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Disease Models & Mechanisms
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October 17, 2019
Drug screens of <i>NGLY1</i> deficiency in worm and fly models reveal catecholamine, NRF2 and anti-inflammatory-pathway activation as potential clinical approaches
Sangeetha Iyer, Joshua D Mast, Hillary Tsang, et al.
Glycobiology
|
October 3, 2024
N-glycoproteomic and proteomic alterations in SRD5A3-deficient fibroblasts
Kishore Garapati, Wasantha Ranatunga, Neha Joshi, et al.
Disease Models & Mechanisms
|
October 23, 2019
Repurposing the aldose reductase inhibitor and diabetic neuropathy drug epalrestat for the congenital disorder of glycosylation PMM2-CDG
Sangeetha Iyer, Feba S Sam, Nina DiPrimio, et al.
Nature Chemical Biology
|
May 9, 2007
Small molecules enhance autophagy and reduce toxicity in Huntington's disease models
Sovan Sarkar, Ethan O Perlstein, Sara Imarisio, et al.
Biorxiv : the Preprint Server for Biology
|
February 6, 2026
Repurposing the HMG-CoA Reductase Inhibitor Atorvastatin for SRD5A3-CDG
Hiba Daghar, Seul Kee Byeon, Claudia Maios, et al.
International Journal of Molecular Sciences
|
August 12, 2022
Systematic Review: Drug Repositioning for Congenital Disorders of Glycosylation (CDG)
Sandra Brasil, Mariateresa Allocca, Salvador C M Magrinho, et al.
Neuron
|
August 12, 2022
Glial control of sphingolipid levels sculpts diurnal remodeling in a circadian circuit
John P Vaughen, Emma Theisen, Irma Magaly Rivas-Serna, et al.
Annals of Neurology
|
October 15, 2021
Sorbitol Is a Severity Biomarker for PMM2-CDG with Therapeutic Implications
Anna N Ligezka, Silvia Radenkovic, Mayank Saraswat, et al.
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Search research articles
Search
Showing results (21-30 of 28) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 28 results.
Disease Models & Mechanisms
|
October 17, 2019
Drug screens of <i>NGLY1</i> deficiency in worm and fly models reveal catecholamine, NRF2 and anti-inflammatory-pathway activation as potential clinical approaches
Sangeetha Iyer, Joshua D Mast, Hillary Tsang, et al.
Glycobiology
|
October 3, 2024
N-glycoproteomic and proteomic alterations in SRD5A3-deficient fibroblasts
Kishore Garapati, Wasantha Ranatunga, Neha Joshi, et al.
Disease Models & Mechanisms
|
October 23, 2019
Repurposing the aldose reductase inhibitor and diabetic neuropathy drug epalrestat for the congenital disorder of glycosylation PMM2-CDG
Sangeetha Iyer, Feba S Sam, Nina DiPrimio, et al.
Nature Chemical Biology
|
May 9, 2007
Small molecules enhance autophagy and reduce toxicity in Huntington's disease models
Sovan Sarkar, Ethan O Perlstein, Sara Imarisio, et al.
Biorxiv : the Preprint Server for Biology
|
February 6, 2026
Repurposing the HMG-CoA Reductase Inhibitor Atorvastatin for SRD5A3-CDG
Hiba Daghar, Seul Kee Byeon, Claudia Maios, et al.
International Journal of Molecular Sciences
|
August 12, 2022
Systematic Review: Drug Repositioning for Congenital Disorders of Glycosylation (CDG)
Sandra Brasil, Mariateresa Allocca, Salvador C M Magrinho, et al.
Neuron
|
August 12, 2022
Glial control of sphingolipid levels sculpts diurnal remodeling in a circadian circuit
John P Vaughen, Emma Theisen, Irma Magaly Rivas-Serna, et al.
Annals of Neurology
|
October 15, 2021
Sorbitol Is a Severity Biomarker for PMM2-CDG with Therapeutic Implications
Anna N Ligezka, Silvia Radenkovic, Mayank Saraswat, et al.
Page
of 3