Relevant bibliographies by topics / Histochemical analysis

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  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Histochemical analysis'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Histochemical analysis"

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Martin, T. P., A. C. Vailas, J. B. Durivage, V. R. Edgerton, and K. R. Castleman. "Quantitative histochemical determination of muscle enzymes: biochemical verification." Journal of Histochemistry & Cytochemistry 33, no. 10 (October 1985): 1053–59. http://dx.doi.org/10.1177/33.10.4045183.

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We established quantitative histochemical assays for the enzymatic activity of succinate dehydrogenase and alpha-glycerol phosphate dehydrogenase for cat skeletal muscle. A computer-enhanced image analysis system was used to quantitate the histochemical enzyme-activity reaction products. We describe a series of experiments that verify the reliability and validity of the assays. Histochemically determined enzyme activities were linear with respect to tissue thickness and reaction time. Biochemically determined enzyme activities were also linear with respect to tissue thickness and incubation time. Consecutive tissue sections, assayed either histochemically or biochemically, were used to establish a linear regression equation that allowed quantitative histochemically determined reaction rates, measured in optical density per minute, to be calibrated as nanomoles per minute.
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Hua, C., X. K. Shu, and C. Lei. "Pancreatoblastoma: a histochemical and immunohistochemical analysis." Journal of Clinical Pathology 49, no. 11 (November 1, 1996): 952–54. http://dx.doi.org/10.1136/jcp.49.11.952.

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de Eguileor, Magda, Sergio Daniel, Franco Cotelli, Roberto Valvassori, and Giulio Lanzavecchia. "Histochemical analysis of oligochaete body wall." Hydrobiologia 180, no. 1 (August 1989): 99–107. http://dx.doi.org/10.1007/bf00027542.

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Schendel, Stephen A., Annette Cholon, and Jean Delaire. "Histochemical Analysis of Cleft Palate Muscle." Plastic and Reconstructive Surgery 94, no. 7 (December 1994): 919–23. http://dx.doi.org/10.1097/00006534-199412000-00003.

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Kristeva, Michaela, Jyotirmay Biswas, Geeta Pararajasegaram, Alex Sevanian, and Narsing A. Rao. "Histochemical Analysis of Experimental Granulomatous Uveitis." Ophthalmic Research 23, no. 2 (1991): 73–78. http://dx.doi.org/10.1159/000267092.

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Stirling, John W. "Freeze Substitution for Histochemical and Immunohistochemical Analysis." American Journal of Clinical Pathology 96, no. 4 (October 1, 1991): 553. http://dx.doi.org/10.1093/ajcp/96.4.553.

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Greve, J. M. D., R. Muszkat, B. Schmidt, J. Chiovatto, T. E. P. Barros, and L. R. Batisttella. "Functional electrical stimulation (FES): muscle histochemical analysis." Spinal Cord 31, no. 12 (December 1993): 764–70. http://dx.doi.org/10.1038/sc.1993.119.

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Marin, M., L. Ascensao, S. Budimir, D. Janošević, S. Duletić-Laušević, and P. Marin. "The Histochemical Analysis ofThymus MalyiRonninger Glandular Trichomes." Biotechnology & Biotechnological Equipment 24, sup1 (January 2010): 39–41. http://dx.doi.org/10.1080/13102818.2010.10817807.

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Karbanová, Jana, and Jaroslav Mokrý. "Histological and histochemical analysis of embryoid bodies." Acta Histochemica 104, no. 4 (January 2002): 361–65. http://dx.doi.org/10.1078/0065-1281-00677.

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Nessim, Maged, Suresh K. Pandey, Liliana Werner, Musadiq Mohammed, and Vinod Kumar. "Histochemical analysis of bandage contact lens precipitates." Contact Lens and Anterior Eye 31, no. 1 (February 2008): 47–49. http://dx.doi.org/10.1016/j.clae.2007.06.004.

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Dissertations / Theses on the topic "Histochemical analysis"

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Seif, Mourad W. "Progress in immuno-histochemical analysis of the endometrial cycle." Thesis, University of Manchester, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.257445.

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Atkins, Elizabeth Ann. "A histochemical analysis of the colonic epithelial glycoproteins from ulcerative colitus, Crohn's disease and diverticular disease." Thesis, University of British Columbia, 1987. http://hdl.handle.net/2429/26161.

