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F Elias

Showing results (271-280 of 283) with videos related to

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Journal of Chemical Neuroanatomy|July 25, 2015
The centrally projecting Edinger-Westphal nucleus--I: Efferents in the rat brainEdmilson D Dos Santos Júnior, André V Da Silva, Kelly R T Da Silva, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 27, 2024
The mouse metabolic phenotyping center (MMPC) live consortium: an NIH resource for in vivo characterization of mouse models of diabetes and obesityMaren Laughlin, Richard McIndoe, Sean H Adams, et al.
Cell Metabolism|April 9, 2010
Direct insulin and leptin action on pro-opiomelanocortin neurons is required for normal glucose homeostasis and fertilityJennifer W Hill, Carol F Elias, Makoto Fukuda, et al.
Journal of Inherited Metabolic Disease|March 12, 2020
Pathogenic variants in SQOR encoding sulfide:quinone oxidoreductase are a potentially treatable cause of Leigh diseaseMarisa W Friederich, Abdallah F Elias, Alice Kuster, et al.
Journal of Inherited Metabolic Disease|February 13, 2019
Clinical, neuroradiological, and biochemical features of SLC35A2-CDG patientsMari-Anne Vals, Angel Ashikov, Pilvi Ilves, et al.
HGG Advances|June 14, 2025
Long-Read Sequencing is Required for Precision Diagnosis of Incontinentia PigmentiMonica H Wojcik, Robin D Clark, Abdallah F Elias, et al.
Research Square|February 20, 2025
Long-Read Sequencing is Required for Precision Diagnosis of Incontinentia PigmentiMonica H Wojcik, Robin D Clark, Abdallah F Elias, et al.
Nature Genetics|July 10, 2012
Loss-of-function mutations in TGFB2 cause a syndromic presentation of thoracic aortic aneurysmMark E Lindsay, Dorien Schepers, Nikhita Ajit Bolar, et al.
Neurology|August 14, 2016
Phenotypic spectrum of GABRA1: From generalized epilepsies to severe epileptic encephalopathiesKatrine Johannesen, Carla Marini, Siona Pfeffer, et al.
Genetics in Medicine Open|June 5, 2025
Autosomal dominant <i>HK1</i>-related neurodevelopmental disorder with visual defects and brain anomalies (NEDVIBA): An emerging mitochondrial disorderBobby G Ng, Erik A Eklund, Jill A Rosenfeld, et al.
Pageof 29

Showing results (271-280 of 283) with videos related to

Sort By:
Pageof 29
Journal of Chemical Neuroanatomy|July 25, 2015
The centrally projecting Edinger-Westphal nucleus--I: Efferents in the rat brainEdmilson D Dos Santos Júnior, André V Da Silva, Kelly R T Da Silva, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 27, 2024
The mouse metabolic phenotyping center (MMPC) live consortium: an NIH resource for in vivo characterization of mouse models of diabetes and obesityMaren Laughlin, Richard McIndoe, Sean H Adams, et al.
Cell Metabolism|April 9, 2010
Direct insulin and leptin action on pro-opiomelanocortin neurons is required for normal glucose homeostasis and fertilityJennifer W Hill, Carol F Elias, Makoto Fukuda, et al.
Journal of Inherited Metabolic Disease|March 12, 2020
Pathogenic variants in SQOR encoding sulfide:quinone oxidoreductase are a potentially treatable cause of Leigh diseaseMarisa W Friederich, Abdallah F Elias, Alice Kuster, et al.
Journal of Inherited Metabolic Disease|February 13, 2019
Clinical, neuroradiological, and biochemical features of SLC35A2-CDG patientsMari-Anne Vals, Angel Ashikov, Pilvi Ilves, et al.
HGG Advances|June 14, 2025
Long-Read Sequencing is Required for Precision Diagnosis of Incontinentia PigmentiMonica H Wojcik, Robin D Clark, Abdallah F Elias, et al.
Research Square|February 20, 2025
Long-Read Sequencing is Required for Precision Diagnosis of Incontinentia PigmentiMonica H Wojcik, Robin D Clark, Abdallah F Elias, et al.
Nature Genetics|July 10, 2012
Loss-of-function mutations in TGFB2 cause a syndromic presentation of thoracic aortic aneurysmMark E Lindsay, Dorien Schepers, Nikhita Ajit Bolar, et al.
Neurology|August 14, 2016
Phenotypic spectrum of GABRA1: From generalized epilepsies to severe epileptic encephalopathiesKatrine Johannesen, Carla Marini, Siona Pfeffer, et al.
Genetics in Medicine Open|June 5, 2025
Autosomal dominant <i>HK1</i>-related neurodevelopmental disorder with visual defects and brain anomalies (NEDVIBA): An emerging mitochondrial disorderBobby G Ng, Erik A Eklund, Jill A Rosenfeld, et al.
Pageof 29