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Brett H Graham

Showing results (51-60 of 92) with videos related to

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Neuron|April 17, 2012
Sox9 and NFIA coordinate a transcriptional regulatory cascade during the initiation of gliogenesisPeng Kang, Hyun Kyoung Lee, Stacey M Glasgow, et al.
Biomolecules|March 25, 2022
Mechanistic Investigation of GHS-R Mediated Glucose-Stimulated Insulin Secretion in Pancreatic IsletsGeetali Pradhan, Jong Han Lee, Chia-Shan Wu, et al.
Molecular Genetics and Metabolism|July 5, 2017
Analyses of SLC13A5-epilepsy patients reveal perturbations of TCA cycleMatthew N Bainbridge, Erin Cooney, Marcus Miller, et al.
Elife|June 26, 2016
Loss of Frataxin induces iron toxicity, sphingolipid synthesis, and Pdk1/Mef2 activation, leading to neurodegenerationKuchuan Chen, Guang Lin, Nele A Haelterman, et al.
American Journal of Medical Genetics. Part A|September 13, 2019
An unusual cause for Coffin-Lowry syndrome: Three brothers with a novel microduplication in RPS6KA3Valerie J Castelluccio, Francesco Vetrini, Ty Lynnes, et al.
Cold Spring Harbor Molecular Case Studies|November 28, 2022
Characterization of a novel deep-intronic variant in <i>DYNC2H1</i> identified by whole-exome sequencing in a patient with a lethal form of a short-rib thoracic dysplasia type IIIMuqsit Buchh, Patrick J Gillespie, Kayla Treat, et al.
Elife|October 15, 2014
Mitochondrial fusion but not fission regulates larval growth and synaptic development through steroid hormone productionHector Sandoval, Chi-Kuang Yao, Kuchuan Chen, et al.
Pediatric Blood & Cancer|October 18, 2016
Renal cell carcinoma harboring somatic TSC2 mutations in a child with methylmalonic acidemiaSamara L Potter, Rajkumar Venkatramani, Scott Wenderfer, et al.
Molecular Genetics and Metabolism|July 20, 2014
Mitochondrial myopathy, lactic acidosis, and sideroblastic anemia (MLASA) plus associated with a novel de novo mutation (m.8969G>A) in the mitochondrial encoded ATP6 geneLindsay C Burrage, Sha Tang, Jing Wang, et al.
Plos Genetics|June 23, 2017
Peroxisomal biogenesis is genetically and biochemically linked to carbohydrate metabolism in Drosophila and mouseMichael F Wangler, Yu-Hsin Chao, Vafa Bayat, et al.
Pageof 10

Showing results (51-60 of 92) with videos related to

Sort By:
Pageof 10
Neuron|April 17, 2012
Sox9 and NFIA coordinate a transcriptional regulatory cascade during the initiation of gliogenesisPeng Kang, Hyun Kyoung Lee, Stacey M Glasgow, et al.
Biomolecules|March 25, 2022
Mechanistic Investigation of GHS-R Mediated Glucose-Stimulated Insulin Secretion in Pancreatic IsletsGeetali Pradhan, Jong Han Lee, Chia-Shan Wu, et al.
Molecular Genetics and Metabolism|July 5, 2017
Analyses of SLC13A5-epilepsy patients reveal perturbations of TCA cycleMatthew N Bainbridge, Erin Cooney, Marcus Miller, et al.
Elife|June 26, 2016
Loss of Frataxin induces iron toxicity, sphingolipid synthesis, and Pdk1/Mef2 activation, leading to neurodegenerationKuchuan Chen, Guang Lin, Nele A Haelterman, et al.
American Journal of Medical Genetics. Part A|September 13, 2019
An unusual cause for Coffin-Lowry syndrome: Three brothers with a novel microduplication in RPS6KA3Valerie J Castelluccio, Francesco Vetrini, Ty Lynnes, et al.
Cold Spring Harbor Molecular Case Studies|November 28, 2022
Characterization of a novel deep-intronic variant in <i>DYNC2H1</i> identified by whole-exome sequencing in a patient with a lethal form of a short-rib thoracic dysplasia type IIIMuqsit Buchh, Patrick J Gillespie, Kayla Treat, et al.
Elife|October 15, 2014
Mitochondrial fusion but not fission regulates larval growth and synaptic development through steroid hormone productionHector Sandoval, Chi-Kuang Yao, Kuchuan Chen, et al.
Pediatric Blood & Cancer|October 18, 2016
Renal cell carcinoma harboring somatic TSC2 mutations in a child with methylmalonic acidemiaSamara L Potter, Rajkumar Venkatramani, Scott Wenderfer, et al.
Molecular Genetics and Metabolism|July 20, 2014
Mitochondrial myopathy, lactic acidosis, and sideroblastic anemia (MLASA) plus associated with a novel de novo mutation (m.8969G>A) in the mitochondrial encoded ATP6 geneLindsay C Burrage, Sha Tang, Jing Wang, et al.
Plos Genetics|June 23, 2017
Peroxisomal biogenesis is genetically and biochemically linked to carbohydrate metabolism in Drosophila and mouseMichael F Wangler, Yu-Hsin Chao, Vafa Bayat, et al.
Pageof 10