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The aim of the present study was to assess whether the changes in the epithelial glycoproteins seen in the mucosa adjacent to tumors are specific premalignant markers or secondary reactive phenomena. A secondary objective was to assess whether ulcerative colitis and Crohn's Disease could be distinguished from one another histochemically. The carbohydrate prosthetic groups from colonic epithelial glycoproteins were characterized histologically and histochemically from 17 cases of ulcerative colitis, 21 cases of Crohn's Disease and 19 cases of diverticular disease. Two histochemical parameters - the relative proportion of sulpho- and sialomucin and the side-chain substitution pattern of O-acetylated sialic acid - were assessed using a battery of seven histochemical techniques. Serial sections from each specimen were also evaluated morphologically, using hematoxylin and eosin. In addition, the patterns of O-acetylated side-chain sialic acid from the three inflammatory bowel diseases were compared to data previously acquired from the mucosa adjacent to colonic tumors. Results indicate that neither focal changes nor the predominance of sialomucins are specific to the mucosa adjacent to tumors. As well, changes in one histochemical parameter were independent of changes in the other parameter. No histochemical class of epithelial glycoproteins was specific to any of the inflammatory bowel diseases and, therefore, it was not possible to distinguish between ulcerative colitis and Crohn's Disease on the basis of the histochemical techniques used in the present study. It was also noted that the histochemical changes in ulcerative colitis, Crohn's Disease and diverticular specimens were not related to the degree of inflammation. Finally, as a group, Crohn's Disease specimens showed a loss of sulphomucin-sialomucin gradient along the length of the crypts.
Medicine, Faculty of
Pathology and Laboratory Medicine, Department of
Graduate
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Au, Wai-ting Doris. "Enzymatic studies of conidial attachment and lectin-gold histochemical investigation of the extracellular mucilages of Lemonniera aquatica de Wild. and Mycocentrospora filiformis (Petersen) Iqbal /." [Hong Kong : University of Hong Kong], 1993. http://sunzi.lib.hku.hk/hkuto/record.jsp?B13456970.

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Schacht, Tanja [Verfasser]. "Biochemical analysis of the inhibition of Ralstonia solanacearum polygalacturonases by polygalacturonase-inhibiting proteins (PGIP) from tomato stems and biochemical, histochemical and molecular analysis of the silicon effect in the tomato (Solanum lycopersicum) - Ralstonia solanacearum interaction / Tanja Schacht." Hannover : Technische Informationsbibliothek und Universitätsbibliothek Hannover, 2010. http://d-nb.info/1004973624/34.

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García, Caballero Gabriel [Verfasser], and Herbert [Akademischer Betreuer] Kaltner. "Chicken (Gallus gallus) as model for network analysis of adhesion-/growth-regulatory galectins : biochemical characterization of C-GRIFIN/C-GRP and first complete histochemical analysis for the galectin family in bursa of Fabricius / Gabriel García Caballero ; Betreuer: Herbert Kaltner." München : Universitätsbibliothek der Ludwig-Maximilians-Universität, 2018. http://d-nb.info/1155407733/34.

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Salvi, Júnior Ademir [UNESP]. "Schinus Terebinthifolius Raddi: estudo anatômico e histoquímico das folhas e investigação do potencial farmacêutico do extrato etanólico e suas frações." Universidade Estadual Paulista (UNESP), 2009. http://hdl.handle.net/11449/96251.

