90 research outputs found

    Phylogenetic relationships of haplolepideous mosses (Dicranidae) inferred from rps4 gene sequences

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    The haplolepideous mosses (Dicranidae) constitute a large group of ecologically and morphologically diverse species recognised primarily by having peristome teeth with a single row of cells on the dorsal surface

    Evolution of the major moss lineages: phylogenetic analyses based on multiple gene sequences and morphology

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    Evolutionary relationships of mosses are still poorly understood, with family, order, and subclass circumscription and relationships remaining especially obscure

    Opportunities for primary and secondary prevention of excess gestational weight gain: General Practitioners' perspectives

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    BackgroundThe impact of excess gestational weight gain (GWG) on maternal and child health outcomes is well documented. Understanding how health care providers view and manage GWG may assist with influencing healthy gestational weight outcomes. This study aimed to assess General Practitioner\u27s (GPs) perspectives regarding the management and assessment of GWG and to understand how GPs can be best supported to provide healthy GWG advice to pregnant women.MethodsDescriptive qualitative research methods utilising semi - structured interview questions to assess GPs perspectives and management of GWG. GPs participating in shared antenatal care in Geelong, Victoria and Sydney, New South Wales were invited to participate in semi - structured, individual interviews via telephone or in person. Interviews were digitally recorded and transcribed verbatim. Data was analysed utilising thematic analysis for common emerging themes.ResultsTwenty eight GPs participated, 14 from each state. Common themes emerged relating to awareness of the implications of excess GWG, advice regarding weight gain, regularity of gestational weighing by GPs, options for GPs to seek support to provide healthy lifestyle behaviour advice and barriers to engaging pregnant women about their weight. GPs perspectives concerning excess GWG were varied. They frequently acknowledged maternal and child health complications resulting from excess GWG yet weighing practices and GWG advice appeared to be inconsistent. The preferred support option to promote healthy weight was referral to allied health practitioners yet GPs noted that cost and limited access were barriers to achieving this.ConclusionsGPs were aware of the importance of healthy GWG yet routine weighing was not standard practice for diverse reasons. Management of GWG and perspectives of the issue varied widely. Time efficient and cost effective interventions may assist GPs in ensuring women are supported in achieving healthy GWG to provide optimal maternal and infant health outcomes.<br /

    Variation in the Glucose Transporter gene <i>SLC2A2 </i>is associated with glycaemic response to metformin

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    Metformin is the first-line antidiabetic drug with over 100 million users worldwide, yet its mechanism of action remains unclear1. Here the Metformin Genetics (MetGen) Consortium reports a three-stage genome-wide association study (GWAS), consisting of 13,123 participants of different ancestries. The C allele of rs8192675 in the intron of SLC2A2, which encodes the facilitated glucose transporter GLUT2, was associated with a 0.17% (P = 6.6 × 10−14) greater metformin-induced reduction in hemoglobin A1c (HbA1c) in 10,577 participants of European ancestry. rs8192675 was the top cis expression quantitative trait locus (cis-eQTL) for SLC2A2 in 1,226 human liver samples, suggesting a key role for hepatic GLUT2 in regulation of metformin action. Among obese individuals, C-allele homozygotes at rs8192675 had a 0.33% (3.6 mmol/mol) greater absolute HbA1c reduction than T-allele homozygotes. This was about half the effect seen with the addition of a DPP-4 inhibitor, and equated to a dose difference of 550 mg of metformin, suggesting rs8192675 as a potential biomarker for stratified medicine

    How parents choose to use CAM: a systematic review of theoretical models

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    Background: Complementary and Alternative Medicine (CAM) is widely used throughout the UK and the Western world. CAM is commonly used for children and the decision-making process to use CAM is affected by numerous factors. Most research on CAM use lacks a theoretical framework and is largely based on bivariate statistics. The aim of this review was to identify a conceptual model which could be used to explain the decision-making process in parental choice of CAM. Methods: A systematic search of the literature was carried out. A two-stage selection process with predetermined inclusion/exclusion criteria identified studies using a theoretical framework depicting the interaction of psychological factors involved in the CAM decision process. Papers were critically appraised and findings summarised. Results: Twenty two studies using a theoretical model to predict CAM use were included in the final review; only one examined child use. Seven different models were identified. The most commonly used and successful model was Andersen's Sociobehavioural Model (SBM). Two papers proposed modifications to the SBM for CAM use. Six qualitative studies developed their own model. Conclusion: The SBM modified for CAM use, which incorporates both psychological and pragmatic determinants, was identified as the best conceptual model of CAM use. This model provides a valuable framework for future research, and could be used to explain child CAM use. An understanding of the decision making process is crucial in promoting shared decision making between healthcare practitioners and parents and could inform service delivery, guidance and policy

    Phylogenetic relationships among the ciliate arthrodontous mosses: evidence from chloroplast and nuclear DNA sequences

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    Parsimony and maximum likelihood analyses of combined trnL (UAA) 5 t exon - trnF (GAA) and rps4 exon cpDNA, and 18S nrDNA sequences of 60 arthrodontous moss taxa indicate strong support for the monophyly of a clade containing the Splachnineae, Orthotrichineae, and diplolepideous alternate sub-orders. A clade including the Splachnineae, Meesiaceae and Leptobryum (Bryaceae) is similarly well supported and forms the sister group to a clade comprising the Orthotrichineae and the other diplolepideous alternate mosses. Within this latter clade a number of weil supported lineages are identified, but relationships among these remain poorly resolved. These analyses indicate that the Splachnaceous and Orthotrichaceous peristomes have been independently derived from an ancestral 'perfect' bryoid peristome

    The bryophyta (mosses): systematic and evolutionary inferences from an rps4 gene (cpDNA) phylogeny

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    Phylogenetic analyses of nucleotide and amino acid sequences of the chloroplast protein coding gene rps4 were performed for 225 species of mosses, representing 84%of families recognized by Vitt (1984. In: Schuster RM, ed. New manual of bryology, vol 2. Nichinan: Hattori Botanical Laboratory), under the criterion of maximum parsimony with Takakia and Sphagnum as outgroups. Most parsimonious topologies converge to a scenario wherein the Andreaeidae are monophyletic and sister to the Bryidae ( peristomate mosses), the Nematodonteae and the Buxbaumiaceae form a monophyletic lineage, the Diphysciaceae are sister to the Arthrodonteae and, within the latter, the Funarineae-Encalyptineae-Timmiaceae-Haplolepideae compose a monophyletic clade sister to remaining diplolepideous mosses. This hypothesis suggests that early in the evolution of the Arthrodonteae, two major lineages diverged, with opposite and alternate peristomes, respectively. Bootstrap support for the deep dichotomies is poor or lacking but increases when protein translations of rps4 sequences are included in the analysis. Several novel systematic hypotheses are raised, including (a) a diplolepideous rather than haplolepideous origin of the Pleurophascaceae; (b) an a nity of the Catascopiaceae with the Funariineae rather than the Bryineae; and (c) a close relationship of the Calomniaceae and Mitteniaceae to the Rhizgoniaceae. The advantages and disadvantages of a single gene phylogeny are discussed with respect to the identi®cation of polyphyletic familial or suprafamilial taxa
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