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Showing results (781-790 of 884) with videos related to

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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.
The International Journal of Eating Disorders|April 21, 2009
Proposed diagnostic criteria for night eating syndromeKelly C Allison, Jennifer D Lundgren, John P O'Reardon, et al.
American Journal of Medical Genetics|October 1, 1998
Evidence for linkage to psychosis and cerebral asymmetry (relative hand skill) on the X chromosomeS H Laval, J C Dann, R J Butler, 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.
Schizophrenia Bulletin|June 26, 2018
"Brain Connectivity Deviates by Sex and Hemisphere in the First Episode of Schizophrenia"-A Route to the Genetic Basis of Language and Psychosis?Qiang Wang, Jie Zhang, Zhaowen Liu, 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 British Journal of Dermatology|August 19, 2015
Unusual cutaneous features associated with a heterozygous gain-of-function mutation in IFIH1: overlap between Aicardi-Goutières and Singleton-Merten syndromesA-C Bursztejn, T A Briggs, Y del Toro Duany, 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 89

Showing results (781-790 of 884) with videos related to

Sort By:
Pageof 89
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.
The International Journal of Eating Disorders|April 21, 2009
Proposed diagnostic criteria for night eating syndromeKelly C Allison, Jennifer D Lundgren, John P O'Reardon, et al.
American Journal of Medical Genetics|October 1, 1998
Evidence for linkage to psychosis and cerebral asymmetry (relative hand skill) on the X chromosomeS H Laval, J C Dann, R J Butler, 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.
Schizophrenia Bulletin|June 26, 2018
"Brain Connectivity Deviates by Sex and Hemisphere in the First Episode of Schizophrenia"-A Route to the Genetic Basis of Language and Psychosis?Qiang Wang, Jie Zhang, Zhaowen Liu, 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 British Journal of Dermatology|August 19, 2015
Unusual cutaneous features associated with a heterozygous gain-of-function mutation in IFIH1: overlap between Aicardi-Goutières and Singleton-Merten syndromesA-C Bursztejn, T A Briggs, Y del Toro Duany, 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 89