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Made available in DSpace on 2014-06-11T19:28:04Z (GMT). No. of bitstreams: 0 Previous issue date: 2009-12-21Bitstream added on 2014-06-13T20:17:46Z : No. of bitstreams: 1 salvijunior_a_me_arafcf.pdf: 1910773 bytes, checksum: 57df20a4c82fceb864c0b8eea2d26d95 (MD5)
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
Schinus terebinthifolius Raddi, pertence à família Anacardiaceae, é popularmente denominada como aroeira-vermelha. Trata-se de uma espécie nativa da América do Sul, especialmente do Brasil, Paraguai e Argentina. No Brasil ocorre ao longo da Mata Atlântica desde o nordeste até o sul do país. Consta oficialmente na primeira edição da Farmacopeia Brasileira, a qual designa as cascas do tronco como seu farmacógeno, embora estudos revelem que folhas e frutos também podem ser utilizados como fonte de substâncias ativas e, devido a este fato, desperta um grande interesse para a pesquisa. Na literatura é citada como cicatrizante, anti-inflamatória, antioxidante, antitumoral e antimicrobiana. Este trabalho teve como objetivos: descrever a anatomia da região mediana de folíolos de Schinus terebinthifolius; realizar testes histoquímicos nas folhas da espécie com fins de caracterização preliminar de constituintes químicos de interesse; realizar o estudo granulométrico da droga vegetal pulverizada proveniente do processo de moagem de folhas de S. terebinthifolius; estabelecer a caracterização físico-química da droga vegetal; realizar a análise fitoquímica preliminar do extrato e frações obtidas; e, avaliar a atividade antimicrobiana do extrato e das frações utilizando-se a técnica de microdiluição em placas. Os resultados da anatomia revelaram as formas das estruturas celulares das folhas e os tipos de inclusões celulares presentes; na análise histoquímica e triagem fitoquímica identificou-se a presença de grupamentos fenólicos, flavonoides e taninos, terpenoides e saponinas de interesse farmacológico; na caracterização físico-química destacou-se importantes informações para o estabelecimento dos parâmetros referentes ao controle da qualidade da droga; na atividade antibacteriana, o extrato...
Schinus terebinthifolius Raddi, belongs to the Anacardiaceae family, is popularly known as Brazilian pepper. It is native from South America, especially Brazil, Paraguay and Argentina. In Brazil it occurs along the Atlantic Forest from the northeast to the south. Officially listed in the first edition of the Brazilian Pharmacopoeia, which means the bark of the trunk as its pharmacogens, although studies show that fruits and leaves can also be used as a source of active substances, and due to this fact, arouses a great interest for search. The literature cited as healing, anti-inflammatory, antioxidant, antitumor and antimicrobial activities. This study aimed to describe the anatomy of the middle region of leaves of Schinus terebinthifolius; perform tests histochemical in leaflets of the species for purposes of preliminary characterization of chemical constituents of interest; perform the study granulometric to the sprayed drug plant from the process of grinding the leaves of S. terebinthifolius; establish the physical-chemical characterization of the drug plant; perform the preliminary phytochemical analysis of extract and fractions obtained; and, to evaluate the antimicrobial activity of the extract and the fractions using the microdilution plates. The results of the anatomy revealed the forms of cellular structures of the leaves and the types of cellular inclusions present; the histochemical analysis and phytochemical screening could identified the presence of phenolic groups, flavonoids and tannins, terpenoids and saponins of pharmacological interest; in physical-chemical characterization to be detached important information for the establishment of the parameters concerning to quality control of drug; of the antibacterial activity, the extract and the fractions were shown to be effective against the Staphylococcus aureus, Enterococcus faecalis... (Complete abstract click electronic access below)
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Salvi, Júnior Ademir. "Schinus Terebinthifolius Raddi : estudo anatômico e histoquímico das folhas e investigação do potencial farmacêutico do extrato etanólico e suas frações /." Araraquara : [s.n.], 2009. http://hdl.handle.net/11449/96251.

