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R Booth

Showing results (531-540 of 596) with videos related to

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Rheumatology (Oxford, England)|January 13, 2006
Clinical and subclinical inflammation in patients with familial Mediterranean fever and in heterozygous carriers of MEFV mutationsH J Lachmann, B Sengül, T U Yavuzşen, et al.
QJM : Monthly Journal of the Association of Physicians|October 1, 1995
A new apolipoprotein Al variant, Trp50Arg, causes hereditary amyloidosisD R Booth, S Y Tan, S E Booth, et al.
Journal of Cognitive Neuroscience|October 1, 2008
Modality- and task-specific brain regions involved in Chinese lexical processingLi Liu, Xiaoxiang Deng, Danling Peng, et al.
Neuroimage|June 15, 2018
Structural correlates of literacy difficulties in the second language: Evidence from Mandarin-speaking children learning EnglishHehui Li, James R Booth, Nathalie N Bélanger, et al.
Nature|April 8, 1993
Human lysozyme gene mutations cause hereditary systemic amyloidosisM B Pepys, P N Hawkins, D R Booth, et al.
Critical Care (London, England)|August 18, 2012
A distinct influenza infection signature in the blood transcriptome of patients with severe community-acquired pneumoniaGrant P Parnell, Anthony S McLean, David R Booth, et al.
Photochemical & Photobiological Sciences : Official Journal of the European Photochemistry Association and the European Society for Photobiology|August 27, 2009
Quality of UVR exposure for different biological systems along a latitudinal gradientMaria Vernet, Susana B Diaz, Humberto A Fuenzalida, et al.
Plos One|November 5, 2011
Altered antibiotic transport in OmpC mutants isolated from a series of clinical strains of multi-drug resistant E. coliHubing Lou, Min Chen, Susan S Black, et al.
Hepatology (Baltimore, Md.)|January 22, 2011
Hepatitis C pharmacogenetics: state of the art in 2010Nezam H Afdhal, John G McHutchison, Stefan Zeuzem, et al.
Human Mutation|March 1, 2000
Transthyretin Ile73Val is associated with familial amyloidotic polyneuropathy in a Bangladeshi family. Mutations in brief no. 158. OnlineD R Booth, J D Gillmore, M R Persey, et al.
Pageof 60

Showing results (531-540 of 596) with videos related to

Sort By:
Pageof 60
Rheumatology (Oxford, England)|January 13, 2006
Clinical and subclinical inflammation in patients with familial Mediterranean fever and in heterozygous carriers of MEFV mutationsH J Lachmann, B Sengül, T U Yavuzşen, et al.
QJM : Monthly Journal of the Association of Physicians|October 1, 1995
A new apolipoprotein Al variant, Trp50Arg, causes hereditary amyloidosisD R Booth, S Y Tan, S E Booth, et al.
Journal of Cognitive Neuroscience|October 1, 2008
Modality- and task-specific brain regions involved in Chinese lexical processingLi Liu, Xiaoxiang Deng, Danling Peng, et al.
Neuroimage|June 15, 2018
Structural correlates of literacy difficulties in the second language: Evidence from Mandarin-speaking children learning EnglishHehui Li, James R Booth, Nathalie N Bélanger, et al.
Nature|April 8, 1993
Human lysozyme gene mutations cause hereditary systemic amyloidosisM B Pepys, P N Hawkins, D R Booth, et al.
Critical Care (London, England)|August 18, 2012
A distinct influenza infection signature in the blood transcriptome of patients with severe community-acquired pneumoniaGrant P Parnell, Anthony S McLean, David R Booth, et al.
Photochemical & Photobiological Sciences : Official Journal of the European Photochemistry Association and the European Society for Photobiology|August 27, 2009
Quality of UVR exposure for different biological systems along a latitudinal gradientMaria Vernet, Susana B Diaz, Humberto A Fuenzalida, et al.
Plos One|November 5, 2011
Altered antibiotic transport in OmpC mutants isolated from a series of clinical strains of multi-drug resistant E. coliHubing Lou, Min Chen, Susan S Black, et al.
Hepatology (Baltimore, Md.)|January 22, 2011
Hepatitis C pharmacogenetics: state of the art in 2010Nezam H Afdhal, John G McHutchison, Stefan Zeuzem, et al.
Human Mutation|March 1, 2000
Transthyretin Ile73Val is associated with familial amyloidotic polyneuropathy in a Bangladeshi family. Mutations in brief no. 158. OnlineD R Booth, J D Gillmore, M R Persey, et al.
Pageof 60