30 research outputs found

    Student mobility and transition : setting your compass for success

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    With increasing levels of student mobility within Victorian schools, many educational settings experience frequent changes to their student population. These changes are often met with an ad hoc array of practices implemented by schools in an attempt to adequately manage them. This thesis addresses the impact of student mobility on an educational community and its stakeholders in Victoria, Australia. The research was undertaken in five Victorian government schools that encompassed diverse geographical locations and socio-economic profiles. Key stakeholders include: school principals, teachers and education support staff, mobile students, parents/carers of mobile students, non-mobile students and their families. Each group offered a unique perspective regarding student mobility and transition processes. Participants in this study were involved in interviews and focus groups, and completed a questionnaire. Socio-economic status was identified as a predominant factor in student mobility for both families and schools. This was evidenced by high levels of often unpredictable mobility in socio-economically disadvantaged and significantly disadvantaged participating schools. The participating non-disadvantaged school experienced mobility related specifically to perceived academic gain or parental promotion. Regardless of socio-economic status, each group was reliant on other stakeholders to be successful. No stakeholder groups stood alone as being able to successfully navigate the process of mobility and transition independently. This study, through the thematic analysis of the data collected, has uncovered many actionable and achievable recommendations for families, schools and the education system itself both within Victoria and nationwide. The participants in this research clearly indicated a need for a more strategic and planned approach to mobility. Educational communities must respond proactively in order to provide optimal academic, social and emotional outcomes for students in these circumstances.Doctor of Philosoph

    Microtubules control cellular shape and coherence in amoeboid migrating cells

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    Cells navigating through complex tissues face a fundamental challenge: while multiple protrusions explore different paths, the cell needs to avoid entanglement. How a cell surveys and then corrects its own shape is poorly understood. Here, we demonstrate that spatially distinct microtubule dynamics regulate amoeboid cell migration by locally promoting the retraction of protrusions. In migrating dendritic cells, local microtubule depolymerization within protrusions remote from the microtubule organizing center triggers actomyosin contractility controlled by RhoA and its exchange factor Lfc. Depletion of Lfc leads to aberrant myosin localization, thereby causing two effects that rate-limit locomotion: (1) impaired cell edge coordination during path finding and (2) defective adhesion resolution. Compromised shape control is particularly hindering in geometrically complex microenvironments, where it leads to entanglement and ultimately fragmentation of the cell body. We thus demonstrate that microtubules can act as a proprioceptive device: they sense cell shape and control actomyosin retraction to sustain cellular coherence

    Finishing the euchromatic sequence of the human genome

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    The sequence of the human genome encodes the genetic instructions for human physiology, as well as rich information about human evolution. In 2001, the International Human Genome Sequencing Consortium reported a draft sequence of the euchromatic portion of the human genome. Since then, the international collaboration has worked to convert this draft into a genome sequence with high accuracy and nearly complete coverage. Here, we report the result of this finishing process. The current genome sequence (Build 35) contains 2.85 billion nucleotides interrupted by only 341 gaps. It covers ∼99% of the euchromatic genome and is accurate to an error rate of ∼1 event per 100,000 bases. Many of the remaining euchromatic gaps are associated with segmental duplications and will require focused work with new methods. The near-complete sequence, the first for a vertebrate, greatly improves the precision of biological analyses of the human genome including studies of gene number, birth and death. Notably, the human enome seems to encode only 20,000-25,000 protein-coding genes. The genome sequence reported here should serve as a firm foundation for biomedical research in the decades ahead
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