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Journal articles on the topic 'Trichromie'

Author: Grafiati
Published: 4 June 2021
Last updated: 2 February 2022

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1

Yu, Yufeng, and Clifford M. Chapman. "Masson Trichrome Stain: Postfixation Substitutes." Journal of Histotechnology 26, no. 2 (June 2003): 131–34. http://dx.doi.org/10.1179/his.2003.26.2.131.

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2

Lee, Dong-Youn, Cho-Rok Kim, and Joo-Heung Lee. "Trichrome vitiligo in segmental type." Photodermatology, Photoimmunology & Photomedicine 27, no. 2 (March 10, 2011): 111–12. http://dx.doi.org/10.1111/j.1600-0781.2011.00572.x.

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3

Kozlov, V. A., S. P. Sapozhnikov, and P. B. Karyshev. "Trichrome Staining for Detection of Amyloid." Cell and Tissue Biology 12, no. 1 (January 2018): 80–84. http://dx.doi.org/10.1134/s1990519x18010121.

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4

Richmond, Robert S. "Gomori Trichrome Stains for Skeletal Muscle." Journal of Histotechnology 17, no. 3 (September 1994): 288. http://dx.doi.org/10.1179/his.1994.17.3.288.

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5

Chaudhary, Anjali, Devesh K. Pathak, Suryakant Mishra, Priyanka Yogi, Pankaj R. Sagdeo, and Rajesh Kumar. "Polythiophene -viologen bilayer for electro-trichromic device." Solar Energy Materials and Solar Cells 188 (December 2018): 249–54. http://dx.doi.org/10.1016/j.solmat.2018.08.029.

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6

Hann, Seung-Kyung, Yi-Sun Kim, Jung Hoan Yoo, and Yoon-Sun Chun. "Clinical and histopathologic characteristics of trichrome vitiligo." Journal of the American Academy of Dermatology 42, no. 4 (April 2000): 589–96. http://dx.doi.org/10.1016/s0190-9622(00)90170-1.

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7

Hann, Seung-Kyung, Yi-Sun Kim, Jung Hoan Yoo, and Yoon-Sun Chun. "Clinical and histopathologic characteristics of trichrome vitiligo." Journal of the American Academy of Dermatology 42, no. 4 (April 2000): 589–96. http://dx.doi.org/10.1067/mjd.2000.104896.

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8

Ghanaati, Shahram, AkinyeleO Adisa, SamuelE Udeabor, Alica Kubesch, and Mike Barbeck. "The utility of azan trichrome staining in Ameloblastoma." Nigerian Postgraduate Medical Journal 23, no. 1 (2016): 44. http://dx.doi.org/10.4103/1117-1936.180187.

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9

Singh, Sanjay, Neetu Bhari, Mamta Rai, and Somesh Gupta. "Orangechrome Due to Carotenemia Presenting as Trichrome Vitiligo." Journal of Cutaneous Medicine and Surgery 22, no. 4 (June 21, 2018): 422. http://dx.doi.org/10.1177/1203475418755764.

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10

Di Chiacchio, N. G., F. R. Ferreira, M. L. de Alvarenga, and R. Baran. "Nail trichrome vitiligo: case report and literature review." British Journal of Dermatology 168, no. 3 (November 2, 2012): 668–69. http://dx.doi.org/10.1111/bjd.12008.

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11

Neimeister, R., A. L. Logan, and J. H. Egleton. "Modified trichrome staining technique with a xylene substitute." Journal of Clinical Microbiology 22, no. 2 (1985): 306–7. http://dx.doi.org/10.1128/jcm.22.2.306-307.1985.

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12

Maynard, James H. "A Trichrome Stain in Glycol Methacrylate That Works." Laboratory Medicine 17, no. 8 (August 1, 1986): 471–73. http://dx.doi.org/10.1093/labmed/17.8.471.

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13

Hinkelman, Laura M., Leon A. Metlay, Charles J. Churukian, and Robert C. Waag. "Modified Gomori Trichrome Stain for Macroscopic Tissue Slices." Journal of Histotechnology 19, no. 4 (December 1996): 321–23. http://dx.doi.org/10.1179/his.1996.19.4.321.

