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Journal articles on the topic 'Mikroarrays'

Author: Grafiati

Published: 4 June 2021

Last updated: 12 February 2022

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1

Niemeyer, Christof M., and Dietmar Blohm. "DNA-Mikroarrays." Angewandte Chemie 111, no. 19 (1999): 3039–43. http://dx.doi.org/10.1002/(sici)1521-3757(19991004)111:19<3039::aid-ange3039>3.0.co;2-0.

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2

von Eggeling, F., and C. Melle. "Protein-Mikroarrays." Der Onkologe 13, no. 10 (2007): 939–45. http://dx.doi.org/10.1007/s00761-007-1256-2.

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3

Jehle, Heinrich, and Holger Eickhoff. "Mikroarrays im Hochdurchsatz." Nachrichten aus der Chemie 52, no. 7-8 (2004): 870–71. http://dx.doi.org/10.1002/nadc.20040520753.

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4

Pohl, Nicola L. "Perfluorierte Marker als Ankergruppen für Mikroarrays." Angewandte Chemie 120, no. 21 (2008): 3930–32. http://dx.doi.org/10.1002/ange.200704801.

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5

Disney, Matthew D., Sophie Magnet, John S. Blanchard, and Peter H. Seeberger. "Aminoglycosid-Mikroarrays für Bindungsstudien an Resistenzproteinen." Angewandte Chemie 116, no. 12 (2004): 1618–20. http://dx.doi.org/10.1002/ange.200353236.

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6

Sültmann, Holger, and Reiner Dahint. "Web Site: Mikroarrays: Die Menge macht's." Angewandte Chemie 115, no. 34 (2003): 4112. http://dx.doi.org/10.1002/ange.200390594.

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7

Demuth, Philipp, Barbara Birk, Nadine Roth, Robert Landsiedel, and Bennard van Ravenzwaay. "Kofaktor-Mikroarrays zur Identifikation von Kernrezeptorliganden." BIOspektrum 25, no. 3 (2019): 303–5. http://dx.doi.org/10.1007/s12268-019-1052-8.

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8

Liedtke, C., and L. Kiesel. "Die Bedeutung von Mikroarrays für das Mammakarzinom." Gynäkologische Endokrinologie 7, no. 2 (2009): 99–110. http://dx.doi.org/10.1007/s10304-009-0303-z.

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9

Lietard, Jory, Dominik Ameur, Masad J. Damha, and Mark M. Somoza. "In‐situ‐Synthese von hochdichten RNA‐Mikroarrays mittels Photolithographie." Angewandte Chemie 130, no. 46 (2018): 15477–81. http://dx.doi.org/10.1002/ange.201806895.

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10

Küster, Simon K., Martin Pabst, Renato Zenobi, and Petra S. Dittrich. "Automatisierte Detektion von Proteinphosphorylierung durch Nanoliter-Enzymreaktionen auf Mikroarrays." Angewandte Chemie 127, no. 5 (2014): 1691–95. http://dx.doi.org/10.1002/ange.201409440.

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11

Suhr, J., P. J. Goebell, K. W. Schmid, K. Worm, H. Rübben, and T. Otto. "Mikroarrays in der Urologie - Möglichkeiten in Forschung und Diagnostik -." Aktuelle Urologie 33, no. 4 (2002): 262–67. http://dx.doi.org/10.1055/s-2002-32831.

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12

Schroeder, Hendrik, Bernhard Ellinger, Christian F W. Becker, Herbert Waldmann, and Christof M Niemeyer. "DNA-vermittelte Immobilisierung spezifischer Zelloberflächenliganden zur Herstellung von Mikroarrays mit lebenden Zellen." Angewandte Chemie 119, no. 22 (2007): 4258–61. http://dx.doi.org/10.1002/ange.200604467.

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13

Lovrinovic, Marina, and Christof M. Niemeyer. "DNA-Mikroarrays als Decodierungswerkzeuge in der kombinatorischen Chemie und der chemischen Biologie." Angewandte Chemie 117, no. 21 (2005): 3241–46. http://dx.doi.org/10.1002/ange.200500645.

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14

Becker, Christian F. W., Ron Wacker, Werner Bouschen, et al. "Direkter Nachweis von Protein-Protein-Wechselwirkungen durch Massenspektrometrie an Protein-DNA-Mikroarrays." Angewandte Chemie 117, no. 46 (2005): 7808–12. http://dx.doi.org/10.1002/ange.200502908.

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15

Wrulich, Oliver A., and Florian Überall. "DNS-Mikroarrays - Verbesserung der analytischen Plattformen zur Beschreibung molekularer Wirkmuster von Naturstoffpräparaten oder Science Fiction?" Schweizerische Zeitschrift für Ganzheitsmedizin / Swiss Journal of Integrative Medicine 21, no. 7-8 (2009): 348–55. http://dx.doi.org/10.1159/000291024.

