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Astrid Rasmussen

Showing results (81-90 of 125) with videos related to

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Advances in Neurology|October 29, 2004
Familial juvenile myoclonic epilepsyMaría Elisa Alonso, Marco T Medina, Iris E Martínez-Juárez, et al.
Annals of Neurology|October 7, 2004
Huntington's Disease-like 2 (HDL2) in North America and JapanRussell L Margolis, Susan E Holmes, Adam Rosenblatt, et al.
Journal of Clinical Medicine|July 12, 2020
Sjögren's Syndrome Minor Salivary Gland CD4<sup>+</sup> Memory T Cells Associate with Glandular Disease Features and have a Germinal Center T Follicular Helper Transcriptional ProfileMichelle L Joachims, Kerry M Leehan, Mikhail G Dozmorov, et al.
The Lancet. Microbe|May 21, 2026
Gene transfer from NDM-5-producing and OXA-48-producing Enterobacter hormaechei ST79 on contaminated dicloxacillin capsules to other Enterobacterales in Europe, 2020-23: a retrospective, observational, molecular epidemiological studyAstrid Rasmussen, Lone J Porsbo, Louise Roer, et al.
JCI Insight|July 1, 2016
Single-cell analysis of glandular T cell receptors in Sjögren's syndromeMichelle L Joachims, Kerry M Leehan, Christina Lawrence, et al.
ACR Open Rheumatology|August 28, 2019
Reproducibility of Ocular Surface Staining in the Assessment of Sjögren Syndrome-Related Keratoconjunctivitis Sicca: Implications on Disease ClassificationAstrid Rasmussen, Donald U Stone, C Erick Kaufman, et al.
Arthritis and Rheumatism|September 18, 2010
Genetically determined Amerindian ancestry correlates with increased frequency of risk alleles for systemic lupus erythematosusElena Sanchez, Ryan D Webb, Astrid Rasmussen, et al.
Nature Genetics|January 31, 2017
A missense variant in NCF1 is associated with susceptibility to multiple autoimmune diseasesJian Zhao, Jianyang Ma, Yun Deng, et al.
Communications Medicine|January 26, 2026
Genomic characterization and sub-clustering of Escherichia coli clonal complex 38 reveal host associated genetic markersLouise Roer, Astrid Rasmussen, Frank Hansen, et al.
Nature Genetics|July 20, 2004
Mutations in EFHC1 cause juvenile myoclonic epilepsyToshimitsu Suzuki, Antonio V Delgado-Escueta, Kripamoy Aguan, et al.
Pageof 13

Showing results (81-90 of 125) with videos related to

Sort By:
Pageof 13
Advances in Neurology|October 29, 2004
Familial juvenile myoclonic epilepsyMaría Elisa Alonso, Marco T Medina, Iris E Martínez-Juárez, et al.
Annals of Neurology|October 7, 2004
Huntington's Disease-like 2 (HDL2) in North America and JapanRussell L Margolis, Susan E Holmes, Adam Rosenblatt, et al.
Journal of Clinical Medicine|July 12, 2020
Sjögren's Syndrome Minor Salivary Gland CD4<sup>+</sup> Memory T Cells Associate with Glandular Disease Features and have a Germinal Center T Follicular Helper Transcriptional ProfileMichelle L Joachims, Kerry M Leehan, Mikhail G Dozmorov, et al.
The Lancet. Microbe|May 21, 2026
Gene transfer from NDM-5-producing and OXA-48-producing Enterobacter hormaechei ST79 on contaminated dicloxacillin capsules to other Enterobacterales in Europe, 2020-23: a retrospective, observational, molecular epidemiological studyAstrid Rasmussen, Lone J Porsbo, Louise Roer, et al.
JCI Insight|July 1, 2016
Single-cell analysis of glandular T cell receptors in Sjögren's syndromeMichelle L Joachims, Kerry M Leehan, Christina Lawrence, et al.
ACR Open Rheumatology|August 28, 2019
Reproducibility of Ocular Surface Staining in the Assessment of Sjögren Syndrome-Related Keratoconjunctivitis Sicca: Implications on Disease ClassificationAstrid Rasmussen, Donald U Stone, C Erick Kaufman, et al.
Arthritis and Rheumatism|September 18, 2010
Genetically determined Amerindian ancestry correlates with increased frequency of risk alleles for systemic lupus erythematosusElena Sanchez, Ryan D Webb, Astrid Rasmussen, et al.
Nature Genetics|January 31, 2017
A missense variant in NCF1 is associated with susceptibility to multiple autoimmune diseasesJian Zhao, Jianyang Ma, Yun Deng, et al.
Communications Medicine|January 26, 2026
Genomic characterization and sub-clustering of Escherichia coli clonal complex 38 reveal host associated genetic markersLouise Roer, Astrid Rasmussen, Frank Hansen, et al.
Nature Genetics|July 20, 2004
Mutations in EFHC1 cause juvenile myoclonic epilepsyToshimitsu Suzuki, Antonio V Delgado-Escueta, Kripamoy Aguan, et al.
Pageof 13