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3 items found in 2 collections [showing 1 - 3]
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Kv1.3 Contains an Alternative C-Terminal ER Exit Motif and is Recruited into COPII Vesicles by Sec24a
Kv1.3 Contains an Alternative C-Terminal ER Exit Motif and is Recruited into COPII Vesicles by Sec24a
Full Title:
Kv1.3 Contains an Alternative C-Terminal ER Exit Motif and is Recruited into COPII Vesicles by Sec24a
Creator:
Stagg, Scott, Spear, John M., Koborssy, Dolly Al, Schwartz, Austin B, Johnson, Adam J, Audhya, Anjon, Fadool, Debra A
Description:
Background Potassium channels play a fundamental role in resetting the resting membrane potential of excitable cells. Determining the intracellular trafficking and localization mechanisms of potassium channels provides a platform to...
Date:
2015-07-10
Format:
text
Collection:
Department of Chemistry and Biochemistry
Identifiers:
FSU_libsubv1_scholarship_submission_1475170159, 10.1186/s12858-015-0045-6
URLs:
http://purl.flvc.org/fsu/fd/FSU_libsubv1_scholarship_submission_1475170159
Repository ID:
fsu:368776
Pathogenic TFG Mutations Underlying Hereditary Spastic Paraplegia Impair Secretory Protein Trafficking and Axon Fasciculation.
Pathogenic TFG Mutations Underlying Hereditary Spastic Paraplegia Impair Secretory Protein Trafficking and Axon Fasciculation.
Full Title:
Pathogenic TFG Mutations Underlying Hereditary Spastic Paraplegia Impair Secretory Protein Trafficking and Axon Fasciculation.
Creator:
Slosarek, Erin L, Schuh, Amber L, Pustova, Iryna, Johnson, Adam, Bird, Jennifer, Johnson, Matthew, Frankel, E B, Bhattacharya, Nilakshee, Hanna, Michael G, Burke, Jordan E, Ruhl, David A, Quinney, Kyle, Block, Samuel, Peotter, Jennifer L, Chapman, Edwin R, Sheets, Michael D, Butcher, Samuel E, Stagg, Scott M, Audhya, Anjon
Description:
Length-dependent axonopathy of the corticospinal tract causes lower limb spasticity and is characteristic of several neurological disorders, including hereditary spastic paraplegia (HSP) and amyotrophic lateral sclerosis. Mutations in...
Date:
2018-08-28
Format:
journal article, text
Collection:
Department of Chemistry and Biochemistry, Institute of Molecular Biophysics
Identifiers:
FSU_pmch_30157421, 10.1016/j.celrep.2018.07.081, PMC6152936, 30157421, S2211-1247(18)31199-9
URLs:
http://purl.flvc.org/fsu/fd/FSU_pmch_30157421
Repository ID:
fsu:710014
Pathogenic Tfg Mutations Underlying Hereditary Spastic Paraplegia Impair Secretory Protein Trafficking And Axon Fasciculation
Pathogenic Tfg Mutations Underlying Hereditary Spastic Paraplegia Impair Secretory Protein Trafficking And Axon Fasciculation
Full Title:
Pathogenic Tfg Mutations Underlying Hereditary Spastic Paraplegia Impair Secretory Protein Trafficking And Axon Fasciculation
Creator:
Slosarek, Erin L., Schuh, Amber L., Pustova, Iryna, Johnson, Adam, Bird, Jennifer, Johnson, Matthew, Frankel, E. B., Bhattacharya, Nilakshee, Hanna, Michael G., Burke, Jordan E., Ruhl, David A., Quinney, Kyle, Block, Samuel, Peotter, Jennifer L., Chapman, Edwin R., Sheets, Michael D., Butcher, Samuel E., Stagg, Scott M., Audhya, Anjon
Description:
Length-dependent axonopathy of the corticospinal tract causes lower limb spasticity and is characteristic of several neurological disorders, including hereditary spastic paraplegia (HSP) and amyotrophic lateral sclerosis. Mutations in...
Date:
2018-08-28
Format:
journal article, text
Collection:
Department of Chemistry and Biochemistry, Institute of Molecular Biophysics
Identifiers:
FSU_libsubv1_wos_000442923900005, 10.1016/j.celrep.2018.07.081
URLs:
http://purl.flvc.org/fsu/fd/FSU_libsubv1_wos_000442923900005
Repository ID:
fsu:607652