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Immunology Letters|July 13, 2010
Human T-cell memory consists mainly of unexpanded clonesPaul L Klarenbeek, Paul P Tak, Barbera D C van Schaik, et al.
Journal of the Neurological Sciences|January 25, 2013
A novel mutation in COQ2 leading to fatal infantile multisystem diseaseBernadette S Jakobs, Lambert P van den Heuvel, Roel J P Smeets, et al.
Annals of Neurology|January 15, 2009
Folinic acid-responsive seizures are identical to pyridoxine-dependent epilepsyRenata C Gallagher, Johan L K Van Hove, Gunter Scharer, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 26, 2015
Cross-strand binding of TFAM to a single mtDNA molecule forms the mitochondrial nucleoidChristian Kukat, Karen M Davies, Christian A Wurm, et al.
Zeitschrift Fur Gastroenterologie|September 11, 2024
Conservative versus surgical therapy for idiopathic and secondary megacolon or megarectum in adults - a retrospective multicentre controlled studyDaniel Schmitz, Emilia Meier, Steffen Axt, et al.
Neurology|March 1, 2006
Alexander disease: ventricular garlands and abnormalities of the medulla and spinal cordM S van der Knaap, V Ramesh, R Schiffmann, et al.
Genome Medicine|August 17, 2021
An epigenetic and transcriptomic signature of immune tolerance in human monocytes through multi-omics integrationXanthe Brands, Bastiaan W Haak, Augustijn M Klarenbeek, et al.
American Journal of Medical Genetics. Part A|February 4, 2005
Two novel mutations in SLC6A8 cause creatine transporter defect and distinctive X-linked mental retardation in two unrelated Dutch familiesG M S Mancini, C E Catsman-Berrevoets, I F M de Coo, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|February 5, 2005
S-adenosylmethionine and 5-methyltetrahydrofolate are associated with endothelial function after controlling for confounding by homocysteine: the Hoorn StudyA M W Spijkerman, Y M Smulders, P J Kostense, et al.
American Journal of Human Genetics|March 19, 2002
X-linked mental retardation with seizures and carrier manifestations is caused by a mutation in the creatine-transporter gene (SLC6A8) located in Xq28Kimberly A Hahn, Gajja S Salomons, Darci Tackels-Horne, et al.
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