Associated Papers
Naturally Occurring Mutations to Muscle-Type Creatine Kinase Impact Its Canonical and Pharmacological Activities in a Substrate-Dependent Manner In Vitro.
Mosher EP et al.
Molecular Pharmacology, 2021
Ancestral contribution of the muscle-specific creatine kinase (CKM) polymorphism rs4884 in the knee osteoarthritis risk: a preliminary study.
Fernández-Torres J et al.
Clinical Rheumatology, 2021
Actionable perturbations of damage responses by TCL1/ATM and epigenetic lesions form the basis of T-PLL.
Schrader A et al.
Nature Communications, 2018
29449575 (PubMed )
Supplement: 41467_2017_2688_MOESM20_ESM.xlsx › c__Freq_TP092
Discovery of genetic variants of the kinases that activate tenofovir among individuals in the United States, Thailand, and South Africa: HPTN067.
Figueroa DB et al.
Plos One, 2018
CKM Glu83Gly Is Associated With Blunted Creatine Kinase Variation, but Not With Myalgia.
Siddiqui MK et al.
Circulation. Cardiovascular Genetics, 2017
Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase.
Kristjansson RP et al.
Nature Communications, 2016
CKM and LILRB5 are associated with serum levels of creatine kinase.
Dubé MP et al.
Circulation. Cardiovascular Genetics, 2014
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