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American Journal of Medical Genetics. Part A|February 12, 2019
Exome sequencing reveals a novel COL2A1 mutation implicated in multiple epiphyseal dysplasiaVinod Dasa, James R B Eastwood, Michal Podgorski, et al.European Journal of Human Genetics : EJHG|November 4, 2004
Mutations in the known genes are not the major cause of MED; distinctive phenotypic entities among patients with no identified mutationsEveliina Jakkula, Outi Mäkitie, Malwina Czarny-Ratajczak, et al.Biogerontology|October 6, 2011
Telomere maintenance genes SIRT1 and XRCC6 impact age-related decline in telomere length but only SIRT1 is associated with human longevitySangkyu Kim, Xiuhua Bi, Malwina Czarny-Ratajczak, et al.American Journal of Medical Genetics. Part A|March 3, 2004
Clinical and radiographic findings in multiple epiphyseal dysplasia caused by MATN3 mutations: description of 12 patientsOuti Mäkitie, Geert R Mortier, Malwina Czarny-Ratajczak, et al.Scientific Reports|August 23, 2017
Ccdc3: A New P63 Target Involved in Regulation Of Liver Lipid MetabolismWenjuan Liao, Hongbing Liu, Yiwei Zhang, et al.American Journal of Physiology. Heart and Circulatory Physiology|November 20, 2016
Aging is associated with impaired angiogenesis, but normal microvascular network structure, in the rat mesenteryRichard S Sweat, David C Sloas, Scott A Stewart, et al.Pageof 2