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16

Kretschy, Nicole, Ann-Katrin Holik, Veronika Somoza, Klaus-Peter Stengele, and Mark M. Somoza. "o-Nitrobenzyl-photolabile Gruppen der nächsten Generation in der lichtgesteuerten Chemie und der Synthese von Mikroarrays." Angewandte Chemie 127, no. 29 (2015): 8675–79. http://dx.doi.org/10.1002/ange.201502125.

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17

Pajestka, Malwina, Hanswilly Müller, Ahmed Ait-Benarrou, Thomas Brandstetter, and Jürgen Rühe. "Mikroarray-basierte Allergiediagnostik mittels Fluoreszenz-Detektionstechnologie." BIOspektrum 19, no. 3 (2013): 282–84. http://dx.doi.org/10.1007/s12268-013-0308-y.

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18

Wilson, David S., and Steffen Nock. "Protein-Mikroarray-Technologie – Prinzipien und neuere Entwicklungen." Angewandte Chemie 115, no. 5 (2003): 510–17. http://dx.doi.org/10.1002/ange.200390118.

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19

Lübbecke, Miriam, Johanna-Gabriela Walter, Frank Stahl, and Thomas Scheper. "Anwendungen von Aptameren in der Mikroarray-Technologie." BIOspektrum 17, no. 2 (2011): 162–64. http://dx.doi.org/10.1007/s12268-011-0022-6.

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20

Haznedar, Bülent, Mustafa Turan Arslan, and Adem Kalınlı. "Karaciğer Mikroarray Kanser Verisinin Sınıflandırılması için Genetik Algoritma Kullanarak ANFIS’in eğitilmesi." SAÜ Fen Bilimleri Enstitüsü Dergisi 21, no. 1 (2017): 54. http://dx.doi.org/10.16984/saufenbilder.283823.

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21

Köhn, Maja, Marta Gutierrez-Rodriguez, Pascal Jonkheijm, et al. "Eine Mikroarray-Strategie zur Untersuchung der Substratspezifitäten von Protein-Tyrosin-Phosphatasen." Angewandte Chemie 119, no. 40 (2007): 7844–47. http://dx.doi.org/10.1002/ange.200701601.

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22

Lanckohr, C., A. Kasprzynski, L. Klein-Hitpass, et al. "Erratum zu: Identifikation überexprimierter Gene in myxoid-rundzelligen Liposarkomen. DNA-Mikroarray-Analyse und immunhistochemische Korrelation." Der Pathologe 31, no. 3 (2010): 198. http://dx.doi.org/10.1007/s00292-010-1283-4.

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23

"Von Mikroarrays und rekombinanten Allergenen." Allergo Journal 14, no. 1 (2005): 20. http://dx.doi.org/10.1007/bf03370385.

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24

"Exom-Sequenzierung beim nicht-immunologischen Hydrops fetalis." Zeitschrift für Geburtshilfe und Neonatologie 225, no. 01 (2021): 7–8. http://dx.doi.org/10.1055/a-1328-1592.

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Ein nicht-immunologischer Hydrops fetalis betrifft etwa eine von 1700 bis 3000 Schwangerschaften. In nur rund einem Viertel der Fälle lässt sich mittels Karyotypisierung oder chromosomaler Mikroarray-Analyse die der Problematik zugrunde liegende genetische Basis klären. Wie häufig Einzelgen-Defekte ursächlich sind und welches Genspektrum hier beteiligt ist, untersuchte nun ein US-Forscherteam mithilfe der Exom-Sequenzierungstechnologie.

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25

KAPLAN, Selçuk, Saim BOZTEPE, and Hilal ARIKOĞLU. "Mikroarray Veritabanlarının Doku Spesifik Genlerin Belirlenmesindeki Potansiyeli." Kafkas Universitesi Veteriner Fakultesi Dergisi, 2015. http://dx.doi.org/10.9775/kvfd.2015.13639.

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26

Kestler, H. A., and R. K�fer. "Wertigkeit und Notwendigkeit bioinformatischer Methoden zur Mikroarray-Datenanalyse." Der Urologe, Ausgabe A 43, no. 6 (2004). http://dx.doi.org/10.1007/s00120-004-0577-7.

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27

"Indikationskriterien und Bewertung der Molekularen Karyotypisierung mittels Mikroarray-Analysen für die genetische Diagnostik konstitutioneller DNA-Veränderungen ? Grundlagen zur Einführung der Abrechnung der Molekularen Karyotypisierung mittels Mikroarray-Analyse in den EBM und die GOÄ." medizinische genetik 22, no. 1 (2010): 20–25. http://dx.doi.org/10.1007/s11825-010-0210-7.

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28

ÖZPINAR, Haydar, Gündüz TEZMEN, İnci GÖKÇE, and İsmail Hakkı TEKİNER. "Detection of Animal Species in Some Meat and Meat Products by Comparatively Using DNA Microarray and Real Time PCR Methods." Kafkas Universitesi Veteriner Fakultesi Dergisi, 2013. http://dx.doi.org/10.9775/kvfd.2012.7616.

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29

Soylu, Mehmet, Ayşe Arslan, Şöhret Aydemir, and Alper Tünger. "Evaluation of Microarray and Lysis Filtration Combined MALDI TOF MS Procedures for the Identification of Gram Negative Bacteremia." Türk Mikrobiyoloji Cemiyeti Dergisi, 2021. http://dx.doi.org/10.5222/tmcd.2021.46320.

