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NS 41850

Funded outputs count: 30
Funder award ID: NS 41850
OpenAlex ID: G3376850671
Differential Mitochondrial Requirements for Radially and Non-radially Migrating Cortical Neurons: Implications for Mitochondrial Disorders
2016 · Erika G. Lin-Hendel, Meagan J. McManus, et al. · Cell Reports · 77
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Differential Gene Expression Reveals Mitochondrial Dysfunction in an Imprinting Center Deletion Mouse Model of Prader–Willi Syndrome
2013 · Puya G. Yazdi, Hailing Su, et al. · Clinical and Translational Science · 27
Mouse mtDNA mutant model of Leber hereditary optic neuropathy
2012 · Chun Shi Lin, Mark S. Sharpley, et al. · Proceedings of the National Academy of Sciences · 237
Toward a mtDNA locus-specific mutation database using the LOVD platform
2012 · Joanna L. Elson, Mary G. Sweeney, et al. · Human Mutation · 9
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mtDNA lineage analysis of mouse L-cell lines reveals the accumulation of multiple mtDNA mutants and intermolecular recombination
2012 · Weiwei Fan, Chun Shi Lin, et al. · Genes & Development · 39
Bioenergetic Origins of Complexity and Disease
2011 · D. C. Wallace · Cold Spring Harbor Symposia on Quantitative Biology · 125
The epigenome and the mitochondrion: bioenergetics and the environment
2010 · Douglas C. Wallace · Genes & Development · 47
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Association between mitochondrial DNA variations and Alzheimer's disease in the ADNI cohort
2010 · Anita Lakatos, Olga Derbeneva, et al. · Neurobiology of Aging · 98
Systemic Mitochondrial Dysfunction and the Etiology of Alzheimer's Disease and Down Syndrome Dementia
2010 · Pinar E. Coskun, Joanne Wyrembak, et al. · Journal of Alzheimer s Disease · 160
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Mitochondrial DNA mutations in disease and aging
2010 · Douglas C. Wallace · Environmental and Molecular Mutagenesis · 623
Mitochondrial Energetics and Therapeutics
2010 · Douglas C. Wallace, Weiwei Fan, et al. · Annual Review of Pathology Mechanisms of Disease · 730
Valosin containing protein associated inclusion body myopathy: abnormal vacuolization, autophagy and cell fusion in myoblasts
2009 · Jouni Vesa, Hailing Su, et al. · Neuromuscular Disorders · 61
Mitochondrial dysfunction in CA1 hippocampal neurons of the UBE3A deficient mouse model for Angelman syndrome
2009 · Hailing Su, Weiwei Fan, et al. · Neuroscience Letters · 80
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A novel NDUFA1 mutation leads to a progressive mitochondrial complex I-specific neurodegenerative disease
2009 · Prasanth Potluri, Antonio Davila, et al. · Molecular Genetics and Metabolism · 102
Role of SUV3 Helicase in Maintaining Mitochondrial Homeostasis in Human Cells
2008 · Lily Khidr, Guikai Wu, et al. · Journal of Biological Chemistry · 59
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MITOCHIP assessment of differential gene expression in the skeletal muscle of Ant1 knockout mice: Coordinate regulation of OXPHOS, antioxidant, and apoptotic genes
2008 · Vaidya Subramaniam, Pawel Golik, et al. · Biochimica et Biophysica Acta (BBA) - Bioenergetics · 29
Life extension through neurofibromin mitochondrial regulation and antioxidant therapy for neurofibromatosis-1 in Drosophila melanogaster
2007 · James Jiayuan Tong, Samuel E Schriner, et al. · Nature Genetics · 122
A novel recurrent mitochondrial DNA mutation in ND3 gene is associated with isolated complex I deficiency causing Leigh syndrome and dystonia
2006 · Emmanuelle Sarzi, Michael D. Brown, et al. · American Journal of Medical Genetics Part A · 104
Detection of Low Levels of the Mitochondrial tRNALeu(UUR) 3243A>G Mutation in Blood Derived from Patients with Diabetes
2006 · Vincent Procaccio, Nicolas Neckelmann, et al. · Molecular Diagnosis & Therapy · 11
A Mutation of β-Actin That Alters Depolymerization Dynamics Is Associated with Autosomal Dominant Developmental Malformations, Deafness, and Dystonia
2006 · Vincent Procaccio, Gloria Salazar, et al. · The American Journal of Human Genetics · 115
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Incapaces de desconectar: La adición al trabajo puede convertirse en uno de los problemas laborales más graves de este siglo
2006 · Marta Molina · Hispana
The basal proton conductance of mitochondria depends on adenine nucleotide translocase content
2005 · Martin D. Brand, Julian L. Pakay, et al. · Biochemical Journal · 408
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Eliminating the Ant1 Isoform Produces a Mouse with CPEO Pathology but Normal Ocular Motility
2005 · Hang Yin, John S. Stahl, et al. · Investigative Ophthalmology & Visual Science · 23
Adeno-associated virus-mediated gene transfer of the heart/muscle adenine nucleotide translocator (ANT) in mouse
2005 · A Flierl, Y Chen, et al. · Gene Therapy · 61
Mitochondrial DNA Diversity in Indigenous Populations of the Southern Extent of Siberia, and the Origins of Native American Haplogroups
2005 · Elena B. Starikovskaya, Rem I. Sukernik, et al. · Annals of Human Genetics · 210
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