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Annals of Clinical and Translational Neurology
|
September 21, 2016
Progression of Friedreich ataxia: quantitative characterization over 5 years
Maya Patel, Charles J Isaacs, Lauren Seyer, et al.
British Journal of Pharmacology
|
February 2, 2025
Assessment of Spinster homologue 2 (Spns2)-dependent transport of sphingosine-1-phosphate as a therapeutic target
Yugesh Kharel, Tao Huang, Kyle Dunnavant, et al.
Oncotarget
|
February 11, 2016
Non-coding RNA LINC00857 is predictive of poor patient survival and promotes tumor progression via cell cycle regulation in lung cancer
Lihui Wang, Yanli He, Weijun Liu, et al.
American Journal of Human Genetics
|
March 6, 2008
ADCK3, an ancestral kinase, is mutated in a form of recessive ataxia associated with coenzyme Q10 deficiency
Clotilde Lagier-Tourenne, Meriem Tazir, Luis Carlos López, et al.
Science Translational Medicine
|
August 17, 2022
Sphingosine 1-phosphate signaling in perivascular cells enhances inflammation and fibrosis in the kidney
Shinji Tanaka, Shuqiu Zheng, Yugesh Kharel, et al.
BMJ Neurology Open
|
April 1, 2026
Peripheral frataxin levels govern long-term clinical progression in Friedreich ataxia
Christian Rummey, Ian A Blair, Clementina Mesaros, et al.
Molecular Metabolism
|
March 18, 2014
Opening of the mitochondrial permeability transition pore links mitochondrial dysfunction to insulin resistance in skeletal muscle
E P Taddeo, R C Laker, D S Breen, et al.
Frontiers in Molecular Biosciences
|
September 22, 2022
A non-synonymous single nucleotide polymorphism in <i>SIRT6</i> predicts neurological severity in Friedreich ataxia
Layne N Rodden, Christian Rummey, Yi Na Dong, et al.
Annals of Clinical and Translational Neurology
|
September 5, 2015
Frataxin levels in peripheral tissue in Friedreich ataxia
Michael Lazaropoulos, Yina Dong, Elisia Clark, et al.
JCI Insight
|
November 5, 2016
Muscle oxidative phosphorylation quantitation using creatine chemical exchange saturation transfer (CrCEST) MRI in mitochondrial disorders
Catherine DeBrosse, Ravi Prakash Reddy Nanga, Neil Wilson, et al.
Page
of 115
Search research articles
Search
Showing results (1091-1100 of 1,148) with videos related to
Sort By:
Page
of 115
Annals of Clinical and Translational Neurology
|
September 21, 2016
Progression of Friedreich ataxia: quantitative characterization over 5 years
Maya Patel, Charles J Isaacs, Lauren Seyer, et al.
British Journal of Pharmacology
|
February 2, 2025
Assessment of Spinster homologue 2 (Spns2)-dependent transport of sphingosine-1-phosphate as a therapeutic target
Yugesh Kharel, Tao Huang, Kyle Dunnavant, et al.
Oncotarget
|
February 11, 2016
Non-coding RNA LINC00857 is predictive of poor patient survival and promotes tumor progression via cell cycle regulation in lung cancer
Lihui Wang, Yanli He, Weijun Liu, et al.
American Journal of Human Genetics
|
March 6, 2008
ADCK3, an ancestral kinase, is mutated in a form of recessive ataxia associated with coenzyme Q10 deficiency
Clotilde Lagier-Tourenne, Meriem Tazir, Luis Carlos López, et al.
Science Translational Medicine
|
August 17, 2022
Sphingosine 1-phosphate signaling in perivascular cells enhances inflammation and fibrosis in the kidney
Shinji Tanaka, Shuqiu Zheng, Yugesh Kharel, et al.
BMJ Neurology Open
|
April 1, 2026
Peripheral frataxin levels govern long-term clinical progression in Friedreich ataxia
Christian Rummey, Ian A Blair, Clementina Mesaros, et al.
Molecular Metabolism
|
March 18, 2014
Opening of the mitochondrial permeability transition pore links mitochondrial dysfunction to insulin resistance in skeletal muscle
E P Taddeo, R C Laker, D S Breen, et al.
Frontiers in Molecular Biosciences
|
September 22, 2022
A non-synonymous single nucleotide polymorphism in <i>SIRT6</i> predicts neurological severity in Friedreich ataxia
Layne N Rodden, Christian Rummey, Yi Na Dong, et al.
Annals of Clinical and Translational Neurology
|
September 5, 2015
Frataxin levels in peripheral tissue in Friedreich ataxia
Michael Lazaropoulos, Yina Dong, Elisia Clark, et al.
JCI Insight
|
November 5, 2016
Muscle oxidative phosphorylation quantitation using creatine chemical exchange saturation transfer (CrCEST) MRI in mitochondrial disorders
Catherine DeBrosse, Ravi Prakash Reddy Nanga, Neil Wilson, et al.
Page
of 115