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R Booth

Showing results (571-580 of 596) with videos related to

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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.
Clinical Immunology (Orlando, Fla.)|January 15, 2016
The low EOMES/TBX21 molecular phenotype in multiple sclerosis reflects CD56+ cell dysregulation and is affected by immunomodulatory therapiesFiona C McKay, Prudence N Gatt, Nicole Fewings, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|October 24, 2014
Antibodies to MOG have a demyelination phenotype and affect oligodendrocyte cytoskeletonRussell C Dale, Esther M Tantsis, Vera Merheb, et al.
Human Molecular Genetics|March 2, 2010
The multiple sclerosis whole blood mRNA transcriptome and genetic associations indicate dysregulation of specific T cell pathways in pathogenesisKaushal S Gandhi, Fiona C McKay, Mathew Cox, et al.
Nature Genetics|September 15, 2009
IL28B is associated with response to chronic hepatitis C interferon-alpha and ribavirin therapyVijayaprakash Suppiah, Max Moldovan, Golo Ahlenstiel, 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.
Journal of Hepatology|April 29, 2014
IFNL3 polymorphisms predict response to therapy in chronic hepatitis C genotype 2/3 infectionMohammed Eslam, Reynold Leung, Manuel Romero-Gomez, et al.
Plos One|December 15, 2010
A transcription factor map as revealed by a genome-wide gene expression analysis of whole-blood mRNA transcriptome in multiple sclerosisCarlos Riveros, Drew Mellor, Kaushal S Gandhi, 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.
Biochemistry|June 29, 2017
Adenosine Monophosphate Binding Stabilizes the KTN Domain of the Shewanella denitrificans Kef Potassium Efflux SystemChristos Pliotas, Samuel C Grayer, Silvia Ekkerman, et al.
Pageof 60

Showing results (571-580 of 596) with videos related to

Sort By:
Pageof 60
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.
Clinical Immunology (Orlando, Fla.)|January 15, 2016
The low EOMES/TBX21 molecular phenotype in multiple sclerosis reflects CD56+ cell dysregulation and is affected by immunomodulatory therapiesFiona C McKay, Prudence N Gatt, Nicole Fewings, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|October 24, 2014
Antibodies to MOG have a demyelination phenotype and affect oligodendrocyte cytoskeletonRussell C Dale, Esther M Tantsis, Vera Merheb, et al.
Human Molecular Genetics|March 2, 2010
The multiple sclerosis whole blood mRNA transcriptome and genetic associations indicate dysregulation of specific T cell pathways in pathogenesisKaushal S Gandhi, Fiona C McKay, Mathew Cox, et al.
Nature Genetics|September 15, 2009
IL28B is associated with response to chronic hepatitis C interferon-alpha and ribavirin therapyVijayaprakash Suppiah, Max Moldovan, Golo Ahlenstiel, 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.
Journal of Hepatology|April 29, 2014
IFNL3 polymorphisms predict response to therapy in chronic hepatitis C genotype 2/3 infectionMohammed Eslam, Reynold Leung, Manuel Romero-Gomez, et al.
Plos One|December 15, 2010
A transcription factor map as revealed by a genome-wide gene expression analysis of whole-blood mRNA transcriptome in multiple sclerosisCarlos Riveros, Drew Mellor, Kaushal S Gandhi, 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.
Biochemistry|June 29, 2017
Adenosine Monophosphate Binding Stabilizes the KTN Domain of the Shewanella denitrificans Kef Potassium Efflux SystemChristos Pliotas, Samuel C Grayer, Silvia Ekkerman, et al.
Pageof 60