Search research articles
Contact Us
Filters
Showing results (91-100 of 101) with videos related to
Page
of 11
Sort By:
Cell Reports
|
November 28, 2019
In Vivo Protein Complementation Demonstrates Presynaptic α-Synuclein Oligomerization and Age-Dependent Accumulation of 8-16-mer Oligomer Species
Martin Kiechle, Bjoern von Einem, Lennart Höfs, et al.
Neuroscience
|
June 17, 2020
Enhanced Hyaluronan Signaling and Autophagy Dysfunction by VPS35 D620N
Abir A Rahman, Alejandro Soto-Avellaneda, Hyun Yong Jin, et al.
BMJ Mental Health
|
August 21, 2025
Evidence for reduced synaptic protein SNAP-25 in cerebrospinal fluid in major depressive disorder and schizophrenia
Petra Steinacker, Leonie Werner, Alexander Tarabuko, et al.
Human Molecular Genetics
|
January 10, 2018
CHCHD10 mutations p.R15L and p.G66V cause motoneuron disease by haploinsufficiency
Sarah J Brockmann, Axel Freischmidt, Patrick Oeckl, et al.
Acta Neuropathologica
|
February 25, 2016
Peripheral monocytes are functionally altered and invade the CNS in ALS patients
Lisa Zondler, Kathrin Müller, Samira Khalaji, et al.
Brain : a Journal of Neurology
|
April 19, 2021
A serum microRNA sequence reveals fragile X protein pathology in amyotrophic lateral sclerosis
Axel Freischmidt, Anand Goswami, Katharina Limm, et al.
Acta Neuropathologica
|
March 18, 2015
Extracellular vesicle sorting of α-Synuclein is regulated by sumoylation
Marcel Kunadt, Katrin Eckermann, Anne Stuendl, et al.
The Journal of Experimental Medicine
|
March 22, 2024
A TBK1 variant causes autophagolysosomal and motoneuron pathology without neuroinflammation in mice
David Brenner, Kirsten Sieverding, Jahnavi Srinidhi, et al.
Brain : a Journal of Neurology
|
January 18, 2018
Hot-spot KIF5A mutations cause familial ALS
David Brenner, Rüstem Yilmaz, Kathrin Müller, et al.
Brain : a Journal of Neurology
|
October 16, 2019
Reply: Adult-onset distal spinal muscular atrophy: a new phenotype associated with KIF5A mutations
David Brenner, Angela Rosenbohm, Rüstem Yilmaz, et al.
Page
of 11
Search research articles
Search
Showing results (91-100 of 101) with videos related to
Sort By:
Page
of 11
Cell Reports
|
November 28, 2019
In Vivo Protein Complementation Demonstrates Presynaptic α-Synuclein Oligomerization and Age-Dependent Accumulation of 8-16-mer Oligomer Species
Martin Kiechle, Bjoern von Einem, Lennart Höfs, et al.
Neuroscience
|
June 17, 2020
Enhanced Hyaluronan Signaling and Autophagy Dysfunction by VPS35 D620N
Abir A Rahman, Alejandro Soto-Avellaneda, Hyun Yong Jin, et al.
BMJ Mental Health
|
August 21, 2025
Evidence for reduced synaptic protein SNAP-25 in cerebrospinal fluid in major depressive disorder and schizophrenia
Petra Steinacker, Leonie Werner, Alexander Tarabuko, et al.
Human Molecular Genetics
|
January 10, 2018
CHCHD10 mutations p.R15L and p.G66V cause motoneuron disease by haploinsufficiency
Sarah J Brockmann, Axel Freischmidt, Patrick Oeckl, et al.
Acta Neuropathologica
|
February 25, 2016
Peripheral monocytes are functionally altered and invade the CNS in ALS patients
Lisa Zondler, Kathrin Müller, Samira Khalaji, et al.
Brain : a Journal of Neurology
|
April 19, 2021
A serum microRNA sequence reveals fragile X protein pathology in amyotrophic lateral sclerosis
Axel Freischmidt, Anand Goswami, Katharina Limm, et al.
Acta Neuropathologica
|
March 18, 2015
Extracellular vesicle sorting of α-Synuclein is regulated by sumoylation
Marcel Kunadt, Katrin Eckermann, Anne Stuendl, et al.
The Journal of Experimental Medicine
|
March 22, 2024
A TBK1 variant causes autophagolysosomal and motoneuron pathology without neuroinflammation in mice
David Brenner, Kirsten Sieverding, Jahnavi Srinidhi, et al.
Brain : a Journal of Neurology
|
January 18, 2018
Hot-spot KIF5A mutations cause familial ALS
David Brenner, Rüstem Yilmaz, Kathrin Müller, et al.
Brain : a Journal of Neurology
|
October 16, 2019
Reply: Adult-onset distal spinal muscular atrophy: a new phenotype associated with KIF5A mutations
David Brenner, Angela Rosenbohm, Rüstem Yilmaz, et al.
Page
of 11