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  • 1
    Book
    Book
    2021
    ISBN: 1474478638  ISBN: 9781474478632 
    Language: English
    Description: Capturing the landscapes, landmarks, poetry and letters of Keats's epic walk, Carol Kyros Walker retraced Keats's footsteps originally in 1978-1979 and again in the autumns of 2015 and 2016 allowing readers to 'walk' alongside him.
    Subject(s): Poets, English-19th century-Correspondence
    ISBN: 1474478638
    ISBN: 9781474478632
    Source: Alma/SFX Local Collection
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  • 2
    Language: English
    In: Journal of neuro-oncology, 2016-02-13, Vol.127 (3), p.463-472
    Description: The ability to diagnose cancer rapidly with high sensitivity and specificity is essential to exploit advances in new treatments to lead significant reductions in mortality and morbidity. Current cancer diagnostic tests observing tissue architecture and specific protein expression for specific cancers suffer from inter-observer variability, poor detection rates and occur when the patient is symptomatic. A new method for the detection of cancer using 1 μl of human serum, attenuated total reflection—Fourier transform infrared spectroscopy and pattern recognition algorithms is reported using a 433 patient dataset (3897 spectra). To the best of our knowledge, we present the largest study on serum mid-infrared spectroscopy for cancer research. We achieve optimum sensitivities and specificities using a Radial Basis Function Support Vector Machine of between 80.0 and 100 % for all strata and identify the major spectral features, hence biochemical components, responsible for the discrimination within each stratum. We assess feature fed-SVM analysis for our cancer versus non-cancer model and achieve 91.5 and 83.0 % sensitivity and specificity respectively. We demonstrate the use of infrared light to provide a spectral signature from human serum to detect, for the first time, cancer versus non-cancer, metastatic cancer versus organ confined, brain cancer severity and the organ of origin of metastatic disease from the same sample enabling stratified diagnostics depending upon the clinical question asked.
    Subject(s): Adolescent ; Adult ; Aged ; Aged, 80 and over ; Algorithms ; Analysis ; ATR-FTIR ; Biomarkers, Tumor - blood ; Brain Neoplasms - blood ; Brain Neoplasms - diagnosis ; Brain tumors ; Cancer ; Case-Control Studies ; Cell Differentiation ; Diagnosis ; Diagnostics ; Early Detection of Cancer ; Female ; Follow-Up Studies ; Glioma ; Gliomas ; Health aspects ; Humans ; Infrared spectroscopy ; Laboratory Investigation ; Male ; Medicine ; Medicine & Public Health ; Metastasis ; Middle Aged ; Mortality ; Neoplasm Grading ; Neurology ; Oncology ; Prognosis ; Rapid ; Serum ; Spectroscopy ; Spectroscopy, Fourier Transform Infrared - methods ; Support Vector Machine ; Young Adult
    ISSN: 0167-594X
    E-ISSN: 1573-7373
    Source: Alma/SFX Local Collection
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  • 3
    Language: English
    In: Nature communications, 2014-06-09, Vol.5 (1), p.4091-4091
    Description: DNA double-strand break (DSB) repair is a highly regulated process performed predominantly by non-homologous end joining (NHEJ) or homologous recombination (HR) pathways. How these pathways are coordinated in the context of chromatin is unclear. Here we uncover a role for histone H3K36 modification in regulating DSB repair pathway choice in fission yeast. We find Set2-dependent H3K36 methylation reduces chromatin accessibility, reduces resection and promotes NHEJ, while antagonistic Gcn5-dependent H3K36 acetylation increases chromatin accessibility, increases resection and promotes HR. Accordingly, loss of Set2 increases H3K36Ac, chromatin accessibility and resection, while Gcn5 loss results in the opposite phenotypes following DSB induction. Further, H3K36 modification is cell cycle regulated with Set2-dependent H3K36 methylation peaking in G1 when NHEJ occurs, while Gcn5-dependent H3K36 acetylation peaks in S/G2 when HR prevails. These findings support an H3K36 chromatin switch in regulating DSB repair pathway choice.