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Orientador: Luis Vitor Silva do Sacramento
Banca: Norberto Peporine Lopes
Banca: Hérida Regina Nunes Salgado
Resumo: Schinus terebinthifolius Raddi, pertence à família Anacardiaceae, é popularmente denominada como aroeira-vermelha. Trata-se de uma espécie nativa da América do Sul, especialmente do Brasil, Paraguai e Argentina. No Brasil ocorre ao longo da Mata Atlântica desde o nordeste até o sul do país. Consta oficialmente na primeira edição da Farmacopeia Brasileira, a qual designa as cascas do tronco como seu farmacógeno, embora estudos revelem que folhas e frutos também podem ser utilizados como fonte de substâncias ativas e, devido a este fato, desperta um grande interesse para a pesquisa. Na literatura é citada como cicatrizante, anti-inflamatória, antioxidante, antitumoral e antimicrobiana. Este trabalho teve como objetivos: descrever a anatomia da região mediana de folíolos de Schinus terebinthifolius; realizar testes histoquímicos nas folhas da espécie com fins de caracterização preliminar de constituintes químicos de interesse; realizar o estudo granulométrico da droga vegetal pulverizada proveniente do processo de moagem de folhas de S. terebinthifolius; estabelecer a caracterização físico-química da droga vegetal; realizar a análise fitoquímica preliminar do extrato e frações obtidas; e, avaliar a atividade antimicrobiana do extrato e das frações utilizando-se a técnica de microdiluição em placas. Os resultados da anatomia revelaram as formas das estruturas celulares das folhas e os tipos de inclusões celulares presentes; na análise histoquímica e triagem fitoquímica identificou-se a presença de grupamentos fenólicos, flavonoides e taninos, terpenoides e saponinas de interesse farmacológico; na caracterização físico-química destacou-se importantes informações para o estabelecimento dos parâmetros referentes ao controle da qualidade da droga; na atividade antibacteriana, o extrato... (Resumo completo, clicar acesso eletrônico abaixo)
Abstract: Schinus terebinthifolius Raddi, belongs to the Anacardiaceae family, is popularly known as Brazilian pepper. It is native from South America, especially Brazil, Paraguay and Argentina. In Brazil it occurs along the Atlantic Forest from the northeast to the south. Officially listed in the first edition of the Brazilian Pharmacopoeia, which means the bark of the trunk as its pharmacogens, although studies show that fruits and leaves can also be used as a source of active substances, and due to this fact, arouses a great interest for search. The literature cited as healing, anti-inflammatory, antioxidant, antitumor and antimicrobial activities. This study aimed to describe the anatomy of the middle region of leaves of Schinus terebinthifolius; perform tests histochemical in leaflets of the species for purposes of preliminary characterization of chemical constituents of interest; perform the study granulometric to the sprayed drug plant from the process of grinding the leaves of S. terebinthifolius; establish the physical-chemical characterization of the drug plant; perform the preliminary phytochemical analysis of extract and fractions obtained; and, to evaluate the antimicrobial activity of the extract and the fractions using the microdilution plates. The results of the anatomy revealed the forms of cellular structures of the leaves and the types of cellular inclusions present; the histochemical analysis and phytochemical screening could identified the presence of phenolic groups, flavonoids and tannins, terpenoids and saponins of pharmacological interest; in physical-chemical characterization to be detached important information for the establishment of the parameters concerning to quality control of drug; of the antibacterial activity, the extract and the fractions were shown to be effective against the Staphylococcus aureus, Enterococcus faecalis... (Complete abstract click electronic access below)
Mestre
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Carvalho, Cristiane de. "Maturação e caracterização morfoanatômica, fisiológica e bioquímica de sementes de pimentão." Universidade de São Paulo, 2014. http://www.teses.usp.br/teses/disponiveis/11/11136/tde-05052014-145310/.

