INT95636
From wiki-pain
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Sentences Mentioned In
Key: | Protein | Mutation | Event | Anatomy | Negation | Speculation | Pain term | Disease term |
Immunohistochemically, these rhabdoid cells were positive for vimentin, epithelial membrane antigen, smooth-muscle actin, cytokeratin, S-100 protein, and glial fibrillary acidic protein. | |||||||||||||||
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The presence of smooth muscle actin in fibroblasts in the torn human rotator cuff. | |||||||||||||||
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Differential expression analysis of the metastatic and primary tumor samples shows that a large number of the most highly downregulated genes such as TAGLN, ACTG2, TPM1, MYH111 and DES have been previously identified as expressed mostly in the prostatic stromal cells [15]. | |||||||||||||||
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The provided tissue (0.5 cm3) was diagnostic for nasopharyngeal angiofibroma after routine hematoxylin and eosin (H&E) staining (Figure 1), the stromal cells were negative for both cluster of differentiation (CD) 34 antigen and smooth muscle actin (SMA) antibodies and C-kit antibody was rarely detected in single cells. | |||||||||||||||
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Fragments of the tumor were fixed in 10% formaldehyde, included in paraffin, and the sections were stained with HE, VG and immunohistochemically with vimentin (VIM), MNF116, SyN, smooth muscle actin (ACT), desmin, CD68, S100, HMB45, and CD117. | |||||||||||||||
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The notable finding of this study was the presence of a contractile actin isoform, alpha-smooth muscle actin (SMA), in nonvascular cells in all of the seven torn human rotator cuff specimens evaluated immunohistochemically. | |||||||||||||||
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Smooth muscle actin (SMA) was positive in two of the four cases of CMF (50%; 2/4) [Figure 5C]. | |||||||||||||||
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The tumor cells were positive for CD99 and bcl-2 in all cases and for CD56 in two cases and negative for CD34 and smooth muscle actin in all cases. | |||||||||||||||
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Immunohistochemical analysis showed that the tumour cells expressed vimentin, but not smooth-muscle actin, CD34, or desmin. | |||||||||||||||
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Immunohistochemical analysis showed that the tumour cells expressed vimentin, but not smooth-muscle actin (SMA), CD34, or desmin. | |||||||||||||||
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Defensin antibodies were visualized with an excitation filter of 555 nm (bandpass of 28 nm) and an emission filter of 617 nm (bandpass of 73 nm) and smooth muscle actin was acquired with an excitation filter of 640 nm (bandpass 20 nm) and emission filter of 685 (bandpass of 40 nm). | |||||||||||||||
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The tumour cells expressed S-100 protein and glial fibrillary acidic protein (GFAP) and were negative for HMB45, melan A, smooth muscle actin (SMA), desmin, CD34 and CD117. | |||||||||||||||
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The majority of GISTs are usually positive for CD117 (near 95% of cases), CD34 (positive in 7080% of cases), smooth muscle actin (positive in 40% of cases), PS 100 (positive near 5% of cases), and desmin (positive in approximately 2% of cases) [1-3]. | |||||||||||||||
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The tumor cells coexpressed CD34 and smooth muscle actin and were negative for staining desmin and S-100 protein. | |||||||||||||||
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In particular, geNorm classifies GAPDH and Act-B as the best two controls of the group (Table 2), while the best position in the stability ranking produced by NormFinder is occupied by Act-B, followed by hCyPB, GAPDH and HPRT1 (Table 2). | |||||||||||||||
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All the four house-keeping genes tested in this work (Act-B, GAPDH, hCyPB, HPRT1) were classified as optimal controls and showed a constant expression in human leukocytes samples. | |||||||||||||||
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All four house-keeping genes considered in this study (Act-B, GAPDH, hCyPB, HPRT1) were classified as optimal controls and showed stable expression in human leukocytes samples. | |||||||||||||||
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To clarify the development of the subepithelial spaces, the basement membrane, demarcating the lamina propria from the epithelial cells, and the underlying network of myofibroblasts within the villus lamina propria were studied, by staining collagen IV and smooth muscle actin (SMA), respectively [29], [30]. | |||||||||||||||
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Tumour cells were strongly immunolabelled for vimentin and some expressed smooth-muscle actin and desmin. | |||||||||||||||
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Typically the IMT is characterized by the expression of vimentin, smooth muscle actin, and cytokeratins, corresponded to that of myofibroblasts along with other inflammatory markers [10]. | |||||||||||||||
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General Comments
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