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Nature Genetics
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January 11, 2011
Tartrate-resistant acid phosphatase deficiency causes a bone dysplasia with autoimmunity and a type I interferon expression signature
Tracy A Briggs, Gillian I Rice, Sarah Daly, et al.
The Lancet. Rheumatology
|
January 24, 2024
Contribution of rare and predicted pathogenic gene variants to childhood-onset lupus: a large, genetic panel analysis of British and French cohorts
Alexandre Belot, Gillian I Rice, Sulliman Ommar Omarjee, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
March 1, 2007
GSK189254, a novel H3 receptor antagonist that binds to histamine H3 receptors in Alzheimer's disease brain and improves cognitive performance in preclinical models
Andrew D Medhurst, Alan R Atkins, Isabel J Beresford, et al.
CNS Neuroscience & Therapeutics
|
May 17, 2008
Preclinical characterization of A-582941: a novel alpha7 neuronal nicotinic receptor agonist with broad spectrum cognition-enhancing properties
Karin R Tietje, David J Anderson, R Scott Bitner, et al.
Science (New York, N.Y.)
|
July 4, 1986
Voyager 2 in the uranian system: imaging science results
B A Smith, L A Soderblom, R Beebe, et al.
Nature Genetics
|
June 16, 2009
Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response
Gillian I Rice, Jacquelyn Bond, Aruna Asipu, et al.
Nature Genetics
|
September 25, 2012
Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature
Gillian I Rice, Paul R Kasher, Gabriella M A Forte, et al.
Neuropediatrics
|
June 1, 2017
Genetic, Phenotypic, and Interferon Biomarker Status in ADAR1-Related Neurological Disease
Gillian I Rice, Naoki Kitabayashi, Magalie Barth, et al.
The Journal of Allergy and Clinical Immunology
|
September 1, 2018
Hypomorphic caspase activation and recruitment domain 11 (CARD11) mutations associated with diverse immunologic phenotypes with or without atopic disease
Batsukh Dorjbal, Jeffrey R Stinson, Chi A Ma, et al.
Human Mutation
|
January 4, 2020
Genetic and phenotypic spectrum associated with IFIH1 gain-of-function
Gillian I Rice, Sehoon Park, Francesco Gavazzi, et al.
Page
of 48
Search research articles
Search
Showing results (461-470 of 475) with videos related to
Sort By:
Page
of 48
Nature Genetics
|
January 11, 2011
Tartrate-resistant acid phosphatase deficiency causes a bone dysplasia with autoimmunity and a type I interferon expression signature
Tracy A Briggs, Gillian I Rice, Sarah Daly, et al.
The Lancet. Rheumatology
|
January 24, 2024
Contribution of rare and predicted pathogenic gene variants to childhood-onset lupus: a large, genetic panel analysis of British and French cohorts
Alexandre Belot, Gillian I Rice, Sulliman Ommar Omarjee, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
March 1, 2007
GSK189254, a novel H3 receptor antagonist that binds to histamine H3 receptors in Alzheimer's disease brain and improves cognitive performance in preclinical models
Andrew D Medhurst, Alan R Atkins, Isabel J Beresford, et al.
CNS Neuroscience & Therapeutics
|
May 17, 2008
Preclinical characterization of A-582941: a novel alpha7 neuronal nicotinic receptor agonist with broad spectrum cognition-enhancing properties
Karin R Tietje, David J Anderson, R Scott Bitner, et al.
Science (New York, N.Y.)
|
July 4, 1986
Voyager 2 in the uranian system: imaging science results
B A Smith, L A Soderblom, R Beebe, et al.
Nature Genetics
|
June 16, 2009
Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response
Gillian I Rice, Jacquelyn Bond, Aruna Asipu, et al.
Nature Genetics
|
September 25, 2012
Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature
Gillian I Rice, Paul R Kasher, Gabriella M A Forte, et al.
Neuropediatrics
|
June 1, 2017
Genetic, Phenotypic, and Interferon Biomarker Status in ADAR1-Related Neurological Disease
Gillian I Rice, Naoki Kitabayashi, Magalie Barth, et al.
The Journal of Allergy and Clinical Immunology
|
September 1, 2018
Hypomorphic caspase activation and recruitment domain 11 (CARD11) mutations associated with diverse immunologic phenotypes with or without atopic disease
Batsukh Dorjbal, Jeffrey R Stinson, Chi A Ma, et al.
Human Mutation
|
January 4, 2020
Genetic and phenotypic spectrum associated with IFIH1 gain-of-function
Gillian I Rice, Sehoon Park, Francesco Gavazzi, et al.
Page
of 48