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Journal of Cell Science
|
April 8, 2026
Biophysical and biochemical studies support PHD inhibitor development as a TPI deficiency therapy
Presley Roberts, Joseph R Figura, Kaitlin McClure, et al.
Addiction Science & Clinical Practice
|
October 18, 2011
Transporting clinical research to community settings: designing and conducting a multisite trial of brief strategic family therapy
Michael S Robbins, Elizabeth Alonso, Viviana E Horigian, et al.
American Journal of Respiratory Cell and Molecular Biology
|
January 27, 2009
CFTR regulation of intracellular pH and ceramides is required for lung endothelial cell apoptosis
Julie Noe, Daniela Petrusca, Natalia Rush, et al.
Plos Genetics
|
April 1, 2016
Structural and Genetic Studies Demonstrate Neurologic Dysfunction in Triosephosphate Isomerase Deficiency Is Associated with Impaired Synaptic Vesicle Dynamics
Bartholomew P Roland, Alison M Zeccola, Samantha B Larsen, et al.
Free Radical Biology & Medicine
|
September 7, 2023
Membrane regulation of 15LOX-1/PEBP1 complex prompts the generation of ferroptotic signals, oxygenated PEs
Thiliban Manivarma, Aleksandr A Kapralov, Svetlana N Samovich, et al.
Biorxiv : the Preprint Server for Biology
|
December 22, 2025
Degraded sensory coding in a mouse model of <i>Scn2a-</i>related disorder and its rescue by CRISPRa gene activation
Kaeli Vandemark, Hannah R Monday, Lucia Rodriguez, et al.
Biochimica Et Biophysica Acta
|
December 3, 2014
Triosephosphate isomerase I170V alters catalytic site, enhances stability and induces pathology in a Drosophila model of TPI deficiency
Bartholomew P Roland, Christopher G Amrich, Charles J Kammerer, et al.
G3 (Bethesda, Md.)
|
July 20, 2024
Characterization of mycobacteriophage Adephagia cytotoxic proteins
Krista G Freeman, Michael J Lauer, Danny Jiang, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease
|
May 11, 2019
Missense variant in TPI1 (Arg189Gln) causes neurologic deficits through structural changes in the triosephosphate isomerase catalytic site and reduced enzyme levels in vivo
Bartholomew P Roland, Kristen R Richards, Stacy L Hrizo, et al.
Genes
|
October 29, 2025
Newly Identified TPI Deficiency Treatments Function for Novel Disease-Causing Allele, <i>TPI1<sup>R5G</sup></i>
Joseph R Figura, Presley Roberts, Riley Sawka, et al.
Page
of 16
Search research articles
Search
Showing results (131-140 of 157) with videos related to
Sort By:
Page
of 16
Journal of Cell Science
|
April 8, 2026
Biophysical and biochemical studies support PHD inhibitor development as a TPI deficiency therapy
Presley Roberts, Joseph R Figura, Kaitlin McClure, et al.
Addiction Science & Clinical Practice
|
October 18, 2011
Transporting clinical research to community settings: designing and conducting a multisite trial of brief strategic family therapy
Michael S Robbins, Elizabeth Alonso, Viviana E Horigian, et al.
American Journal of Respiratory Cell and Molecular Biology
|
January 27, 2009
CFTR regulation of intracellular pH and ceramides is required for lung endothelial cell apoptosis
Julie Noe, Daniela Petrusca, Natalia Rush, et al.
Plos Genetics
|
April 1, 2016
Structural and Genetic Studies Demonstrate Neurologic Dysfunction in Triosephosphate Isomerase Deficiency Is Associated with Impaired Synaptic Vesicle Dynamics
Bartholomew P Roland, Alison M Zeccola, Samantha B Larsen, et al.
Free Radical Biology & Medicine
|
September 7, 2023
Membrane regulation of 15LOX-1/PEBP1 complex prompts the generation of ferroptotic signals, oxygenated PEs
Thiliban Manivarma, Aleksandr A Kapralov, Svetlana N Samovich, et al.
Biorxiv : the Preprint Server for Biology
|
December 22, 2025
Degraded sensory coding in a mouse model of <i>Scn2a-</i>related disorder and its rescue by CRISPRa gene activation
Kaeli Vandemark, Hannah R Monday, Lucia Rodriguez, et al.
Biochimica Et Biophysica Acta
|
December 3, 2014
Triosephosphate isomerase I170V alters catalytic site, enhances stability and induces pathology in a Drosophila model of TPI deficiency
Bartholomew P Roland, Christopher G Amrich, Charles J Kammerer, et al.
G3 (Bethesda, Md.)
|
July 20, 2024
Characterization of mycobacteriophage Adephagia cytotoxic proteins
Krista G Freeman, Michael J Lauer, Danny Jiang, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease
|
May 11, 2019
Missense variant in TPI1 (Arg189Gln) causes neurologic deficits through structural changes in the triosephosphate isomerase catalytic site and reduced enzyme levels in vivo
Bartholomew P Roland, Kristen R Richards, Stacy L Hrizo, et al.
Genes
|
October 29, 2025
Newly Identified TPI Deficiency Treatments Function for Novel Disease-Causing Allele, <i>TPI1<sup>R5G</sup></i>
Joseph R Figura, Presley Roberts, Riley Sawka, et al.
Page
of 16