Search Results - MacGregor Steele
- Showing 1 - 2 results of 2
-
1
A new genetic subgroup of chronic granulomatous disease with autosomal recessive mutations in p40phox and selective defects in neutrophil NADPH oxidase activity by Juan D. Matute, Andrés A. Arias, Nicola Wright, Iwona Wrobel, Christopher C. M. Waterhouse, Xing Jun Li, Christophe C. Marchal, Natalie D. Stull, David B. Lewis, MacGregor Steele, James D. Kellner, Weiming Yu, Samy O. Meroueh, William M. Nauseef, Mary C. Dinauer
Published 2009Artigo -
2
Improving diagnostic precision, care and syndrome definitions using comprehensive next-generation sequencing for the inherited bone marrow failure syndromes by Ibrahim Ghemlas, Hongbing Li, Bozana Zlateska, Robert J. Klaassen, Conrad V. Fernandez, Rochelle Yanofsky, John K. Wu, Yves D. Pastore, Mariana Silva, Jeff H. Lipton, Josée Brossard, Bruno Michon, Sharon Abish, MacGregor Steele, Roona Sinha, Mark Belletrutti, Vicky R. Breakey, Lawrence Jardine, Lisa Goodyear, Lillian Sung, Santhosh Dhanraj, Emma Reble, Amanda Wagner, Joseph Beyene, Peter N. Ray, M. Stephen Meyn, Michaela Cada, Yigal Dror
Published 2015Artigo
Search Tools:
Related Subjects
Biology
Gene
Mutation
Biochemistry
Bioinformatics
Bone marrow failure
Chronic granulomatous disease
Compound heterozygosity
DNA repair
DNA sequencing
Enzyme
Fanconi anemia
Genetic testing
Genetics
Genotype
Genotyping
Haematopoiesis
Immunology
Medicine
Molecular biology
NADPH oxidase
P22phox
Phagocyte
Phagocytosis
Phenotype
Reactive oxygen species
Sanger sequencing
Stem cell
Superoxide