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Showing 1 to 19 of 19 for “"Differential Modulation"”.

  1. Differential modulation and non-coherent detection in wireless relay networks

    … bypass the requirement of channel information, differential modulation together with non-coherent detection can be deployed. This thesis is concerned with various issues related to differential modulation and non-coherent detection in cooperative networks. Specifically, the thesis examines the …

    sask Repository record for Differential modulation and non-coherent detection in wireless relay networks (opens in a new tab)

  2. LL-37 and citrullinated LL-37: differential modulation of the oxylipin - chemokine axis

    Inflammation plays a crucial role in the host immune system, and it involves a complex network of cellular and molecular events. In the lungs, human bronchial epithelial cells release cytokines/chemokines, and other mediators such as bioactive lipids and cationic host defence peptides (CHDPs) to …

    manitoba Repository record for LL-37 and citrullinated LL-37: differential modulation of the oxylipin - chemokine axis (opens in a new tab)

  3. Differential modulation of T-type voltage gated calcium channels by G-protein coupled receptors.

    … largely unexplored. Investigations into T-type modulation within native neuronal systems have been complicated by the presence of multiple GPCR subtypes and a lack of pharmacological tools to separate currents generated by the three T-type isoforms; Cav3.1, Cav3.2, and Cav3.3. We hypothesize …

    ubc Repository record for Differential modulation of T-type voltage gated calcium channels by G-protein coupled receptors. (opens in a new tab)

  4. Differential modulation of HIV-1 capsid uncoating kinetics revealed by a novel single-particle uncoating assay

    … the two phases of uncoating can be modulated differentially. Binding of factors to the CANTD-CTD hexameric interface, such as PF74 and CPSF6p, accelerate or do not alter capsid opening but strongly stabilise the remaining lattice. In contrast, binding of polyanions to the central capsid pore, …

    unsw Repository record for Differential modulation of HIV-1 capsid uncoating kinetics revealed by a novel single-particle uncoating assay (opens in a new tab)

  5. Differential MMSE: A New Approach for Adaptive Interference Suppression Over Time-Varying Channels

    … noncoherent communication over such channels is differential modulation and demodulation, which obviates the need to track amplitude and phase by exploiting the fact that channel variations over successive symbols are negligible. However, there are no known methods for adaptive interference …

    uiuc Repository record for Differential MMSE: A New Approach for Adaptive Interference Suppression Over Time-Varying Channels (opens in a new tab)

  6. Monoaminergic Signaling in the Human Brain: New Insights

    … emotional Stroop task and identified there were differential modulation of monoamines during the presentation of valenced words in the thalamus and anterior cingulate cortex. In a separate experiment, patients with Parkinson's disease or essential tremors played a social reward task. We observed …

    vt Repository record for Monoaminergic Signaling in the Human Brain: New Insights (opens in a new tab)

  7. Common and Distinct Neural Mechanisms of Fear Acquisition and Reversal in comorbid Autism with Social Anxiety and Social Anxiety Disorder uncomplicated by Autism

    … observed, but within-group differences indicated differential modulation of the ITG in the ASD with SAD group in the Social condition compared to the Nonsocial condition. The SAD group demonstrated differential activation between conditioning stimuli in the Nonsocial condition, but not in the …

    vt Repository record for Common and Distinct Neural Mechanisms of Fear Acquisition and Reversal in comorbid Autism with Social Anxiety and Social Anxiety Disorder uncomplicated by Autism (opens in a new tab)

  8. Starved State Dependent Modulation of Olfactory Receptor Neuron Function in Drosophila melanogaster larvae

    … sensory neuron responses to food odorants and modulation of these responses by hunger, much less is known about the extent of modulation that exists among individual sensory neurons and its impact on driving behavioral output. We hypothesized that starvation differentially alters the …

    unr Repository record for Starved State Dependent Modulation of Olfactory Receptor Neuron Function in Drosophila melanogaster larvae (opens in a new tab)

  9. Presenilins Modulate Cellular Activity of Ryanodine Receptors

    … and presenilin 2 (PS2NTF) that resulted in differential modulation of the RyR open probability and mean Ca2+ current at the RyR single channel level. We herein tested the hypothesis that PS1NTF and PS2NTF functionally modulate RyRs in a physiologically relevant in vitro model resulting in …

    tdl Repository record for Presenilins Modulate Cellular Activity of Ryanodine Receptors (opens in a new tab)

