681 research outputs found

    Winter Predation of Mustela Erminea in Northern Canada

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    Weasels are the most widely distributed mammalian predators in North America. This paper reports the results of a study of short-tail weasel predation in northern Alberta and the Northwest Territories during the winter of 1964-65. ..

    The visual orbits of the spectroscopic binaries HD 6118 and HD 27483 from the Palomar Testbed Interferometer

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    We present optical interferometric observations of two double-lined spectroscopic binaries, HD 6118 and HD 27483, taken with the Palomar Testbed Interferometer (PTI) in the K band. HD 6118 is one of the most eccentric spectroscopic binaries and HD 27483 a spectroscopic binary in the Hyades open cluster. The data collected with PTI in 2001-2002 allow us to determine astrometric orbits and when combined with the radial velocity measurements derive all physical parameters of the systems. The masses of the components are 2.65 +/- 0.27 M_Sun and 2.36 +/- 0.24 M_Sun for HD 6118 and 1.38 +/- 0.13 M_Sun and 1.39 +/- 0.13 M_Sun for HD 27483. The apparent semi-major axis of HD 27483 is only 1.2 mas making it the closest binary successfully observed with an optical interferometer.Comment: submitted to Ap

    Subgroup-specific structural variation across 1,000 medulloblastoma genomes

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    Abstract Medulloblastoma, the most common malignant paediatric brain tumour, is currently treated with nonspecific cytotoxic therapies including surgery, whole-brain radiation, and aggressive chemotherapy. As medulloblastoma exhibits marked intertumoural heterogeneity, with at least four distinct molecular variants, previous attempts to identify targets for therapy have been underpowered because of small samples sizes. Here we report somatic copy number aberrations (SCNAs) in 1,087 unique medulloblastomas. SCNAs are common in medulloblastoma, and are predominantly subgroup-enriched. The most common region of focal copy number gain is a tandem duplication of SNCAIP, a gene associated with Parkinson's disease, which is exquisitely restricted to Group 4Ī±. Recurrent translocations of PVT1, including PVT1-MYC and PVT1-NDRG1, that arise through chromothripsis are restricted to Group 3. Numerous targetable SCNAs, including recurrent events targeting TGF-Ī² signalling in Group 3, and NF-ĪŗB signalling in Group 4, suggest future avenues for rational, targeted therapy

    Rapid, reliable, and reproducible molecular sub-grouping of clinical medulloblastoma samples

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    The diagnosis of medulloblastoma likely encompasses several distinct entities, with recent evidence for the existence of at least four unique molecular subgroups that exhibit distinct genetic, transcriptional, demographic, and clinical features. Assignment of molecular subgroup through routine profiling of high-quality RNA on expression microarrays is likely impractical in the clinical setting. The planning and execution of medulloblastoma clinical trials that stratify by subgroup, or which are targeted to a specific subgroup requires technologies that can be economically, rapidly, reliably, and reproducibly applied to formalin-fixed paraffin embedded (FFPE) specimens. In the current study, we have developed an assay that accurately measures the expression level of 22 medulloblastoma subgroup-specific signature genes (CodeSet) using nanoString nCounter Technology. Comparison of the nanoString assay with Affymetrix expression array data on a training series of 101 medulloblastomas of known subgroup demonstrated a high concordance (Pearson correlation rĀ =Ā 0.86). The assay was validated on a second set of 130 non-overlapping medulloblastomas of known subgroup, correctly assigning 98% (127/130) of tumors to the appropriate subgroup. Reproducibility was demonstrated by repeating the assay in three independent laboratories in Canada, the United States, and Switzerland. Finally, the nanoString assay could confidently predict subgroup in 88% of recent FFPE cases, of which 100% had accurate subgroup assignment. We present an assay based on nanoString technology that is capable of rapidly, reliably, and reproducibly assigning clinical FFPE medulloblastoma samples to their molecular subgroup, and which is highly suited for future medulloblastoma clinical trials

    Deterministically Computing Reduction Numbers of Polynomial Ideals

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    We discuss the problem of determining reduction number of a polynomial ideal I in n variables. We present two algorithms based on parametric computations. The first one determines the absolute reduction number of I and requires computation in a polynomial ring with (n-dim(I))dim(I) parameters and n-dim(I) variables. The second one computes via a Grobner system the set of all reduction numbers of the ideal I and thus in particular also its big reduction number. However,it requires computations in a ring with n.dim(I) parameters and n variables.Comment: This new version replaces the earlier version arXiv:1404.1721 and it has been accepted for publication in the proceedings of CASC 2014, Warsaw, Polna

