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Human Gene Therapy
|
February 20, 2025
Adeno-Associated Virus Gene Therapy Development: Early Planning and Regulatory Considerations to Advance the Platform Vector Gene Therapy Program
Richa Madan Lomash, Jean Dehdashti, Oleg A Shchelochkov, et al.
Human Gene Therapy
|
June 19, 2026
Adeno-Associated Virus Gene Therapy Translation: Lessons from Early Regulatory Meetings
Rodica Stan, Richa Madan Lomash, Oleg A Shchelochkov, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 19, 2021
Severity modeling of propionic acidemia using clinical and laboratory biomarkers
Oleg A Shchelochkov, Irini Manoli, Paul Juneau, et al.
American Journal of Human Genetics
|
September 10, 2013
An X-linked cobalamin disorder caused by mutations in transcriptional coregulator HCFC1
Hung-Chun Yu, Jennifer L Sloan, Gunter Scharer, et al.
Plos One
|
May 14, 2021
Validation of protein arginine methyltransferase 5 (PRMT5) as a candidate therapeutic target in the spontaneous canine model of non-Hodgkin lymphoma
Shelby L Sloan, Kyle A Renaldo, Mackenzie Long, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine
|
August 30, 2020
Quantification of Macrophage-Driven Inflammation During Myocardial Infarction with <sup>18</sup>F-LW223, a Novel TSPO Radiotracer with Binding Independent of the rs6971 Human Polymorphism
Mark G MacAskill, Agne Stadulyte, Lewis Williams, et al.
Brain : a Journal of Neurology
|
February 1, 2022
ZBTB11 dysfunction: spectrum of brain abnormalities, biochemical signature and cellular consequences
Dulika Sumathipala, Petter Strømme, Zohreh Fattahi, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 31, 2013
Targeting proximal tubule mitochondrial dysfunction attenuates the renal disease of methylmalonic acidemia
Irini Manoli, Justin R Sysol, Lingli Li, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 6, 2021
1-<sup>13</sup>C-propionate breath testing as a surrogate endpoint to assess efficacy of liver-directed therapies in methylmalonic acidemia (MMA)
Irini Manoli, Alexandra R Pass, Elizabeth A Harrington, et al.
Circulation Research
|
November 3, 2017
Mitochondrial Reactive Oxygen Species in Lipotoxic Hearts Induce Post-Translational Modifications of AKAP121, DRP1, and OPA1 That Promote Mitochondrial Fission
Kensuke Tsushima, Heiko Bugger, Adam R Wende, et al.
Page
of 27
Search research articles
Search
Showing results (251-260 of 267) with videos related to
Sort By:
Page
of 27
Human Gene Therapy
|
February 20, 2025
Adeno-Associated Virus Gene Therapy Development: Early Planning and Regulatory Considerations to Advance the Platform Vector Gene Therapy Program
Richa Madan Lomash, Jean Dehdashti, Oleg A Shchelochkov, et al.
Human Gene Therapy
|
June 19, 2026
Adeno-Associated Virus Gene Therapy Translation: Lessons from Early Regulatory Meetings
Rodica Stan, Richa Madan Lomash, Oleg A Shchelochkov, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 19, 2021
Severity modeling of propionic acidemia using clinical and laboratory biomarkers
Oleg A Shchelochkov, Irini Manoli, Paul Juneau, et al.
American Journal of Human Genetics
|
September 10, 2013
An X-linked cobalamin disorder caused by mutations in transcriptional coregulator HCFC1
Hung-Chun Yu, Jennifer L Sloan, Gunter Scharer, et al.
Plos One
|
May 14, 2021
Validation of protein arginine methyltransferase 5 (PRMT5) as a candidate therapeutic target in the spontaneous canine model of non-Hodgkin lymphoma
Shelby L Sloan, Kyle A Renaldo, Mackenzie Long, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine
|
August 30, 2020
Quantification of Macrophage-Driven Inflammation During Myocardial Infarction with <sup>18</sup>F-LW223, a Novel TSPO Radiotracer with Binding Independent of the rs6971 Human Polymorphism
Mark G MacAskill, Agne Stadulyte, Lewis Williams, et al.
Brain : a Journal of Neurology
|
February 1, 2022
ZBTB11 dysfunction: spectrum of brain abnormalities, biochemical signature and cellular consequences
Dulika Sumathipala, Petter Strømme, Zohreh Fattahi, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 31, 2013
Targeting proximal tubule mitochondrial dysfunction attenuates the renal disease of methylmalonic acidemia
Irini Manoli, Justin R Sysol, Lingli Li, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 6, 2021
1-<sup>13</sup>C-propionate breath testing as a surrogate endpoint to assess efficacy of liver-directed therapies in methylmalonic acidemia (MMA)
Irini Manoli, Alexandra R Pass, Elizabeth A Harrington, et al.
Circulation Research
|
November 3, 2017
Mitochondrial Reactive Oxygen Species in Lipotoxic Hearts Induce Post-Translational Modifications of AKAP121, DRP1, and OPA1 That Promote Mitochondrial Fission
Kensuke Tsushima, Heiko Bugger, Adam R Wende, et al.
Page
of 27