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Lancashire Teaching Hospitals NHS Trust, Preston, U.K. and

Title: Lancashire Teaching Hospitals NHS Trust, Preston, U.K. and
Authors: Michael J. Walsh; Maneesh N. Singh; Helen F. Stringfellow; Hubert M. Pollock; Azzedine Hammiche; Olaug Grude; Nigel J. Fullwood; Mark A. Pitt; Pierre L. Martin-hirsch; Francis L. Martin
Contributors: The Pennsylvania State University CiteSeerX Archives
Source: ftp://ftp.ncbi.nlm.nih.gov/pub/pmc/ec/04/Biomark_Insights_2008_Mar_25_3_179-189.tar.gz
Collection: CiteSeerX
Subject Terms: biomarker; cervical cytology; Fourier-transform infrared microspectroscopy; high-grade; low-grade; principal
Description: Infrared (IR) absorbance of cellular biomolecules generates a vibrational spectrum, which can be exploited as a “biochemical fingerprint ” of a particular cell type. Biomolecules absorb in the mid-IR (2–20 μm) and Fourier-transform infrared (FTIR) microspectroscopy applied to discriminate different cell types (exfoliative cervical cytology collected into buffered fixative solution) was evaluated. This consisted of cervical cytology free of atypia (i.e. normal; n = 60), specimens categorised as containing low-grade changes (i.e. CIN1 or LSIL; n = 60) and a further cohort designated as high-grade (CIN2/3 or HSIL; n = 60). IR spectral analysis was coupled with principal component analysis (PCA), with or without subsequent linear discriminant analysis (LDA), to determine if normal versus low-grade versus high-grade exfoliative cytology could be segregated. With increasing severity of atypia, decreases in absorbance intensity were observable throughout the 1,500 cm −1 to 1,100 cm −1 spectral region; this included proteins (1,460 cm −1), glycoproteins (1,380 cm −1), amide III (1,260 cm −1), asymmetric (ν as) PO 2 (1,225 cm
Document Type: text
File Description: application/zip
Language: English
Relation: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.275.8105
Availability: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.275.8105
Rights: Metadata may be used without restrictions as long as the oai identifier remains attached to it.
Accession Number: edsbas.CC17F6F1
Database: BASE