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T Emrick

Showing results (11-20 of 37) with videos related to

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Meta Gene|November 21, 2014
The effect of citrulline and arginine supplementation on lactic acidemia in MELAS syndromeAyman W El-Hattab, Lisa T Emrick, Kaitlin C Williamson, et al.
ACS Nano|February 25, 2009
Linear dipole behavior in single CdSe-oligo(phenylene vinylene) nanostructuresK T Early, K D McCarthy, M Y Odoi, et al.
Neurology. Genetics|February 8, 2021
<i>EIF2AK2</i>-related Neurodevelopmental Disorder With Leukoencephalopathy, Developmental Delay, and Episodic Neurologic Regression Mimics Pelizaeus-Merzbacher DiseaseDaniel G Calame, Meagan Hainlen, Danielle Takacs, et al.
American Journal of Medical Genetics. Part A|August 21, 2024
Recessive loss-of-function variants in DPH1 identified as the molecular cause in a sibling pair previously diagnosed with Fine-Lubinsky syndromeEmily R Waskow, , Lisa T Emrick, et al.
Nano Letters|July 28, 2007
Fluorescence lifetimes and correlated photon statistics from single CdSe/oligo(phenylene vinylene) composite nanostructuresM Y Odoi, N I Hammer, K T Early, et al.
Mitochondrion|August 3, 2014
Glucose metabolism derangements in adults with the MELAS m.3243A>G mutationAyman W El-Hattab, Lisa T Emrick, Jean W Hsu, et al.
Nanotechnology|July 7, 2011
Blinking suppression and intensity recurrences in single CdSe-oligo(phenylene vinylene) nanostructures: experiment and kinetic modelK T Early, K D McCarthy, N I Hammer, et al.
Molecular Genetics and Metabolism|February 7, 2016
Impaired nitric oxide production in children with MELAS syndrome and the effect of arginine and citrulline supplementationAyman W El-Hattab, Lisa T Emrick, Jean W Hsu, et al.
Molecular Genetics and Metabolism|February 14, 2012
Restoration of impaired nitric oxide production in MELAS syndrome with citrulline and arginine supplementationAyman W El-Hattab, Jean W Hsu, Lisa T Emrick, et al.
BMC Neurology|March 4, 2024
Expanded clinical phenotype and untargeted metabolomics analysis in RARS2-related mitochondrial disorder: a case reportAmeya S Walimbe, Keren Machol, Stephen F Kralik, et al.
Pageof 4

Showing results (11-20 of 37) with videos related to

Sort By:
Pageof 4
Meta Gene|November 21, 2014
The effect of citrulline and arginine supplementation on lactic acidemia in MELAS syndromeAyman W El-Hattab, Lisa T Emrick, Kaitlin C Williamson, et al.
ACS Nano|February 25, 2009
Linear dipole behavior in single CdSe-oligo(phenylene vinylene) nanostructuresK T Early, K D McCarthy, M Y Odoi, et al.
Neurology. Genetics|February 8, 2021
<i>EIF2AK2</i>-related Neurodevelopmental Disorder With Leukoencephalopathy, Developmental Delay, and Episodic Neurologic Regression Mimics Pelizaeus-Merzbacher DiseaseDaniel G Calame, Meagan Hainlen, Danielle Takacs, et al.
American Journal of Medical Genetics. Part A|August 21, 2024
Recessive loss-of-function variants in DPH1 identified as the molecular cause in a sibling pair previously diagnosed with Fine-Lubinsky syndromeEmily R Waskow, , Lisa T Emrick, et al.
Nano Letters|July 28, 2007
Fluorescence lifetimes and correlated photon statistics from single CdSe/oligo(phenylene vinylene) composite nanostructuresM Y Odoi, N I Hammer, K T Early, et al.
Mitochondrion|August 3, 2014
Glucose metabolism derangements in adults with the MELAS m.3243A>G mutationAyman W El-Hattab, Lisa T Emrick, Jean W Hsu, et al.
Nanotechnology|July 7, 2011
Blinking suppression and intensity recurrences in single CdSe-oligo(phenylene vinylene) nanostructures: experiment and kinetic modelK T Early, K D McCarthy, N I Hammer, et al.
Molecular Genetics and Metabolism|February 7, 2016
Impaired nitric oxide production in children with MELAS syndrome and the effect of arginine and citrulline supplementationAyman W El-Hattab, Lisa T Emrick, Jean W Hsu, et al.
Molecular Genetics and Metabolism|February 14, 2012
Restoration of impaired nitric oxide production in MELAS syndrome with citrulline and arginine supplementationAyman W El-Hattab, Jean W Hsu, Lisa T Emrick, et al.
BMC Neurology|March 4, 2024
Expanded clinical phenotype and untargeted metabolomics analysis in RARS2-related mitochondrial disorder: a case reportAmeya S Walimbe, Keren Machol, Stephen F Kralik, et al.
Pageof 4