Browse study websites

Discover. Prevent. Cure.

Menu Fundraise Donate

    Recommended pages

      Do you mean

        145-156 of 538 results for 'Gene'

        Refine research

        Research

        Vitamin D receptor polymorphisms are associated with severity of wheezing illnesses and asthma exacerbations in children

        These findings suggest that genetic variants at the VDR locus may play a role in acute wheeze/asthma severity in children ...

        Research

        Towards a PBMC "virogram assay" for precision medicine: Concordance between ex vivo and in vivo viral infection transcriptomes

        In this rhinovirus study, we first hypothesized that ex vivo human cells response to virus can serve as a proxy for otherwise controversial in vivo human... ...

        Research

        Common variation contributes to the genetic architecture of social communication traits

        Andrew Whitehouse Watch and listen to Andrew AJ PhD Angela Wright Bennett Professor of Autism Research at Telethon Kids Institute; Director, CliniKids Andrew.Whitehouse@telethonkids.org.au Angela Wright Bennett Professor of Autism Research at ...

        Research

        Multiomic neuropathology improves diagnostic accuracy in pediatric neuro-oncology

        The large diversity of central nervous system (CNS) tumor types in children and adolescents results in disparate patient outcomes and renders accurate diagnosis challenging. In this study, we prospectively integrated DNA methylation profiling and targeted gene panel sequencing with blinded neuropathological reference diagnostics for a population-based cohort of more than 1,200 newly diagnosed pediatric patients with CNS tumors, to assess their utility in routine neuropathology. ...

        Research

        A brief history of MECP2 duplication syndrome: 20-years of clinical understanding

        MECP2 duplication syndrome (MDS) is a rare, X-linked, neurodevelopmental disorder caused by a duplication of the methyl-CpG-binding protein 2 (MECP2) gene-a gene in which loss-of-function mutations lead to Rett syndrome (RTT). MDS has an estimated live birth prevalence in males of 1/150,000. ...

        Research

        Risk of childhood acute lymphoblastic leukaemia following parental occupational exposure to extremely low frequency electromagnetic fields

        Risk of childhood acute lymphoblastic leukaemia following parental occupational exposure to extremely low frequency electromagnetic fields British Journal.. ...

        Research

        Heterogeneity in mechanisms of emergent resistance in pediatric T-cell acute lymphoblastic leukemia

        Biological changes associated with T-ALL relapse and resistance are stochastic and highly individual ...

        Research

        Expanding the phenotype of the CDKL5 deficiency disorder: Are seizures mandatory?

        These cases, both without seizures but with apparent behavioral symptomatology, together question whether seizures are mandatory in this disorder ...

        Research

        Evolutionary genomics of epidemic visceral leishmaniasis in the Indian subcontinent

        Our results reveal the complexity of Leishmania donovani evolution in the Indian subcontinent in response to drug treatment ...

        Research

        ANRIL Promoter DNA Methylation: A Perinatal Marker for Later Adiposity

        Experimental studies show a substantial contribution of early life environment to obesity risk through epigenetic processes. ...

        Research

        An integrated expression atlas of miRNAs and their promoters in human and mouse

        We provided a broad atlas of miRNA expression and promoters in primary mammalian cells, establishing a foundation for detailed analysis of miRNA. ...

        Research

        Silencing of GATA3 defines a novel stem cell-like subgroup of ETP-ALL

        GATA3low ETP-ALL is a novel stem cell-like leukemia with implications for the use of myeloid-derived therapies ...

        Page 13 of 45