    East Midlands Research into Ageing Network (EMRAN) Discussion Paper Series

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    Academic geriatric medicine in Leicester . There has never been a better time to consider joining us. We have recently appointed a Professor in Geriatric Medicine, alongside Tom Robinson in stroke and Victoria Haunton, who has just joined as a Senior Lecturer in Geriatric Medicine. We have fantastic opportunities to support students in their academic pursuits through a well-established intercalated BSc programme, and routes on through such as ACF posts, and a successful track-record in delivering higher degrees leading to ACL post. We collaborate strongly with Health Sciences, including academic primary care. See below for more detail on our existing academic set-up. Leicester Academy for the Study of Ageing We are also collaborating on a grander scale, through a joint academic venture focusing on ageing, the ā€˜Leicester Academy for the Study of Ageingā€™ (LASA), which involves the local health service providers (acute and community), De Montfort University; University of Leicester; Leicester City Council; Leicestershire County Council and Leicester Age UK. Professors Jayne Brown and Simon Conroy jointly Chair LASA and have recently been joined by two further Chairs, Professors Kay de Vries and Bertha Ochieng. Karen Harrison Dening has also recently been appointed an Honorary Chair. LASA aims to improve outcomes for older people and those that care for them that takes a person-centred, whole system perspective. Our research will take a global perspective, but will seek to maximise benefits for the people of Leicester, Leicestershire and Rutland, including building capacity. We are undertaking applied, translational, interdisciplinary research, focused on older people, which will deliver research outcomes that address domains from: physical/medical; functional ability, cognitive/psychological; social or environmental factors. LASA also seeks to support commissioners and providers alike for advice on how to improve care for older people, whether by research, education or service delivery. Examples of recent research projects include: ā€˜Local History CafĆ©ā€™ project specifically undertaking an evaluation on loneliness and social isolation; ā€˜Better Visitsā€™ project focused on improving visiting for family members of people with dementia resident in care homes; and a study on health issues for older LGBT people in Leicester. Clinical Geriatric Medicine in Leicester We have developed a service which recognises the complexity of managing frail older people at the interface (acute care, emergency care and links with community services). There are presently 17 consultant geriatricians supported by existing multidisciplinary teams, including the largest complement of Advance Nurse Practitioners in the country. Together we deliver Comprehensive Geriatric Assessment to frail older people with urgent care needs in acute and community settings. The acute and emergency frailty units ā€“ Leicester Royal Infirmary This development aims at delivering Comprehensive Geriatric Assessment to frail older people in the acute setting. Patients are screened for frailty in the Emergency Department and then undergo a multidisciplinary assessment including a consultant geriatrician, before being triaged to the most appropriate setting. This might include admission to in-patient care in the acute or community setting, intermediate care (residential or home based), or occasionally other specialist care (e.g. cardiorespiratory). Our new emergency department is the countyā€™s first frail friendly build and includes fantastic facilities aimed at promoting early recovering and reducing the risk of hospital associated harms. There is also a daily liaison service jointly run with the psychogeriatricians (FOPAL); we have been examining geriatric outreach to oncology and surgery as part of an NIHR funded study. We are home to the Acute Frailty Network, and those interested in service developments at the national scale would be welcome to get involved. Orthogeriatrics There are now dedicated hip fracture wards and joint care with anaesthetists, orthopaedic surgeons and geriatricians. There are also consultants in metabolic bone disease that run clinics. Community work Community work will consist of reviewing patients in clinic who have been triaged to return to the community setting following an acute assessment described above. Additionally, primary care colleagues refer to outpatients for sub-acute reviews. You will work closely with local GPs with support from consultants to deliver post-acute, subacute, intermediate and rehabilitation care services. Stroke Medicine 24/7 thrombolysis and TIA services. The latter is considered one of the best in the UK and along with the high standard of vascular surgery locally means one of the best performances regarding carotid intervention

    Molecular subgroups of medulloblastoma: the current consensus

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    Medulloblastoma, a small blue cell malignancy of the cerebellum, is a major cause of morbidity and mortality in pediatric oncology. Current mechanisms for clinical prognostication and stratification include clinical factors (age, presence of metastases, and extent of resection) as well as histological subgrouping (classic, desmoplastic, and large cell/anaplastic histology). Transcriptional profiling studies of medulloblastoma cohorts from several research groups around the globe have suggested the existence of multiple distinct molecular subgroups that differ in their demographics, transcriptomes, somatic genetic events, and clinical outcomes. Variations in the number, composition, and nature of the subgroups between studies brought about a consensus conference in Boston in the fall of 2010. Discussants at the conference came to a consensus that the evidence supported the existence of four main subgroups of medulloblastoma (Wnt, Shh, Group 3, and Group 4). Participants outlined the demographic, transcriptional, genetic, and clinical differences between the four subgroups. While it is anticipated that the molecular classification of medulloblastoma will continue to evolve and diversify in the future as larger cohorts are studied at greater depth, herein we outline the current consensus nomenclature, and the differences between the medulloblastoma subgroups

    On certain infinite extensions of the rationals with Northcott property

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    A set of algebraic numbers has the Northcott property if each of its subsets of bounded Weil height is finite. Northcott's Theorem, which has many Diophantine applications, states that sets of bounded degree have the Northcott property. Bombieri, Dvornicich and Zannier raised the problem of finding fields of infinite degree with this property. Bombieri and Zannier have shown that \IQ_{ab}^{(d)}, the maximal abelian subfield of the field generated by all algebraic numbers of degree at most dd, is such a field. In this note we give a simple criterion for the Northcott property and, as an application, we deduce several new examples, e.g. \IQ(2^{1/d_1},3^{1/d_2},5^{1/d_3},7^{1/d_4},11^{1/d_5},...) has the Northcott property if and only if 21/d1,31/d2,51/d3,71/d4,111/d5,...2^{1/d_1},3^{1/d_2},5^{1/d_3},7^{1/d_4},11^{1/d_5},... tends to infinity
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