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

Yanick J Crow

Showing results (141-150 of 234) with videos related to

Pageof 24
Sort By:
Journal of Clinical Immunology|February 8, 2023
Type I Interferonopathy due to a Homozygous Loss-of-Inhibitory Function Mutation in STAT2Gaofeng Zhu, Mihaly Badonyi, Lina Franklin, et al.
Neuropediatrics|September 23, 2014
Mutations in ADAR1, IFIH1, and RNASEH2B presenting as spastic paraplegiaYanick J Crow, Maha S Zaki, Mohamed S Abdel-Hamid, et al.
Annals of the Rheumatic Diseases|June 8, 2014
Aicardi-Goutières syndrome harbours abundant systemic and brain-reactive autoantibodiesEloy Cuadrado, Adeline Vanderver, Kristy J Brown, et al.
American Journal of Human Genetics|June 5, 2002
Identification of microcephalin, a protein implicated in determining the size of the human brainAndrew P Jackson, Helen Eastwood, Sandra M Bell, et al.
European Journal of Immunology|May 26, 2025
Mutations in RNU4ATAC Are Associated With Chilblain-Like Lesions and Enhanced Type I Interferon SignallingNic Robertson, Aakash Joshi, Francesca Ritchie, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|July 9, 2016
Tartrate-Resistant Acid Phosphatase Deficiency in the Predisposition to Systemic Lupus ErythematosusJie An, Tracy A Briggs, Audrey Dumax-Vorzet, et al.
The Journal of Allergy and Clinical Immunology|May 26, 2018
Severe combined immunodeficiency in stimulator of interferon genes (STING) V154M/wild-type miceDelphine Bouis, Peggy Kirstetter, Florent Arbogast, et al.
The Journal of Clinical Investigation|November 18, 2014
Inherited STING-activating mutation underlies a familial inflammatory syndrome with lupus-like manifestationsNadia Jeremiah, Bénédicte Neven, Matteo Gentili, et al.
Nature Genetics|August 5, 2008
ADAMTSL2 mutations in geleophysic dysplasia demonstrate a role for ADAMTS-like proteins in TGF-beta bioavailability regulationCarine Le Goff, Fanny Morice-Picard, Nathalie Dagoneau, et al.
Developmental Medicine and Child Neurology|July 27, 2010
Intracerebral large artery disease in Aicardi-Goutières syndrome implicates SAMHD1 in vascular homeostasisVenkateswaran Ramesh, Bruno Bernardi, Altin Stafa, et al.
Pageof 24

Showing results (141-150 of 234) with videos related to

Sort By:
Pageof 24
Journal of Clinical Immunology|February 8, 2023
Type I Interferonopathy due to a Homozygous Loss-of-Inhibitory Function Mutation in STAT2Gaofeng Zhu, Mihaly Badonyi, Lina Franklin, et al.
Neuropediatrics|September 23, 2014
Mutations in ADAR1, IFIH1, and RNASEH2B presenting as spastic paraplegiaYanick J Crow, Maha S Zaki, Mohamed S Abdel-Hamid, et al.
Annals of the Rheumatic Diseases|June 8, 2014
Aicardi-Goutières syndrome harbours abundant systemic and brain-reactive autoantibodiesEloy Cuadrado, Adeline Vanderver, Kristy J Brown, et al.
American Journal of Human Genetics|June 5, 2002
Identification of microcephalin, a protein implicated in determining the size of the human brainAndrew P Jackson, Helen Eastwood, Sandra M Bell, et al.
European Journal of Immunology|May 26, 2025
Mutations in RNU4ATAC Are Associated With Chilblain-Like Lesions and Enhanced Type I Interferon SignallingNic Robertson, Aakash Joshi, Francesca Ritchie, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|July 9, 2016
Tartrate-Resistant Acid Phosphatase Deficiency in the Predisposition to Systemic Lupus ErythematosusJie An, Tracy A Briggs, Audrey Dumax-Vorzet, et al.
The Journal of Allergy and Clinical Immunology|May 26, 2018
Severe combined immunodeficiency in stimulator of interferon genes (STING) V154M/wild-type miceDelphine Bouis, Peggy Kirstetter, Florent Arbogast, et al.
The Journal of Clinical Investigation|November 18, 2014
Inherited STING-activating mutation underlies a familial inflammatory syndrome with lupus-like manifestationsNadia Jeremiah, Bénédicte Neven, Matteo Gentili, et al.
Nature Genetics|August 5, 2008
ADAMTSL2 mutations in geleophysic dysplasia demonstrate a role for ADAMTS-like proteins in TGF-beta bioavailability regulationCarine Le Goff, Fanny Morice-Picard, Nathalie Dagoneau, et al.
Developmental Medicine and Child Neurology|July 27, 2010
Intracerebral large artery disease in Aicardi-Goutières syndrome implicates SAMHD1 in vascular homeostasisVenkateswaran Ramesh, Bruno Bernardi, Altin Stafa, et al.
Pageof 24