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Journal of Pediatric Hematology/Oncology|June 26, 2018
Novel IL2RG Mutation Causes Leaky TLOWB+NK+ SCID With Nodular Regenerative Hyperplasia and Normal IL-15 STAT5 PhosphorylationJoão F Neves, Catarina Martins, Ana I Cordeiro, et al.
Human Gene Therapy|July 21, 2018
Age-Related Seroprevalence of Antibodies Against AAV-LK03 in a UK Population CohortDany P Perocheau, Sharon Cunningham, Juhee Lee, et al.
Journal of Clinical Immunology|November 28, 2024
Griscelli Syndrome Type 2: Comprehensive Analysis of 149 New and Previously Described Patients with RAB27A DeficiencyJesmeen Maimaris, Adriel Roa-Bautista, Mahreen Sohail, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|April 10, 2016
Deficiency of Adenosine Deaminase Type 2: A Description of Phenotype and Genotype in Fifteen CasesSira Nanthapisal, Claire Murphy, Ebun Omoyinmi, et al.
Journal of Clinical Immunology|September 13, 2019
Novel Gain-of-Function Mutation in Stat1 Sumoylation Site Leads to CMC/CID Phenotype Responsive to RuxolitinibTariq Al Shehri, Kimberly Gilmour, Florian Gothe, et al.
Molecular Genetics and Metabolism|November 23, 2024
The effects of casein glycomacropeptide on general health status in children with PKU: A randomized crossover trialAlex Pinto, Anne Daly, Camille Newby, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|August 30, 2023
Socioeconomic and Demographic Risk Factors for SARS-CoV-2 Seropositivity Among Healthcare Workers in a UK Hospital: A Prospective Cohort StudyTanya Lam, Anja Saso, Arturo Torres Ortiz, et al.
Nature Communications|March 13, 2021
Long-term lymphoid progenitors independently sustain naïve T and NK cell production in humansNatalia Izotova, Christine Rivat, Cristina Baricordi, et al.
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