Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Astrid Rasmussen

Showing results (41-50 of 125) with videos related to

Pageof 13
Sort By:
International Journal of Molecular Sciences|September 28, 2021
Defective Efferocytosis in a Murine Model of Sjögren's Syndrome Is Mediated by Dysfunctional Mer Tyrosine Kinase ReceptorRichard Witas, Astrid Rasmussen, Robert H Scofield, et al.
The Journal of Rheumatology|May 17, 2019
Sjögren Syndrome without Focal Lymphocytic Infiltration of the Salivary GlandsRohan Sharma, Kaustubh S Chaudhari, Biji T Kurien, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|February 28, 2014
Genome-wide DNA methylation patterns in naive CD4+ T cells from patients with primary Sjögren's syndromeNezam Altorok, Patrick Coit, Travis Hughes, et al.
Plos One|April 17, 2020
Correction: Pulse-Field capillary electrophoresis of repeat-primed PCR amplicons for analysis of large repeats in Spinocerebellar Ataxia Type 10Vera Hashem, Anjana Tiwari, Brittani Bewick, et al.
Clinical and Experimental Rheumatology|July 13, 2018
Antibodies to periodontogenic bacteria are associated with higher disease activity in lupus patientsHarini Bagavant, Micah L Dunkleberger, Nina Wolska, et al.
Plos One|March 12, 2020
Pulse-Field capillary electrophoresis of repeat-primed PCR amplicons for analysis of large repeats in Spinocerebellar Ataxia Type 10Vera Hashem, Anjana Tiwari, Brittani Bewick, et al.
European Journal of Human Genetics : EJHG|February 28, 2013
Paradoxical effects of repeat interruptions on spinocerebellar ataxia type 10 expansions and repeat instabilityKaren N McFarland, Jilin Liu, Ivette Landrian, et al.
Frontiers in Immunology|December 28, 2020
Single Cell Transcriptomics Implicate Novel Monocyte and T Cell Immune Dysregulation in SarcoidosisLori Garman, Richard C Pelikan, Astrid Rasmussen, et al.
Human Molecular Genetics|June 4, 2024
Extended haplotype with rs41524547-G defines the ancestral origin of SCA10Karen N McFarland, Anjana Tiwari, Vera Hashem, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 13, 2007
Distinct distribution of autosomal dominant spinocerebellar ataxia in the Mexican populationElisa Alonso, Leticia Martínez-Ruano, Irene De Biase, et al.
Pageof 13

Showing results (41-50 of 125) with videos related to

Sort By:
Pageof 13
International Journal of Molecular Sciences|September 28, 2021
Defective Efferocytosis in a Murine Model of Sjögren's Syndrome Is Mediated by Dysfunctional Mer Tyrosine Kinase ReceptorRichard Witas, Astrid Rasmussen, Robert H Scofield, et al.
The Journal of Rheumatology|May 17, 2019
Sjögren Syndrome without Focal Lymphocytic Infiltration of the Salivary GlandsRohan Sharma, Kaustubh S Chaudhari, Biji T Kurien, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|February 28, 2014
Genome-wide DNA methylation patterns in naive CD4+ T cells from patients with primary Sjögren's syndromeNezam Altorok, Patrick Coit, Travis Hughes, et al.
Plos One|April 17, 2020
Correction: Pulse-Field capillary electrophoresis of repeat-primed PCR amplicons for analysis of large repeats in Spinocerebellar Ataxia Type 10Vera Hashem, Anjana Tiwari, Brittani Bewick, et al.
Clinical and Experimental Rheumatology|July 13, 2018
Antibodies to periodontogenic bacteria are associated with higher disease activity in lupus patientsHarini Bagavant, Micah L Dunkleberger, Nina Wolska, et al.
Plos One|March 12, 2020
Pulse-Field capillary electrophoresis of repeat-primed PCR amplicons for analysis of large repeats in Spinocerebellar Ataxia Type 10Vera Hashem, Anjana Tiwari, Brittani Bewick, et al.
European Journal of Human Genetics : EJHG|February 28, 2013
Paradoxical effects of repeat interruptions on spinocerebellar ataxia type 10 expansions and repeat instabilityKaren N McFarland, Jilin Liu, Ivette Landrian, et al.
Frontiers in Immunology|December 28, 2020
Single Cell Transcriptomics Implicate Novel Monocyte and T Cell Immune Dysregulation in SarcoidosisLori Garman, Richard C Pelikan, Astrid Rasmussen, et al.
Human Molecular Genetics|June 4, 2024
Extended haplotype with rs41524547-G defines the ancestral origin of SCA10Karen N McFarland, Anjana Tiwari, Vera Hashem, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 13, 2007
Distinct distribution of autosomal dominant spinocerebellar ataxia in the Mexican populationElisa Alonso, Leticia Martínez-Ruano, Irene De Biase, et al.
Pageof 13