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American Journal of Human Genetics|July 27, 1999
Identification of a mutation cluster in mevalonate kinase deficiency, including a new mutation in a patient of Mennonite ancestryD D Hinson, R M Ross, S Krisans, et al.Molecular and Cellular Endocrinology|November 15, 2016
Activation of AMP-activated protein kinase rapidly suppresses multiple pro-inflammatory pathways in adipocytes including IL-1 receptor-associated kinase-4 phosphorylationSarah J Mancini, Anna D White, Silvia Bijland, et al.Nucleic Acids Research|August 14, 2013
Tracking in atomic detail the functional specializations in viral RecA helicases that occur during evolutionKamel El Omari, Christoph Meier, Denis Kainov, et al.European Journal of Medical Genetics|February 14, 2006
Spectrum and distribution of MECP2 mutations in 424 Rett syndrome patients: a molecular updateC Philippe, L Villard, N De Roux, et al.The Journal of Pediatrics|October 16, 2002
Cutaneous manifestations of hyper-IgE syndrome in infants and childrenSarah L Chamlin, Timothy H McCalmont, Bari B Cunningham, et al.Journal of the American Academy of Dermatology|August 11, 2007
Information about infantile hemangiomas on the Internet: how accurate is it?Karen Minzer-Conzetti, Maria C Garzon, Anita N Haggstrom, et al.Journal of Medicinal Chemistry|December 8, 1995
Cyclooxygenase-2 inhibitors. Synthesis and pharmacological activities of 5-methanesulfonamido-1-indanone derivativesC S Li, W C Black, C C Chan, et al.British Journal of Cancer|March 4, 2010
Participants' uptake of clinical trial results: a randomised experimentJ Mancini, D Genre, F Dalenc, et al.Journal of the American Academy of Dermatology|February 8, 2020
Topical calcineurin inhibitors for pediatric periorificial dermatitisAyelet Ollech, Rame Yousif, Lacey Kruse, et al.Journal of the American Academy of Dermatology|July 18, 2006
Incontinentia pigmenti in male patientsTheresa R Pacheco, Moise Levy, James C Collyer, et al.Pageof 39