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14

Anton, Elsa. "Detection of Apoptosis by a Modified Trichrome Technique." Journal of Histotechnology 22, no. 4 (December 1999): 301–4. http://dx.doi.org/10.1179/his.1999.22.4.301.

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15

WHITTAKER, P. "Assessment of myocardial fibrosis: Underestimation using trichrome staining." Journal of Molecular and Cellular Cardiology 24 (June 1992): S39. http://dx.doi.org/10.1016/0022-2828(92)92971-e.

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16

Li, X., and A. Pandya. "064 Genetic and histologic characterization of trichrome vitiligo." Journal of Investigative Dermatology 136, no. 5 (May 2016): S11. http://dx.doi.org/10.1016/j.jid.2016.02.089.

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17

Ahmad Ghazali, W. A. A., H. Al-Talib, and A. B. Zaini. "Microsporidiosis: Identification by a simple modified trichrome stain." International Journal of Infectious Diseases 101 (December 2020): 430. http://dx.doi.org/10.1016/j.ijid.2020.09.1129.

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18

Cotton, F. Albert, Lee M. Daniels, Carlos A. Murillo, and Isabel Pascual. "Compounds with Linear, Bonded Trichromium Chains." Journal of the American Chemical Society 119, no. 42 (October 1997): 10223–24. http://dx.doi.org/10.1021/ja971998+.

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19

Saxena, Rashmil. "Dual Immunohistochemistry—Aniline Blue Stain: The Trichrome Stain Revisited." Journal of Histotechnology 33, no. 1 (March 2010): 25–29. http://dx.doi.org/10.1179/his.2010.33.1.25.

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20

Kannan, Shruti, Laura A. Morgan, Benjamin Liang, McKenzie G. Cheung, Christopher Q. Lin, Dan Mun, Ralph G. Nader, et al. "Segmentation of Glomeruli Within Trichrome Images Using Deep Learning." Kidney International Reports 4, no. 7 (July 2019): 955–62. http://dx.doi.org/10.1016/j.ekir.2019.04.008.

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21

Novaes, Rômulo D., Marli C. Cupertino, Mariaurea M. Sarandy, André Souza, Evelise A. Soares, and Reggiani V. Gonçalves. "Time-Dependent Resolution of Collagen Deposition During Skin Repair in Rats: A Correlative Morphological and Biochemical Study." Microscopy and Microanalysis 21, no. 6 (November 5, 2015): 1482–90. http://dx.doi.org/10.1017/s1431927615015366.

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AbstractSkin samples were used to compare microscopy methods used to quantify collagen with potential applicability to resolve time-dependent collagen deposition during skin wound healing in rats. Skin wounds by secondary intention were made in rats and tissue fragments were collected every 7 days for 21 days. Collagen content determined by biochemical analysis was compared with collagen measured by point counting (PC) on histological skin sections stained by Gomori’s trichrome method (Trichrome/PC), Sirius red under polarized light (PL) microscopy (Sirius red/PL-PC), and computational color segmentation (CS) applied to sections stained with Sirius red (Sirius red/PL-CS). All microscopy methods investigated resolved the time-dependent dynamics of collagen deposition in scar tissue during skin wound healing in rats. Collagen content measured by Sirius red/PL-PC and Sirius red/PL-CS was significantly lower when compared with Trichrome/PC. The Trichrome/PC method provided overestimated values of collagen compared with biochemical analysis. In the early stages of wound healing, which shows high production of noncollagenous molecules, Sirius red/PL-CS and Sirius red/PL-PC methods were more suitable for quantification of collagen fibers. Trichrome staining did not allow clear separation between collagenous and noncollagenous elements in skin samples, introducing a marked bias in collagen quantification.
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22

Gorbanzadeh, B., and J. Sadraei. "PP-171 Detection of Microsporidia and Cryptosporidium in stool specimens from AIDS patients by Modified Trichrome-Blue and Acid-Fast Trichrome staining methods." International Journal of Infectious Diseases 15 (July 2011): S93. http://dx.doi.org/10.1016/s1201-9712(11)60323-8.