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Objective: Each hour of delay in antibiotics administration increases mortality in sepsis. The aim of this study was to decrease the bacteria identification time to initiate appropriate antibiotic treatment as early as possible. Method: Tests were applied to 39 Gram negative bacteria isolated from blood cultures sent to our laboratory from intensive care units between November 2015- February 2016. The results of bacterial identification tested on both microarray and LFM methods were compared. Results: In the comparison of MALDI-TOF MS after sub-culture, MALDI-TOF after lysis centrifugation and microarray methods, sensitivity was determined as 82% (32/39) in LFM and as 87.1% (34/39) in the microarray method. All three methods had a concordance of 76.9% (30/39). Most common species identified in this study were Acinetobacter spp., Klebsiella spp. and Escherichia spp., and their Cohen’s Kappa coefficients for LFM and post-subculture MALDI were calculated as 0.715, 0.843, and 0.938, respectively. In addition, their BC-GN microarray and post-subculture MALDI concordance rates calculated with Cohen’s Kappa were 0.935, 0.753 and 0.938, respectively. Both methods showed good correlations with the post-culture MALDI method. Conclusion: Lysis centrifugation and microarray platforms decrease the identification time in blood culture processing successfully. Results of this study suggest that for the laboratories with MALDI-TOF mass spectrophotometer, the lysis filtration method is a fast and cost-effective method that may be suitable for routine procedures.

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30

Henke, C., M. Ruebner, PL Strissel, et al. "Regulation der Genexpression in einzelnen Zellkompartimenten der humanen Plazenta mittels Laser micro-dissection Mikroskopie und Mikroarray." Geburtshilfe und Frauenheilkunde 74, S 01 (2014). http://dx.doi.org/10.1055/s-0034-1388061.

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31

Bhonde, MR, D. Moorthy, M.-L. Hanski, et al. "Mikroarray-Analyse der p53-abhängigen und p53-unabhängigen transkriptionellen Antwort von Kolonkarzinomzellen auf DNA-Schädigung durch Irinotecan." Zeitschrift für Gastroenterologie 41, no. 08 (2015). http://dx.doi.org/10.1055/s-0035-1555441.

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32

Øvstebø, Reidun, Peter Kierulf, and Kari Bente Foss Haug. "Circulating nucleic acids in blood as biomarkers." Norsk Epidemiologi 16, no. 1 (2009). http://dx.doi.org/10.5324/nje.v16i1.204.

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<p>This short review on a rapidly expanding domain in biomarkers focuses on the value of markers derived from either circulating intracellular DNA and RNA (leukocytes) or from free DNA and RNA in plasma or serum. In circulating intracellular DNA biomarkers, importance has been pointed to reside in the ever increasing number of SNPs directly related to disease such as hemochromatosis or associated with genetic make up that leads to different drug-susceptibility. Quantitative gene expression profiling, increasingly using global expression platforms, is gaining momentum in various disease states such as cancer, inflammation, cardiovascular disease and diabetes. Circulating free nucleic acids in plasma or serum gain in importance as biomarkers particularly in cancer and foeto-maternal understanding. The surprising recent findings of circulating free mRNA carries the potential of examining normal and diseased plasma for global gene expression profiling – opening avenues to new biomarkers. When appropriate, this review gives reference to methodological considerations and refers the readers to important literature in the fields</p><p>I denne korte oversiktsartikkelen redegjøres det for et biomarkørfelt som utvikler seg hurtig. Gjennom en blodprøve kan man få kjennskap til forandringer i sirkulerende leucocytter, intracellulære nukleinsyrer (DNA og RNA) og fritt DNA og RNA fra plasma eller serum. Single Nucleotide Polymorphisms (SNPs) i DNA har allerede bekreftet sine muligheter som biomarkører (f.eks. Hemokromatose, Faktor V Leiden, Cytochrom P450 (CYP’er)). Stadig flere SNP’er vinner innpass i klinisk sammenheng. Siden sirkulerende hvite blodlegemer kan sies kontinuerlig å overvåke kroppens organer og vev, og dette avspeiles i disse blodcellers genekspresjon (RNA), knyttes det i dag forventninger til sykdomsspesifikke genekspresjonsprofiler. Både ved visse kreftformer, betennelsestilstander og hjertekar-sykdom viser hvite blodlegemer mer eller mindre tydelig sykdomsspesifikke genekspresjonsprofiler. Denne type sykdomsspesifikke genekspresjonsmarkører vil bli økende viktig fremover. Ved slike markører vil man kunne ha nytte av kvantitativ måling av enkeltmarkører, og også globale genekspresjonsprofiler på mikroarray-plattformer. Sirkulerende fritt DNA og kanskje særlig RNA i plasma åpner for nye sykdomsmarkører i første rekke ved forskjellige kreftformer og ved foeto-maternelle problemstillinger. Oversikten gir også en henvisning til metodologiske referanser i disse feltene.</p>

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