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Durante a maturação da semente, a partir da fertilização do óvulo, há alterações inerentes à formação da semente, com destaque para as variações do tamanho, do teor de água, das massas da matéria fresca e seca e da germinação das sementes. Paralelamente, para os frutos carnosos há alterações visíveis nos frutos relacionados à forma, à cor e à senescência. Não há, todavia, relatos de quais mudanças (morfológica, anatômica, fisiológica e bioquímica) ocorrem nas sementes que se desenvolvem no interior de frutos carnosos mantidos em repouso por diferentes períodos de tempo. O objetivo dessa pesquisa foi avaliar a fase final da formação das sementes de pimentão, considerando as variações da morfologia externa dos frutos e do parâmetro fisiológico, da morfologia interna, da enzima endo-?-mananase, da anatomia e do acúmulo de substâncias de reservas e do ciclo celular das sementes, visando verificar se essas mudanças explicam as alterações fisiológicas das sementes de pimentão após o repouso pós-colheita do fruto e durante o armazenamento das sementes. As sementes foram extraídas de frutos em diferentes estádios de maturação, (cores verde, verde-avermelhada e vermelha), mantidos em repouso por 3, 7 ou 14 dias ou sem repouso, e avaliadas logo após a colheita e durante o armazenamento. Os frutos foram avaliados quanto à coloração, dimensões e massa. As sementes foram avaliadas quanto ao teor de água, massa de matéria seca, massa de 1000 sementes, germinação e vigor, além da avaliação de imagens de raios X para o estudo da morfologia interna das sementes, da atividade da enzima endo-?-mananase pelo método da difusão em gel, análises histoquímicas para o estudo da anatomia e de substâncias de reserva e a avaliação do ciclo celular. A colheita das sementes de pimentão pode ser caracterizada pela coloração dos frutos. Em função do repouso há alteração da cor do fruto, do ciclo celular das sementes hidratadas, da atividade da enzima endo-?-mananase e de algumas substâncias de reserva, interferindo positivamente na qualidade das sementes de pimentão. Entretanto, o repouso de frutos, que estão em estágio avançado de desenvolvimento, causa redução da qualidade das sementes. O teor de água, a massa de matéria seca e a morfologia interna da semente, a anatomia das células do endosperma e a presença de substâncias de reservas das sementes não são alterados durante o repouso do fruto, mas estão relacionados ao estádio de formação das sementes. Na medida em que há a deterioração natural das sementes durante o armazenamento, há redução da germinação e do vigor, da atividade da endo-?-mananase, da quantidade de lipídios, proteínas e polissacarídeos das células do embrião e do endosperma. Durante o repouso do fruto por 14 dias, as sementes extraídas de frutos verdes têm tolerância à desidratação, caracterizada principalmente pelo aumento da germinação após a secagem das sementes. A maturidade fisiológica das sementes é caracterizada pela coloração verde-avermelhada dos frutos e também pela estabilização do teor de água das sementes (30%), pela quantidade de matéria seca e pelo conteúdo de DNA 4C; não há coincidência entre maturidade fisiológica e máxima germinação.
During seed maturation there are some significant alterations in seed size, moisture content, fresh and dry matter and germination. Furthermore, for fleshy fruits, visible alterations occur as the fruit shape, color and senescence. There are not reports about which morphological, anatomical, physiological and biochemical alterations occur in seeds that develop inside fleshy fruits during the rest of them, for different periods of time. The objective of this research was to evaluate the final stage of the bell pepper seed formation and it was considered the variations of the external morphology of the fruit, and the physiological parameter, internal morphology, activity of endo-?-mannanase, anatomy and the reserve substances accumulation, and cell cycle of the seeds to verify if these changes explain the physiological changes of the bell pepper seeds after the fruit resting and during the seed storage. The seeds were extracted from fruits at different maturation stages (colors green, reddish-green and red), with (3, 7 or 14 days) or without fruit resting, and during the seed storage. The fruits were evaluated by color, and the measurements and weight. The seeds were evaluated for moisture content, dry mass, mass of 1000 seeds, germination and vigor and X-ray imaging to study the internal morphology of the seeds, endo-?-mannanase activity by gel diffusion assay, histochemical analyzes to study seed anatomy and reserve substances, and flow cytometry to assess the cell cycle. The harvest of bell peppers seeds can be made by the color of the fruits. The fruit resting alters the fruit color, germination, vigor, endo-?-mannanase activity, some storage substances and cell cycle improving bell pepper seed quality. However it has a negative role when the fruits are in advanced stage of development (red fruits and resting time more than 7 days). The moisture content, dry matter and the internal morphology of the seeds do not change by the fruit resting, but because of the seed maturation stage. It was observed reduction of all the physiological parameters, including the amount of lipids in the cells and endo-?-mannanase activity. During fruit resting, the endo-?-mannanase activity and the 4C DNA content of the cells decrease and there is an increased rate of germination and vigor. The water content, dry matter, internal morphology and anatomy of the cells of the endosperm and the presence of reserves substances in the seeds are not changed due to the rest of the fruit, but are related to the seed formation stage. There is natural seed deterioration during storage and a reduction of germination and vigor, endo-?-mannanase activity, amount of lipids, proteins and polysaccharides in the embryo and endosperm cells. During the fruit resting (14 days), the seeds extracted from green fruits have desiccation tolerance, characterized by increased of the seed germination after drying. The physiological maturity is reached when the fruits are reddish-green, characterized by stabilizing the water content of the seeds (30 %), amount of dry matter and the 4C DNA content. There is not a coincidence between physiological maturity and maximum germination.
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Reuther, Theresa Maria. "Vergleich der Stabilität von Schanzschrauben im Knochen im externen Fixateurverbund zu ausgewählten Zeitpunkten am Schafmodell." Doctoral thesis, Humboldt-Universität zu Berlin, Medizinische Fakultät - Universitätsklinikum Charité, 2006. http://dx.doi.org/10.18452/15482.

