AIF3 splicing switch triggers neurodegeneration
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T. Dawson | V. Dawson | M. Sasaki | K. Hatanpaa | W. Luo | Jennifer E. Wang | Yingfei Wang | V. Rajaram | A. Lemoff | Mi Zhou | Yanan Wang | Calvin Chang | Shuiqiao Liu | Z. Ruan | Kalyani Nambiar
[1] C. Brenner,et al. AIF meets the CHCHD4/Mia40-dependent mitochondrial import pathway. , 2020, Biochimica et Biophysica Acta - Molecular Basis of Disease.
[2] P. Nicotera,et al. A disease-associated Aifm1 variant induces severe myopathy in knockin mice , 2018, Molecular metabolism.
[3] J. Prehn,et al. Apoptosis-Inducing Factor (AIF) in Physiology and Disease: The Tale of a Repented Natural Born Killer , 2018, EBioMedicine.
[4] Publisher's Note , 2018, Anaesthesia.
[5] R. Dortch,et al. A novel missense mutation in AIFM1 results in axonal polyneuropathy and misassembly of OXPHOS complexes , 2017, European journal of neurology.
[6] C. Marco-Marín,et al. A newly distal hereditary motor neuropathy caused by a rare AIFM1 mutation , 2017, neurogenetics.
[7] S. Humphray,et al. X-linked hypomyelination with spondylometaphyseal dysplasia (H-SMD) associated with mutations in AIFM1 , 2017, neurogenetics.
[8] Sanjay P. Prabhu,et al. AIFM1 mutation presenting with fatal encephalomyopathy and mitochondrial disease in an infant , 2017, Cold Spring Harbor molecular case studies.
[9] Deborah A. Levine,et al. Post-stroke dementia – a comprehensive review , 2017, BMC Medicine.
[10] E. Obersztyn,et al. Spondyloepimetaphyseal dysplasia with neurodegeneration associated with AIFM1 mutation – a novel phenotype of the mitochondrial disease , 2017, Clinical genetics.
[11] J. Qian,et al. A nuclease that mediates cell death induced by DNA damage and poly(ADP-ribose) polymerase-1 , 2016, Science.
[12] I. Sevrioukova. Structure/Function Relations in AIFM1 Variants Associated with Neurodegenerative Disorders. , 2016, Journal of molecular biology.
[13] Rufus Akinyemi,et al. Stroke injury, cognitive impairment and vascular dementia , 2016, Biochimica et biophysica acta.
[14] E. Bertini,et al. A novel AIFM1 mutation expands the phenotype to an infantile motor neuron disease , 2015, European Journal of Human Genetics.
[15] Elena Vecino,et al. Glia–neuron interactions in the mammalian retina , 2016, Progress in Retinal and Eye Research.
[16] K. Rajewsky,et al. Efficient generation of Rosa26 knock-in mice using CRISPR/Cas9 in C57BL/6 zygotes , 2016, BMC Biotechnology.
[17] E. Lamantea,et al. A slowly progressive mitochondrial encephalomyopathy widens the spectrum of AIFM1 disorders , 2015, Neurology.
[18] P. Huppke,et al. From ventriculomegaly to severe muscular atrophy: expansion of the clinical spectrum related to mutations in AIFM1. , 2015, Mitochondrion.
[19] D. Lowy,et al. Isolation of Mouse Embryo Fibroblasts. , 2013, Bio-protocol.
[20] M. Hegde,et al. Mitochondrial dysfunction in psychiatric and neurological diseases: Cause(s), consequence(s), and implications of antioxidant therapy , 2013, BioFactors.
[21] Qian-Quan Sun,et al. Distribution of CaMKIIα expression in the brain in vivo, studied by CaMKIIα-GFP mice , 2013, Brain Research.
[22] K. Fischbeck,et al. Cowchock syndrome is associated with a mutation in apoptosis-inducing factor. , 2012, American journal of human genetics.
[23] T. Dawson,et al. Poly(ADP-Ribose) (PAR) Binding to Apoptosis-Inducing Factor Is Critical for PAR Polymerase-1–Dependent Cell Death (Parthanatos) , 2011, Science Signaling.
