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Transforming automated inspection & non-destructive testing: world-leading Open Access research on robotics, sensors & ultrasonics

Strathprints makes available scholarly Open Access content by researchers within the Centre for Ultrasonic Engineering, based within Electronic & Electrical Engineering.

Research at CUE brings together next generation robotics with sensing technology to enable inspection of high value components, such as aerospace components, at the point of manufacture. Non-destructive testing techniques using ultrasound and other sensors can then be deployed to assess components for structural faults or damage and thereby ensure they are built correctly and more efficiently. Research at CUE is to be stimulated by the construction of a new £2.5 million state-of-the-art Robotically-Enabled Sensing (RES) hub within the Department of Electronic & Electrical Engineering (EEE).

Explore the Open Access research by EEE, or explore all of Strathclyde's Open Access research...

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Group by: Publication Date | Item type | No Grouping
Jump to: 2018 | 2015 | 2012 | 2005 | 2002
Number of items: 7.

2018

Choi, Jason C and Wu, Wei and Phillips, Elizabeth and Plevin, Robin and Sera, Fusako and Homma, Shunichi and Worman, Howard J (2018) Elevated dual specificity protein phosphatase 4 in cardiomyopathy caused by lamin A/C gene mutation is primarily ERK1/2-dependent and its depletion improves cardiac function and survival. Human Molecular Genetics, 27 (13). pp. 2290-2305. ISSN 0964-6906

2015

Sposito, Teresa and Preza, Elisavet and Mahoney, Colin J. and Setó-Salvia, Núria and Ryan, Natalie S. and Morris, Huw R. and Arber, Charles and Devine, Michael J. and Houlden, Henry and Warner, Thomas T. and Bushell, Trevor J. and Zagnoni, Michele and Kunath, Tilo and Livesey, Frederick J. and Fox, Nick C. and Rossor, Martin N. and Hardy, John and Wray, Selina (2015) Developmental regulation of tau splicing is disrupted in stem cell derived neurons from frontotemporal dementia patients with the 10+16 splice-site mutation in MAPT. Human Molecular Genetics, 24 (18). pp. 5260-5269. ISSN 0964-6906

2012

Winchester, Catherine and Ohzeki, Hiromitsu and Vouyiouklis, Demetrius and Thompson, Rhiannon and Yamagami, Keiji and Norrie, John and Hunter, Robert and Pratt, Judith and Morris, Brian J (2012) Converging evidence that sequence variations in the novel candidate gene MAP2K7 (MKK7) are functionally associated with schizophrenia. Human Molecular Genetics, 21 (22). pp. 4910-4921.

2005

Warby, Simon C and Chan, Edmond Y and Metzler, Martina and Gan, Lu and Singaraja, Roshni R and Crocker, Susan F and Robertson, Harold A and Hayden, Michael R (2005) Huntingtin phosphorylation on serine 421 is significantly reduced in the striatum and by polyglutamine expansion in vivo. Human Molecular Genetics, 14 (11). pp. 1569-1577. ISSN 0964-6906

2002

Luthi-Carter, Ruth and Hanson, Sarah A and Strand, Andrew D and Bergstrom, Donald A and Chun, Wanjoo and Peters, Nikki L and Woods, Annette M and Chan, Edmond Y and Kooperberg, Charles and Krainc, Dimitri and Young, Anne B and Tapscott, Stephen J and Olson, James M (2002) Dysregulation of gene expression in the R6/2 model of polyglutamine disease : parallel changes in muscle and brain. Human Molecular Genetics, 11 (17). pp. 1911-1926. ISSN 0964-6906

Chan, Edmond Y W and Luthi-Carter, Ruth and Strand, Andrew and Solano, Steven M and Hanson, Sarah A and DeJohn, Molly M and Kooperberg, Charles and Chase, Kathryn O and DiFiglia, Marian and Young, Anne B and Leavitt, Blair R and Cha, Jang-Ho J and Aronin, Neil and Hayden, Michael R and Olson, James M (2002) Increased huntingtin protein length reduces the number of polyglutamine-induced gene expression changes in mouse models of Huntington's disease. Human Molecular Genetics, 11 (17). pp. 1939-1951. ISSN 0964-6906

Chan, Edmond Y W and Nasir, Jamal and Gutekunst, Claire-Anne and Coleman, Sarah and Maclean, Alan and Maas, Alex and Metzler, Martina and Gertsenstein, Marina and Ross, Christopher A and Nagy, Andràs and Hayden, Michael R (2002) Targeted disruption of Huntingtin-associated protein-1 (Hap1) results in postnatal death due to depressed feeding behavior. Human Molecular Genetics, 11 (8). pp. 945-959. ISSN 0964-6906

This list was generated on Thu Apr 2 08:37:41 2020 BST.