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Stephan Züchner

Showing results (21-30 of 198) with videos related to

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Biochemical and Biophysical Research Communications|September 12, 2013
Ascorbate-induced generation of 5-hydroxymethylcytosine is unaffected by varying levels of iron and 2-oxoglutarateKevin M Dickson, Christopher B Gustafson, Juan I Young, et al.
Annals of Neurology|January 4, 2022
A Recurrent KPNA3 Missense Variant Causing Infantile Pure Spastic ParaplegiaJonathan De Winter, Liedewei Van de Vondel, Stephan Züchner, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 25, 2014
Rapid in vivo forward genetic approach for identifying axon death genes in DrosophilaLukas J Neukomm, Thomas C Burdett, Michael A Gonzalez, et al.
Nature Communications|March 24, 2021
Axonal chemokine-like Orion induces astrocyte infiltration and engulfment during mushroom body neuronal remodelingAna Boulanger, Camille Thinat, Stephan Züchner, et al.
International Journal of Molecular Sciences|October 28, 2015
Abnormal Paraplegin Expression in Swollen Neurites, τ- and α-Synuclein Pathology in a Case of Hereditary Spastic Paraplegia SPG7 with an Ala510Val MutationDietmar R Thal, Stephan Züchner, Stephan Gierer, et al.
Experimental Neurology|June 24, 2018
The human motor neuron axonal transcriptome is enriched for transcripts related to mitochondrial function and microtubule-based axonal transportRenata Maciel, Dana M Bis, Adriana P Rebelo, et al.
Brain : a Journal of Neurology|March 5, 2003
A novel nonsense mutation in the ABC1 gene causes a severe syringomyelia-like phenotype of Tangier diseaseStephan Züchner, Anne D Sperfeld, Jan Senderek, et al.
Biochimica Et Biophysica Acta. Molecular Cell Research|December 4, 2016
Abl2 kinase phosphorylates Bi-organellar regulator MNRR1 in mitochondria, stimulating respirationSiddhesh Aras, Hassan Arrabi, Neeraja Purandare, et al.
Brain : a Journal of Neurology|February 26, 2016
Severe axonal Charcot-Marie-Tooth disease with proximal weakness caused by de novo mutation in the MORC2 genePetra Laššuthová, Dana Šafka Brožková, Marcela Krůtová, et al.
Communications Biology|December 18, 2021
Restoring Shank3 in the rostral brainstem of shank3ab-/- zebrafish autism models rescues sensory deficitsRobert A Kozol, David M James, Ivan Varela, et al.
Pageof 20

Showing results (21-30 of 198) with videos related to

Sort By:
Pageof 20
Biochemical and Biophysical Research Communications|September 12, 2013
Ascorbate-induced generation of 5-hydroxymethylcytosine is unaffected by varying levels of iron and 2-oxoglutarateKevin M Dickson, Christopher B Gustafson, Juan I Young, et al.
Annals of Neurology|January 4, 2022
A Recurrent KPNA3 Missense Variant Causing Infantile Pure Spastic ParaplegiaJonathan De Winter, Liedewei Van de Vondel, Stephan Züchner, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 25, 2014
Rapid in vivo forward genetic approach for identifying axon death genes in DrosophilaLukas J Neukomm, Thomas C Burdett, Michael A Gonzalez, et al.
Nature Communications|March 24, 2021
Axonal chemokine-like Orion induces astrocyte infiltration and engulfment during mushroom body neuronal remodelingAna Boulanger, Camille Thinat, Stephan Züchner, et al.
International Journal of Molecular Sciences|October 28, 2015
Abnormal Paraplegin Expression in Swollen Neurites, τ- and α-Synuclein Pathology in a Case of Hereditary Spastic Paraplegia SPG7 with an Ala510Val MutationDietmar R Thal, Stephan Züchner, Stephan Gierer, et al.
Experimental Neurology|June 24, 2018
The human motor neuron axonal transcriptome is enriched for transcripts related to mitochondrial function and microtubule-based axonal transportRenata Maciel, Dana M Bis, Adriana P Rebelo, et al.
Brain : a Journal of Neurology|March 5, 2003
A novel nonsense mutation in the ABC1 gene causes a severe syringomyelia-like phenotype of Tangier diseaseStephan Züchner, Anne D Sperfeld, Jan Senderek, et al.
Biochimica Et Biophysica Acta. Molecular Cell Research|December 4, 2016
Abl2 kinase phosphorylates Bi-organellar regulator MNRR1 in mitochondria, stimulating respirationSiddhesh Aras, Hassan Arrabi, Neeraja Purandare, et al.
Brain : a Journal of Neurology|February 26, 2016
Severe axonal Charcot-Marie-Tooth disease with proximal weakness caused by de novo mutation in the MORC2 genePetra Laššuthová, Dana Šafka Brožková, Marcela Krůtová, et al.
Communications Biology|December 18, 2021
Restoring Shank3 in the rostral brainstem of shank3ab-/- zebrafish autism models rescues sensory deficitsRobert A Kozol, David M James, Ivan Varela, et al.
Pageof 20