Genetic deficiency of the mitochondrial protein PGAM5 causes a Parkinson’s-like movement disorder
Wei Lü(National Institute of Allergy and Infectious Diseases), Michael J. Lenardo(National Institutes of Health)
Cited by 175
Related Papers
A guide to cancer immunotherapy: from T cell basic science to clinical practice
|Nature reviews. Immunology|2020|4.1k
Heterozygous splice mutation in <i>PIK3R1</i> causes human immunodeficiency with lymphoproliferation due to dominant activation of PI3K
|The Journal of Experimental Medicine|2014|282
Mitochondrial Protein PGAM5 Regulates Mitophagic Protection against Cell Necroptosis
|PLoS ONE|2016|157
Specification of DNA Binding Activity of NF- B Proteins
|Cold Spring Harbor Perspectives in Biology|2009|136
Defective glycosylation and multisystem abnormalities characterize the primary immunodeficiency XMEN disease
|Journal of Clinical Investigation|2019|103