    Subject(s): Acetylation ; Acetyltransferases - metabolism ; Chromatin - metabolism ; DNA End-Joining Repair ; DNA Repair ; DNA, Fungal - metabolism ; Histone-Lysine N-Methyltransferase - metabolism ; Histones - metabolism ; Methylation ; Recombinational DNA Repair ; Schizosaccharomyces - genetics ; Schizosaccharomyces - metabolism ; Schizosaccharomyces pombe Proteins - metabolism
    ISSN: 2041-1723
    E-ISSN: 2041-1723
    Source: Nature Open Access
    Source: PubMed Central
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  • 4
    Language: English
    In: Science (American Association for the Advancement of Science), 2012-06-29, Vol.336 (6089), p.1704-1708
    Description: Noscapine is an antitumor alkaloid from opium poppy that binds tubulin, arrests metaphase, and induces apoptosis in dividing human cells. Elucidation of the biosynthetic pathway will enable improvement in the commercial production of noscapine and related bioactive molecules. Transcriptomic analysis revealed the exclusive expression of 10 genes encoding five distinct enzyme classes in a high noscapine-producing poppy variety, HN1. Analysis of an F₂ mapping population indicated that these genes are tightly linked in HN1, and bacterial artificial chromosome sequencing confirmed that they exist as a complex gene cluster for plant alkaloids. Virus-induced gene silencing resulted in accumulation of pathway intermediates, allowing gene function to be linked to noscapine synthesis and a novel biosynthetic pathway to be proposed.
    Subject(s): Alkaloids ; Anticancer properties ; Antineoplastic Agents, Phytogenic - biosynthesis ; Biological and medical sciences ; Biosynthesis ; Capsules ; Classical genetics, quantitative genetics, hybrids ; Clusters ; Cough ; Enzymes ; Flowers & plants ; Fundamental and applied biological sciences. Psychology ; Gene silencing ; Genes ; Genes, Plant ; Genetic aspects ; Genetics of eukaryotes. Biological and molecular evolution ; Genomes ; Latex ; Libraries ; Low level ; Molecular Sequence Data ; Morphinans ; Multigene Family ; Narcotics ; Noscapine - metabolism ; Open reading frames ; Papaver - enzymology ; Papaver - genetics ; Papaver - metabolism ; Papaver somniferum ; Pharmaceutical sciences ; Physiological aspects ; Plant biology ; Poppies ; Pteridophyta, spermatophyta ; REPORTS ; Research ; Synthesis ; Vegetals
    ISSN: 0036-8075
    E-ISSN: 1095-9203
    Source: JSTOR Life Sciences
    Source: Academic Search Ultimate
    Source: Alma/SFX Local Collection
    Source: Get It Now
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  • 5
    Language: English
    In: TechTrends, 2011-02-06, Vol.55 (2), p.31-38
    Description: Understanding the covert events surrounding the undergraduate students’ experience is essential to educators’ and counselors’ involvement in their success. Research into bullying behaviors has documented victims’ feelings of anger, sadness and poor concentration. Affordable technologies have propagated this concern into cyberspace. This exploratory study evaluated the instances of cyberbullying experienced by undergraduate students. Additionally, the forms of technology utilized in cyberbullying were queried. A 27-item survey was distributed to 120 undergraduate students in social science, technology and education departments. The majority of all respondents (54%) and 100% of male respondents indicated they knew someone who had been cyberbullied. The perpetrators primarily used cell phones, Facebook and instant messaging. The study results provide legitimate concerns regarding the undergraduate students’ exposure to cyberbullying and numerous areas for future research.
