Published in Invest Ophthalmol Vis Sci on December 01, 2005
Adenine nucleotide translocase 1 deficiency results in dilated cardiomyopathy with defects in myocardial mechanics, histopathological alterations, and activation of apoptosis. JACC Cardiovasc Imaging (2011) 1.60
Severity of cardiomyopathy associated with adenine nucleotide translocator-1 deficiency correlates with mtDNA haplogroup. Proc Natl Acad Sci U S A (2013) 0.97
Mouse models of oxidative phosphorylation defects: powerful tools to study the pathobiology of mitochondrial diseases. Biochim Biophys Acta (2008) 0.90
The mitochondrial ADP/ATP carrier: functional and structural studies in the route of elucidating pathophysiological aspects. J Bioenerg Biomembr (2008) 0.82
Dynamics of abducens nucleus neurons in the awake mouse. J Neurophysiol (2012) 0.80
Mitochondrial Diseases Part II: Mouse models of OXPHOS deficiencies caused by defects in regulatory factors and other components required for mitochondrial function. Mitochondrion (2015) 0.80
Retinal function and structure in Ant1-deficient mice. Invest Ophthalmol Vis Sci (2010) 0.78
ANT1-mediated fatty acid-induced uncoupling as a target for improving myocellular insulin sensitivity. Diabetologia (2016) 0.77
Human adenine nucleotide translocases physically and functionally interact with respirasomes. Mol Biol Cell (2017) 0.75
Extension of murine life span by overexpression of catalase targeted to mitochondria. Science (2005) 10.11
Natural selection shaped regional mtDNA variation in humans. Proc Natl Acad Sci U S A (2002) 6.95
Effects of purifying and adaptive selection on regional variation in human mtDNA. Science (2004) 5.87
The ADP/ATP translocator is not essential for the mitochondrial permeability transition pore. Nature (2004) 5.85
The American Society of Anesthesiologists Postoperative Visual Loss Registry: analysis of 93 spine surgery cases with postoperative visual loss. Anesthesiology (2006) 5.66
Teaching ophthalmoscopy to medical students (the TOTeMS study). Am J Ophthalmol (2013) 4.69
mtDNA mutations increase tumorigenicity in prostate cancer. Proc Natl Acad Sci U S A (2005) 4.66
An enhanced MITOMAP with a global mtDNA mutational phylogeny. Nucleic Acids Res (2006) 4.51
A mouse model of mitochondrial disease reveals germline selection against severe mtDNA mutations. Science (2008) 3.95
A back migration from Asia to sub-Saharan Africa is supported by high-resolution analysis of human Y-chromosome haplotypes. Am J Hum Genet (2002) 3.71
Ischemic Optic Neuropathies. N Engl J Med (2015) 3.53
Nonmydriatic ocular fundus photography among headache patients in an emergency department. Neurology (2013) 3.36
MITOMAP: a human mitochondrial genome database--2004 update. Nucleic Acids Res (2005) 3.35
Most cases labeled as "retinal migraine" are not migraine. J Neuroophthalmol (2007) 3.20
Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss. Nat Genet (2011) 3.16
Nonmydriatic digital ocular fundus photography on the iPhone 3G: the FOTO-ED study. Arch Ophthalmol (2012) 3.12
Asymmetric papilledema in idiopathic intracranial hypertension. J Neuroophthalmol (2015) 2.84
Nonmydriatic ocular fundus photography in the emergency department. N Engl J Med (2011) 2.81
A chronic inflammatory response dominates the skeletal muscle molecular signature in dystrophin-deficient mdx mice. Hum Mol Genet (2002) 2.80
Alzheimer's brains harbor somatic mtDNA control-region mutations that suppress mitochondrial transcription and replication. Proc Natl Acad Sci U S A (2004) 2.77
Feasibility of nonmydriatic ocular fundus photography in the emergency department: Phase I of the FOTO-ED study. Acad Emerg Med (2011) 2.46
Profiles of obesity, weight gain, and quality of life in idiopathic intracranial hypertension (pseudotumor cerebri). Am J Ophthalmol (2007) 2.44
Treatment of nonarteritic anterior ischemic optic neuropathy. Surv Ophthalmol (2009) 2.23
Meningoceles in idiopathic intracranial hypertension. AJR Am J Roentgenol (2014) 2.21
Congruency in homonymous hemianopia. Am J Ophthalmol (2007) 2.17
Structural and functional MRI reveals multiple retinal layers. Proc Natl Acad Sci U S A (2006) 2.15
