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Virulence|May 24, 2023
Evolution of Mycobacterium abscessus in the human lung: Cumulative mutations and genomic rearrangement of porin genes in patient isolatesShamira J Shallom, Hervé Tettelin, Prabha Chandrasekaran, et al.Annals of the American Thoracic Society|January 28, 2014
Inhaled amikacin for treatment of refractory pulmonary nontuberculous mycobacterial diseaseKenneth N Olivier, Pamela A Shaw, Tanya S Glaser, et al.Journal of Clinical Immunology|February 23, 2020
Correction to: Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert CommitteeStuart G Tangye, Waleed Al-Herz, Aziz Bousfiha, et al.Journal of Clinical Immunology|January 19, 2020
Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert CommitteeStuart G Tangye, Waleed Al-Herz, Aziz Bousfiha, et al.Biorxiv : the Preprint Server for Biology|June 26, 2025
A novel frameshift mutation in Phosphoinositide 3-kinase regulatory subunit 1 (PIK3R1) causes immunodeficiency and Amyotrophic Lateral Sclerosis (ALS)Brice Calco, Colin L Sweeney, Joseph Steiner, et al.Journal of Immunology (Baltimore, Md. : 1950)|December 1, 2017
STAT5B: A Differential Regulator of the Life and Death of CD4+ Effector Memory T CellsSonia S Majri, Jill M Fritz, Alejandro V Villarino, et al.Journal of Clinical Immunology|August 9, 2017
Emerging Infections and Pertinent Infections Related to Travel for Patients with Primary ImmunodeficienciesKathleen E Sullivan, Hamid Bassiri, Ahmed A Bousfiha, et al.Blood|February 1, 2013
Mutations in GATA2 cause human NK cell deficiency with specific loss of the CD56(bright) subsetEmily M Mace, Amy P Hsu, Linda Monaco-Shawver, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|October 8, 2014
An AAVS1-targeted minigene platform for correction of iPSCs from all five types of chronic granulomatous diseaseRandall K Merling, Colin L Sweeney, Jessica Chu, et al.Journal of Medical Genetics|October 3, 2023
Spectrum of LYST mutations in Chediak-Higashi syndrome: a report of novel variants and a comprehensive review of the literatureMarie Morimoto, Elena-Raluca Nicoli, Chulaluck Kuptanon, et al.Pageof 68