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23

Ding, Cheng-Rong, Zhi-Min Jin, Hai-Bin Wang, Mao-Lin Hu, and He Lin. "1,4-Diazabicyclo[2.2.2]octane-1,4-diium trichromate." Acta Crystallographica Section C Crystal Structure Communications 60, no. 5 (April 21, 2004): m203—m204. http://dx.doi.org/10.1107/s0108270104004007.

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24

Joseph, A. A., and G. O. Popoola. "Comparison of various staining techniques in the diagnosis of Coccidian parasitosis in HIV infection." Journal of Medical and Biomedical Sciences 5, no. 3 (June 12, 2017): 28–35. http://dx.doi.org/10.4314/jmbs.v5i3.3.

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Diarrhoea due to oppourtunistic coccidian parasites is a common clinical presentation in HIV infection. Its management differs from that of diarrhoea due to other protozoa, improvement of immune status being the mainstay while specific drug treatment is available for other aetiologies, hence, the need for its accurate identification when present. This can be achieved via various diagnostic techniques, commonly microscopy in this environment, hence the need to compare the efficacy of the commonly used stains in our locality. The objective of the study is to identify the most effective of the commonly used stains in identifying these parasites. Diarrhea stool samples from 250 adult HIV positives and an equal number of age and sex matched HIV negative controls were screened, staining with trichrome, auramine and modified Ziehl Neelsen stain. A positivity rate of 55% was reported. Modified Ziehl Neelsen, when compared with trichrome staining had 81% sensitivity, 77.3% specificity, positive predictive value of 70.4%, negative predictive value of 85.9% and when compared to auramine staining, had 80% sensitivity, 76.7% specificity, positive predictive value of 69.9%, negative predictive value of 85.2% in test subjects. There was a significant moderate level of agreement between the staining methods though trichrome showed a stronger agreement than auramine when compared with Modified ZN in test (κ value 0.569 and 0.553 respectively), and a significant, fair level of agreement between the methods with Auramine showing a stronger agreement than trichrome when both were compared with Modified ZN (κ value 0.399 and 0.332 respectively) in controls. Auramine and trichrome techniques are preferred for screening and diagnosis based on findings. Of these two techniques, auramine is preferred.Journal of Medical and Biomedical Sciences (2016) 5(3), 28-35Keywords: comparison, trichrome, auramine, modified ziehl neelsen, HIV
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25

Al-Mahmood, Saevan S. "Improving light microscopic detection of collagen by trichrome stain modification." Iraqi Journal of Veterinary Sciences 34, no. 2 (May 17, 2020): 273–81. http://dx.doi.org/10.33899/ijvs.2019.126176.1256.

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26

Salleh, Fatmah Md, Tengku Shahrul Anuar, Azlin Mohd Yasin, and Norhayati Moktar. "Wintergreen oil: A novel method in Wheatley's trichrome staining technique." Journal of Microbiological Methods 91, no. 1 (October 2012): 174–78. http://dx.doi.org/10.1016/j.mimet.2012.08.004.

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27

Young, David G. "Improvements to Collagen and Nuclear Staining of the Masson's Trichrome." Journal of Histotechnology 24, no. 4 (December 2001): 271–73. http://dx.doi.org/10.1179/his.2001.24.4.271.

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28

Osheroff, Merrill R., and Richard N. Ruffing. "An Improved Trichrome Procedure For Glycol Methacrylate-Embedded Lung Tissue." Journal of Histotechnology 8, no. 2 (June 1985): 92–94. http://dx.doi.org/10.1179/his.1985.8.2.92.

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29

Skinner, Robert A. "Modified Osheroff-Ruffing: An Improved Trichrome Procedure for Glycol Methacrylate." Journal of Histotechnology 10, no. 4 (December 1987): 249–50. http://dx.doi.org/10.1179/his.1987.10.4.249.

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30

Moore, Joyce. "Citrate Buffer Alternative to Picric Acid for Masson Trichrome Stain." Journal of Histotechnology 19, no. 4 (December 1996): 341–42. http://dx.doi.org/10.1179/his.1996.19.4.341.

