sirius Kit (Advansta, CA, USA) was used for antibody detection, and an AE-9300 Ez capture MG (ATTO, Tokyo, Japan) was used for image data capture.…”
Section: Methodsmentioning
confidence: 99%
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“…The PD-L1, P53 and CK17 expression OSCC tissues were evaluated from serial deparaffinized sections. The OSCC biopsy specimens had been fixed with formalin from 24 to 48 h at room temperature and treated with routine processing as in a previous study [12, 13]. Four micrometer-thick sections of paraffin-embedded tissues were mounted on precoated slides and air-dried overnight at 58°C.…”
Section: Methodsmentioning
confidence: 99%
“…Four micrometer-thick sections of paraffin-embedded tissues were mounted on precoated slides and air-dried overnight at 58°C. The serial sections were prepared for staining and were incubated with primary antibodies for 12 h. Immunohistochemistry (IHC) was performed using a Discovery Auto-Stainer with automated protocols (Ventana Medical Systems, Inc.; Roche) as previously described [13, 14].…”
Section: Methodsmentioning
confidence: 99%