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Grace Yoon

Showing results (91-100 of 177) with videos related to

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Stem Cell Reports|November 19, 2019
Adult Human Dermal Progenitor Cell Transplantation Modulates the Functional Outcome of Split-Thickness Skin XenograftsNatacha A Agabalyan, Holly D Sparks, Samar Tarraf, et al.
Molecular Genetics & Genomic Medicine|November 2, 2018
Triple A syndrome presenting as complicated hereditary spastic paraplegiaEtienne Leveille, Hernan D Gonorazky, Marie-France Rioux, et al.
Human Mutation|April 14, 2016
High Frequency of Pathogenic Rearrangements in SPG11 and Extensive Contribution of Mutational Hotspots and Founder AllelesSven Günther, Ewelina Elert-Dobkowska, Anne S Soehn, et al.
BMC Bioinformatics|March 8, 2017
Ultra-high dimensional variable selection with application to normative aging study: DNA methylation and metabolic syndromeGrace Yoon, Yinan Zheng, Zhou Zhang, et al.
American Journal of Human Genetics|January 8, 2021
De novo variants in POLR3B cause ataxia, spasticity, and demyelinating neuropathyDjurdja Djordjevic, Maxime Pinard, Marie-Soleil Gauthier, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|April 26, 2011
A population-based study of dystrophin mutations in CanadaJean K Mah, Kathryn Selby, Craig Campbell, et al.
American Journal of Human Genetics|April 8, 2022
De novo variants in POLR3B cause ataxia, spasticity, and demyelinating neuropathyDjurdja Djordjevic, Maxime Pinard, Marie-Soleil Gauthier, et al.
Human Molecular Genetics|October 11, 2018
Bi-allelic mutations of LONP1 encoding the mitochondrial LonP1 protease cause pyruvate dehydrogenase deficiency and profound neurodegeneration with progressive cerebellar atrophyGraeme A M Nimmo, Sundararajan Venkatesh, Ashutosh K Pandey, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|May 26, 2016
Survival Impact of Early Post-Transplant Toxicities in Pediatric and Adolescent Patients Undergoing Allogeneic Hematopoietic Cell Transplantation for Malignant and Nonmalignant Diseases: Recognizing Risks and Optimizing OutcomesNaima Al Mulla, Justine M Kahn, Zhezhen Jin, et al.
American Journal of Medical Genetics. Part A|May 29, 2012
Definition of a critical genetic interval related to kidney abnormalities in the Potocki-Lupski syndromeElaine Suk-Ying Goh, Irene C Perez, Cesar P Canales, et al.
Pageof 18

Showing results (91-100 of 177) with videos related to

Sort By:
Pageof 18
Stem Cell Reports|November 19, 2019
Adult Human Dermal Progenitor Cell Transplantation Modulates the Functional Outcome of Split-Thickness Skin XenograftsNatacha A Agabalyan, Holly D Sparks, Samar Tarraf, et al.
Molecular Genetics & Genomic Medicine|November 2, 2018
Triple A syndrome presenting as complicated hereditary spastic paraplegiaEtienne Leveille, Hernan D Gonorazky, Marie-France Rioux, et al.
Human Mutation|April 14, 2016
High Frequency of Pathogenic Rearrangements in SPG11 and Extensive Contribution of Mutational Hotspots and Founder AllelesSven Günther, Ewelina Elert-Dobkowska, Anne S Soehn, et al.
BMC Bioinformatics|March 8, 2017
Ultra-high dimensional variable selection with application to normative aging study: DNA methylation and metabolic syndromeGrace Yoon, Yinan Zheng, Zhou Zhang, et al.
American Journal of Human Genetics|January 8, 2021
De novo variants in POLR3B cause ataxia, spasticity, and demyelinating neuropathyDjurdja Djordjevic, Maxime Pinard, Marie-Soleil Gauthier, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|April 26, 2011
A population-based study of dystrophin mutations in CanadaJean K Mah, Kathryn Selby, Craig Campbell, et al.
American Journal of Human Genetics|April 8, 2022
De novo variants in POLR3B cause ataxia, spasticity, and demyelinating neuropathyDjurdja Djordjevic, Maxime Pinard, Marie-Soleil Gauthier, et al.
Human Molecular Genetics|October 11, 2018
Bi-allelic mutations of LONP1 encoding the mitochondrial LonP1 protease cause pyruvate dehydrogenase deficiency and profound neurodegeneration with progressive cerebellar atrophyGraeme A M Nimmo, Sundararajan Venkatesh, Ashutosh K Pandey, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|May 26, 2016
Survival Impact of Early Post-Transplant Toxicities in Pediatric and Adolescent Patients Undergoing Allogeneic Hematopoietic Cell Transplantation for Malignant and Nonmalignant Diseases: Recognizing Risks and Optimizing OutcomesNaima Al Mulla, Justine M Kahn, Zhezhen Jin, et al.
American Journal of Medical Genetics. Part A|May 29, 2012
Definition of a critical genetic interval related to kidney abnormalities in the Potocki-Lupski syndromeElaine Suk-Ying Goh, Irene C Perez, Cesar P Canales, et al.
Pageof 18