Hasil Pencarian - Jesse Slone

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  1. 1
    Mitochondrial Genome Variants as a Cause of Mitochondrial Cardiomyopathy

    Mitochondrial Genome Variants as a Cause of Mitochondrial Cardiomyopathy oleh Teresa Campbell, Jesse Slone, Taosheng Huang

    Diterbitkan 2022-09-01
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  2. 2
    Perspective: Is Random Monoallelic Expression a Contributor to Phenotypic Variability of Autosomal Dominant Disorders?

    Perspective: Is Random Monoallelic Expression a Contributor to Phenotypic Variability of Autosomal Dominant Disorders? oleh Baoheng Gui, Baoheng Gui, Jesse Slone, Taosheng Huang

    Diterbitkan 2017-11-01
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  3. 3
    Identification of a Drosophila glucose receptor using Ca2+ imaging of single chemosensory neurons.

    Identification of a Drosophila glucose receptor using Ca2+ imaging of single chemosensory neurons. oleh Tetsuya Miyamoto, Yan Chen, Jesse Slone, Hubert Amrein

    Diterbitkan 2013-01-01
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  4. 4
    Mitochondrial DNA Variants and Common Diseases: A Mathematical Model for the Diversity of Age-Related mtDNA Mutations

    Mitochondrial DNA Variants and Common Diseases: A Mathematical Model for the Diversity of Age-Related mtDNA Mutations oleh Huanzheng Li, Jesse Slone, Lin Fei, Taosheng Huang

    Diterbitkan 2019-06-01
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  5. 5
    Nanoscopic quantification of sub-mitochondrial morphology, mitophagy and mitochondrial dynamics in living cells derived from patients with mitochondrial diseases

    Nanoscopic quantification of sub-mitochondrial morphology, mitophagy and mitochondrial dynamics in living cells derived from patients with mitochondrial diseases oleh Weiwei Zou, Qixin Chen, Jesse Slone, Li Yang, Xiaoting Lou, Jiajie Diao, Taosheng Huang

    Diterbitkan 2021-05-01
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  6. 6
    Systemic Delivery of AAV-Fdxr Mitigates the Phenotypes of Mitochondrial Disorders in Fdxr Mutant Mice

    Systemic Delivery of AAV-Fdxr Mitigates the Phenotypes of Mitochondrial Disorders in Fdxr Mutant Mice oleh Li Yang, Jesse Slone, Weiwei Zou, Luis F. Queme, Michael P. Jankowski, Fei Yin, Taosheng Huang

    Diterbitkan 2020-09-01
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  7. 7
    Clinical study of ferredoxin-reductase-related mitochondriopathy: Genotype-phenotype correlation and proposal of ancestry-based carrier screening in the Mexican population

    Clinical study of ferredoxin-reductase-related mitochondriopathy: Genotype-phenotype correlation and proposal of ancestry-based carrier screening in the Mexican population oleh Teresa Campbell, Jesse Slone, Hallie Metzger, Wensheng Liu, Stephanie Sacharow, Amy Yang, Mariya Moosajee, Chiara La Morgia, Valerio Carelli, Flavia Palombo, Matthew A. Lines, A. Micheil Innes, Rebecca J. Levy, Derek Neilson, Nicola Longo, Taosheng Huang

    Diterbitkan 2024-01-01
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  8. 8
    PINK1-mediated Drp1S616 phosphorylation modulates synaptic development and plasticity via promoting mitochondrial fission

    PINK1-mediated Drp1S616 phosphorylation modulates synaptic development and plasticity via promoting mitochondrial fission oleh Qingtao Gao, Runyi Tian, Hailong Han, Jesse Slone, Caifang Wang, Xiao Ke, Tongmei Zhang, Xiangyu Li, Yuhong He, Panlin Liao, Fang Wang, Ye Chen, Shiqing Fu, Kexuan Zhang, Fangfang Zeng, Yingxuan Yang, Zhuo Li, Jieqiong Tan, Jiada Li, Youming Lu, Taosheng Huang, Zhonghua Hu, Zhuohua Zhang

    Diterbitkan 2022-04-01
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