39 research outputs found
Auxin–Cytokinin Interaction Regulates Meristem Development
Plant hormones regulate many aspects of plant growth and development. Both auxin and cytokinin have been known for a long time to act either synergistically or antagonistically to control several significant developmental processes, such as the formation and maintenance of meristem. Over the past few years, exciting progress has been made to reveal the molecular mechanisms underlying the auxin–cytokinin action and interaction. In this review, we shall briefly discuss the major progress made in auxin and cytokinin biosynthesis, auxin transport, and auxin and cytokinin signaling. The frameworks for the complicated interaction of these two hormones in the control of shoot apical meristem and root apical meristem formation as well as their roles in in vitro organ regeneration are the major focus of this review
Complement and clusterin in the spinal cord dorsal horn and gracile nucleus following sciatic nerve injury in the adult rat
Counter-radicalization Policies and Policing in Education : Making a Case for Human Security in Europe
Research on counter-radicalization policies and policing in education in Europe is currently patchy and often focused on the United Kingdom. Scholars have observed that counter-radicalization policing in education is a threat to human freedom, human rights and dignity, and safe learning environments. However, scholars generally have not examined this issue from the viewpoint of human security. This paper examines the policing policy matter from the perspective of the personal security form of human security. The concern is that such a policing policy-related threat is antithetical to the concept of human security promoted by the United Nations (UN) and which the European Union (EU) and some European states had adopted. The study aims to find out how the current educational counter-radicalization initiatives and their effects could be used to argue for human security in Europe. The goal is to see how we can learn from past mistakes and improve future directions. The primary data are sourced from selected national, EU and UN policy documents, and a national media report. This work employs descriptive discourse analysis to analyse its data. The findings reveal that the present educational counterradicalization policies of selected cases are grossly and/or explicitly deficient in the principles and language of human security. This has a negative impact on our understanding of the counter-radicalization policy effects in Europe. The study shows that the counter-radicalization strategy could trigger insecurity and negative security-oriented education for citizenship than we previously acknowledged in the literature. This piece suggests that the adverse consequences and tendencies could have been prevented had the appropriate human security elements been used in formulating and promoting the policy/strategy.Peer reviewe
Mammography and the Risk of Thyroid and Hematological Cancers: A Nationwide Population-based Study
18F-AV-1451 and CSF T-tau and P-tau as biomarkers in Alzheimer's disease
To elucidate the relationship between cerebrospinal fluid (CSF) total-tau (T-tau) and phosphorylated tau (P-tau) with the tau PET ligand 18F-AV-1451 in Alzheimer's disease (AD), we examined 30 cognitively healthy elderly (15 with preclinical AD), 14 prodromal AD, and 39 AD dementia patients. CSF T-tau and P-tau were highly correlated (R = 0.92, P < 0.001), but they were only moderately associated with retention of 18F-AV-1451, and mainly in demented AD patients. 18F-AV-1451, but not CSF T-tau or P-tau, was strongly associated with atrophy and cognitive impairment. CSF tau was increased in preclinical AD, despite normal 18F-AV-1451 retention. However, not all dementia AD patients exhibited increased CSF tau, even though 18F-AV-1451 retention was always increased at this disease stage. We conclude that CSF T-tau and P-tau mainly behave as biomarkers of "disease state", since they appear to be increased in many cases of AD at all disease stages, already before the emergence of tau aggregates. In contrast, 18F-AV-1451 is a biomarker of "disease stage", since it is increased in clinical stages of the disease, and is associated with brain atrophy and cognitive decline