[24] K. Sakata,et al. Lack of promoter IV‐driven BDNF transcription results in depression‐like behavior , 2010, Genes, brain, and behavior.
[25] Severe X-linked mitochondrial encephalomyopathy associated with a mutation in apoptosis-inducing factor. , 2010, American journal of human genetics.
[26] P. Bénit,et al. A brain-specific isoform of mitochondrial apoptosis-inducing factor: AIF2 , 2010, Cell Death and Differentiation.
[27] O. Ottersen,et al. Outer mitochondrial membrane localization of apoptosis-inducing factor: mechanistic implications for release , 2009, ASN neuro.
[28] T. Dawson,et al. Poly(ADP-ribose) signals to mitochondrial AIF: A key event in parthanatos , 2009, Experimental Neurology.
[29] P. Bénit,et al. The Variability of the Harlequin Mouse Phenotype Resembles that of Human Mitochondrial-Complex I-Deficiency Syndromes , 2008, PloS one.
[30] S. Ackerman,et al. Loss of Apoptosis-Inducing Factor Results in Cell-Type-Specific Neurogenesis Defects , 2008, The Journal of Neuroscience.
[31] P. Bénit,et al. Targeted Deletion of AIF Decreases Mitochondrial Oxidative Phosphorylation and Protects from Obesity and Diabetes , 2007, Cell.
[32] David S. Park,et al. Dissociating the dual roles of apoptosis‐inducing factor in maintaining mitochondrial structure and apoptosis , 2006, The EMBO journal.
[33] V. Yuste,et al. Identification and Characterization of AIFsh2, a Mitochondrial Apoptosis-inducing Factor (AIF) Isoform with NADH Oxidase Activity* , 2006, Journal of Biological Chemistry.
[34] J. Bellalou,et al. AIFsh, a Novel Apoptosis-inducing Factor (AIF) Pro-apoptotic Isoform with Potential Pathological Relevance in Human Cancer* , 2006, Journal of Biological Chemistry.
[35] P. Bénit,et al. Muscle-Specific Loss of Apoptosis-Inducing Factor Leads to Mitochondrial Dysfunction, Skeletal Muscle Atrophy, and Dilated Cardiomyopathy , 2005, Molecular and Cellular Biology.
[36] T. Dawson,et al. Bcl-x Is Required for Proper Development of the Mouse Substantia Nigra , 2005, The Journal of Neuroscience.
[37] K. Mihara,et al. Export of mitochondrial AIF in response to proapoptotic stimuli depends on processing at the intermembrane space , 2005, The EMBO journal.
[38] P. Bénit,et al. AIF deficiency compromises oxidative phosphorylation , 2004, The EMBO journal.
[39] Wayne N. Frankel,et al. The harlequin mouse mutation downregulates apoptosis-inducing factor , 2002, Nature.
[40] G. Kroemer,et al. DNA binding is required for the apoptogenic action of apoptosis inducing factor , 2002, Nature Structural Biology.
[41] T. Dawson,et al. Mediation of Poly(ADP-Ribose) Polymerase-1-Dependent Cell Death by Apoptosis-Inducing Factor , 2002, Science.
[42] Ahmed Haouz,et al. The crystal structure of the mouse apoptosis-inducing factor AIF , 2002, Nature Structural Biology.
[43] T. Lemberger,et al. A CamKIIα iCre BAC allows brain‐specific gene inactivation , 2001 .
[44] G. Kroemer,et al. NADH Oxidase Activity of Mitochondrial Apoptosis-inducing Factor* , 2001, The Journal of Biological Chemistry.
[45] T. Lemberger,et al. A CamKIIalpha iCre BAC allows brain-specific gene inactivation. , 2001, Genesis.
[46] S. Zeitlin,et al. CaMKIIalpha-Cre transgene expression and recombination patterns in the mouse brain. , 2000, Genesis.
[47] Ruedi Aebersold,et al. Molecular characterization of mitochondrial apoptosis-inducing factor , 1999, Nature.
[48] J. McCaffery,et al. Localization of GTPases by indirect immunofluorescence and immunoelectron microscopy. , 1995, Methods in enzymology.
[49] T. Dawson,et al. Mechanisms of nitric oxide-mediated neurotoxicity in primary brain cultures , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.