  10. Carbon Catabolite Regulation of Yersinia pestis Pathogenesis

    … sources induce robust biofilm development. The differential modulation of Y. pestis biofilm production was found to be facilitated by the cAMP receptor protein, CRP. The microevolution of Y. pestis biovar Orientalis is characterized by loss of glycerol fermentation resulting from dysfunction of …

    utmb Repository record for Carbon Catabolite Regulation of Yersinia pestis Pathogenesis (opens in a new tab)

  11. Studies in Multiple-Antenna Wireless Communications

    … these methods are analyzed.</p> <p>Trained and differential modulation are simple coding techniques for single-user time-varying channels. The performance of these coding methods is characterized for a channel having a constant specular component plus a time-varying diffuse component. A first- …

    byu Repository record for Studies in Multiple-Antenna Wireless Communications (opens in a new tab)

  12. The Octopaminergic Modulatory Circuitry of the Drosophila Larval Mushroom Body Calyx

    … express different neuromodulatory receptors for differential modulation. Here I aimed to use the simple and genetically amenable Drosophila larval Mushroom Body (MB) calyx, a higher order processing area involved in learned odour discrimination, as a model to map octopamine (OA) neuromodulatory …

    cambridge Repository record for The Octopaminergic Modulatory Circuitry of the Drosophila Larval Mushroom Body Calyx (opens in a new tab)

  13. Novel DWT-DAPSK based transceivers for DVB-T transmission and next generation mobile networks

    … small spectral coefficients. Several types of modulation schemes such as DPSK, QAM are employed in OFDM systems, which introduce certain penalties such as increased bandwidth and complexity of the system design. So a multilevel differential modulation technique namely Differential Amplitude and …

    liverpool-jm Repository record for Novel DWT-DAPSK based transceivers for DVB-T transmission and next generation mobile networks (opens in a new tab)

  14. Probiotic Modulation of Mucosal Immune Responses in an In Vitro Co-Culture Model

    … benefits through many mechanisms including modulation of the gut immune system. Gut mucosal macrophages play a pivotal role in driving mucosal immune responses. The local environment and macrophage subset determine immune response: tolerance, associated with an M2-like, regulatory macrophage …

    plymouth Repository record for Probiotic Modulation of Mucosal Immune Responses in an In Vitro Co-Culture Model (opens in a new tab)

  15. Role of second generation phosphodiesterase inhibitors on mammalian sperm mobility

    … type-specific phosphodiesterase inhibitors, differential modulation of sperm motility can be achieved without affecting other sperm function such as acrosome reaction. Additionally, by enhancing sperm function through PDE inhibition, there is a possibility of increasing IVF rates. The …

    abertay Repository record for Role of second generation phosphodiesterase inhibitors on mammalian sperm mobility (opens in a new tab)

  16. Estrogen Signaling in Trigeminal Nociception

    … inflammation increased GPR30 but not ERα. Differential modulation of these ERK-coupled receptors by estrogen and inflammation may play a role in increased trigeminal pain during periods of falling estrogen.

    ku Repository record for Estrogen Signaling in Trigeminal Nociception (opens in a new tab)

  17. NEUROACTIVE AGENTS-MEDIATED CHANGES IN NEURONAL NETWORK ACTIVITY CONTROLS SUSCEPTIBILITY TO SUDDEN UNEXPECTED DEATH IN EPILEPSY (SUDEP)

    … seizure (AGSz) network and respiratory modulation in other models. The goal of my dissertation is to understand the mechanisms by which adenosine could cause SUDEP susceptibility, the neuronal networks in the DBA/1 mice that lead to S-IRA and how fluoxetine modulates the neuronal …

    siu-theses Repository record for NEUROACTIVE AGENTS-MEDIATED CHANGES IN NEURONAL NETWORK ACTIVITY CONTROLS SUSCEPTIBILITY TO SUDDEN UNEXPECTED DEATH IN EPILEPSY (SUDEP) (opens in a new tab)