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Anika L Burrell

Showing results (1-10 of 12) with videos related to

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Biochemical Society Transactions|February 22, 2022
IMPDH dysregulation in disease: a mini reviewAnika L Burrell, Justin M Kollman
Molecular Biology of the Cell|May 29, 2020
Freedom of assembly: metabolic enzymes come togetherJacqueline C Simonet, Anika L Burrell, Justin M Kollman, et al.
The Journal of Biological Chemistry|November 23, 2021
A highly conserved zebrafish IMPDH retinal isoform produces the majority of guanine and forms dynamic protein filaments in photoreceptor cellsWhitney M Cleghorn, Anika L Burrell, Michelle M Giarmarco, et al.
The Journal of Cell Biology|February 7, 2024
Light-sensitive phosphorylation regulates retinal IMPDH1 activity and filament assemblyS John Calise, Audrey G O'Neill, Anika L Burrell, et al.
Biorxiv : the Preprint Server for Biology|October 4, 2023
Light-sensitive phosphorylation regulates enzyme activity and filament assembly of human IMPDH1 retinal splice variantsS John Calise, Audrey G O'Neill, Anika L Burrell, et al.
Nature Structural & Molecular Biology|January 11, 2022
IMPDH1 retinal variants control filament architecture to tune allosteric regulationAnika L Burrell, Chuankai Nie, Meerit Said, et al.
Biorxiv : the Preprint Server for Biology|March 30, 2023
Point mutations in IMPDH2 which cause early-onset neurodevelopmental disorders disrupt enzyme regulation and filament structureAudrey G O'Neill, Anika L Burrell, Michael Zech, et al.
The Journal of Biological Chemistry|July 6, 2023
Neurodevelopmental disorder mutations in the purine biosynthetic enzyme IMPDH2 disrupt its allosteric regulationAudrey G O'Neill, Anika L Burrell, Michael Zech, et al.
Molecular Biology of the Cell|August 11, 2017
Reconstituted IMPDH polymers accommodate both catalytically active and inactive conformationsSajitha A Anthony, Anika L Burrell, Matthew C Johnson, et al.
Disease Models & Mechanisms|August 18, 2025
Retinopathy-associated inosine monophosphate dehydrogenase 1 mutations cause metabolic and filament defects in conesKaitlyn M Rutter, Michelle M Giarmarco, Vivian Truong, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Biochemical Society Transactions|February 22, 2022
IMPDH dysregulation in disease: a mini reviewAnika L Burrell, Justin M Kollman
Molecular Biology of the Cell|May 29, 2020
Freedom of assembly: metabolic enzymes come togetherJacqueline C Simonet, Anika L Burrell, Justin M Kollman, et al.
The Journal of Biological Chemistry|November 23, 2021
A highly conserved zebrafish IMPDH retinal isoform produces the majority of guanine and forms dynamic protein filaments in photoreceptor cellsWhitney M Cleghorn, Anika L Burrell, Michelle M Giarmarco, et al.
The Journal of Cell Biology|February 7, 2024
Light-sensitive phosphorylation regulates retinal IMPDH1 activity and filament assemblyS John Calise, Audrey G O'Neill, Anika L Burrell, et al.
Biorxiv : the Preprint Server for Biology|October 4, 2023
Light-sensitive phosphorylation regulates enzyme activity and filament assembly of human IMPDH1 retinal splice variantsS John Calise, Audrey G O'Neill, Anika L Burrell, et al.
Nature Structural & Molecular Biology|January 11, 2022
IMPDH1 retinal variants control filament architecture to tune allosteric regulationAnika L Burrell, Chuankai Nie, Meerit Said, et al.
Biorxiv : the Preprint Server for Biology|March 30, 2023
Point mutations in IMPDH2 which cause early-onset neurodevelopmental disorders disrupt enzyme regulation and filament structureAudrey G O'Neill, Anika L Burrell, Michael Zech, et al.
The Journal of Biological Chemistry|July 6, 2023
Neurodevelopmental disorder mutations in the purine biosynthetic enzyme IMPDH2 disrupt its allosteric regulationAudrey G O'Neill, Anika L Burrell, Michael Zech, et al.
Molecular Biology of the Cell|August 11, 2017
Reconstituted IMPDH polymers accommodate both catalytically active and inactive conformationsSajitha A Anthony, Anika L Burrell, Matthew C Johnson, et al.
Disease Models & Mechanisms|August 18, 2025
Retinopathy-associated inosine monophosphate dehydrogenase 1 mutations cause metabolic and filament defects in conesKaitlyn M Rutter, Michelle M Giarmarco, Vivian Truong, et al.
Pageof 2