This study demonstrates the application of High Power Ultrasonic Microembossing Technology (HPUMT) in producing microfeatures on polymer substrates. The work reviews a novel method of obtaining flash free and precise microfeatures by manipulating the material density through microcellular foaming. The microfeatures created on the polymer substrates were further characterized by analyzing the feature depth with respect to the critical ultrasonic embossing operating parameters such as embossing heating times (s), embossing amplitude (ym) at a constant embossing trigger force (N). An experiment design was constructed and performed to characterize the parameters on foamed and unfoamed (or regular) versions of polystyrene (PS) and polypropylene ...
Microfluidics is a promising technology that is used extensively in biomedical devices, so called la...
Long INterspersed Element-1 (LINE-1 or L1) is the only active autonomous retrotransposon in the huma...
Fabry disease is a rare, X-linked lysosomal storage disease arising from deficiency of the lysosomal...
This dissertation presents work that aims to address the current limitations of latent fingerprint a...
Silica-based nanocomposites with core/shell configurations have diverse functionalities and applicat...
Dye-sensitized solar cells (DSSCs) and quantum dot-sensitized solar cells (QDSSCs) are two promising...
This thesis presents work on advancements and applications of methodology for the analysis of biolog...
Organic semiconductors have evolved rapidly over the last decades and currently are considered as th...
The main goal of the presented research is development of nanoparticle based matrix-assisted laser d...
This thesis presents efforts in the advancement and application of high-spatial resolution matrix-as...
In the neuron, neurotransmitter release is mediated by SNARE (soluble NSF (N-ethylmaleimide-sensitiv...
Our understanding of how metabolic networks are structured and regulated is limited by the multicell...
Silencing of the Fragile X Mental Retardation Protein (FMRP)-encoding gene Fmr1 causes Fragile X Syn...
High-throughput screening (HTS) represents a powerful tool for drug discovery by allowing tens of th...
The need of prevention and occurrence reduction of work related musculoskeletal disorders is the ici...
Microfluidics is a promising technology that is used extensively in biomedical devices, so called la...
Long INterspersed Element-1 (LINE-1 or L1) is the only active autonomous retrotransposon in the huma...
Fabry disease is a rare, X-linked lysosomal storage disease arising from deficiency of the lysosomal...
This dissertation presents work that aims to address the current limitations of latent fingerprint a...
Silica-based nanocomposites with core/shell configurations have diverse functionalities and applicat...
Dye-sensitized solar cells (DSSCs) and quantum dot-sensitized solar cells (QDSSCs) are two promising...
This thesis presents work on advancements and applications of methodology for the analysis of biolog...
Organic semiconductors have evolved rapidly over the last decades and currently are considered as th...
The main goal of the presented research is development of nanoparticle based matrix-assisted laser d...
This thesis presents efforts in the advancement and application of high-spatial resolution matrix-as...
In the neuron, neurotransmitter release is mediated by SNARE (soluble NSF (N-ethylmaleimide-sensitiv...
Our understanding of how metabolic networks are structured and regulated is limited by the multicell...
Silencing of the Fragile X Mental Retardation Protein (FMRP)-encoding gene Fmr1 causes Fragile X Syn...
High-throughput screening (HTS) represents a powerful tool for drug discovery by allowing tens of th...
The need of prevention and occurrence reduction of work related musculoskeletal disorders is the ici...
Microfluidics is a promising technology that is used extensively in biomedical devices, so called la...
Long INterspersed Element-1 (LINE-1 or L1) is the only active autonomous retrotransposon in the huma...
Fabry disease is a rare, X-linked lysosomal storage disease arising from deficiency of the lysosomal...