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D R Booth

Showing results (41-50 of 52) with videos related to

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Nature|April 8, 1993
Human lysozyme gene mutations cause hereditary systemic amyloidosisM B Pepys, P N Hawkins, D R Booth, 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.
Nature|February 27, 1997
Instability, unfolding and aggregation of human lysozyme variants underlying amyloid fibrillogenesisD R Booth, M Sunde, V Bellotti, et al.
Genes and Immunity|September 23, 2011
The role of SNPs in the α-chain of the IL-7R gene in CD4+ T-cell recovery in HIV-infected African patients receiving suppressive cARTR Rajasuriar, D R Booth, M Gouillou, et al.
Genes and Immunity|December 17, 2013
Hepatic metallothionein expression in chronic hepatitis C virus infection is IFNL3 genotype-dependentK S O'Connor, G Parnell, E Patrick, et al.
Genes and Immunity|June 17, 2016
IFNL3/4 genotype is associated with altered immune cell populations in peripheral blood in chronic hepatitis C infectionK S O'Connor, S A Read, M Wang, et al.
The Journal of Clinical Investigation|June 15, 1996
Hereditary hepatic and systemic amyloidosis caused by a new deletion/insertion mutation in the apolipoprotein AI geneD R Booth, S Y Tan, S E Booth, et al.
Genes and Immunity|April 19, 2013
CCR5-Δ32 genotype does not improve predictive value of IL28B polymorphisms for treatment response in chronic HCV infectionV Suppiah, N J Armstrong, K S O'Connor, et al.
Data in Brief|March 10, 2017
Data characterizing the ZMIZ1 molecular phenotype of multiple sclerosisN Fewings, P N Gatt, F C McKay, et al.
Journal of Autoimmunity|January 9, 2017
The autoimmune risk gene ZMIZ1 is a vitamin D responsive marker of a molecular phenotype of multiple sclerosisN L Fewings, P N Gatt, F C McKay, et al.
Pageof 6

Showing results (41-50 of 52) with videos related to

Sort By:
Pageof 6
Nature|April 8, 1993
Human lysozyme gene mutations cause hereditary systemic amyloidosisM B Pepys, P N Hawkins, D R Booth, 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.
Nature|February 27, 1997
Instability, unfolding and aggregation of human lysozyme variants underlying amyloid fibrillogenesisD R Booth, M Sunde, V Bellotti, et al.
Genes and Immunity|September 23, 2011
The role of SNPs in the α-chain of the IL-7R gene in CD4+ T-cell recovery in HIV-infected African patients receiving suppressive cARTR Rajasuriar, D R Booth, M Gouillou, et al.
Genes and Immunity|December 17, 2013
Hepatic metallothionein expression in chronic hepatitis C virus infection is IFNL3 genotype-dependentK S O'Connor, G Parnell, E Patrick, et al.
Genes and Immunity|June 17, 2016
IFNL3/4 genotype is associated with altered immune cell populations in peripheral blood in chronic hepatitis C infectionK S O'Connor, S A Read, M Wang, et al.
The Journal of Clinical Investigation|June 15, 1996
Hereditary hepatic and systemic amyloidosis caused by a new deletion/insertion mutation in the apolipoprotein AI geneD R Booth, S Y Tan, S E Booth, et al.
Genes and Immunity|April 19, 2013
CCR5-Δ32 genotype does not improve predictive value of IL28B polymorphisms for treatment response in chronic HCV infectionV Suppiah, N J Armstrong, K S O'Connor, et al.
Data in Brief|March 10, 2017
Data characterizing the ZMIZ1 molecular phenotype of multiple sclerosisN Fewings, P N Gatt, F C McKay, et al.
Journal of Autoimmunity|January 9, 2017
The autoimmune risk gene ZMIZ1 is a vitamin D responsive marker of a molecular phenotype of multiple sclerosisN L Fewings, P N Gatt, F C McKay, et al.
Pageof 6