    Subject(s): Article ; Bullying ; College students ; Cyberbullying ; Education ; Educational Technology ; Instant messaging ; Internet ; Learning and Instruction ; Studies ; Universities and colleges ; University students
    ISSN: 8756-3894
    E-ISSN: 1559-7075
    Source: Academic Search Ultimate
    Source: Alma/SFX Local Collection
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  • 6
    Article
    Article
    2015
    ISSN: 1354-4187 
    Language: English
    In: British journal of learning disabilities, 2015-12, Vol.43 (4), p.246-253
    Description: Accessible summary More people with learning disabilities are living longer. This is a good news story! But, the bad news is that they do not live as long as the rest of the population. Health and other services need to be better organised to ensure that people with learning disabilities get better healthcare and other services which would help them lead more healthy lives. Most older people with learning disabilities live at home with their Mum or Dad, who are getting older too and find life more difficult. Care and support services need to adapt as families' needs change, but often this does not happen. We need to know more about these problems, which people with learning disabilities and their family carers face as they get older. This article looks at what we know and what more we need to find out to help older people with learning disabilities and their family carers live happier and healthier lives. Background: Growing numbers of people with learning disabilities are now living into older age. This study aims to examine the state of knowledge about their lives and the challenges that ageing has for both family carers and policymakers and practitioners. Materials and Methods: The article synthesises existing research in the fields of learning disability, ageing and family and social care with a view to learning lessons from these separate fields, identifying possibilities for collaboration and identifying gaps in knowledge. Results: The article concludes that existing research in the fields of ageing and family and social care can add significantly to an understanding of the impact of ageing on people with learning disabilities and their carers but, to date, there has been little collaboration or sharing of knowledge between the three areas. Conclusion: The article concludes that further research is required to fully understand the impact of ageing on the quality of life of people with learning disabilities and their family carers and to inform the design and delivery of services. A useful and productive way forward would be learn from and to work with researchers in cogniscent fields, notably, but not only, in the fields of social gerontology and family and social care.
    Subject(s): Family ; health & social care policy and practice ; Health care industry ; learning (intellectual) disabilities ; Learning disabilities ; Learning disabled ; research ; Target marketing
    ISSN: 1354-4187
    E-ISSN: 1468-3156
    Source: Hellenic Academic Libraries Link
    Source: Academic Search Ultimate
    Source: Alma/SFX Local Collection
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  • 7
    Language: English
    In: Science (American Association for the Advancement of Science), 2015-07-17, Vol.349 (6245), p.309-312
    Description: Morphinan alkaloids from the opium poppy are used for pain relief. The direction of metabolites to morphinan biosynthesis requires isomerization of (S)- to (R)-reticuline. Characterization of high-reticuline poppy mutants revealed a genetic locus, designated STORR [(S)- to (R)-reticuline] that encodes both cytochrome P450 and oxidoreductase modules, the latter belonging to the aldo-keto reductase family. Metabolite analysis of mutant alleles and heterologous expression demonstrate that the P450 module is responsible for the conversion of (S)-reticuline to 1,2-dehydroreticuline, whereas the oxidoreductase module converts 1,2-dehydroreticuline to (R)-reticuline rather than functioning as a P450 redox partner. Proteomic analysis confirmed that these two modules are contained on a single polypeptide in vivo. This modular assembly implies a selection pressure favoring substrate channeling. The fusion protein STORR may enable microbial-based morphinan production.
    Subject(s): Biosynthesis ; Enzymes ; Metabolites ; Modules ; Morphine ; Narcotics ; Pathways ; Poppies ; Proteins ; REPORTS
    ISSN: 0036-8075
    E-ISSN: 1095-9203
    Source: JSTOR Life Sciences
    Source: Academic Search Ultimate
    Source: Alma/SFX Local Collection
    Source: Get It Now
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  • 8
    Article
    Article
    2018
    ISSN: 0002-5240 
    Language: English
    In: Algebra universalis, 2018-04-20, Vol.79 (2), p.1-31
    Description: For L a complete lattice L and X = ( X , ( R i ) I ) a relational structure, we introduce the convolution algebra L X . This algebra consists of the lattice L X equipped with an additional n i -ary operation f i for each n i + 1 -ary relation R i of X . For α 1 , … , α n i ∈ L X and x ∈ X we set f i ( α 1 , … , α n i ) ( x ) = ⋁ { α 1 ( x 1 ) ∧ ⋯ ∧ α n i ( x n i ) : ( x 1 , … , x n i , x ) ∈ R i } . For the 2-element lattice 2, 2 X is the reduct of the familiar complex algebra X + obtained by removing Boolean complementation from the signature. It is shown that this construction is bifunctorial and behaves well with respect to one-one and onto maps and with respect to products. When L is the reduct of a complete Heyting algebra, the operations of L X are completely additive in each coordinate and L X is in the variety generated by 2 X . Extensions to the construction are made to allow for completely multiplicative operations defined through meets instead of joins, as well as modifications to allow for convolutions of relational structures with partial orderings. Several examples are given.
