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Multiple Sclerosis and Related Disorders|September 27, 2022
Peripheral nerve vulnerability as risk factor for multiple sclerosis: Possible insights from Neurofibromatosis type 2 (NF2)Alexander Schulz, Anna Cecilia Lawson McLean, Steffen K Rosahl
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|April 22, 2004
Uptake of a fluorescent dye as a swift and simple indicator of organelle intactness: import-competent chloroplasts from soil-grown ArabidopsisAlexander Schulz, Jürgen Knoetzel, Henrik V Scheller, et al.
Cell and Tissue Research|June 7, 2014
Syncytin-1 in differentiating human myoblasts: relationship to caveolin-3 and myogeninBolette Bjerregard, Iwona Ziomkiewicz, Alexander Schulz, et al.
Trends in Plant Science|October 18, 2005
Phytoplasmas and their interactions with hostsNynne M Christensen, Kristian B Axelsen, Mogens Nicolaisen, et al.
Plant Signaling & Behavior|August 26, 2009
Dimerization and endocytosis of the sucrose transporter StSUT1 in mature sieve elementsJohannes Liesche, Alexander Schulz, Undine Krügel, et al.
Chaos (Woodbury, N.Y.)|January 27, 2025
Singularity of Lévy walks in the lifted Pomeau-Manneville mapSamuel Brevitt, Alexander Schulz, Dominic Pegler, et al.
The Journal of Biological Chemistry|December 18, 2001
Post-translational modification of plant plasma membrane H(+)-ATPase as a requirement for functional complementation of a yeast transport mutantThomas P Jahn, Alexander Schulz, Jan Taipalensuu, et al.
Physical Review. E, Statistical, Nonlinear, and Soft Matter Physics|November 7, 2014
Diffusion and bulk flow in phloem loading: a theoretical analysis of the polymer trap mechanism for sugar transport in plantsJulia Dölger, Hanna Rademaker, Johannes Liesche, et al.
Physiologia Plantarum|November 13, 2018
Arabidopsis PLDs with C2-domain function distinctively in hypoxiaAlbert Premkumar, Sylvia Lindberg, Ida Lager, et al.
Translational Neurodegeneration|December 31, 2016
Stroke-like onset of brain stem degeneration presents with unique MRI sign and heterozygous NMNAT2 variant: a case reportAlexander Schulz, Franziska Wagner, Martin Ungelenk, et al.
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