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31

Yu, Hsin Her, and Leslie J. Fina. "Trichroic Infrared Studies of Oriented Nylon 11." Macromolecules 27, no. 21 (October 1994): 6192–200. http://dx.doi.org/10.1021/ma00099a039.

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32

Kellogg, James A., and Carol J. Elder. "Justification for Use of a Single Trichrome Stain as the Sole Means for Routine Detection of Intestinal Parasites in Concentrated Stool Specimens." Journal of Clinical Microbiology 37, no. 3 (1999): 835–37. http://dx.doi.org/10.1128/jcm.37.3.835-837.1999.

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Of 12,321 stool samples analyzed over a 6-year interval, 870 (7.1%) were positive for a total of 1,019 parasites, of which 1,011 (99.2%) were found in trichrome-stained smears of unconcentrated specimens while only 479 (47.0%) were detected in iodine-stained smears of concentrated samples. Stool specimens were next analyzed by trichrome staining of both unconcentrated and concentrated specimens preserved in either mercury-polyvinyl alcohol (PVA) or cupric PVA. Of 2,198 specimens, 171 (7.8%) were positive for a total of 208 parasites, 192 (92.3%) and 204 (98.1%) of which were found in the unconcentrated and concentrated specimens, respectively (P < 0.05). In our patient population, examination of a single trichrome-stained smear of a concentrated stool specimen is a cost-effective alternative to routinely analyzing both concentrated and unconcentrated specimens for parasites.
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33

Florentine, Barbara D., Arno A. Roscher, Jerry Garrett, and Nancy E. Warner. "Necrotic Seminoma of the Testis." Archives of Pathology & Laboratory Medicine 126, no. 2 (February 1, 2002): 205–6. http://dx.doi.org/10.5858/2002-126-0205-nsott.

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Abstract We describe an infarcted mass in the testis containing “ghost” cells suspicious for neoplasm. The entire lesion was necrotic. A Masson trichrome stain greatly improved nuclear and cytologic detail, confirming the suspicion of neoplasm. Placental alkaline phosphatase revealed specific membrane staining of the neoplastic cells and established a diagnosis of seminoma. Masson trichrome plus selected immunostains offer a promising approach to the diagnosis of certain necrotic neoplasms.
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34

Chioralia, Gabriela, Thomas Trammer, Helge Kampen, and Hanns M. Seitz. "Relevant Criteria for Detecting Microsporidia in Stool Specimens." Journal of Clinical Microbiology 36, no. 8 (1998): 2279–83. http://dx.doi.org/10.1128/jcm.36.8.2279-2283.1998.

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By using different staining techniques, 479 stool specimens from 212 diarrheic patients with AIDS were examined for microsporidian spores. Calcofluor fluorescence staining of 119 specimens revealed fluorescent ovoid structures of microsporidian size. Staining of these samples according to the method of Weber et al. (R. Weber, R. T. Bryan, R. L. Owen, C. M. Wilcox, L. Gorelkin, and G. S. Visvesvara, N. Engl. J. Med. 326:161–166, 1992) with trichrome produced six specimens with pinkish spores containing the characteristic microsporidian belt-like structure. The 6 specimens were processed for transmission electron microscopy, as were another 21 specimens which did not present the belt-like structure after trichrome staining but which looked highly suspicious after fluorescence staining. In these 21 samples, only fungal spores and, particularly, bacterial Clostridium spores were demonstrated, whereas in the 6 samples diagnosed positive after trichrome staining, the existence of microsporidia could be verified by electron microscopy. Based on our observations, we propose that the belt-like structure seen with the Weber stains in microsporidian spores corresponds to structures existing in priming-stage spores. The results suggest that routine microscopical fecal diagnosis for microsporidian infection should include a screening by fluorescence staining and, subsequently, a confirmatory viewing of fluorescence-positive samples after trichrome staining.
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35

Cotton, F. Albert, Peng Lei, and Carlos A. Murillo. "Linear trichromium(II) chains wrapped by unsymmetrical formamidinates." Inorganica Chimica Acta 349 (June 2003): 173–81. http://dx.doi.org/10.1016/s0020-1693(03)00093-8.