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Externe Fixateure werden häufig für die Stabilisierung und Behandlung schwerer Frakturen genutzt. Schraubenkanalinfektionen können dabei zu Komplikationen, wie Osteomyelitis und Stabilitätsverlusten führen. Es ist unklar, ob Schraubenkanalinfektionen zu Schraubenlockerungen führen, oder aber ob der Stabilitätsverlust von Schrauben in Schraubenkanalinfektionen resultiert. Das Ziel dieser Studie ist es, einen Zusammenhang zwischen der mechanischen Stabilität, dem Auftreten von Infektionen und der osseären Verankerung darzustellen. An 27 Schafen wurde eine standardisierte Osteotomie (3mm weiter Frakturspalt) der rechten Tibia durchgeführt und mit einem monolateralem Fixateur externe stabilisiert. Während der täglichen Pinpflege wurde die Haut um die Schraubeneintrittsstellen begutachtet. Radiologische Verlaufskontrollen erfolgten in wöchentlichen Abständen. Nach 3, 6 und 9 Wochen wurden die Tiere getötet, die Ausdrehmomente der Schrauben gemessen und mikrobiologische Abstriche genommen. Knochenschnitte durch die Schraubenkanäle wurden für histologische, histochemische und histomorphometrische Analysen genommen. In dieser Studie scheint es zu einer Zunahme der Stabilisierung der osseären Verankerung während des Heilungsverlaufes zu kommen. Da die kortikale Knochendichte über die Zeit abnimmt, kann die zunehmend stabilere Verankerung der Schrauben einzig über eine gleichzeitige periostale Kallusdichtezunahme erklärt werden. Die größten Ausdrehmomente des neugebildeten periostalen Kallus wurden zum Sechswochenzeitpunkt gemessen. Danach nimmt die periostale Kallusfläche ab, wohingegen die Kallusdichte zunimmt. Die mikrobiologische Besiedelungsrate (15%) war dreifach höher als die klinisch bestätigten Infektionen. Hingegen war die Osteolyserate (28%) doppelt so hoch wie die mikrobiologisch bestätigte Infektionsrate. Eine Korrelation zwischen Infektion, Osteolyse und Pinlockerung konnte nicht gefunden werden.
External fixators are frequently used for the stabilization and the treatment of problematic fractures. Pin track infections have been shown to cause complications such as osteomyelitis and loss of stability of osteosynthesis. It remains unclear, whether pin track infection provokes pin loosening, or loss of the pin stability results in pin track infections. The aim of this study was to investigate the correlation between the mechanical stability of pins, the incidence of pin track infections and the osseus anchorage of pins. 27 sheep underwent a standardized osteotomy (3 mm gap) of the right tibia. The tibiae were stabilized by a monolateral external fixator. Within the daily pin care routine, the skin around the pin entries was scored. Radiographs were taken at weekly intervals. After 3, 6 and 9 weeks, the animals were sacrificed, the extraction torque of all pins was determined and microbiological analyses were taken. Bone sections through the pintracks were taken for histological, histochemical and histomorphometrical analysis. This study reveals an increasing stability of osseous pinanchorage over the course of healing. As the cortical bone density decreased over time, the increased anchorage-stability of the pins can only be explained by the simultaneous increase of the periosteal callus bone density. The magnitude of the extraction force is determined by the newbuilt periosteal callus, which is at its biggest value at six weeks. Afterwards, the periosteal callus area abates, while the callus bone density accumulates. The microbiologically affirmed infection rate (15%) was three times higher than the one clinical ascertained. In contrast the evidence of osteolysis (28%) was twice as high as the microbiologically diagnosed infection-rate. Despite the low infection rate, evidence of cortical lysis coud not be prevented. No correlation could be found between infection, osteolysis and pin loosening.
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Strabala, Timothy John. "Analysis of functional elements in and histochemical localization of expression of the Agrobacterium tumefaciens pTiA6 ipt gene promoter." 1991. http://catalog.hathitrust.org/api/volumes/oclc/25770265.html.

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Books on the topic "Histochemical analysis"

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Mason, Gillian Ivy. In situ quantification of enzyme histochemical reactions using TV image analysis. Birmingham: University of Birmingham, 1993.

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Larsson, Olof. Peptides as cotransmitters in salivary secretion: Histochemical, biochemical and functional studies of parotid and submandibular glands. [S.l: s.n.], 1989.

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Larsson, Olof. Peptides as cotransmitters in salivary secretion: Histochemical, biochemical and functional studies of parotid and submandibular glands. Stockholm: Kongl. Carolinska Medico Chirurgiska Institutet, 1989.

