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Page 1
Fibroblast dedifferentiation as a determinant of successful regeneration.
Lin TY, Gerber T, Taniguchi-Sugiura Y, Murawala P, Hermann S, Grosser L, Shibata E, Treutlein B, Tanaka EM. Lin TY, et al. Among authors: grosser l. Dev Cell. 2021 May 17;56(10):1541-1551.e6. doi: 10.1016/j.devcel.2021.04.016. Dev Cell. 2021. PMID: 34004152 Free PMC article.
Fasting as an intervention to alter the impact of simulated night-shift work on glucose metabolism in healthy adults: a cluster randomised controlled trial.
Centofanti S, Heilbronn LK, Wittert G, Dorrian J, Coates AM, Kennaway D, Gupta C, Stepien JM, Catcheside P, Yates C, Grosser L, Matthews RW, Banks S. Centofanti S, et al. Among authors: grosser l. Diabetologia. 2024 Oct 18. doi: 10.1007/s00125-024-06279-1. Online ahead of print. Diabetologia. 2024. PMID: 39422718
Cortisol and shiftwork: A scoping review.
Grosser L, Knayfati S, Yates C, Dorrian J, Banks S. Grosser L, et al. Sleep Med Rev. 2022 Aug;64:101581. doi: 10.1016/j.smrv.2021.101581. Epub 2021 Nov 27. Sleep Med Rev. 2022. PMID: 35872400 Review.
Functional Characterization of Rare RAB12 Variants and Their Role in Musician's and Other Dystonias.
Hebert E, Borngräber F, Schmidt A, Rakovic A, Brænne I, Weissbach A, Hampf J, Vollstedt EJ, Größer L, Schaake S, Müller M, Manzoor H, Jabusch HC, Alvarez-Fischer D, Kasten M, Kostic VS, Gasser T, Zeuner KE, Kim HJ, Jeon B, Bauer P, Altenmüller E, Klein C, Lohmann K. Hebert E, et al. Among authors: grosser l. Genes (Basel). 2017 Oct 18;8(10):276. doi: 10.3390/genes8100276. Genes (Basel). 2017. PMID: 29057844 Free PMC article. Review.
Translating slow-binding inhibition kinetics into cellular and in vivo effects.
Walkup GK, You Z, Ross PL, Allen EK, Daryaee F, Hale MR, O'Donnell J, Ehmann DE, Schuck VJ, Buurman ET, Choy AL, Hajec L, Murphy-Benenato K, Marone V, Patey SA, Grosser LA, Johnstone M, Walker SG, Tonge PJ, Fisher SL. Walkup GK, et al. Among authors: grosser la. Nat Chem Biol. 2015 Jun;11(6):416-23. doi: 10.1038/nchembio.1796. Epub 2015 Apr 20. Nat Chem Biol. 2015. PMID: 25894085 Free PMC article.
Mutations in POGLUT1, encoding protein O-glucosyltransferase 1, cause autosomal-dominant Dowling-Degos disease.
Basmanav FB, Oprisoreanu AM, Pasternack SM, Thiele H, Fritz G, Wenzel J, Größer L, Wehner M, Wolf S, Fagerberg C, Bygum A, Altmüller J, Rütten A, Parmentier L, El Shabrawi-Caelen L, Hafner C, Nürnberg P, Kruse R, Schoch S, Hanneken S, Betz RC. Basmanav FB, et al. Among authors: grosser l. Am J Hum Genet. 2014 Jan 2;94(1):135-43. doi: 10.1016/j.ajhg.2013.12.003. Am J Hum Genet. 2014. PMID: 24387993 Free PMC article.
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