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36

Lin, Amy Y., Andrew J. Maniotis, Klara Valyi-Nagy, Dibyen Majumdar, Suman Setty, Shri Hari Kadkol, Lu Leach, Jacob Pe'er, and Robert Folberg. "Distinguishing Fibrovascular Septa From Vasculogenic Mimicry Patterns." Archives of Pathology & Laboratory Medicine 129, no. 7 (July 1, 2005): 884–92. http://dx.doi.org/10.5858/2005-129-884-dfsfvm.

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Abstract Context.—Molecular analyses indicate that periodic acid–Schiff (PAS)–positive (laminin-rich) patterns in melanomas are generated by invasive tumor cells by vasculogenic mimicry. Some observers, however, consider these patterns to be fibrovascular septa, generated by a stromal host response. Objective.—To delineate differences between vasculogenic mimicry patterns and fibrovascular septa in primary uveal melanomas. Design.—Frequency distributions, associations with outcome, and thicknesses of trichrome-positive and PAS-positive looping patterns were determined in 234 primary uveal melanomas. Sequential sections of 13 additional primary uveal melanomas that contained PAS-positive/trichrome-negative looping patterns were stained for type I and type IV collagens, laminin, and fibronectin. Real-time quantitative polymerase chain reaction was performed on RNA from cultured uveal melanoma cells for the expression of COL1A1, COL4A2, and fibronectin. Results.—Trichrome-positive loops were encountered less frequently than PAS-positive loops (10% vs 56%, respectively). Death from metastatic melanoma was strongly associated with PAS-positive (P &lt; .001) but not with trichrome-positive (P = .57) loops. Trichrome-positive loops were significantly thicker than PAS-positive loops (P &lt; .001). The PAS-positive patterns stained positive for laminin, type I and type IV collagens, and fibronectin. Type I collagen was detected within melanoma cells and focally within some PAS-positive patterns. Real-time quantitative polymerase chain reaction revealed 3-fold, 25-fold, and 97-fold increases, respectively, in expression of COL4A2, fibronectin, and COL1A1 by invasive pattern-forming primary melanoma cells compared with poorly invasive non– pattern-forming cells. Conclusions.—Fibrovascular septa are rare and prognostically insignificant in uveal melanomas, whereas vasculogenic mimicry patterns are associated with increased mortality. Type I collagen, seen focally in some vasculogenic mimicry patterns, may be synthesized by tumor cells, independent of a host stromal response.
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37

Trentini Lopes Ribeiro, Fernanda, Maria Laura Medeiros Assef, and Silvana Maris Círio. "HISTOPATHOLOGIC STUDY OF CUTANEOUS FIBROSARCOMA IN DOGS (Canis familiares, Linnaeus, 1758) WITH DIFFERENT STAINING TECHNIQUES." Revista Acadêmica: Ciência Animal 7, no. 3 (July 15, 2009): 341. http://dx.doi.org/10.7213/cienciaanimal.v7i3.10017.

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Fibrosarcoma is characterized as an invasive nodular tumor of mesodermal origin, with elongated normochromatic nuclei. The histopathologic analysis using specific staining techniques is efficient in detailing the neoplastic architecture and the relations with surrounding tissues. In the present study, the canine skin fibrosarcoma was histologically characterized using Hematoxilin-Eosin stain, Mallory’s Trichrome stain and Shorr’s Trichrome stain as routine staining for conjunctive tissue, Toluidine Blue to highlight the mitosis and Picrosirius-Hematoxilin Trichrome to characterize the collagen type. It was concluded that the Picrosirius stain characterized the existing collagen type as type I and III; the Toluidine Blue staining highlighted the mitoses together with Shorr’s staining, as this one also provided a marking for the conjunctive tissue and the formed bands. The Mallory’s staining technique highlighted the conjunctive tissue and the bands that are spread; the Hematoxilin-Eosin stain highlighted with emphasis the neoplastic cells.
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38

Miller, Marian L., Anastasia Andringa, Kathleen Dixon, and Michael P. Carty. "Insights into UV-induced apoptosis: ultrastructure, trichrome stain and spectral imaging." Micron 33, no. 2 (January 2002): 157–66. http://dx.doi.org/10.1016/s0968-4328(01)00014-2.

