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The American Journal of Bioethics : AJOB
|
September 28, 2022
Clarifying the Blurry Boundaries between Research and Clinical Care
Forough Noohi, Lainie F Ross
The Journal of Law, Medicine & Ethics : a Journal of the American Society of Law, Medicine & Ethics
|
November 18, 2022
Mitochondrial Replacement Therapy: In Whose Interests?
Forough Noohi, Vardit Ravitsky, Bartha Maria Knoppers, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 22, 2023
Diagnosis, treatment and disclosure: A qualitative exploration of participant challenges in a Monogenic Diabetes Registry
Forough Noohi, Manu S Sundaresan, Rochelle N Naylor, et al.
Journal of Clinical and Translational Science
|
January 17, 2024
Investigator and participant expectations for returning non-genetic results: insights from the Rare and Atypical Diabetes Network (RADIANT) study
Forough Noohi, Manu S Sundaresan, Rochelle N Naylor, et al.
Frontiers in Genetics
|
December 22, 2016
Empirical Validation of a Hypothesis of the Hormetic Selective Forces Driving the Evolution of Longevity Regulation Mechanisms
Alejandra Gomez-Perez, Pavlo Kyryakov, Michelle T Burstein, et al.
Journal of Obstetrics and Gynaecology Canada : JOGC = Journal D'Obstetrique Et Gynecologie Du Canada : JOGC
|
July 23, 2017
Mitochondrial Replacement Therapy: The Road to the Clinic in Canada
Bartha Maria Knoppers, Arthur Leader, Stacey Hume, et al.
Cell Cycle (Georgetown, Tex.)
|
August 17, 2012
Lithocholic acid extends longevity of chronologically aging yeast only if added at certain critical periods of their lifespan
Michelle T Burstein, Pavlo Kyryakov, Adam Beach, et al.
Healthcare Policy = Politiques De Sante
|
March 30, 2018
Research on Human Embryos and Reproductive Materials: Revisiting Canadian Law and Policy
Ubaka Ogbogu, Amy Zarzeczny, Jay Baltz, et al.
Molecular Brain
|
April 15, 2017
Absence of neurological abnormalities in mice homozygous for the Polr3a G672E hypomyelinating leukodystrophy mutation
Karine Choquet, Sharon Yang, Robyn D Moir, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 9) with videos related to
Sort By:
Page
of 1
The American Journal of Bioethics : AJOB
|
September 28, 2022
Clarifying the Blurry Boundaries between Research and Clinical Care
Forough Noohi, Lainie F Ross
The Journal of Law, Medicine & Ethics : a Journal of the American Society of Law, Medicine & Ethics
|
November 18, 2022
Mitochondrial Replacement Therapy: In Whose Interests?
Forough Noohi, Vardit Ravitsky, Bartha Maria Knoppers, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 22, 2023
Diagnosis, treatment and disclosure: A qualitative exploration of participant challenges in a Monogenic Diabetes Registry
Forough Noohi, Manu S Sundaresan, Rochelle N Naylor, et al.
Journal of Clinical and Translational Science
|
January 17, 2024
Investigator and participant expectations for returning non-genetic results: insights from the Rare and Atypical Diabetes Network (RADIANT) study
Forough Noohi, Manu S Sundaresan, Rochelle N Naylor, et al.
Frontiers in Genetics
|
December 22, 2016
Empirical Validation of a Hypothesis of the Hormetic Selective Forces Driving the Evolution of Longevity Regulation Mechanisms
Alejandra Gomez-Perez, Pavlo Kyryakov, Michelle T Burstein, et al.
Journal of Obstetrics and Gynaecology Canada : JOGC = Journal D'Obstetrique Et Gynecologie Du Canada : JOGC
|
July 23, 2017
Mitochondrial Replacement Therapy: The Road to the Clinic in Canada
Bartha Maria Knoppers, Arthur Leader, Stacey Hume, et al.
Cell Cycle (Georgetown, Tex.)
|
August 17, 2012
Lithocholic acid extends longevity of chronologically aging yeast only if added at certain critical periods of their lifespan
Michelle T Burstein, Pavlo Kyryakov, Adam Beach, et al.
Healthcare Policy = Politiques De Sante
|
March 30, 2018
Research on Human Embryos and Reproductive Materials: Revisiting Canadian Law and Policy
Ubaka Ogbogu, Amy Zarzeczny, Jay Baltz, et al.
Molecular Brain
|
April 15, 2017
Absence of neurological abnormalities in mice homozygous for the Polr3a G672E hypomyelinating leukodystrophy mutation
Karine Choquet, Sharon Yang, Robyn D Moir, et al.
Page
of 1