    Subject(s): Algebra ; Article ; Boolean algebra ; Construction ; Convolution ; In memory of Bjarni Jónsson ; Mathematics ; Mathematics and Statistics
    ISSN: 0002-5240
    E-ISSN: 1420-8911
    Source: Alma/SFX Local Collection
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  • 9
    Language: English
    In: Nucleic acids research, 2020-02-20, Vol.48 (3), p.1271-1284
    Description: Abstract The healing of broken chromosomes by de novo telomere addition, while a normal developmental process in some organisms, has the potential to cause extensive loss of heterozygosity, genetic disease, or cell death. However, it is unclear how de novo telomere addition (dnTA) is regulated at DNA double-strand breaks (DSBs). Here, using a non-essential minichromosome in fission yeast, we identify roles for the HR factors Rqh1 helicase, in concert with Rad55, in suppressing dnTA at or near a DSB. We find the frequency of dnTA in rqh1Δ rad55Δ cells is reduced following loss of Exo1, Swi5 or Rad51. Strikingly, in the absence of the distal homologous chromosome arm dnTA is further increased, with nearly half of the breaks being healed in rqh1Δ rad55Δ or rqh1Δ exo1Δ cells. These findings provide new insights into the genetic context of highly efficient dnTA within HR intermediates, and how such events are normally suppressed to maintain genome stability.
    Subject(s): Chromosomes, Fungal - genetics ; DNA Breaks, Double-Stranded ; DNA Helicases - genetics ; DNA-Binding Proteins - genetics ; Exodeoxyribonucleases - genetics ; Gene Expression Regulation, Fungal - genetics ; Genome Integrity, Repair and ; Genome, Fungal - genetics ; Genomic Instability - genetics ; Loss of Heterozygosity - genetics ; Rad51 Recombinase - genetics ; Recombinational DNA Repair - genetics ; Schizosaccharomyces - genetics ; Schizosaccharomyces pombe Proteins - genetics ; Telomere - genetics
    ISSN: 0305-1048
    E-ISSN: 1362-4962
    Source: PubMed Central
    Source: DOAJ Directory of Open Access Journals - Not for CDI Discovery
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  • 10
    Language: English
    In: Nucleic acids research, 2014-05-01, Vol.42 (9), p.5644-5656
    Description: DNA double-strand breaks (DSBs) can cause chromosomal rearrangements and extensive loss of heterozygosity (LOH), hallmarks of cancer cells. Yet, how such events are normally suppressed is unclear. Here we identify roles for the DNA damage checkpoint pathway in facilitating homologous recombination (HR) repair and suppressing extensive LOH and chromosomal rearrangements in response to a DSB. Accordingly, deletion of Rad3ATR, Rad26ATRIP, Crb253BP1 or Cdc25 overexpression leads to reduced HR and increased break-induced chromosome loss and rearrangements. We find the DNA damage checkpoint pathway facilitates HR, in part, by promoting break-induced Cdt2-dependent nucleotide synthesis. We also identify additional roles for Rad17, the 9-1-1 complex and Chk1 activation in facilitating break-induced extensive resection and chromosome loss, thereby suppressing extensive LOH. Loss of Rad17 or the 9-1-1 complex results in a striking increase in break-induced isochromosome formation and very low levels of chromosome loss, suggesting the 9-1-1 complex acts as a nuclease processivity factor to facilitate extensive resection. Further, our data suggest redundant roles for Rad3ATR and Exo1 in facilitating extensive resection. We propose that the DNA damage checkpoint pathway coordinates resection and nucleotide synthesis, thereby promoting efficient HR repair and genome stability.
    Subject(s): Cell Cycle Checkpoints ; Checkpoint Kinase 2 - metabolism ; Chromosomes, Fungal - genetics ; Comparative Genomic Hybridization ; DNA Breaks, Double-Stranded ; DNA Cleavage ; Exodeoxyribonucleases - metabolism ; Genome Integrity, Repair and ; Genome, Fungal ; Genomic Instability ; Loss of Heterozygosity ; Nucleotides - biosynthesis ; Recombinational DNA Repair ; Schizosaccharomyces - genetics ; Schizosaccharomyces - metabolism ; Schizosaccharomyces pombe ; Schizosaccharomyces pombe Proteins - metabolism
    ISSN: 0305-1048
    E-ISSN: 1362-4962
    Source: PubMed Central
    Source: DOAJ Directory of Open Access Journals - Not for CDI Discovery
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