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        193-204 of 538 results for 'Gene'

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        Comparative analysis of the full genome of Helicobacter pylori isolate sahul64 identifies genes of high divergence

        Genome sequence of Sahul64, an H. pylori strain isolated from an indigenous Australian ...

        Research

        Promoter polymorphisms in two overlapping 6p25 genes implicate mitochondrial proteins in cognitive deficit in schizophrenia

        Association mapping of a 10 Mb interval identified a 260 kb region with a cluster of single-nucleotide polymorphisms (SNPs) significantly associated with CD... ...

        Research

        Exposure to diagnostic radiological procedures and the risk of childhood acute lymphoblastic leukemia

        Diagnostic irradiation of the mother during pregnancy increases the risk of childhood acute lymphoblastic leukemia ...

        Research

        Infant feeding practices and childhood acute leukemia: Findings from the Childhood Cancer & Leukemia International Consortium

        Increasing evidence suggests that breastfeeding may protect from childhood acute lymphoblastic leukemia and acute myeloid leukemia. However, most studies have limited their analyses to any breastfeeding, and only a few data have examined exclusive breastfeeding, or other exposures such as formula milk. ...

        Research

        Serotonergic contributions to human brain aggression networks

        We investigated the influence of brain serotonin modulation and MAOA genotype on functional amygdala connectivity during aggressive behavior ...

        Research

        Characterization of regulatory dendritic cells differentiated from the bone marrow of UV-irradiated mice

        In summary, UV-BMDCs do not express the classical phenotypic or gene expression properties of DCs reported by others as 'regulatory' or 'tolerogenic'. ...

        Research

        NTNG1 mutations are a rare cause of Rett syndrome

        A translocation that disrupted the netrin G1 gene (NTNG1) was recently reported in a patient with the early seizure variant of Rett syndrome (RTT). ...

        Research

        Characterising the development of molecular and hormonal circadian rhythm development in preterm infants

        Jane Pillow JP BMedSci (Dist) MBBS, PhD (Dist) FRACP Research Theme Head, Early Environment; Team Lead, Chronobiology jane.pillow@telethonkids.org.au Research Theme Head, Early Environment; Team Lead, Chronobiology Professor Jane Pillow is an ...

        Research

        Inherited balanced translocation t(9;17)(q33.2;q25.3) concomitant with a 16p13.1 duplication in a patient with schizophrenia.

        We report two rare genetic aberrations in a schizophrenia patient that may act together to confer disease susceptibility. ...

        Research

        Clinical Implications of Minimal Residual Disease Detection in Infants With KMT2A-Rearranged Acute Lymphoblastic Leukemia Treated on the Interfant-06 Protocol

        Infant acute lymphoblastic leukemia (ALL) is characterized by a high incidence of KMT2A gene rearrangements and poor outcome. We evaluated the value of minimal residual disease (MRD) in infants with KMT2A-rearranged ALL treated within the Interfant-06 protocol, which compared lymphoid-style consolidation (protocol IB) versus myeloid-style consolidation (araC, daunorubicin, etoposide/mitoxantrone, araC, etoposide). ...

        Research

        A genome-wide approach to children's aggressive behavior: The EAGLE consortium

        Common variants at 2p12 show suggestive evidence for association with childhood aggression ...

        Research

        Elucidation of pathways driving asthma pathogenesis: Development of a systems-level analytic strategy

        Whereas asthma was rare in the late 1800s and early 1900s, the marked increase in its incidence and prevalence since the 1960s points to substantial gene ×... ...

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