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Molecular Histochemical Techniques. Springer, 2012.

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Koji, Takehiko. Molecular Histochemical Techniques. Springer, 2012.

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Koji, Takehiko. Molecular Histochemical Techniques. Springer, 2000.

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Histochemical and Immunohistochemical Techniques: Applications to pharmacology and toxicology. Springer, 1991.

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H, Bach P., and Baker John R. J, eds. Histochemical and immunohistochemical techniques: Applications to pharmacology and toxicology. London: Chapman and Hall, 1991.

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Ali, Arlene Cheryl Yasmin. The most acidic urinary protein complex: development of specific antibodies, histochemical localization, disease associations, and amino acid analysis. 1985.

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Studies of intercellular communication and intracellular metabolic responses by bone cells to simulated weightlessness: Final NASA report. [Washington, DC: National Aeronautics and Space Administration, 1997.

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Book chapters on the topic "Histochemical analysis"

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Passonneau, Janet V., and Oliver H. Lowry. "Histochemical Analyses." In Enzymatic Analysis, 353–62. Totowa, NJ: Humana Press, 1993. http://dx.doi.org/10.1007/978-1-60327-407-4_12.

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Hacker, Hans Jörg, Gabriele Seelmann-Eggebert, Fritz Klimek, Peter Peschke, and Rolf F. Kletzien. "Histochemical Analysis of Hepatocarcinogenesis." In Experimental Hepatocarcinogenesis, 105–18. Boston, MA: Springer US, 1988. http://dx.doi.org/10.1007/978-1-4613-0957-4_9.

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Ploem, J. S. "Image Analysis, Fluorescence and Laser Microscopy." In Histochemical and Immunohistochemical Techniques, 53–69. Dordrecht: Springer Netherlands, 1991. http://dx.doi.org/10.1007/978-94-011-3094-3_3.

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de Eguileor, Magda, Sergio Daniel, Franco Cotelli, Roberto Valvassori, and Giulio Lanzavecchia. "Histochemical analysis of oligochaete body wall." In Aquatic Oligochaete Biology, 99–107. Dordrecht: Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-2393-5_11.

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Demarco, Diego. "Histochemical Analysis of Plant Secretory Structures." In Methods in Molecular Biology, 313–30. New York, NY: Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-6788-9_24.

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Centeno, José A., Todor Todorov, Joseph P. Pestaner, Florabel G. Mullick, and Wayne B. Jonas. "Histochemical and Microprobe Analysis in Medical Geology." In Essentials of Medical Geology, 717–26. Dordrecht: Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-94-007-4375-5_32.

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Yabe, Tomio, and Nobuaki Maeda. "Histochemical Analysis of Heparan Sulfate 3-O-Sulfotransferase Expression in Mouse Brain." In Methods in Molecular Biology, 377–87. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-1714-3_29.

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Fujii, Yasuhisa, Nobuhiko Ohno, Nobuo Terada, and Shinichi Ohno. "Morphological and Histochemical Analysis of Living Mouse Livers by New “Cryobiopsy” Technique." In In Vivo Cryotechnique in Biomedical Research and Application for Bioimaging of Living Animal Organs, 249–53. Tokyo: Springer Japan, 2016. http://dx.doi.org/10.1007/978-4-431-55723-4_47.

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Kobayashi, K., K. Awai, H. Shimada, T. Masuda, K. Takamiya, and H. Ohta. "Histochemical Analysis of Three MGD Genes Using Promoter-GUS Fusion System in Arabidopsis." In Advanced Research on Plant Lipids, 199–202. Dordrecht: Springer Netherlands, 2003. http://dx.doi.org/10.1007/978-94-017-0159-4_46.

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Ito, N., K. Nishi, M. Nakajima, A. Ishitani, K. Nakajima, and T. Hirota. "Histochemical Analysis of the Chemical Structure of Blood-group-related Carbohydrate Chains in Human Pancreas." In Advances in Forensic Haemogenetics, 187–89. Berlin, Heidelberg: Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-75496-8_56.

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Conference papers on the topic "Histochemical analysis"

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Brennan III, James F., Tjeerd J. Roemer, Yang Wang, Maryann Fitzmaurice, Robert S. Lees, John R. Kramer, Jr., and Michael S. Feld. "Histochemical analysis of human coronary artery using near-infrared Raman spectroscopy." In International Symposium on Biomedical Optics Europe '94, edited by Rinaldo Cubeddu, Renato Marchesini, Serge R. Mordon, Katarina Svanberg, Herbert H. Rinneberg, and Georges A. Wagnieres. SPIE, 1995. http://dx.doi.org/10.1117/12.198710.

