M. Schülke

发表

Human muscle-derived CLEC14A-positive cells regenerate muscle independent of PAX7

C. Kocks, N. Rajewsky, A. Spuler, 2019, Nature Communications.

New evidence for a mutation hotspot in exon 37 of the NF1 gene

P. Robinson, P. Nürnberg, S. Tinschert, 1997 .

Diffusivity, permeability and solubility of H2, Ar, N2, and CO2 in poly(tetrafluoroethylene) between room temperature and 180 °C

G. Kiss, B. Sebők, M. Schülke, 2016 .

Critically Ill Patients With Icu-Acquired Weakness Show Reduced Density of Myosin in Electron Microscope Early After Onset of Critical Illness

T. Wollersheim, S. Weber-Carstens, M. Krebs, 2015, Intensive Care Medicine Experimental.

International Workshop: Outcome measures and clinical trial readiness in primary mitochondrial myopathies in children and adults. Consensus recommendations. 16–18 November 2016, Rome, Italy

M. Zeviani, H. Prokisch, M. Mancuso, 2017, Neuromuscular Disorders.

A novel mutation L1425p in the GAP‐region of the NF1 gene detected by temperature gradient gel electrophoresis (TGGE);

R. Fahsold, H. Peters, M. Schülke, 1999, Human mutation.

New evidence for a mutation hotspot in exon 37 of the NF1 gene.

P. Robinson, P. Nürnberg, S. Tinschert, 1997, Human Mutation.

Met and Cxcr4 cooperate to protect skeletal muscle stem cells against inflammation-induced damage during regeneration

Jie Chen, Joscha Griger, Ines Lahmann, 2021, eLife.

PORTEVIN-LeCHATELIER EFFECT AND OBSERVATION OF SLIP BAND GROWTH IN Cu-Al SINGLE CRYSTALS

H. Neuhäuser, J. Plessing, M. Schülke, 1989 .

Dynamic Studies of Slip Line Formation on Single Crystals of fcc Solid solutions

A. Hampel, H. Neuhäuser, M. Schülke, 1989 .

Complex surface analytical investigations on hydrogen absorption and desorption processes of a TiMn2-based alloy

K. Sankaran, G. Kiss, K. Müller, 2009, Analytical and bioanalytical chemistry.

Influence of surface contaminations on the hydrogen storage behaviour of metal hydride alloys

G. Kiss, K. Müller, M. Lammers, 2008, Analytical and bioanalytical chemistry.

Next-generation phenotyping integrated in a national framework for patients with ultra-rare disorders improves genetic diagnostics and yields new molecular findings

Heinen, Heiko, Kehrer, 2023, medRxiv.

International Workshop: Outcome measures and clinical trial readiness in primary mitochondrial myopathies in children and adults. Consensus recommendations. 16–18 November 2016, Rome, Italy

M. Zeviani, H. Prokisch, M. Mancuso, 2017, Neuromuscular Disorders.