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39

KIMACHI, Akira, You-Wu YAO, and Shigeru ANDO. "Velocity Field Sensing System Using Color TV Camera and Trichrome Stroboscope." IEEJ Transactions on Sensors and Micromachines 119, no. 1 (1999): 20–26. http://dx.doi.org/10.1541/ieejsmas.119.20.

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40

Birchall, Ian E. "Evaluation of Renal Biopsies with the Silver Methenamine/Masson Trichrome Technique." Journal of Histotechnology 17, no. 2 (June 1994): 131–35. http://dx.doi.org/10.1179/his.1994.17.2.131.

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41

Saxena, Sandeep, and Carsten H. Meyer. "A Trichrome RGB Endoillumination Prototype System: A Novel Application for Chromovitrectomy." Ophthalmologica 230, s2 (2013): 73–76. http://dx.doi.org/10.1159/000354168.

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42

Li, Hui, Gene-Hsiang Lee, and Shie-Ming Peng. "Synthesis and crystal structure of trichromium metal string complex." Journal of Molecular Structure 707, no. 1-3 (November 2004): 179–86. http://dx.doi.org/10.1016/j.molstruc.2004.07.037.

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43

Cotton, F. Albert, Lee M. Daniels, Carlos A. Murillo, and Isabel Pascual. "Tuning metal-to-metal distances in linear trichromium units." Inorganic Chemistry Communications 1, no. 1 (January 1998): 1–3. http://dx.doi.org/10.1016/s1387-7003(98)00002-1.

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44

Higgins, Gerald Vincent. "lodine-Trichrome Staining Technique: A Replacement of Iodine Solution in Fecal Examination." Laboratory Medicine 19, no. 12 (December 1, 1988): 824–25. http://dx.doi.org/10.1093/labmed/19.12.824.

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45

Meyer, Richard, Gwendolyn C. Claussen, and Shin J. Oh. "Modified trichrome staining technique of the nerve to determine proximal nerve viability." Microsurgery 16, no. 3 (1995): 129–32. http://dx.doi.org/10.1002/micr.1920160302.

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46

Allison, Russ, and Sally Tanswell. "Unexpected Results of Trichrome Staining of Quenched Epithelial Tissue Following Delayed Fixation." Journal of Histotechnology 16, no. 4 (December 1993): 343–48. http://dx.doi.org/10.1179/his.1993.16.4.343.

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47

MacNiven, Iain. "Stable Trichrome for the Demonstration of the Intermyofibrillary Network in Muscle Biopsies." Journal of Histotechnology 17, no. 1 (March 1994): 59–61. http://dx.doi.org/10.1179/his.1994.17.1.59.

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48

Valaitis, Jonas, Yolanda Trujillo, Diane Burica, and Lucia Tirva. "Detection of Early Acute Myocardial Infarction by Gomori Trichrome Aniline Blue Stain." Journal of Histotechnology 17, no. 2 (June 1994): 127–30. http://dx.doi.org/10.1179/his.1994.17.2.127.

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49

Garvey, W., F. Bigelow, A. Fathi, C. Jimenez, and B. Carpenter. "Modified Gomori Trichrome Stain for Frozen Skeletal Muscle and Paraffin Embedded Sections." Journal of Histotechnology 19, no. 4 (December 1996): 329–33. http://dx.doi.org/10.1179/his.1996.19.4.329.

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50

Sam-Yellowe, Tobili Y., Kush Addepalli, Raghavendra Yadavalli, and John W. Peterson. "New trichrome stains identify cysts of Colpodella sp. (Apicomplexa) and Bodo caudatus." International Microbiology 23, no. 2 (November 20, 2019): 303–11. http://dx.doi.org/10.1007/s10123-019-00104-1.

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