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G Will

Showing results (51-60 of 173) with videos related to

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Nucleic Acids Research|July 25, 1991
Single-base mutational analysis of cancer and genetic diseases using membrane bound modified oligonucleotidesY Zhang, M Y Coyne, S G Will, et al.
Archives of Disease in Childhood|January 8, 2004
Variations in neurodegenerative disease across the UK: findings from the national study of Progressive Intellectual and Neurological Deterioration (PIND)G Devereux, L Stellitano, C M Verity, et al.
Neuroepidemiology|March 21, 2009
Survival and re-operation rates after neurosurgical procedures in Scotland: implications for targeted surveillance of sub-clinical variant Creutzfeldt-Jakob diseaseSheila M Bird, Elizabeth L C Merrall, Hester J T Ward, et al.
Histopathology|August 10, 2000
Laboratory diagnosis of variant Creutzfeldt-Jakob diseaseJ W Ironside, M W Head, J E Bell, et al.
British Journal of Pharmacology|March 1, 1985
Competitive antagonism at thromboxane receptors in human plateletsR A Armstrong, R L Jones, V Peesapati, et al.
Journal of the Royal Society, Interface|October 4, 2006
Factors determining the potential for onward transmission of variant Creutzfeldt-Jakob disease via surgical instrumentsTini Garske, Hester J T Ward, Paul Clarke, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 30, 2009
Is there evidence of vertical transmission of variant Creutzfeldt-Jakob disease?Katy Murray, James Peters, Lesley Stellitano, et al.
IEEE Transactions on Cybernetics|April 29, 2022
Hierarchical One-Class Model With Subnetwork for Representation Learning and Outlier DetectionWandong Zhang, Q M Jonathan Wu, W G Will Zhao, et al.
Neuroscience Letters|July 25, 2014
Sexual experience influences mating-induced activity in nitric oxide synthase-containing neurons in the medial preoptic areaVictoria L Nutsch, Ryan G Will, Tomoko Hattori, et al.
BMC Medical Genetics|December 29, 2009
PRNP variation in UK sporadic and variant Creutzfeldt Jakob disease highlights genetic risk factors and a novel non-synonymous polymorphismMatthew T Bishop, Catherine Pennington, Craig A Heath, et al.
Pageof 18

Showing results (51-60 of 173) with videos related to

Sort By:
Pageof 18
Nucleic Acids Research|July 25, 1991
Single-base mutational analysis of cancer and genetic diseases using membrane bound modified oligonucleotidesY Zhang, M Y Coyne, S G Will, et al.
Archives of Disease in Childhood|January 8, 2004
Variations in neurodegenerative disease across the UK: findings from the national study of Progressive Intellectual and Neurological Deterioration (PIND)G Devereux, L Stellitano, C M Verity, et al.
Neuroepidemiology|March 21, 2009
Survival and re-operation rates after neurosurgical procedures in Scotland: implications for targeted surveillance of sub-clinical variant Creutzfeldt-Jakob diseaseSheila M Bird, Elizabeth L C Merrall, Hester J T Ward, et al.
Histopathology|August 10, 2000
Laboratory diagnosis of variant Creutzfeldt-Jakob diseaseJ W Ironside, M W Head, J E Bell, et al.
British Journal of Pharmacology|March 1, 1985
Competitive antagonism at thromboxane receptors in human plateletsR A Armstrong, R L Jones, V Peesapati, et al.
Journal of the Royal Society, Interface|October 4, 2006
Factors determining the potential for onward transmission of variant Creutzfeldt-Jakob disease via surgical instrumentsTini Garske, Hester J T Ward, Paul Clarke, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 30, 2009
Is there evidence of vertical transmission of variant Creutzfeldt-Jakob disease?Katy Murray, James Peters, Lesley Stellitano, et al.
IEEE Transactions on Cybernetics|April 29, 2022
Hierarchical One-Class Model With Subnetwork for Representation Learning and Outlier DetectionWandong Zhang, Q M Jonathan Wu, W G Will Zhao, et al.
Neuroscience Letters|July 25, 2014
Sexual experience influences mating-induced activity in nitric oxide synthase-containing neurons in the medial preoptic areaVictoria L Nutsch, Ryan G Will, Tomoko Hattori, et al.
BMC Medical Genetics|December 29, 2009
PRNP variation in UK sporadic and variant Creutzfeldt Jakob disease highlights genetic risk factors and a novel non-synonymous polymorphismMatthew T Bishop, Catherine Pennington, Craig A Heath, et al.
Pageof 18