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Stephan Müller

Showing results (71-80 of 78) with videos related to

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Biorxiv : the Preprint Server for Biology|November 24, 2025
Neuronal compartmentalization results in "impoverished" axonal mitochondriaAdrian Marti Pastor, Liam S C Lewis, Stephan Müller, et al.
Scientific Reports|April 29, 2017
Decreased body mass index in the preclinical stage of autosomal dominant Alzheimer's diseaseStephan Müller, Oliver Preische, Hamid R Sohrabi, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|September 30, 2018
Relationship between physical activity, cognition, and Alzheimer pathology in autosomal dominant Alzheimer's diseaseStephan Müller, Oliver Preische, Hamid R Sohrabi, et al.
Cell Stem Cell|March 12, 2013
Genetic correction of a LRRK2 mutation in human iPSCs links parkinsonian neurodegeneration to ERK-dependent changes in gene expressionPeter Reinhardt, Benjamin Schmid, Lena F Burbulla, et al.
Scientific Reports|August 27, 2017
Tau plasma levels in subjective cognitive decline: Results from the DELCODE studyStephan Müller, Oliver Preische, Jens C Göpfert, et al.
Cell|December 23, 2022
Spatial proteomics in three-dimensional intact specimensHarsharan Singh Bhatia, Andreas-David Brunner, Furkan Öztürk, et al.
Human Mutation|May 25, 2012
PRRT2 mutations are the major cause of benign familial infantile seizuresJulian Schubert, Roberta Paravidino, Felicitas Becker, et al.
Nature Genetics|March 10, 2015
De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathySteffen Syrbe, Ulrike B S Hedrich, Erik Riesch, et al.
Pageof 8

Showing results (71-80 of 78) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 78 results.
Biorxiv : the Preprint Server for Biology|November 24, 2025
Neuronal compartmentalization results in "impoverished" axonal mitochondriaAdrian Marti Pastor, Liam S C Lewis, Stephan Müller, et al.
Scientific Reports|April 29, 2017
Decreased body mass index in the preclinical stage of autosomal dominant Alzheimer's diseaseStephan Müller, Oliver Preische, Hamid R Sohrabi, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|September 30, 2018
Relationship between physical activity, cognition, and Alzheimer pathology in autosomal dominant Alzheimer's diseaseStephan Müller, Oliver Preische, Hamid R Sohrabi, et al.
Cell Stem Cell|March 12, 2013
Genetic correction of a LRRK2 mutation in human iPSCs links parkinsonian neurodegeneration to ERK-dependent changes in gene expressionPeter Reinhardt, Benjamin Schmid, Lena F Burbulla, et al.
Scientific Reports|August 27, 2017
Tau plasma levels in subjective cognitive decline: Results from the DELCODE studyStephan Müller, Oliver Preische, Jens C Göpfert, et al.
Cell|December 23, 2022
Spatial proteomics in three-dimensional intact specimensHarsharan Singh Bhatia, Andreas-David Brunner, Furkan Öztürk, et al.
Human Mutation|May 25, 2012
PRRT2 mutations are the major cause of benign familial infantile seizuresJulian Schubert, Roberta Paravidino, Felicitas Becker, et al.
Nature Genetics|March 10, 2015
De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathySteffen Syrbe, Ulrike B S Hedrich, Erik Riesch, et al.
Pageof 8