The basal proton conductance of mitochondria depends on adenine nucleotide translocase content. Biochem J (2005) 2.05
Fulminant idiopathic intracranial hypertension. Neurology (2007) 2.02
Evidence for adaptive selection acting on the tRNA and rRNA genes of human mitochondrial DNA. Hum Mutat (2006) 1.98
Life extension through neurofibromin mitochondrial regulation and antioxidant therapy for neurofibromatosis-1 in Drosophila melanogaster. Nat Genet (2007) 1.98
Elevated male European and female African contributions to the genomes of African American individuals. Hum Genet (2006) 1.97
Data structures and compression algorithms for genomic sequence data. Bioinformatics (2009) 1.96
Quality of nonmydriatic digital fundus photography obtained by nurse practitioners in the emergency department: the FOTO-ED study. Ophthalmology (2012) 1.95
The mitochondrial theory of aging and its relationship to reactive oxygen species damage and somatic mtDNA mutations. Proc Natl Acad Sci U S A (2005) 1.88
Clinical course of idiopathic intracranial hypertension with transverse sinus stenosis. Neurology (2012) 1.83
Succinate dehydrogenase is a direct target of sirtuin 3 deacetylase activity. PLoS One (2011) 1.73
Functional estrogen receptors in the mitochondria of breast cancer cells. Mol Biol Cell (2006) 1.72
The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J. Hum Genet (2002) 1.65
Diffusion-weighted magnetic resonance imaging in Shaken Baby Syndrome. Am J Ophthalmol (2002) 1.65
The dual origin and Siberian affinities of Native American Y chromosomes. Am J Hum Genet (2001) 1.65
Adenine nucleotide translocase 1 deficiency results in dilated cardiomyopathy with defects in myocardial mechanics, histopathological alterations, and activation of apoptosis. JACC Cardiovasc Imaging (2011) 1.60
Ancient mtDNA genetic variants modulate mtDNA transcription and replication. PLoS Genet (2009) 1.58
Control region mtDNA variants: longevity, climatic adaptation, and a forensic conundrum. Proc Natl Acad Sci U S A (2003) 1.57
MicroRNA-206 is overexpressed in the diaphragm but not the hindlimb muscle of mdx mouse. Am J Physiol Cell Physiol (2007) 1.57
Mitochondrial DNA diversity in indigenous populations of the southern extent of Siberia, and the origins of Native American haplogroups. Ann Hum Genet (2005) 1.54
A mitochondrial etiology of Alzheimer and Parkinson disease. Biochim Biophys Acta (2011) 1.52
Deafness and blindness as a presentation of colorectal meningeal carcinomatosis. Clin Adv Hematol Oncol (2010) 1.51
The neuro-ophthalmology of mitochondrial disease. Surv Ophthalmol (2010) 1.51
A novel NDUFA1 mutation leads to a progressive mitochondrial complex I-specific neurodegenerative disease. Mol Genet Metab (2009) 1.47
Identification of the gene and the mutation responsible for the mouse nob phenotype. Invest Ophthalmol Vis Sci (2003) 1.47
Ischemic optic neuropathies. Curr Opin Neurol (2004) 1.45
Third nerve palsies. Semin Neurol (2007) 1.45
Update on the pathophysiology and management of idiopathic intracranial hypertension. J Neurol Neurosurg Psychiatry (2012) 1.42
Mitochondrial DNA-like sequences in the nucleus (NUMTs): insights into our African origins and the mechanism of foreign DNA integration. Hum Mutat (2004) 1.39
Multiple brain infarcts after orbital inflammation. Rev Neurol Dis (2009) 1.38
A patient with headache and increased intracranial pressure. Rev Neurol Dis (2008) 1.37
Mitochondrial variants in schizophrenia, bipolar disorder, and major depressive disorder. PLoS One (2009) 1.36
Isolated third, fourth, and sixth cranial nerve palsies from presumed microvascular versus other causes: a prospective study. Ophthalmology (2013) 1.36
Diagnostic accuracy and use of nonmydriatic ocular fundus photography by emergency physicians: phase II of the FOTO-ED study. Ann Emerg Med (2013) 1.35
Mouse mtDNA mutant model of Leber hereditary optic neuropathy. Proc Natl Acad Sci U S A (2012) 1.35
VCP associated inclusion body myopathy and paget disease of bone knock-in mouse model exhibits tissue pathology typical of human disease. PLoS One (2010) 1.34
Update on idiopathic intracranial hypertension. Am J Ophthalmol (2011) 1.33
Adaptive selection of mitochondrial complex I subunits during primate radiation. Gene (2006) 1.31
