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        205-216 of 538 results for 'Gene'

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        Lack of replication for the myosin-18B association with mathematical ability in independent cohorts

        Twin studies indicate that dyscalculia (or mathematical disability) is caused partly by a genetic component, which is yet to be understood at the molecular... ...

        Research

        CAGE-defined promoter regions of the genes implicated in Rett Syndrome

        A comprehensive picture of the regulatory regions of the three genes involved in Rett Syndrome ...

        Research

        The anti-inflammatory actions of IL-4 in human monocytes are not mediated by IL-10, RP105 or the kinase activity of RIPK2

        The anti-inflammatory actions of IL-4 in activated human monocytes may reflect transcriptional regulation of genes involved in TLR signaling pathways. ...

        Research

        A positive feedback loop between alpha1-adrenoceptors and inflammatory cytokines in keratinocytes

        Our results suggest that reciprocal influences between alpha1-adrenoceptors and inflammatory cytokines may play a role in normal inflammatory responses ...

        Research

        A retrospective study of Babesia macropus associated with morbidity and mortality

        This is a retrospective study of 38 cases of infection by Babesia macropus, associated with a syndrome of anaemia and debility in hand-reared or free-ranging... ...

        Research

        ARHGEF12 influences the risk of glaucoma by increasing intraocular pressure.

        Two important risk factors for this disease are a positive family history and elevated intraocular pressure (IOP), which is also highly heritable. ...

        Research

        Silencing of TESTIN by dense biallelic promoter methylation

        Aberrant promoter DNA methylation has been reported in childhood acute lymphoblastic leukaemia and has the potential to contribute to its onset and outcome ...

        Research

        Prenatal origins and health outcomes of male reproductive congenital anomalies diagnosed at birth and testicular cancer in adulthood

        Liz Milne E MPH PhD Honorary Emeritus Fellow Honorary Emeritus Fellow Liz is an epidemiologist specialising in the aetiology and prevention of childhood cancers and other chronic diseases. For over a decade, her research has had a strong focus on ...

        Research

        Identification of epithelial phospholipase A2 receptor 1 as a potential target in asthma

        PLA2R1 is increased in the airway epithelium in asthma, and serves as a regulator of airway hyperresponsiveness, airway permeability, antigen sensitization, and airway inflammation ...

        Research

        Two females with mutations in USP9X highlight the variable expressivity of the intellectual disability syndrome

        The genetic causes of intellectual disability (ID) are heterogeneous and include both chromosomal and monogenic etiologies. ...

        Research

        Analysis of the human monocyte-derived macrophage transcriptome and response to lipopolysaccharide provides new insights into genetic aetiology of inflammatory bowel disease.

        We propose that this system provides a model for the differentiation and adaptation of monocytes entering the intestinal lamina propria. ...

        Research

        Acute viral bronchiolitis in infants and young children

        Deborah Pat Strickland Holt DH PG PhD PhD, DSc, FRCPath, FRCPI, FAA Program Head, Immunobiology and Immunotherapeutic Program Emeritus Honorary Researcher Deb.Strickland@telethonkids.org.au Patrick.Holt@telethonkids.org.au Program Head, ...

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