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The Journal of Dermatology|April 7, 2020
Fatal neonatal nephrocutaneous syndrome in 18 Roma children with EGFR deficiencyStella Mazurova, Marketa Tesarova, Jiri Zeman, et al.Investigative Ophthalmology & Visual Science|July 12, 2011
Large proteoglycan complexes and disturbed collagen architecture in the corneal extracellular matrix of mucopolysaccharidosis type VII (Sly syndrome)Robert D Young, Petra Liskova, Christian Pinali, et al.Molecular Genetics and Metabolism Reports|March 4, 2022
Clinical and genetic characteristics of two patients with tyrosinemia type 1 in Slovenia - A novel fumarylacetoacetate hydrolase (FAH) intronic disease-causing variantJaka Sikonja, Jernej Brecelj, Mojca Zerjav Tansek, et al.Current Biology : CB|May 13, 2022
Surface flow for colonial integration in reef-building coralsThibault Bouderlique, Julian Petersen, Louis Faure, et al.Nature Communications|May 27, 2023
Directionality of developing skeletal muscles is set by mechanical forcesKazunori Sunadome, Alek G Erickson, Delf Kah, et al.Science Advances|August 6, 2016
Analysis of neural crest-derived clones reveals novel aspects of facial developmentMarketa Kaucka, Evgeny Ivashkin, Daniel Gyllborg, et al.Nature Communications|November 14, 2022
Altered developmental programs and oriented cell divisions lead to bulky bones during salamander limb regenerationMarketa Kaucka, Alberto Joven Araus, Marketa Tesarova, et al.Brain : a Journal of Neurology|April 20, 2006
Phenotypic spectrum associated with mutations of the mitochondrial polymerase gamma geneRita Horvath, Gavin Hudson, Gianfrancesco Ferrari, et al.Elife|June 14, 2018
Signals from the brain and olfactory epithelium control shaping of the mammalian nasal capsule cartilageMarketa Kaucka, Julian Petersen, Marketa Tesarova, et al.Journal of Medical Genetics|December 28, 2011
Mutation screening of 75 candidate genes in 152 complex I deficiency cases identifies pathogenic variants in 16 genes including NDUFB9Tobias B Haack, Florence Madignier, Martina Herzer, et al.Pageof 5