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A Messing

Showing results (91-100 of 104) with videos related to

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Neuron|May 15, 1998
Deletion of the K(V)1.1 potassium channel causes epilepsy in miceS L Smart, V Lopantsev, C L Zhang, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 26, 1996
Absence of the beta subunit (cchb1) of the skeletal muscle dihydropyridine receptor alters expression of the alpha 1 subunit and eliminates excitation-contraction couplingR G Gregg, A Messing, C Strube, et al.
The Journal of Cell Biology|March 8, 2000
P(0) glycoprotein overexpression causes congenital hypomyelination of peripheral nervesL Wrabetz, M L Feltri, A Quattrini, et al.
The Journal of Cell Biology|November 22, 2000
Epitope-tagged P(0) glycoprotein causes Charcot-Marie-Tooth-like neuropathy in transgenic miceS C Previtali, A Quattrini, M Fasolini, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 25, 1996
Targeted deletion in astrocyte intermediate filament (Gfap) alters neuronal physiologyM A McCall, R G Gregg, R R Behringer, et al.
Experimental Neurology|December 17, 1997
Generation and transplantation of EGF-responsive neural stem cells derived from GFAP-hNGF transgenic miceM K Carpenter, C Winkler, R Fricker, et al.
Protein Expression and Purification|May 16, 2026
High yield production of C-terminally processed KRAS4a, HRAS, and NRAS for biophysical studyShelley Perkins, Sophie Krahnke, Erik K Larsen, et al.
The Journal of Comparative Neurology|October 23, 1997
Grafts of EGF-responsive neural stem cells derived from GFAP-hNGF transgenic mice: trophic and tropic effects in a rodent model of Huntington's diseaseJ H Kordower, E Y Chen, C Winkler, et al.
Nature Communications|March 3, 2016
A Helitron transposon reconstructed from bats reveals a novel mechanism of genome shuffling in eukaryotesIvana Grabundzija, Simon A Messing, Jainy Thomas, et al.
American Journal of Human Genetics|September 22, 2001
Infantile Alexander disease: spectrum of GFAP mutations and genotype-phenotype correlationD Rodriguez, F Gauthier, E Bertini, et al.
Pageof 11

Showing results (91-100 of 104) with videos related to

Sort By:
Pageof 11
Neuron|May 15, 1998
Deletion of the K(V)1.1 potassium channel causes epilepsy in miceS L Smart, V Lopantsev, C L Zhang, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 26, 1996
Absence of the beta subunit (cchb1) of the skeletal muscle dihydropyridine receptor alters expression of the alpha 1 subunit and eliminates excitation-contraction couplingR G Gregg, A Messing, C Strube, et al.
The Journal of Cell Biology|March 8, 2000
P(0) glycoprotein overexpression causes congenital hypomyelination of peripheral nervesL Wrabetz, M L Feltri, A Quattrini, et al.
The Journal of Cell Biology|November 22, 2000
Epitope-tagged P(0) glycoprotein causes Charcot-Marie-Tooth-like neuropathy in transgenic miceS C Previtali, A Quattrini, M Fasolini, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 25, 1996
Targeted deletion in astrocyte intermediate filament (Gfap) alters neuronal physiologyM A McCall, R G Gregg, R R Behringer, et al.
Experimental Neurology|December 17, 1997
Generation and transplantation of EGF-responsive neural stem cells derived from GFAP-hNGF transgenic miceM K Carpenter, C Winkler, R Fricker, et al.
Protein Expression and Purification|May 16, 2026
High yield production of C-terminally processed KRAS4a, HRAS, and NRAS for biophysical studyShelley Perkins, Sophie Krahnke, Erik K Larsen, et al.
The Journal of Comparative Neurology|October 23, 1997
Grafts of EGF-responsive neural stem cells derived from GFAP-hNGF transgenic mice: trophic and tropic effects in a rodent model of Huntington's diseaseJ H Kordower, E Y Chen, C Winkler, et al.
Nature Communications|March 3, 2016
A Helitron transposon reconstructed from bats reveals a novel mechanism of genome shuffling in eukaryotesIvana Grabundzija, Simon A Messing, Jainy Thomas, et al.
American Journal of Human Genetics|September 22, 2001
Infantile Alexander disease: spectrum of GFAP mutations and genotype-phenotype correlationD Rodriguez, F Gauthier, E Bertini, et al.
Pageof 11