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The Journal of Investigative Dermatology|August 8, 2002
Defolliculated (dfl): a dominant mouse mutation leading to poor sebaceous gland differentiation and total elimination of pelage folliclesRebecca M Porter, Colin A B Jahoda, Declan P Lunny, et al.The Journal of Biological Chemistry|October 10, 2012
Keratin K18 increases cystic fibrosis transmembrane conductance regulator (CFTR) surface expression by binding to its C-terminal hydrophobic patchYuanyuan Duan, Ying Sun, Fan Zhang, et al.Nature Reviews. Disease Primers|September 25, 2020
Epidermolysis bullosaAjoy Bardhan, Leena Bruckner-Tuderman, Iain L C Chapple, et al.Journal of Cell Science|November 8, 2012
Keratin 1 maintains skin integrity and participates in an inflammatory network in skin through interleukin-18Wera Roth, Vinod Kumar, Hans-Dietmar Beer, et al.The EMBO Journal|March 10, 2022
Keratin filaments mediate the expansion of extra-embryonic membranes in the post-gastrulation mouse embryoWallis Nahaboo, Sema Elif Eski, Evangéline Despin-Guitard, et al.American Journal of Human Genetics|February 9, 2006
Loss-of-function mutations in the keratin 5 gene lead to Dowling-Degos diseaseRegina C Betz, Laura Planko, Sibylle Eigelshoven, et al.European Journal of Human Genetics : EJHG|February 19, 2020
A dominant vimentin variant causes a rare syndrome with premature agingBenjamin Cogné, Jamal-Eddine Bouameur, Gaëlle Hayot, et al.Ebiomedicine|May 13, 2019
Treatment of keratinocytes with 4-phenylbutyrate in epidermolysis bullosa: Lessons for therapies in keratin disordersMarina Spörrer, Ania Prochnicki, Regine C Tölle, et al.The Journal of Cell Biology|December 9, 2015
A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activityVinod Kumar, Jamal-Eddine Bouameur, Janina Bär, et al.Translational Oncology|November 16, 2018
High Keratin 8/18 Ratio Predicts Aggressive Hepatocellular Cancer PhenotypeNicole Golob-Schwarzl, Kira Bettermann, Anita Kuldeep Mehta, et al.Pageof 13