Landscape of the mitochondrial Hsp90 metabolome in tumours. Nat Commun (2013) 1.29
Mitochondrial DNA haplogroups influence AIDS progression. AIDS (2008) 1.29
Analysis of mitochondrial DNA diversity in the aleuts of the commander islands and its implications for the genetic history of beringia. Am J Hum Genet (2002) 1.29
Anemia and papilledema. Am J Ophthalmol (2003) 1.27
Prophylaxis for second eye involvement in leber hereditary optic neuropathy: an open-labeled, nonrandomized multicenter trial of topical brimonidine purite. Am J Ophthalmol (2005) 1.27
Neuroprotective effect of subretinal implants in the RCS rat. Invest Ophthalmol Vis Sci (2005) 1.27
Traces of early Eurasians in the Mansi of northwest Siberia revealed by mitochondrial DNA analysis. Am J Hum Genet (2002) 1.27
Mitochondrial DNA haplogroups associated with age-related macular degeneration. Invest Ophthalmol Vis Sci (2009) 1.26
Diagnosis and management of MELAS. Expert Rev Mol Diagn (2004) 1.24
Magnetic resonance imaging of tissue and vascular layers in the cat retina. J Magn Reson Imaging (2006) 1.24
Mitochondrial DNA haplogroups influence lipoatrophy after highly active antiretroviral therapy. J Acquir Immune Defic Syndr (2009) 1.24
The molecular mechanisms of OPA1-mediated optic atrophy in Drosophila model and prospects for antioxidant treatment. PLoS Genet (2008) 1.24
Valosin containing protein associated inclusion body myopathy: abnormal vacuolization, autophagy and cell fusion in myoblasts. Neuromuscul Disord (2009) 1.23
Immunohistochemical analysis of the outer plexiform layer in the nob mouse shows no abnormalities. Vis Neurosci (2003) 1.23
A mitochondrial etiology of neurodegenerative diseases: evidence from Parkinson's disease. Ann N Y Acad Sci (2008) 1.22
Differences of sperm motility in mitochondrial DNA haplogroup U sublineages. Gene (2005) 1.21
Mitochondrial DNA variant associated with Leber hereditary optic neuropathy and high-altitude Tibetans. Proc Natl Acad Sci U S A (2012) 1.21
Subretinal implantation of semiconductor-based photodiodes: durability of novel implant designs. J Rehabil Res Dev (2002) 1.20
Erectile dysfunction drugs and nonarteritic anterior ischemic optic neuropathy. Am J Ophthalmol (2005) 1.20
Persistent over-expression of specific CC class chemokines correlates with macrophage and T-cell recruitment in mdx skeletal muscle. Neuromuscul Disord (2003) 1.19
Systemic mitochondrial dysfunction and the etiology of Alzheimer's disease and down syndrome dementia. J Alzheimers Dis (2010) 1.19
Reactive oxygen species and fatigue-induced prolonged low-frequency force depression in skeletal muscle fibres of rats, mice and SOD2 overexpressing mice. J Physiol (2007) 1.18
Blood flow magnetic resonance imaging of retinal degeneration. Invest Ophthalmol Vis Sci (2008) 1.18
Tool from ancient pharmacopoeia prevents vision loss. Mol Vis (2006) 1.17
The artificial silicon retina in retinitis pigmentosa patients (an American Ophthalmological Association thesis). Trans Am Ophthalmol Soc (2010) 1.17
Homonymous hemianopia in stroke. J Neuroophthalmol (2006) 1.17
Mitochondrial content and distribution changes specific to mouse diaphragm after chronic normobaric hypoxia. Am J Physiol Regul Integr Comp Physiol (2009) 1.16
Mitochondrial cardiomyopathies: how to identify candidate pathogenic mutations by mitochondrial DNA sequencing, MITOMASTER and phylogeny. Eur J Hum Genet (2010) 1.15
Association of mitochondrial SOD deficiency with salt-sensitive hypertension and accelerated renal senescence. J Appl Physiol (1985) (2006) 1.15
Thrombolysis for central retinal artery occlusion. J Neuroophthalmol (2007) 1.13
Ischemic optic neuropathy following spine surgery. J Neurosurg Anesthesiol (2005) 1.13
Perinatal exercise improves glucose homeostasis in adult offspring. Am J Physiol Endocrinol Metab (2012) 1.13
Layer-specific anatomical, physiological and functional MRI of the retina. NMR Biomed (2008) 1.13
ARL2 and BART enter mitochondria and bind the adenine nucleotide transporter. Mol Biol Cell (2002) 1.11
MITOMASTER: a bioinformatics tool for the analysis of mitochondrial DNA sequences. Hum Mutat (2009) 1.10