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Trimanto, Trimanto, Lia Hapsari, and Dini Dwiyanti. "Alpinia galanga (L.) willd: Plant morphological characteristic, histochemical analysis and review on pharmacological." In INTERNATIONAL CONFERENCE ON LIFE SCIENCES AND TECHNOLOGY (ICoLiST 2020). AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0052687.

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Brennan III, James F., Tjeerd J. Roemer, Anna M. Tercyak, Yang Wang, Maryann Fitzmaurice, Robert S. Lees, John R. Kramer, Jr., Ramachandra R. Dasari, and Michael S. Feld. "In-situ histochemical analysis of human coronary artery by Raman spectroscopy compared with biochemical assay." In Photonics West '95, edited by Joseph R. Lakowicz. SPIE, 1995. http://dx.doi.org/10.1117/12.208528.

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Sulisetijono, Eko Sri Sulasmi, Murni Sapta Sari, and Kuni Mawaddah. "Where do bioactive compounds accumulate in fern? A histochemical analysis of seven therapeutic pteris from Tahura Soeryo." In PROCEEDINGS OF THE 3RD INTERNATIONAL SEMINAR ON METALLURGY AND MATERIALS (ISMM2019): Exploring New Innovation in Metallurgy and Materials. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0002439.

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Kesler, Gavriel, Rumelia Koren, Anat Kesler, Don Kristt, and Rivka Gal. "Periodontal plastic surgery: thermal effect analysis using Erbium:YAG Kesler's handpiece. Histochemical evaluation by Picrosirius red stain and polarization microscopy for collagen determination: in." In BiOS 2000 The International Symposium on Biomedical Optics, edited by John D. B. Featherstone, Peter Rechmann, and Daniel Fried. SPIE, 2000. http://dx.doi.org/10.1117/12.380808.

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Moake, J. L., M. A. Harris, C. E. Whitley, and C. P. Alfrey. "RAPID, SENSITIVE N0N-RADI0ACTIVE QUANTIFICATION AND ANALYSIS OF PLASMA VON WILLEBRAND FACTOR (vWF) MULTIMERS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644085.

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Abstract:
Assessment of plasma vWF abnormalities by clinical coagulation laboratories is difficult because the available test systems for vWF antigen quantification and multimer analysis are expensive, laborious, and require days, radioactive anti-vWF antibodies and autoradiographic methods. We have devised simple, rapid, sensitive alternative techniques for vWF quantification and multimer analysis that can be readily installed in clinical laboratories. Plasma vWF antigen quantification is by a 2 hour enzyme immunoassay that accurately detects levels as low as 0.23% of normal. Plasma vWF to be quantified is bound to polyclonal monospecific antihuman vWF attached to small glass beads, and anti-human vWF conjugated with alkaline phosphatase is added to make an insoluble "sandwich." A substrate solution consisting of phenylphosphate and 4-amino-antipurine is added, followed by potassium ferricyanide. Optical density (at 490-510 nm) of the red color that develops is directly proportional to the plasma concentration of vWF antigen. Plasma vWF multimeric analysis is by a one-day electrophoretic immunobiot procedure. Plasma vWF multimer forms are solubilized in SDS-urea-Tris-EDTA, separated by horizontal 1% agarose gel electrophoresis, and transferred to a cationic membrane. Other protein binding sites on the membrane are blocked with milk proteins, and the membrane is overlaid with anti-vWF IgG linked to alkaline phosphatase. vWF multimers are then displayed as blue bands by soaking the membrane in an alkaline solution of the histochemical stain, fast blue RR (commonly used for leukocyte alkaline phosphatase scoring) dissolved in naphtol AS-MX phosphate. These simple, non-radioactive procedures performed together permit the rapid distinction of classical (Type I) von Willebrand's disease (vWD), characterized by low vWF antigen and normal multimers, from the Type II vWD syndromes, characterized by a relative deficiency of the largest plasma vWF forms. Unusually large vWF multimers, present in remission plasma of patients with chronic relapsing thrombotic thrombocytopenic purpura (TTP), are also easily detected using this rapid system of multimer analysis.
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